KR20230101172A - 포유류 비병원성 및 발육란 고증식성 재조합 인플루엔자 바이러스 - Google Patents
포유류 비병원성 및 발육란 고증식성 재조합 인플루엔자 바이러스 Download PDFInfo
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Abstract
본 발명은 포유류 비병원성 및 발육란 고증식성을 갖는 재조합 인플루엔자 바이러스, 상기 재조합 인플루엔자 바이러스를 포함하는 백신 조성물 및 이의 제조방법과 상기 재조합 인플루엔자 바이러스를 제작하기 위한 재조합 벡터 및 재조합 인플루엔자 바이러스 제조용 조성물에 관한 것으로, 본 발명의 재조합 인플루엔자 바이러스는 아미노산 변이를 포함하는 중합효소 염기성 단백질 2(PB2)를 포함하며, 인체에 대한 비-병원성과 높은 면역원성, 그리고 발육란에서 높은 증식을 통해 우수한 생산성을 가져, 조류 인플루엔자 바이러스 백신주로서 효과적으로 사용될 수 있다.
Description
본 발명은 포유류 비병원성 및 발육란 고증식성 특성을 갖는 재조합 인플루엔자 바이러스, 상기 재조합 인플루엔자 바이러스를 포함하는 백신 조성물 및 이의 제조방법과 상기 재조합 인플루엔자 바이러스를 제작하기 위한 재조합 벡터 및 재조합 인플루엔자 바이러스 제조용 조성물에 관한 것이다.
인플루엔자는 전 세계적으로 매년 10억 명이 감염되고 3~5백만 명이 중증으로 진행, 29만~65만 명이 사망하는 전염성이 강한 급성호흡기감염증병이다. 조류 인플루엔자 A H5N1, H5N6, H7N4 및 H7N9 바이러스에서 사람 감염이 확인되었고, 새로운 조류 인플루엔자의 사람 감염이 지속적으로 발생하고 있다. 대유행 인플루엔자 발생의 필수 요소인 사람간 전파 능력은 간단한 유전자 변이 만으로도 획득될 수 있다는 사실이 밝혀지고 있고, WHO는 인플루엔자 바이러스가 계속 변이를 일으키고 있어 전 세계가 인플루엔자 대유행의 가능성에 여전히 취약하며 지속적인 감시가 필요하다고 밝혔다.
국내 조류 인플루엔자는 주로 저병원성 H9N2 아형의 바이러스에 의한 저병원성 조류인플루엔자로 1996년 최초 발생 이후 발생이 없다가 1999년 발생 이후부터 2004년까지 매년 발생하고 있으며, 그 빈도는 20-30% 정도로 국내 계군에 만연해 있으며, 외국의 경우처럼 산란율 저하 및 폐사로 경제적인 피해를 초래하고 있다 (Lee et al., 2000, Avian Dis, 44:527-535). 1996년 및 최근에 분리된 H9N2 바이러스들은 계태아 증식성이 낮아 (이 등., 1998, 서울대학교 대학원 석사학위논문) 불활화 백신 제조 시 적게는 10배에서 많게는 100배를 농축하여야만 효과를 얻을 수 있는 것으로 생각되고 있다.
인플루엔자 바이러스는 오소믹소바이러스에 속하며, 음성의 단일가닥 RNA 절편 8개를 게놈으로 갖는 바이러스로서, 상기 8개의 RNA 절편으로부터 헤마글루티닌(hemagglutinin; HA), 뉴라미니다제(neuraminidase, NA), 핵단백질(nucleoprotein; NP), 매트릭스 단백질 1 및 2 (matrix, M1, M2), 중합효소 염기성 단백질 1 및 2, 중합효소 산성 단백질(polymerase base protein 1, polymerase base protein 2, polymerase acidic protein; 각각 PB1, PB2, PA), 및 비구조 단백질 1 및 2 (nonstructural protein 1 & 2; 각각 NS1, NS2)가 만들어진다.
역유전학(reversed genetics) 시스템은 인플루엔자 A 바이러스에서 바이러스 게놈의 조작을 가능하게 한다. 최근 연구 결과, pol I 프로모터로부터 8개의 모든 vRNA를 플라스미드 발현시키고 중합효소 복합체 단백질을 공동발현 시키면 감염성 인플루엔자 A 바이러스가 형성되는 것으로 확인되었다(Neumann et al., Proc. Natl. Acad. Sci. USA 1999, 246:9345; Fodor et al., J. Virol. 1999, 73:9679). 플라스미드로부터 완전히 활성화된 인플루엔자 A 바이러스를 생성하는데 헬퍼 바이러스를 사용한 감염을 필요로 하지 않는 이러한 방법은 기술적 제한없이 모든 유전자 단편의 조작을 가능하게 한다.
인플루엔자 바이러스의 증식성은 HA와 NA 활성의 조화가 중요한 것으로 알려져 있다. 일반적으로 발육란(계태아)에서의 바이러스 생산성은 세포배양과는 달리, 병원성이 높은 바이러스의 경우 계태아의 폐사를 초래하므로 요막강 내 바이러스 역가는 낮으며, 계태아의 조기 폐사로 인해 수확되는 요막액의 양이 줄어들어 바이러스 생산성이 감소하는 것으로 알려져 있다.
인체 인플루엔자 A 바이러스 백신주의 경우 역유전학을 통한 바이러스의 변이를 유도할 수 있기 때문에 고병원성 H5N1 바이러스의 병원성을 약화시키고, 계태아나 세포주에서의 증식성을 증가시키는 방향으로 개발이 이루어질 수 있었다.
이와 달리 조류에서 사용하는 저병원성 조류인플루엔자 백신은 저병원성 H9N2 조류인플루엔자 A/chicken/Korea/01310/2001(H9N2)(01310)를 발육란에서 20번 계대한 바이러스를 불활화한 백신을 사용하고 있다. 그러나, 20번 계대하는 과정에서 발육란 요막액 내에서의 증식성이 높아졌으나, 계태아에 대한 병원성이 매우 높아 접종 후 48시간 내 중사율이 증가하는 문제가 있다.
한편, H9N2 아형 조류 인플루엔자 바이러스 KBNP-0028(KCTC 10866BP)는 발육란 고생산성 및 계태아 병원성이 없어, 생산성이 높으며 포유류에 대한 병원성과 관련된 돌연변이를 갖지 않아 안전한 백신주로 국내 특허등록(특허 제0708593호) 된 바이러스이다. KBNP-0028의 NS 게놈 절편을 PR8 바이러스의 나머지 7개 게놈 절편과 함께 재조합 바이러스(rPR-NS(0028))를 제작하는 경우, 마우스에서의 병원성이 낮고, 면역원성이 높으며 발육란에서의 증식성이 높은 것으로 알려져 있으며 이러한 특성과 관련된 아미노산의 변이가 특정[G139D, S151T, PL motif 변이 (GSEV > EPEV)] 되어 있다(특허 제 10-1426407호). 그러나, 이 경우에도 포유류 증식성은 잔존하는 것으로 알려져 있다.
조류인플루엔자 바이러스는 오랜 기간 동안 인간과 더불어 역사를 같이한 바이러스로 인체 내 면역 반응이 전무하기 때문에, 인간에서 인간으로 전파력은 기존 인간 독감 바이러스보다 훨씬 빠른 것으로 예상된다. 따라서, 조류 인플루엔자 바이러스의 발생을 조기에 막을 수 있는 예방 백신의 개발이 국민의 보건, 국가 경제력 및 국방력 제고에 필요하다.
상기한 문제를 해결하고 포유류에 비 병원성이면서도 우수한 면역원성과 증식성을 갖는 인플루엔자 바이러스 백신주의 개발을 위해, 본 발명의 발명자가 예의 노력한 결과, 인플루엔자 바이러스 A/CHICKEN/KOREA/01310/2001(H9N2) 의 중합효소 염기성 단백질 2(PB2) 단백질에 아미노산 변이를 포함하는 변이 단백질 및/또는 이를 코딩하는 게놈을 포함하는 재조합 인플루엔자 바이러스는 발육란에서 고증식성을 가지면서도, 인체에 대한 감염위험이 매우 낮은 재조합 인플루엔자 바이러스를 제조할 수 있음을 확인하고, 본 발명을 완성하였다.
상기 목적을 달성하기 위한 수단으로서, 본 발명은 인플루엔자 바이러스 A/CHICKEN/KOREA/01310/2001(H9N2)의 중합효소 염기성 단백질 2(polymerase basic protein 2: PB2)에서 66번 아이소루신(I)을 메티오닌(M)으로, 109번 아이소루신(I)을 발린(V)으로 그리고 133번 아이소루신(I)을 발린(V)으로 변이시킨 단백질을 포함하는 재조합 인플루엔자 바이러스를 제공한다.
상기 재조합 인플루엔자 바이러스는 인플루엔자 바이러스의 헤마글루티닌(hemagglutinin: HA) 단백질 및 뉴라미니다제(neuraminidase: NA)를 더 포함할 수 있다.
상기 재조합 인플루엔자 바이러스는 인플루엔자 바이러스의 중합효소 염기성 단백질 1(polymerase basic protein 1: PB1), 중합효소 산성 단백질(polymerase acidic protein: PA), 핵단백질(nucleoprotein: NP), 매트릭스 단백질(matrix: M) 및 비구조 단백질(nonstructural protein: NS)로 이루어진 군으로부터 선택된 하나 이상의 단백질을 더 포함할 수 있다.
상기 염기성 단백질 2(polymerase basic protein 2: PB2) 단백질은 서열번호 1의 아미노산 서열을 갖는 것일 수 있다.
상기 헤마글루티닌(hemagglutinin: HA) 단백질 및 뉴라미니다제(neuraminidase: NA)는 아형 H9N2 조류 인플루엔자 바이러스의 헤마글루티닌(hemagglutinin: HA) 단백질 및 뉴라미니다제(neuraminidase: NA)일 수 있다.
상기 뉴라미니다제(neuraminidase: NA)는 인플루엔자 바이러스 Y280 lineage (A/CHICKEN/KOREA/SL20/2020)(H9N2)의 뉴라미다제(neuraminidase; NA)일 수 있다.
상기 헤마글루티닌(hemagglutinin: HA) 단백질은 인플루엔자 바이러스 Y280 lineage (A/CHICKEN/KOREA/SL20/2020)(H9N2)의 헤마글루티닌(hemagglutinin; HA) 또는 인플루엔자 바이러스 Y280 lineage (A/CHICKEN/KOREA/SL20/2020)(H9N2)의 헤마글루티닌(hemagglutinin; HA)에서 226번 류신이 글루타민으로 변이된 것 일 수 있다.
상기 헤마글루티닌(hemagglutinin: HA) 단백질은 서열번호 3 또는 서열번호 4의 아미노산 서열로 구성되는 것 일 수 있다.
상기 뉴라미니다제(neuraminidase: NA)는 서열번호 5의 아미노산 서열로 구성되는 것 일 수 있다.
상기 인플루엔자 바이러스의 PB1, PA, NP, M 및 NS 단백질은 인플루엔자 바이러스 A/Perto Rico/8 (H1N1)의 PB1, PA, NP, M 및 NS 단백질일 수 있다.
상기 중합효소 염기성 단백질 1(polymerase basic protein 1: PB1)은 서열번호 6의 아미노산 서열로 구성되는 것일 수 있다.
상기 중합효소 산성 단백질(polymerase acidic protein: PA)는 서열번호 7의 아미노산 서열로 구성되는 것일 수 있다.
상기 핵단백질(nucleoprotein: NP)는 서열번호 8의 아미노산 서열로 구성되는 것 일 수 있다.
상기 매트릭스 단백질(matrix: M)은 서열번호 9의 아미노산 서열로 구성되는 것 일 수 있다.
상기 비구조 단백질(nonstructural protein: NS)은 서열번호 10의 아미노산 서열로 구성되는 것 일 수 있다.
본 발명의 다른 형태로, 기탁번호 KCTC 14691BP의 재조합 인플루엔자 바이러스에 관한 것이다.
본 발명의 또 다른 형태로, 상기한 재조합 인플루엔자 바이러스를 포함하는 인플루엔자 바이러스 백신에 관한 것이다.
상기 백신은 사독 백신 또는 생독 백신 일 수 있다.
본 발명의 또 다른 형태로, 인플루엔자 바이러스 A/CHICKEN/KOREA/01310/2001(H9N2)의 염기성 단백질 2(polymerase basic protein 2: PB2)에서 66번 아이소루신(I)이 메티오닌(M)으로, 109번 아이소루신(I)이 발린(V)으로 그리고 133번 아이소루신(I)이 발린(V)으로 변이된 PB2 단백질을 코딩하는 폴리뉴클레오타이드를 포함하는 재조합 벡터에 관한 것이다.
중합효소 염기성 단백질 2(PB2)를 코딩하는 폴리뉴클레오타이드는 서열번호 1의 서열로 구성되는 아미노산 서열에서 66번 아이소루신(I)이 메티오닌(M)으로, 109번 아이소루신(I)이 발린(V)으로 그리고 133번 아이소루신(I)이 발린(V)으로 치환된 단백질을 코딩하는 것 일 수 있다.
본 발명의 또 다른 형태로, 인플루엔자 바이러스의 헤마글루티닌(hemagglutinin: HA) 단백질을 코딩하는 폴리뉴클레오타이드; 인플루엔자 바이러스의 뉴라미니다제(neuraminidase: NA)를 코딩하는 폴리뉴클레오타이드; 및 인플루엔자 바이러스 A/CHICKEN/KOREA/01310/2001(H9N2)의 염기성 단백질 2(polymerase basic protein 2: PB2)에서 66번 아이소루신(I)이 메티오닌(M)으로, 109번 아이소루신(I)이 발린(V)으로 그리고 133번 아이소루신(I)이 발린(V)으로 변이된 PB2 단백질을 코딩하는 폴리뉴클레오타이드를 포함하는 재조합 인플루엔자 바이러스 제조용 조성물에 관한 것이다.
상기 조성물은 인플루엔자 바이러스의 중합효소 염기성 단백질 1(polymerase basic protein 1: PB1)을 코딩하는 폴리뉴클레오타이드, 중합효소 산성 단백질(polymerase acidic protein: PA)을 코딩하는 폴리뉴클레오타이드, 핵단백질(nucleoprotein: NP)를 코딩하는 폴리뉴클레오타이드, 매트릭스 단백질(matrix: M)을 코딩하는 폴리뉴클레오타이드 및 비구조 단백질(nonstructural protein: NS)을 코딩하는 폴리뉴클레오타이드로 이루어진 군으로부터 선택된 하나 이상을 더 포함할 수 있다.
상기 폴리뉴클레오타이드는 벡터에 포함된 것 일 수 있다.
상기 중합효소 염기성 단백질 2(PB2)를 코딩하는 폴리뉴클레오타이드는 서열번호 1의 서열로 구성되는 아미노산 서열에서 66번 아이소루신(I)이 메티오닌(M)으로, 109번 아이소루신(I)이 발린(V)으로 그리고 133번 아이소루신(I)이 발린(V)으로 치환된 PB2 단백질을 코딩하는 것 일 수 있다.
본 발명의 또 다른 형태로, 상기 재조합 벡터 또는 재조합 인플루엔자 바이러스 제조용 조성물을 발육란에 접종하는 단계를 포함하는 재조합 인플루엔자 바이러스 제조방법에 관한 것이다.
상기 제조방법은 접종된 발육란을 배양하는 단계를 더 포함할 수 있다.
본 발명의 재조합 인플루엔자 바이러스는 아미노산 변이를 포함하는 중합효소 염기성 단백질 2(PB2)를 포함하며, 인체에 대한 비-병원성과 높은 면역원성, 그리고 발육란에서 높은 증식을 통해 우수한 생산성을 가져, 조류 인플루엔자 바이러스 백신주로서 효과적으로 사용될 수 있다.
도 1a는 본 발명의 일 실시예에 따른 재조합 인플루엔자 바이러스(rSL20(P), rSL20(P)-L226Q, rSL20(P)-310PB2 및 rSL20(P)-MVV310PB2)와 야생형 조류 인플루엔자 바이러스(Y280 wild type, rPR8)의 MDCK 세포주에서 증식성을 보여주는 그래프이다.
도 1b은 본 발명의 일 실시예에 따른 재조합 인플루엔자 바이러스(rSL20(P), rSL20(P)-L226Q, rSL20(P)-310PB2 및 rSL20(P)-MVV310PB2)와 야생형 조류 인플루엔자 바이러스(Y280 wild type, rPR8)의 A549 세포주에서 증식성을 보여주는 그래프이다.
도 2a는 본 발명의 일 실시예에 따른 재조합 인플루엔자 바이러스 rSL20(P), rSL20(P)-L226Q 및 rSL20(P)-MVV310PB2를 각각 접종한 마우스의 체중 변화를 보여주는 그래프이다.
도 2b는 본 발명의 일 실시예에 따른 재조합 인플루엔자 바이러스 rSL20(P), rSL20(P)-L226Q 및 rSL20(P)-MVV310PB2를 각각 접종한 마우스의 생존률을 확인한 결과를 보여주는 그래프이다.
도 1b은 본 발명의 일 실시예에 따른 재조합 인플루엔자 바이러스(rSL20(P), rSL20(P)-L226Q, rSL20(P)-310PB2 및 rSL20(P)-MVV310PB2)와 야생형 조류 인플루엔자 바이러스(Y280 wild type, rPR8)의 A549 세포주에서 증식성을 보여주는 그래프이다.
도 2a는 본 발명의 일 실시예에 따른 재조합 인플루엔자 바이러스 rSL20(P), rSL20(P)-L226Q 및 rSL20(P)-MVV310PB2를 각각 접종한 마우스의 체중 변화를 보여주는 그래프이다.
도 2b는 본 발명의 일 실시예에 따른 재조합 인플루엔자 바이러스 rSL20(P), rSL20(P)-L226Q 및 rSL20(P)-MVV310PB2를 각각 접종한 마우스의 생존률을 확인한 결과를 보여주는 그래프이다.
이하에서, 본 발명을 보다 상세하기 설명한다.
본 발명은 인플루엔자 바이러스 A/CHICKEN/KOREA/01310/2001(H9N2)의 중합효소 염기성 단백질 2(polymerase basic protein 2: PB2)에서 66번 아이소루신(I)을 메티오닌(M)으로, 109번 아이소루신(I)을 발린(V)으로 그리고 133번 아이소루신(I)을 발린(V)으로 변이(I66M, I109V, 및 I133V)시킨 단백질을 포함하는 재조합 인플루엔자 바이러스를 제공한다.
또한, 본 발명은 인플루엔자 바이러스 A/CHICKEN/KOREA/01310/2001(H9N2)의 중합효소 염기성 단백질 2(polymerase basic protein 2: PB2) 단백질에서 66번 아이소루신(I)을 메티오닌(M)으로, 109번 아이소루신(I)을 발린(V)으로 그리고 133번 아이소루신(I)을 발린(V)으로 변이시킨 단백질을 코딩하는 폴리뉴클레오타이드를 포함하는 게놈을 포함하는 재조합 인플루엔자 바이러스를 제공한다.
조류 인플루엔자 바이러스는 11-12개의 단백질들을 발현하는 8개의 조각난 단일가닥 RNA를 게놈(genome)으로 가지고 있으며, 이 RNA들은 4개의 바이러스 단백질인 핵단백질 (nucleoprotein, NP), 중합효소 염기성 단백질 1(polymerase basic protein 1; PB1), 중합효소 염기성 단백질 2(polymerase basic protein 2; PB2), 중합효소 산성 단백질(polymerase acidic protein; PA)과 함께 리보핵단백질(ribonucleoprotein, RNP)을 형성하고, 감염된 세포 내에서 RNA 의존성 RNA 중합효소(RNA-dependent RNA polymerase)에 의해 전사 및 복제된다. 이 RNA 중합효소는 capped RNA와 결합, 핵산내부가수분해효소 절단, RNA전사 활동(RNA-directed RNA transcription activity)을 포함한 여러 활성을 가지고 있다. 조류 인플루엔자 바이러스의 RNA 중합효소는 헤테로트라이머 구조를 가지며, 세 개의 단위체(subunit) PB1(polymerase basic 1), PB2(polymerase basic 2), 그리고 PA(polymerase acidic)로 구성된다. 상기 RNA 중합효소는 바이러스 게놈의 복제와 바이러스의 mRNA 합성을 수행한다. 그 중 중합효소 단위체 PB2는 감염된 숙주 세포의 mRNA의 캡 구조에 결합하는 단백질로 알려져 있다.
본 발명에서 중합효소 염기성 단백질 2(polymerase basic protein 2; PB2)는 중합효소 단위체 B2(polymerase subunit B2) 또는 PB2라고도 지칭될 수 있다. 본 발명의 재조합 인플루엔자 바이러스에 포함되는 PB2는 인플루엔자 바이러스는 한국에서 2001년에 분리된 저벙원성 조류 인플루엔자 바이러스 A/CHICKEN/KOREA/01310/2001(H9N2)의 PB2 단백질의 아미노산 서열을 기초 66번 아이소루신(I)을 메티오닌(M)으로, 109번 아이소루신(I)을 발린(V)으로 그리고 133번 아이소루신(I)을 발린(V)으로 치환한 변이를 포함하는데 기술적 특징이 있다. 상기한 치환 변이를 포함하는 PB2 단백질을 포함하는 재조합 인플루엔자 바이러스는 포유류에서 우수한 면역원성을 유지하면서도 병원성은 나타내지 않으며, 발육란에서 증식성이 우수해, 백신주로 활용되는데 유리한 특성을 갖는다.
상기한 PB2 단백질은 서열번호 1의 아미노산 서열에서 I66M, I109V, 및 I133V 변이를 포함하는 아미노산 서열로 구성된 것 일 수 있다.
일 예로, 본 발명의 재조합 인플루엔자 바이러스에 포함되는 PB2 단백질은 서열번호 2의 아미노산 서열로 구성된 것 일 수 있다.
본 발명에서 "서열로 구성되는"은 해당 서열만으로 이루어지거나 해당 서열을 포함하면서 서열이 상이해지지 않는 조건으로 서열의 양 말단에 추가의 서열을 포함하는 것도 본 발명에 포함되는 것으로 이해된다. 일 예로, 서열번호 2의 아미노산 서열로 구성된 단백질은 서열번호 2에 개시된 아미노산 서열만으로 이루어진 경우뿐 아니라, 서열번호 2의 아미노산 서열을 포함하면서, 양쪽 말단에 추가의 아미노산 서열을 포함하는 경우까지, 본 발명에 해당한다.
다른 일 예로, 본 발명의 재조합 인플루엔자 바이러스에 포함되는 PB2 단백질은 서열번호 12의 염기서열을 포함하는 폴리뉴클레오타이드에 의하여 코딩되는 것 일 수 있다.
본 발명의 재조합 인플루엔자 바이러스는 바이러스의 종류, 아형, 균주(strain) 등에 상관없이 역유전학 방법에 의해 제조될 수 있는 모든 인플루엔자 바이러스를 포함한다. 일 예로 본 발명의 재조합 인플루엔자 바이러스는 바이러스에 재조합되는 헤마글루티닌(hemagglutinin: HA) 단백질 및 뉴라미니다제(neuraminidase: NA)의 종류에 따라 아형이 결정될 수 있다. 일 예로, H9 형의 HA와 N2형의 NA 단백질을 재조합 한 경우, H9N2 아형의 재조합 인플루엔자 바이러스 일 수 있다.
본 발명의 재조합 인플루엔자 바이러스는 인플루엔자 바이러스의 헤마글루티닌(hemagglutinin: HA) 단백질 및 뉴라미니다제(neuraminidase: NA)를 더 포함할 수 있다.
또한, 본 발명의 재조합 인플루엔자 바이러스의 게놈은 헤마글루티닌(hemagglutinin: HA) 단백질 및 뉴라미니다제(neuraminidase: NA)를 코딩하는 폴리뉴클레오타이드 서열을 더 포함할 수 있다.
상기 HA와 NA 단백질은 백신을 투여하는 개체에 목적하는 면역원성을 부여하기 위해 적절한 인플루엔자 바이러스로부터 분리하여 본 발명의 재조합 인플루엔자 바이러스에 재조합 될 수 있다. 따라서, 본 발명의 재조합 인플루엔자 바이러스는 아형의 제한없이 제조될 수 있어, 백신주로서 활용이 더욱 용이하다.
일 예로, A/H1 내지 A/H16 중 선택된 아형의 HA와 N1 내지 N9로 이루어진 군에서 선택된 아형의 NA를 포함할 수 있다. 구체적으로, 국내에서 분리되고, 인체 감염 가능성이 높은 A형 조류 인플루엔자 바이러스 중, A/H1, A/H2, A/H3, A/H4, A/H5, A/H6, A/H7, A/H9 및 A/H10 중 선택된 HA와 N1, N2, 및 N7 중 선택된 NA를 포함할 수 있다.
본 발명의 일 실시예에서는 A/H9형의 HA와 N2형의 NA 단백질을 포함하도록 H9N2 아형의 조류 인플루엔자 바이러스의 헤마글루티닌(hemagglutinin: HA) 단백질 및 뉴라미니다제(neuraminidase: NA)를 포함하는 재조합 인플루엔자 바이러스를 구축하여, 백신주로서 활용 가능성을 확인하였다.
보다 구체적인 일 예로, 본 발명의 재조합 인플루엔자 바이러스는 상기한 PB2 변이 단백질과 함께 2020년 한국에서 분리된 인플루엔자 바이러스 Y280 lineage (A/CHICKEN/KOREA/SL20/2020)(H9N2)의 헤마글루티닌(HA) 및 뉴라미다제(NA); 또는 이 들의 게놈을 포함할 수 있다.
다른 구체적인 일 예로, 본 발명의 재조합 인플루엔자 바이러스는 Y280 lineage (A/CHICKEN/KOREA/SL20/2020)(H9N2)의 뉴라미다제(NA) 및 상기 바이러스는 Y280 lineage (A/CHICKEN/KOREA/SL20/2020)(H9N2)의 헤마글루티닌(HA)에서 226번 류신을 글루타민으로 치환한 변이를 포함하는 HA 변이 단백질을 포함하거나; 이들의 게놈을 포함할 수 있다.
일 예로, 상기 헤마글루티닌(HA)은 서열번호 3 또는 서열번호 4의 아미노산 서열로 구성된 아미노산 서열을 포함할 수 있고, 다른 일 예로, 서열번호 13 또는 서열번호 14의 염기서열을 포함하는 폴리뉴클레오타이드 서열로 코딩되는 것 일 수 있다.
다른 일 예로, 상기 뉴라미다제(NA)는 서열번호 5의 아미노산 서열로 구성된 아미노산 서열을 포함할 수 있고, 다른 일 예로, 서열번호 15의 염기서열을 포함하거나, 이로 이루어진 폴리뉴클레오타이드로 코딩되는 것 일 수 있다.
본 발명의 재조합 인플루엔자 바이러스는 상기 치환 변이를 포함하는 PB2 단백질과 함께 인플루엔자 바이러스의 중합효소 염기성 단백질 1(polymerase basic protein 1: PB1), 중합효소 산성 단백질(polymerase acidic protein: PA), 핵단백질(nucleoprotein: NP), 매트릭스 단백질(matrix: M) 및 비구조 단백질(nonstructural protein: NS)로 이루어진 군으로부터 선택된 하나 이상을 더 포함할 수 있다.
또한, 또한, 본 발명의 재조합 인플루엔자 바이러스의 게놈은 중합효소 염기성 단백질 1(polymerase basic protein 1: PB1), 중합효소 산성 단백질(polymerase acidic protein: PA), 핵단백질(nucleoprotein: NP), 매트릭스 단백질(matrix: M) 및 비구조 단백질(nonstructural protein: NS)로 이루어진 군으로부터 선택된 하나 이상을 코딩하는 폴리뉴클레오타이드 서열을 더 포함할 수 있다.
바람직한 일 예로, PB1, PA, NP, M 및 NS 단백질을 모두 포함할 수 있으나, 상기 각 단백질은 단일 종의 바이러스에 유래되거나 다 종의 바이러스로부터 각각 유래된 것 일 수 있다. 또한, 상기 PB1, PA, NP, M 및 NS 단백질은 본 기술분야에 공지된 인플루엔자 바이러스로부터 유래되는 것 또는 이의 돌연변이를 제한없이 사용할 수 있다.
상기 중합효소 염기성 단백질 1(polymerase basic protein 1: PB1)은 인플루엔자 바이러스의 중합효소를 구성하는 단위체(subunit)로 중합효소 단위체 B1(polymerase subunit B1)이라고도 지칭된다. 일 예로, PB1 단백질은 A/Puerto Rico/8/34(H1N1)의 PB1 단백질 일 수 있다. 다른 일 예로, PB1 단백질은 서열번호 6의 아미노산 서열로 구성되는 것일 수 있다. 또 다른 일 예로, 상기 중합효소 염기성 단백질 1(PB1)은 서열번호 16의 염기서열을 포함하거나, 이로 이루어진 폴리뉴클레오타이드로 코딩되는 것 일 수 있다.
상기 중합효소 산성 단백질(polymerase acidic protein: PA)은 인플루엔자 바이러스의 중합효소를 구성하는 단위체(subunit)로 중합효소 단위체 A(polymerase subunit A)이라고도 지칭된다. 일 예로, PA 단백질은 A/Perto Rico/8/34(H1N1)의 PA 단백질 일 수 있다. 다른 일 예로, PA 단백질은 서열번호 7의 아미노산 서열로 구성되거는 것일 수 있다. 다른 일 예로, 상기 중합효소 산성 단백질(polymerase acidic protein: PA)는 단백질은 서열번호 17의 염기서열을 포함하거나, 이로 이루어진 폴리뉴클레오타이드로 코딩되는 것 일 수 있다.
상기 핵단백질(nucleoprotein: NP)은 바이러스의 음성 가닥 RNA를 캡슐화하는 구조 단백질로, 핵단백질(NP)은 종의 특이성을 결정하는 주요 요인 중 하나이다. 상기 핵단백질(NP)은 일 예로 A/Perto Rico/8/34(H1N1)의 NP 단백질 일 수 있다. 다른 일 예로, 상기 핵단백질(NP)는 서열번호 8의 아미노산 서열로 구성되는 것 일 수 있다. 또 다른 일 예로, 상기 핵단백질(NP)은 서열번호 18의 염기서열을 포함하거나, 이로 이루어진 폴리뉴클레오타이드로 코딩되는 것 일 수 있다.
상기 매트릭스 단백질(matrix: M)은 일 예로 A/Perto Rico/8/34(H1N1)의 M 단백질 일 수 있다. 다른 일 예로 상기 매트릭스 단백질(M)은 서열번호 9의 아미노산 서열로 구성되는 것 일 수 있다. 또 다른 일 예로, 상기 매트릭스 단백질(M)은 서열번호 19의 염기서열을 포함하거나, 이로 이루어진 폴리뉴클레오타이드로 코딩되는 것 일 수 있다.
상기 비구조 단백질(nonstructural protein: NS)은 일 예로 A/Perto Rico/8/34(H1N1)의 NS 단백질 일 수 있다. 다른 일 예로, 상기 비구조 단백질(NS)은 서열번호 10의 아미노산 서열로 구성되는 것 일 수 있다. 또 다른 일 예로, 상기 비구조 단백질(NS)은 서열번호 20의 염기서열을 포함하거나, 이로 이루어진 폴리뉴클레오타이드로 코딩되는 것 일 수 있다.
일 예로, 본 발명의 재조합 인플루엔자 바이러스는 상기한 변이를 포함하는 PB2 단백질과 함께, A/Perto Rico/8/34(H1N1)의 중합효소 염기성 단백질 1(polymerase basic protein 1: PB1), 중합효소 산성 단백질(polymerase acidic protein: PA), 핵단백질(nucleoprotein: NP), 매트릭스 단백질(matrix: M) 및/또는 비구조 단백질(nonstructural protein: NS)을 포함할 수 있다. 이러한 재조합 인플루엔자 바이러스의 경우, 포유류에 대한 비병원성, 높은 면역원성 및 증식률을 가져 백신주로서 활용이 우수하다.
구체적인 일 예로, 본 발명의 재조합 인플루엔자 바이러스는 서열번호 2의 아미노산 서열을 포함하는 PB2 단백질, 서열번호 3의 아미노산 서열을 포함하는 HA 단백질, 서열번호 5의 아미노산 서열을 포함하는 NA 단벡질, 서열번호 6의 아미노산 서열을 포함하는 PB1 단백질, 서열번호 7의 아미노산 서열을 포함하는 PA 단백질, 서열번호 8의 아미노산 서열을 포함하는 NP 단백질, 서열번호 9의 아미노산 서열을 포함하는 M 단백질 및 서열번호 10의 아미노산 서열을 포함하는 NS 단백질을 포함하거나; 상기한 단백질들을 코딩하는 게놈을 포함할 수 있다.
상기한 본 발명의 재조합 인플루엔자 바이러스는, 본 명세서에서는 rSL20(P)-MVV310PB2로 명명되었고, 2021년 9월 1일 국제기탁기관인 생물자원센터(KCTC)에 수탁되어, KCTC 14691BP의 기탁번호를 부여 받았다.
따라서, 본 발명은 기탁번호 KCTC 14691BP의 재조합 인플루엔자 바이러스를 제공한다.
또 다른 형태로, 본 발명읜 상기한 재조합 인플루엔자 바이러스를 포함하는 인플루엔자 바이러스 백신을 제공한다.
본 발명에서 상기 백신은 백신 제조에 사용되는 백신용 조성물을 포함하는 의미이며, 본 발명의 재조합 인플루엔자 바이러스를 유효성분으로 포함하는 백신 조성물을 포함하는 것으로 이해된다.
일 예로 상기 백신은 바이러스 균주를 그대로 포함하는 생독 백신 일 수 있다.
다른 일 예로, 상기 백신은 사독 백신일 수 있다. 구체적으로, 본 발명의 재조합 인플루엔자 바이러스는 불활화 처리되어 동물용 또는 인체용 불활화 백신으로 제공될 수 있다. 상기 바이러스의 불활화 방법은 본 발명 기술분야에서 통상적으로 이용되는 백신 제조방법 또는 바이러스 불활화 방법을 이용할 수 있고, 구체적인 실시예에 기재된 방법으로 한정되는 것은 아니다. 본 발명의 치환 변이를 갖는 PB2 단백질 또는 이를 코딩하는 게놈을 포함하는 재조합 인플루엔자 바이러스는 포유류에 대한 병원성을 나타내지 않으며, 면역원성과 계태아에서 증식성이 우수해, 백신주로서 우수한 특성을 갖는다. 따라서, 이를 유효성분으로 포함하는 백신은 투여 개체의 감염 위험성을 낮추면서 우수한 백신 효과를 얻을 수 있다.
본 발명의 일 실시예에서, 재조합 인플루엔자 바이러스를 각각 접종한 마우스에 접종한 결과, 본 발명의 치환 변이를 포함하는 PB2 단백질을 갖는 rSL20(P)-MVV310PB2 재조합 바이러스를 접종한 마우스에서는 체중 감소 및 마우스 폐사가 나타나지 않아, 백신으로서 유용할 것으로 판단된다
또 다른 일 실시예에서 재조합 바이러스들의 계태아에서의 증식역가(50% embryo infection dose, EID50/ml)를 측정한 결과, 본 발명의 rSL20(P)-MVV310PB2 재조합 바이러스를 접종한 경우 가장 높은 계태아 증식성을 가짐을 확인했고, rSL20(P)-MVV310PB2 재조합 바이러스와 동일한 유래의 HA, NA, PB1, PB2, PA, NP, M 및 NS 단백질을 포함하면서, PB2에 변이를 포함하지 않는 rSL20(P)-310PB2 재조합 바이러스의 경우 계태아 증식성이 10배 가량 감소함을 확인하였다. 이에 따라, PB2 단백질에서 I66M, I109V 및 I133V 변이를 포함하는 경우 계태아 증식성이 높아 백신으로 활용이 우수하다.
본 발명의 재조합 인플루엔자 바이러스와 함께 혼합될 수 있는 부형제의 종류는 특별히 한정되지 않고, 백신의 효과를 유지 또는 향상시키거나, 백신의 안정성 등을 높이기 위한 부형제라면 제한없이 본 발명의 백신에 포함하여 사용될 수 있다. 또한, 백신의 효과 개선을 위한 아쥬반트를 더 포함하여 사용할 수 있다.
일 예로, Montanide ISA70(SEPPIC, France), 수산화알루미늄젤(Al(OH)3-gel), Arlacel A special(ICI, USA), 및/또는 Freund's adjuvant 등을 포함할 수 있으나, 이에 제한되는 것은 아니다.
상기 백신은 닭과 오리 등의 조류뿐 아니라 인간, 돼지, 개, 마우스 등을 포함하는 포유류에도 적용 가능하다. 특히, 본 발명의 PB2 단백질 또는 이의 게놈을 포함하는 인플루엔자 바이러스의 경우 포유류에 비병원성이면서 면역원성 및 증식성이 높아, 우수한 백신 효율을 갖는다.
본 발명은 또 다른 형태로, 인플루엔자 바이러스 A/CHICKEN/KOREA/01310/2001(H9N2)의 중합효소 염기성 단백질 2(polymerase basic protein 2: PB2)에서 66번 아이소루신(I)이 메티오닌(M)으로, 109번 아이소루신(I)이 발린(V)으로 그리고 133번 아이소루신(I)이 발린(V)으로 치환된 단백질을 코딩하는 폴리뉴클레오타이드를 포함하는 재조합 벡터를 제공한다.
상기 재조합 벡터는 역유전학(reserved genetics)을 이용해서 재조합 인플루엔자 바이러스를 제조하는데 사용될 수 있다. 상기한 변이를 포함하는 PB2 단백질을 코딩하는 폴리뉴클레오타이드를 포함하는 벡터를 이용해 역유전학 법으로 생산된 재조합 인플루엔자 바이러스는 PB2 단백질의 변이를 포함하여 포유류에서 병원성을 나타내지 않는 특성을 갖는다.
본 발명에서 폴리뉴클레오타이드는 단백질 또는 폴리펩타이드를 코딩하기 위한 뉴클레오타이드의 중합 사슬로, 용어 염기서열, 유전자 또는 게놈서열과 상호 교환적으로 사용될 수 있다.
상기 중합효소 염기성 단백질 2(PB2)를 코딩하는 폴리뉴클레오타이드는 서열번호 1의 서열로 구성되는 아미노산 서열에서 66번 아이소루신(I)이 메티오닌(M)으로, 109번 아이소루신(I)이 발린(V)으로 그리고 133번 아이소루신(I)이 발린(V)으로 치환된 단백질을 코딩하는 것 일 수 있고, 다른 일 예로, 서열번호 2의 아미노산로 구성되는 PB2 단백질을 코딩하는 것 일 수 있다. 또 다른 일 예로, 서열번호 12의 염기서열로 구성되거나 이로 이루어진 것 일 수 있다.
또 다른 형태로, 본 발명은 인플루엔자 바이러스의 헤마글루티닌(hemagglutinin: HA) 단백질을 코딩하는 폴리뉴클레오타이드; 인플루엔자 바이러스의 뉴라미니다제(neuraminidase: NA)를 코딩하는 폴리뉴클레오타이드; 및 인플루엔자 바이러스 A/CHICKEN/KOREA/01310/2001(H9N2)의 염기성 단백질 2(polymerase basic protein 2: PB2)에서 66번 아이소루신(I)이 메티오닌(M)으로, 109번 아이소루신(I)이 발린(V)으로 그리고 133번 아이소루신(I)이 발린(V)으로 치환된 단백질을 코딩하는 폴리뉴클레오타이드를 포함하는 재조합 인플루엔자 바이러스 제조용 조성물을 제공한다.
상기 조성물은 인플루엔자 바이러스의 중합효소 염기성 단백질 1(polymerase basic protein 1: PB1)을 코딩하는 폴리뉴클레오타이드, 중합효소 산성 단백질(polymerase acidic protein: PA)을 코딩하는 폴리뉴클레오타이드, 핵단백질(nucleoprotein: NP)를 코딩하는 폴리뉴클레오타이드, 매트릭스 단백질(matrix: M)을 코딩하는 폴리뉴클레오타이드 및 비구조 단백질(nonstructural protein: NS)을 코딩하는 폴리뉴클레오타이드로 이루어진 군으로부터 선택된 하나 이상을 더 포함할 수 있다.
일 예로, 본 발명의 재조합 인플루엔자 바이러스 제조용 조성물은 인플루엔자 바이러스의 헤마글루티닌(hemagglutinin: HA) 단백질을 코딩하는 폴리뉴클레오타이드; 뉴라미니다제(neuraminidase: NA)를 코딩하는 폴리뉴클레오타이드; A/CHICKEN/KOREA/01310/2001(H9N2)의 염기성 단백질 2(polymerase basic protein 2: PB2)에서 66번 아이소루신(I)이 메티오닌(M)으로, 109번 아이소루신(I)이 발린(V)으로 그리고 133번 아이소루신(I)이 발린(V)으로 치환된 단백질을 코딩하는 폴리뉴클레오타이드; 중합효소 염기성 단백질 1(polymerase basic protein 1: PB1)을 코딩하는 폴리뉴클레오타이드; 중합효소 산성 단백질(polymerase acidic protein: PA)을 코딩하는 폴리뉴클레오타이드; 핵단백질(nucleoprotein: NP)를 코딩하는 폴리뉴클레오타이드; 매트릭스 단백질(matrix: M)을 코딩하는 폴리뉴클레오타이드 및 비구조 단백질(nonstructural protein: NS)을 코딩하는 폴리뉴클레오타이드를 포함할 수 있다.
상기 폴리뉴클레오타이드는 벡터에 포함된 것 일 수 있다. 상기 폴리뉴클레오타이드는 각각 하나의 벡터에 포함되거나 하나의 벡터에 하나 이상 단백질을 코딩하는 폴리뉴클레오타이드가 포함될 수 있다.
상기 중합효소 염기성 단백질 2(PB2)를 코딩하는 폴리뉴클레오타이드는 서열번호 1의 서열로 구성되는 아미노산 서열에서 66번 아이소루신(I)이 메티오닌(M)으로, 109번 아이소루신(I)이 발린(V)으로 그리고 133번 아이소루신(I)이 발린(V)으로 치환된 단백질을 코딩하는 것 일 수 있고, 다른 일 예로, 서열번호 2의 아미노산로 구성되는 PB2 단백질을 코딩하는 것 일 수 있다. 또 다른 일 예로, 서열번호 12의 염기서열을 포함하거나 이로 이루어진 것 일 수 있다.
일 예로 헤마글루티닌(hemagglutinin: HA) 단백질을 코딩하는 폴리뉴클레오타이드는 Y280 lineage (A/CHICKEN/KOREA/SL20/2020)(H9N2)의 헤마글루티닌(HA)에서 226번 류신을 글루타민으로 치환한 변이를 포함하는 HA 변이 단백질을 코딩하는 것 일 수 있다. 다른 일 예로 서열번호 3 또는 서열번호 4의 아미노산 서열로 구성된 HA 단백질을 코딩하는 것 일 수 있다. 또 다른 일 예로, 서열번호 13의 염기서열 또는 서열번호 14의 염기서열을 포함하거나, 이로 이루어진 것 일 수 있다.
일 예로 뉴라미니다제(neuraminidase: NA)를 코딩하는 폴리뉴클레오타이드는 Y280 lineage (A/CHICKEN/KOREA/SL20/2020)(H9N2)의 뉴라미다제(NA)를 코딩하는 것 일 수 있다. 다른 일 예로 서열번호 5의 아미노산 서열로 구성된 NA 단백질을 코딩하는 것 일 수 있다. 또 다른 일 예로, 서열번호 15의 염기서열을 포함하거나, 이로 이루어진 것 일 수 있다.
일 예로, 중합효소 염기성 단백질 1(polymerase basic protein 1: PB1)을 코딩하는 폴리뉴클레오타이드는 A/Perto Rico/8/34(H1N1)의 PB1 단백질을 코딩하는 것 일 수 있다. 다른 일 예로, 서열번호 6의 아미노산 서열로 구성되는 PB1 단백질을 코딩하는 것 일 수 있다. 또 다른 일 예로, 서열번호 16의 염기서열을 포함하거나, 이로 이루어진 것 일 수 있다.
일 예로, 중합효소 산성 단백질(polymerase acidic protein: PA)을 코딩하는 폴리뉴클레오타이드는 A/Perto Rico/8/34(H1N1)의 PA 단백질을 코딩하는 것 일 수 있다. 다른 일 예로, 서열번호 7의 아미노산 서열로 구성되는 PA 단백질을 코딩하는 것 일 수 있다. 또 다른 일 예로, 서열번호 17의 염기서열을 포함하거나, 이로 이루어진 것 일 수 있다.
일 예로, 핵단백질(nucleoprotein: NP)를 코딩하는 폴리뉴클레오타이드는 A/Perto Rico/8/34(H1N1)의 NP 단백질을 코딩하는 것 일 수 있다. 다른 일 예로, 서열번호 8의 아미노산 서열로 구성되는 NP 단백질을 코딩하는 것 일 수 있다. 또 다른 일 예로, 서열번호 18의 염기서열을 포함하거나, 이로 이루어진 것 일 수 있다.
일 예로, 매트릭스 단백질(matrix: M)을 코딩하는 폴리뉴클레오타이드는 A/Perto Rico/8/34(H1N1)의 M 단백질을 코딩하는 것 일 수 있다. 다른 일 예로, 서열번호 9의 아미노산 서열로 구성되는 M 단백질을 코딩하는 것 일 수 있다. 또 다른 일 예로, 서열번호 19의 염기서열을 포함하거나, 이로 이루어진 것 일 수 있다.
일 예로, 비구조 단백질(nonstructural protein: NS)을 코딩하는 폴리뉴클레오타이드는 A/Perto Rico/8/34(H1N1)의 NS 단백질을 코딩하는 것 일 수 있다. 다른 일 예로, 서열번호 10의 아미노산 서열로 구성되는 NS 단백질을 코딩하는 것 일 수 있다. 또 다른 일 예로, 서열번호 20의 염기서열을 포함하거나, 이로 이루어진 것 일 수 있다.
본 발명의 재조합 인플루엔자 바이러스 제조용 조성물은 역유전학을 통해 상기 조성물에 포함된 폴리뉴클레오타이드로 재조합 인플루엔자 바이러스를 제조할 수 있다. 일 예로, 각각의 폴리뉴클레오타이드를 각각 Pol I과 Pol II를 포함하는 벡터에 클로닝하고, 8개 벡터를 세포 또는 발육란에 공동 형질감염(co-transfection)하여 재조합 바이러스를 생산할 수 있다.
이러한 측면에서, 본 발명은 또 다른 형태로, 인플루엔자 바이러스 A/CHICKEN/KOREA/01310/2001(H9N2)의 중합효소 염기성 단백질 2(polymerase basic protein 2: PB2)에서 66번 아이소루신(I)이 메티오닌(M)으로, 109번 아이소루신(I)이 발린(V)으로 그리고 133번 아이소루신(I)이 발린(V)으로 치환된 단백질을 코딩하는 폴리뉴클레오타이드를 포함하는 재조합 벡터 또는
인플루엔자 바이러스 A/CHICKEN/KOREA/01310/2001(H9N2)의 중합효소 염기성 단백질 2(polymerase basic protein 2: PB2)에서 66번 아이소루신(I)이 메티오닌(M)으로, 109번 아이소루신(I)이 발린(V)으로 그리고 133번 아이소루신(I)이 발린(V)으로 치환된 단백질을 코딩하는 폴리뉴클레오타이드; 및 헤마글루티닌(hemagglutinin: HA) 단백질을 코딩하는 폴리뉴클레오타이드, 인플루엔자 바이러스의 뉴라미니다제(neuraminidase: NA)를 코딩하는 폴리뉴클레오타이드 중합효소 염기성 단백질 1(polymerase basic protein 1: PB1)을 코딩하는 폴리뉴클레오타이드, 중합효소 산성 단백질(polymerase acidic protein: PA)을 코딩하는 폴리뉴클레오타이드, 핵단백질(nucleoprotein: NP)를 코딩하는 폴리뉴클레오타이드, 매트릭스 단백질(matrix: M)을 코딩하는 폴리뉴클레오타이드 및 비구조 단백질(nonstructural protein: NS)을 코딩하는 폴리뉴클레오타이드로 이루어진 군으로부터 선택된 하나 이상을 포함하는 조류 인플루엔자 바이러스 제조용 조성물을 세포 또는 발육란에 접종하는 것을 포함하는 재조합 인플루엔자 바이러스 제조방법을 제공한다.
상기 세포 또는 발육란은 상기한 벡터 또는 이를 포함하는 조성물로 형질 감염시키고, 배양을 통해서 바이러스를 증식시키는 방법으로 바이러스를 생산할 수 있는 것이라면 종류에 제한없이 본 발명에 사용될 수 있다. 한편 본 발명의 재조합 인플루엔자 바이러스는 포유류 세포에서는 낮은 증식성을 나타내어 인체에 대한 매우 낮은 감염 위험성을 나타내는 것을 특징으로 하므로, 상기 세포는 포유류 세포를 제외한 세포인 것이 바람직하다.
상기 제조방법은 형질감염된 세포 또는 발육란을 배양하는 것을 더 포함할 수 있다. 상기 세포 또는 발육란의 배양은 본 발명 기술분야에서 통상적으로 사용되는 배양 조건, 배지 등을 이용하여 수행될 수 있다.
일 예로, A/KOREA/01310/2001(H9N2)의 PB2 단백질에서 66번 아미노산을 아이소루신(I)에서 메티오닌(M)으로, 109번 아미노산을 아이소루신(I)에서 메티오닌(M)으로, 133번 아미노산을 아이소루신(I)에서 발린(V)으로 변이시킨 단백질을 코딩하는 폴리뉴클레오타이드(서열번호 12)를 클로닝한 벡터 또는
상기 서열번호 12의 폴리뉴클레오타이드를 클로닝한 벡터, HA를 코딩하는 뉴클레오타이드(서열번호 13)를 클로닝한 벡터, NA를 코딩하는 뉴클레오타이드(서열번호 15)를 클로닝한 벡터, PB1을 코딩하는 뉴클레오타이드(서열번호 16)를 클로닝한 벡터, PA을 코딩하는 뉴클레오타이드(서열번호 17)를 클로닝한 벡터, NP를 코딩하는 뉴클레오타이드(서열번호 18)를 클로닝한 벡터, M을 코딩하는 뉴클레오타이드(서열번호 19)를 클로닝한 벡터 및/또는 NS(서열번호 20)를 클로닝한 벡터를 포함하는 재조합 인플루엔자 바이러스 제조용 조성물을 세포로 공동 형질감염하거나, 발육란에 요막강 경로로 접종하여 배양한 후 바이러스를 얻었다. 상기에서 얻어진 본 발명의 재조합 인플루엔자 바이러스는 바이러스 역가(EID50/ml(log10))가 우수해 높은 계태아 증식성을 가지며, 포유류 세포주에서 증식하지 못해, 포유류에 비병원성인, 즉, 인체에 대한 낮은 감염 위험을 가짐을 확인하였다.
중복된 기재를 피하기 위해서, 별도의 언급이 없는 한, 재조합 인플루엔자 바이러스 부분에서 기술한 본 발명 각 구성에 대한 정의 및 설명은 재조합 벡터, 백신, 재조합 인플루엔자 바이러스 제조용 조성물 및 재조합 인플루엔자 바이러스 제조방법에 그대로 준용된다.
이하, 본 발명을 실시예에 의해 상세히 설명한다. 단, 하기 실시예는 본 발명을 예시하는 것일 뿐, 본 발명이 하기 실시예에 의해 한정되는 것은 아니다.
실시예 1. 재조합 바이러스 제작
1-1. 재조합 바이러스 제작
재조합 인플루엔자 바이러스 제작을 위하여, 호프만 박사의 역유전학 벡터시스템(특허 제0862758호)을 사용하였다. 벡터 구성은 특허에 기재된 내용과 동일한 벡터 pHW2000를 분양받아 실험에 사용하였다.
구체적으로, 2020년 한국에서 분리된 인플루엔자 바이러스 Y280 lineage (A/chicken/KOREA/SL20/2020)(H9N2)의 헤마글루티닌(hemagglutinin; HA)의 게놈 절편(서열번호 13), 뉴라미다제(neuraminidase; NA) 게놈 절편(서열번호 15)이 클로닝된 호프만 벡터;
상기 Y280 lineage H9N2 바이러스의 헤마글루티닌(hemagglutinin; HA) 유전자의 226번 아미노산을 류신에서 글루타민으로 변이시킨 유전자(서열번호 14)를 클로닝한 호프만 벡터(Y280-L226Q);
국내 저병원성 조류 인플루엔자 바이러스 01310(A/chicken/Korea/01310/2001)(H9N2)의 염기성 단백질 2(polymerase basic protein 2: PB2) 게놈 절편(서열번호 11)이 클로닝된 호프만 벡터;
인플루엔자 바이러스 01310(A/chicken/Korea/01310/2001)(H9N2)의 PB2 단백질에서 66번 아미노산을 아이소루신(I)에서 메티오닌(M)으로, 109번 아미노산을 아이소루신(I)에서 발린(V)으로, 133번 아미노산을 아이소루신(I)에서 발린(V)으로 변이시킨 단백질을 코딩하는 유전자(서열번호 12)를 클로닝한 호프만 벡터(01310-MVV);
인플루엔자 바이러스 A/Puerto Rico/8/34(H1N1)의 PB2(서열번호 22), PB1(서열번호 16), PA(서열번호 17), NP(서열번호 18), M(서열번호 19) 또는 NS(서열번호 20)의 게놈 절편을 각각 클로닝한 호프만 벡터 플라스미드를 준비하였다.
8개 단백질에 대한 각각의 벡터 플라스미드를 조합하여 재조합바이러스를 제조하였고, 각 재조합 바이러스의 유전자 구성은 하기의 표 1에 나타난 바와 같다.
재조합바이러스 | HA | NA | PB2 | PB1 | PA | NP | M | NS |
Y280 야생형 | Y280 | Y280 | Y280 | Y280 | Y280 | Y280 | Y280 | Y280 |
rSL20(P) | Y280 | Y280 | PR8 | PR8 | PR8 | PR8 | PR8 | PR8 |
rSL20 (P) -L226Q |
Y280 -L226Q |
Y280 | PR8 | PR8 | PR8 | PR8 | PR8 | PR8 |
rSL20 (P) -310PB2 |
Y280 | Y280 | 01310 | PR8 | PR8 | PR8 | PR8 | PR8 |
rSL20 (P)-MVV310PB2 | Y280 | Y280 | 01310-MVV | PR8 | PR8 | PR8 | PR8 | PR8 |
구체적으로, 293T 세포(생명자원센터, KCTC)를 6-웰 세포배양용기에 5%(v/v) FBS를 함유한 DMEM(GIBCO BRL) 배지에 2X106개/2ml 부유하여 각 웰에 첨가한 후 3 내지 4시간 부착시켰다. 배지를 제거한 후, Opti-MEM 배지(Invitrogen Co. USA) 2ml를 첨가하였다. 재조합 바이러스에 포함시킬 HA, NA,
PB2,
PB1,
PA,
NP,
M, 및 NS 게놈을 클로닝한 플라스미드 8개를 모두 하나의 1.5ml 튜브에 각각 300ng씩의 양으로 넣고, 최종 25㎕가 되도록 Opti-MEM 배지를 첨가하였다. 또 다른 1.5ml 튜브에 plus reagent(Invitrogen Co. USA) 6㎕와 Opti-MEM 배지 69㎕를 첨가하여 혼합한 후 플라스미드가 들어있는 1.5ml 튜브에 첨가하여 혼합한 후 실온에서 15분간 반응시켰다. 기다리는 동안 리포펙타민(lipofectamine) 4㎕(Invitrogen Co)와 Opti-MEM 96㎕를 혼합하여 15분간 반응한 후 100㎕를 취하여 상기 플라스미드가 있는 튜브에 첨가한 후 15분간 추가 반응시켰다. 얻어진 반응 생성물을 상기293T 세포가 들어있는 각 웰에 100㎕를 첨가하였다. 6-웰 배양용기를 5% CO2, 37℃에서 20시간 배양한 후, 각 웰 당 트립신 10㎍(2.5㎍/4㎕)을 첨가하고, 24시간 후 상층액을 수확하였다. 상기 수확된 상층액 200㎕를 10 내지 11일령 SPF 발육란(Sunrise Co., NY)에 요막강 경로로 접종하였다. 상기 접종된 발육란을 37℃에서 3일간 배양한 후 요막액을 수확하여 혈구응집 여부를 확인한 결과 모두 혈구응집 양성을 보였다.
이 재조합 바이러스의 혈구응집역가를 측정하고, 100배 희석하여 동일한 방법으로 발육란에서 증식시킨 바이러스를 -70℃에서 보관하며 실험에 사용하였다.
1-2. 바이러스 역가 측정
상기의 재조합 바이러스들의 계태아에서의 증식역가(50% embryo infection dose, EID50/ml)를 측정하기 위하여, 각각의 재조합 바이러스들을 인산완충용액으로 10-1 내지 10-9까지 10진 희석하여 각 희석 배수 별로 10 내지 11일령의 SPF 발육란 5개에 요막강 경로로 100㎕씩 접종하였다. 그 후 3일간 배양한 후, 요막액을 수확하여 닭의 적혈구로 혈구응집여부를 확인하여 Reed-Muench 계산식에 따라 바이러스 역가(EID50/ml)를 측정하였다.
그 결과 얻어진 바이러스 역가(EID50/ml(log10))를 아래의 표 2에 나타내었다.
재조합 바이러스 | EID 50 /ml(log10) |
Y280 야생형 | 9.67 ± 0.29 |
rSL20(P) | 9.41 ± 0.12 |
rSL20(P)-L226Q | 9.42 ± 0.14 |
rSL20(P)-310PB2 | 8.57 ± 0.46 |
rSL20(P)-MVV310PB2 | 9.58 ± 0.14 |
표 2에 나타낸 바와 같이, 바이러스 역가(EID50/ml(log10))를 살펴보면, rSL20(P)의 경우 109.41와 rSL20(P)-L226Q는 109.42 로 비슷하였고, rSL20(P)-310PB2의 경우 108.57 로 10배 가량 감소하였으나, MVV 변이를 갖는 PB2 단백질을 포함하는 유전자를 갖는 rSL20(P)-MVV310PB2 재조합 바이러스는 109.58 EID50/ml로 높은 계태아 증식성을 가짐을 확인하였다.
실시예 2: 재조합 바이러스의 포유류 병원성 평가
2-1. 포유류 세포주에서의 재조합 바이러스의 증식성 평가
실시예 1에서 제조한 재조합 바이러스의 포유류에서의 증식성을 확인하기 위해, 야생형 인플루엔자 바이러스 Y280(Y280 wild-type), 실시예 1의 네 가지 재조합 바이러스, 그리고 인플루엔자 바이러스 PR8의 전체 유전자를 역유전학을 사용해 재생성한 바이러스(rPR8)를 1 MOI로 MDCK 세포주(생물자원센터, 한국)와 A549 세포주(생물자원센터, 한국)에 접종하고 0, 24, 48, 72시간 마다 상층액을 수득하여 시간대별 증식한 바이러스의 양을 TCID50/0.1ml로 측정하였다.
도 1a 및 도 1b에 나타낸 바와 같이, 야생형 인플루엔자 바이러스 Y280은 MDCK 에서만 증식가능 하였고, PR8 바이러스의 6개 내부 유전자를 가진 rSL20(P)와 rSL20(P)-L226Q 재조합 바이러스의 경우 두 세포주에서 야생형 인플루엔자 바이러스 PR8(rPR8) 이상의 높은 증식성을 보였으며, A549 세포주에서는 rSL20(P)가 rSL20(P)-L226Q보다 더 높은 증식성을 나타냈다.
그러나, 01310의 PB2 게놈을 갖는 rSL20(P)-310PB2와 변이를 포함하는 MVVPB2를 가진 rSL20(P)-MVV310PB2 두 바이러스는 두 세포주 모두에서 증식하지 못하여, 인체에 대한 매우 낮은 감염 위험을 가짐을 확인하였다. 상기와 같은 결과를 통해, 상기 두 종류의 바이러스는 상호 유사한 수준의 낮은 포유류 독성을 나타내는 것을 확인하였고, 상기 실시예 1-2에서 확인한 바와 같이 계태아에서의 증식역가 측면에서는 rSL20(P)-MVV310PB2 가 현저히 우수하므로, 종합적으로 rSL20(P)-MVV310PB2 가 사독 백신주로 더욱 적합한 바이러스가 될 수 있음을 확인하였다.
2-2. 마우스에서 재조합 바이러스의 병원성 평가
실시예 1의 재조합 바이러스가 포유류에서 병원성을 갖는지 확인하기 위해, rSL20(P), rSL20(P)-L226Q 및 rSL20(P)-MVV310PB2의 재조합 바이러스 각각을 6주령 BALB/c 암컷 마우스에 106 EID50/0.05ml으로 비강 내 접종하고, 1주간 체중을 측정하여 병원성을 확인하였다. 그리고, 3일째 폐를 샘플링하여 폐 내 증식성을 확인하였다.
도 2a에 나타낸 바와 같이, rSL20(P) 재조합 바이러스를 접종한 경우, 7일째까지 지속적으로 체중이 감소하였고, rSL20(P)L226Q 재조합 바이러스를 접종한 경우 3일째에 이미 60%가 안락사 기준의 체중으로 감소하였으며 4일째에는 모든 개체가 폐사하여, rSL20(P)L226Q 재조합 바이러스가 가장 병원성이 높음을 알 수 있었다. 그러나, rSL20(P)-MVV310PB2 재조합 바이러스를 접종한 경우, 마우스에서 체중 감소가 확인되지 않았다. 이러한 결과는 도 2b에서도 확인할 수 있었다. rSL20(P) 재조합 바이러스와 rSL20(P)L226Q 재조합 바이러스를 접종한 경우 각각 4일 이후 또는 6일 이후에 마우스 개체가 폐사하였으나, rSL20(P)-MVV310PB2 재조합 바이러스를 접종한 경우 마우스의 폐사가 나타나지 않았다.
또한, 3일째에 샘플링한 폐에서 폐 유제액을 10일령 발육란에 각각 접종하고, 증식한 바이러스를 10진 희석하여 TCID50/0.1ml로 역가를 측정하는 방법으로 폐에서 증식한 바이러스의 양을 확인하였다. TCID50/0.1ml 값은 3회 측정한 값의 평균으로 나타내었다.
Recombinant virus | Virus isolation rate | Log10 TCID50/0.1 ml |
rSL20(P) | 3/3 | 4.00 ± 0.25 |
rSL20(P)-L226Q | 3/3 | 5.00 ± 0.25 |
rSL20(P)-MVV310PB2 | 0/3 | 0.00 ± 0.00 |
표 3에 나타낸 바와 같이, 다른 바이러스 접종군에서는 마우스의 폐에서 바이러스가 검출되었으나, rSL20(P)-MVV310PB2 재조합 바이러스를 접종한 마우스의 폐에서는 바이러스가 검출되지 않아, 포유류에 대하여 본 발명의 재조합 바이러스가 병원성이 없음을 확인하였다.
실시예 3: 재조합 바이러스의 항체 형성능 평가
3-1. 재조합 바이러스의 닭에서 항체 형성능 평가
실시예 1의 재조합바이러스가 사독 백신주로 사용될 수 있는지 확인하기 위해서, rSL20(P), rSL20(P)-L226Q 및 rSL20(P)-MVV310PB2 재조합 바이러스를 각각 포르말린으로 불활화하여 발육란에 접종하고, 불활화 여부를 확인하였다. 이 후, 재조합 바이러스와 ISA70을 3:7 (v/v) 로 섞어 그룹당 각 3주령 SPF 닭 5마리에 피하로 0.5ml을 접종하였다. 접종 3, 4주 후에 채혈하여 혈청을 RDE 및 비동화 처리 후 세 가지 항원을 이용하여 HI test를 하였다. 결과는 표 4 나타내었다.
불활화 재조합 바이러스 |
백신접종 후 주(week) (wpv) |
HI 역가의 기하평균(GMT)a | ||
Antigen | ||||
rSL20(P) | rSL20(P)-L226Q | rSL20(P)-MVV310PB2 | ||
rSL20(P) | 3 wpv | 1195 (756 - 1633)b |
256 (256 - 256)b |
1195 (756 - 1633)b |
4 wpv | 2303 (721 - 3884)b |
288 (90 - 486)b |
1195 (461 - 1929)b |
|
rSL20(P)-L226Q | 3 wpv | 1741 (888 - 2594)b |
256 (61 - 451)b |
1075 (283 - 1867)b |
4 wpv | 1638 (942 - 2355)b |
307 (66 - 548)b |
1331 (478 - 2184)b |
|
rSL20(P)-MVV310PB2 | 3 wpv | 2560 (653 - 4467)b |
371 (117 - 625)b |
2304 (125 - 4483)b |
4 wpv | 2048 (491 - 3605)b |
666 (239 - 1092)b |
1434 (737 - 2130)b |
|
a Geomatric mean of HI titer b GMT 계산한 값의 95% 신뢰도의 신뢰구간 |
표 4에 나타낸 바와 같이, 모든 바이러스 백신 접종군에서 항체가 검출되었고, 실시예 1의 재조합 바이러스가 면역원성을 가짐을 확인하였다. 특히, rSL20(P)-MVV310PB2 재조합 바이러스 백신을 접종한 경우 높은 항체가 검출됨을 확인되어, 포유류에 병원성을 가지지 않으면서도, 높은 면역원성을 가져 백신주로서 개발에 유용함을 확인하였다.
<110> Geniner Co., Ltd.
<120> MAMMALIAN AVIRULENT AND EMBRYONATED EGG HIGHLY REPLICATIVE
RECOMBINANT INFLUENZA VIRUS
<130> G1.1P
<160> 22
<170> KoPatentIn 3.0
<210> 1
<211> 760
<212> PRT
<213> Artificial Sequence
<220>
<223> PB2 wild of 01310
<400> 1
Met Glu Arg Ile Lys Glu Leu Arg Asp Leu Met Ser Gln Ser Arg Thr
1 5 10 15
Arg Glu Ile Leu Thr Lys Thr Thr Val Asp His Met Ala Ile Ile Lys
20 25 30
Lys Tyr Thr Ser Gly Arg Gln Glu Lys Asn Pro Ala Leu Arg Met Lys
35 40 45
Trp Met Met Ala Met Lys Tyr Pro Ile Thr Ala Asp Lys Arg Ile Met
50 55 60
Glu Ile Ile Pro Glu Arg Asn Glu Gln Gly Gln Thr Leu Trp Ser Lys
65 70 75 80
Thr Asn Asp Ala Gly Ser Asp Lys Val Met Val Ser Pro Leu Ala Val
85 90 95
Thr Trp Trp Asn Arg Asn Gly Pro Thr Thr Ser Thr Val His Tyr Pro
100 105 110
Lys Val Tyr Lys Thr Tyr Phe Glu Lys Val Glu Arg Leu Lys His Gly
115 120 125
Thr Phe Gly Pro Ile His Phe Arg Asn Gln Val Lys Ile Arg Arg Arg
130 135 140
Val Asp Ile Asn Pro Gly His Ala Asp Leu Ser Ala Arg Glu Ala Gln
145 150 155 160
Asp Val Ile Met Glu Val Val Phe Pro Asn Glu Val Gly Ala Arg Ile
165 170 175
Leu Thr Ser Glu Ser Gln Leu Thr Ile Thr Lys Glu Lys Lys Glu Glu
180 185 190
Leu Gln Asp Cys Lys Ile Ala Pro Leu Met Val Ala Tyr Met Leu Glu
195 200 205
Arg Glu Leu Val Arg Lys Thr Arg Phe Leu Pro Val Ala Gly Gly Thr
210 215 220
Ser Ser Val Tyr Ile Glu Val Leu His Leu Thr Gln Gly Thr Cys Trp
225 230 235 240
Glu Gln Met Tyr Thr Pro Gly Gly Glu Val Arg Asn Asp Asp Val Asp
245 250 255
Gln Ser Leu Ile Ile Ala Ala Arg Asn Ile Val Arg Arg Ala Thr Val
260 265 270
Ser Ala Asp Pro Leu Ala Ser Leu Leu Glu Met Cys His Gly Thr Gln
275 280 285
Ile Gly Gly Ile Arg Met Val Asp Ile Leu Arg Gln Asn Pro Thr Glu
290 295 300
Glu Gln Ala Val Asp Ile Cys Lys Ala Ala Ile Gly Leu Arg Ile Ser
305 310 315 320
Ser Ser Phe Ser Phe Gly Gly Phe Thr Phe Lys Arg Thr Ser Gly Ser
325 330 335
Ser Val Lys Lys Glu Glu Glu Val Leu Thr Gly Asn Leu Gln Thr Leu
340 345 350
Lys Ile Arg Val His Glu Gly Tyr Glu Glu Phe Thr Met Val Gly Arg
355 360 365
Arg Ala Thr Ala Leu Leu Arg Lys Ala Thr Arg Arg Leu Ile Gln Leu
370 375 380
Ile Val Ser Gly Arg Asp Glu Gln Ser Ile Ala Glu Ala Ile Ile Val
385 390 395 400
Ala Met Val Phe Ser Gln Glu Asp Cys Met Ile Lys Ala Val Arg Gly
405 410 415
Asp Leu Asn Phe Val Asn Arg Ala Asn Gln Arg Leu Asn Pro Met His
420 425 430
Gln Leu Leu Arg His Phe Gln Lys Asp Ala Lys Val Leu Phe Gln Asn
435 440 445
Trp Gly Ile Glu Pro Ile Asp Asn Val Met Gly Met Ile Gly Ile Leu
450 455 460
Pro Asp Met Thr Pro Ser Thr Glu Met Ser Leu Arg Gly Val Arg Val
465 470 475 480
Ser Lys Met Gly Val Asp Glu Tyr Ser Ser Thr Glu Arg Val Val Val
485 490 495
Ser Ile Asp Arg Phe Leu Arg Val Arg Asp Gln Arg Gly Asn Ile Leu
500 505 510
Leu Ser Pro Glu Glu Val Ser Glu Thr Gln Gly Thr Glu Lys Leu Thr
515 520 525
Ile Thr Tyr Ser Ser Ser Met Met Trp Glu Ile Asn Gly Pro Glu Ser
530 535 540
Val Leu Val Asn Thr Tyr Gln Trp Ile Ile Arg Asn Trp Glu Thr Val
545 550 555 560
Lys Ile Gln Trp Ser Gln Asp Pro Thr Met Leu Tyr Asn Lys Val Glu
565 570 575
Phe Glu Pro Phe Gln Ser Leu Val Pro Lys Ala Ala Arg Gly Gln Tyr
580 585 590
Ser Gly Phe Val Arg Thr Leu Phe Gln Gln Met Arg Asp Val Leu Gly
595 600 605
Thr Phe Asp Thr Val Gln Ile Ile Lys Leu Leu Pro Phe Ala Ala Ala
610 615 620
Pro Pro Glu Gln Ser Arg Met Gln Phe Ser Ser Leu Thr Val Asn Val
625 630 635 640
Arg Gly Ser Gly Met Arg Ile Leu Val Arg Gly Asn Ser Pro Val Phe
645 650 655
Asn Tyr Asn Lys Ala Thr Lys Arg Leu Thr Val Leu Gly Lys Asp Ala
660 665 670
Gly Ala Leu Thr Glu Asp Pro Asp Glu Gly Thr Ala Gly Val Glu Ser
675 680 685
Ala Val Leu Arg Gly Phe Leu Ile Leu Gly Lys Glu Asp Lys Arg Tyr
690 695 700
Gly Pro Ala Leu Ser Ile Asn Glu Leu Ser Asn Leu Ala Lys Gly Glu
705 710 715 720
Lys Ala Asn Val Leu Ile Gly Gln Gly Asp Val Val Leu Val Met Lys
725 730 735
Arg Lys Arg Asp Ser Ser Ile Leu Thr Asp Ser Gln Thr Ala Thr Lys
740 745 750
Arg Ile Arg Met Ala Ile Asn ***
755 760
<210> 2
<211> 760
<212> PRT
<213> Artificial Sequence
<220>
<223> PB2 MVV mutant
<400> 2
Met Glu Arg Ile Lys Glu Leu Arg Asp Leu Met Ser Gln Ser Arg Thr
1 5 10 15
Arg Glu Ile Leu Thr Lys Thr Thr Val Asp His Met Ala Ile Ile Lys
20 25 30
Lys Tyr Thr Ser Gly Arg Gln Glu Lys Asn Pro Ala Leu Arg Met Lys
35 40 45
Trp Met Met Ala Met Lys Tyr Pro Ile Thr Ala Asp Lys Arg Ile Met
50 55 60
Glu Met Ile Pro Glu Arg Asn Glu Gln Gly Gln Thr Leu Trp Ser Lys
65 70 75 80
Thr Asn Asp Ala Gly Ser Asp Lys Val Met Val Ser Pro Leu Ala Val
85 90 95
Thr Trp Trp Asn Arg Asn Gly Pro Thr Thr Ser Thr Ile His Tyr Pro
100 105 110
Lys Val Tyr Lys Thr Tyr Phe Glu Lys Val Glu Arg Leu Lys His Gly
115 120 125
Thr Phe Gly Pro Val His Phe Arg Asn Gln Val Lys Ile Arg Arg Arg
130 135 140
Val Asp Ile Asn Pro Gly His Ala Asp Leu Ser Ala Arg Glu Ala Gln
145 150 155 160
Asp Val Ile Met Glu Val Val Phe Pro Asn Glu Val Gly Ala Arg Ile
165 170 175
Leu Thr Ser Glu Ser Gln Leu Thr Ile Thr Lys Glu Lys Lys Glu Glu
180 185 190
Leu Gln Asp Cys Lys Ile Ala Pro Leu Met Val Ala Tyr Met Leu Glu
195 200 205
Arg Glu Leu Val Arg Lys Thr Arg Phe Leu Pro Val Ala Gly Gly Thr
210 215 220
Ser Ser Val Tyr Ile Glu Val Leu His Leu Thr Gln Gly Thr Cys Trp
225 230 235 240
Glu Gln Met Tyr Thr Pro Gly Gly Glu Val Arg Asn Asp Asp Val Asp
245 250 255
Gln Ser Leu Ile Ile Ala Ala Arg Asn Ile Val Arg Arg Ala Thr Val
260 265 270
Ser Ala Asp Pro Leu Ala Ser Leu Leu Glu Met Cys His Gly Thr Gln
275 280 285
Ile Gly Gly Ile Arg Met Val Asp Ile Leu Arg Gln Asn Pro Thr Glu
290 295 300
Glu Gln Ala Val Asp Ile Cys Lys Ala Ala Ile Gly Leu Arg Ile Ser
305 310 315 320
Ser Ser Phe Ser Phe Gly Gly Phe Thr Phe Lys Arg Thr Ser Gly Ser
325 330 335
Ser Val Lys Lys Glu Glu Glu Val Leu Thr Gly Asn Leu Gln Thr Leu
340 345 350
Lys Ile Arg Val His Glu Gly Tyr Glu Glu Phe Thr Met Val Gly Arg
355 360 365
Arg Ala Thr Ala Leu Leu Arg Lys Ala Thr Arg Arg Leu Ile Gln Leu
370 375 380
Ile Val Ser Gly Arg Asp Glu Gln Ser Ile Ala Glu Ala Ile Ile Val
385 390 395 400
Ala Met Val Phe Ser Gln Glu Asp Cys Met Ile Lys Ala Val Arg Gly
405 410 415
Asp Leu Asn Phe Val Asn Arg Ala Asn Gln Arg Leu Asn Pro Met His
420 425 430
Gln Leu Leu Arg His Phe Gln Lys Asp Ala Lys Val Leu Phe Gln Asn
435 440 445
Trp Gly Ile Glu Pro Ile Asp Asn Val Met Gly Met Ile Gly Ile Leu
450 455 460
Pro Asp Met Thr Pro Ser Thr Glu Met Ser Leu Arg Gly Val Arg Val
465 470 475 480
Ser Lys Met Gly Val Asp Glu Tyr Ser Ser Thr Glu Arg Val Val Val
485 490 495
Ser Ile Asp Arg Phe Leu Arg Val Arg Asp Gln Arg Gly Asn Ile Leu
500 505 510
Leu Ser Pro Glu Glu Val Ser Glu Thr Gln Gly Thr Glu Lys Leu Thr
515 520 525
Ile Thr Tyr Ser Ser Ser Met Met Trp Glu Ile Asn Gly Pro Glu Ser
530 535 540
Val Leu Val Asn Thr Tyr Gln Trp Ile Ile Arg Asn Trp Glu Thr Val
545 550 555 560
Lys Ile Gln Trp Ser Gln Asp Pro Thr Met Leu Tyr Asn Lys Val Glu
565 570 575
Phe Glu Pro Phe Gln Ser Leu Val Pro Lys Ala Ala Arg Gly Gln Tyr
580 585 590
Ser Gly Phe Val Arg Thr Leu Phe Gln Gln Met Arg Asp Val Leu Gly
595 600 605
Thr Phe Asp Thr Val Gln Ile Ile Lys Leu Leu Pro Phe Ala Ala Ala
610 615 620
Pro Pro Glu Gln Ser Arg Met Gln Phe Ser Ser Leu Thr Val Asn Val
625 630 635 640
Arg Gly Ser Gly Met Arg Ile Leu Val Arg Gly Asn Ser Pro Val Phe
645 650 655
Asn Tyr Asn Lys Ala Thr Lys Arg Leu Thr Val Leu Gly Lys Asp Ala
660 665 670
Gly Ala Leu Thr Glu Asp Pro Asp Glu Gly Thr Ala Gly Val Glu Ser
675 680 685
Ala Val Leu Arg Gly Phe Leu Ile Leu Gly Lys Glu Asp Lys Arg Tyr
690 695 700
Gly Pro Ala Leu Ser Ile Asn Glu Leu Ser Asn Leu Ala Lys Gly Glu
705 710 715 720
Lys Ala Asn Val Leu Ile Gly Gln Gly Asp Val Val Leu Val Met Lys
725 730 735
Arg Lys Arg Asp Ser Ser Ile Leu Thr Asp Ser Gln Thr Ala Thr Lys
740 745 750
Arg Ile Arg Met Ala Ile Asn ***
755 760
<210> 3
<211> 560
<212> PRT
<213> Artificial Sequence
<220>
<223> HA wild of Y280
<400> 3
Met Glu Thr Val Ser Leu Ile Thr Ile Leu Val Val Ala Thr Val Ser
1 5 10 15
Ser Ala Asp Lys Ile Cys Ile Gly Tyr Gln Ser Thr Asn Ser Thr Glu
20 25 30
Thr Val Asp Thr Leu Thr Glu Asn Asn Val Pro Val Thr His Ala Lys
35 40 45
Glu Leu Leu His Thr Glu His Asn Gly Met Leu Cys Ala Thr Ser Leu
50 55 60
Gly His Pro Leu Ile Leu Asp Thr Cys Thr Ile Glu Gly Leu Ile Tyr
65 70 75 80
Gly Asn Pro Ser Cys Asp Pro Leu Leu Gly Gly Arg Glu Trp Ser Tyr
85 90 95
Ile Val Glu Arg Pro Ser Ala Val Asn Gly Leu Cys Tyr Pro Gly Asn
100 105 110
Val Glu Asn Leu Glu Glu Leu Arg Ser Leu Phe Ser Ser Ser Arg Ser
115 120 125
Tyr Gln Arg Ile Gln Ile Phe Pro Asp Thr Ile Trp Asn Val Ser Tyr
130 135 140
Ser Gly Thr Ser Lys Ala Cys Ser Asp Ser Phe Tyr Arg Ser Met Arg
145 150 155 160
Trp Leu Thr Gln Lys Asn Asn Ala Tyr Pro Thr Gln Asp Ala Gln Tyr
165 170 175
Thr Asn Asn Gln Gly Lys Asn Ile Leu Leu Met Trp Gly Ile Asn His
180 185 190
Pro Pro Thr Asp Asp Val Gln Thr Asn Leu Tyr Thr Arg Thr Asp Thr
195 200 205
Thr Thr Ser Val Ala Thr Glu Glu Met Asn Arg Val Phe Lys Pro Leu
210 215 220
Ile Gly Pro Arg Pro Leu Val Asn Gly Leu Met Gly Arg Ile Asp Tyr
225 230 235 240
Tyr Trp Ser Val Leu Lys Pro Gly Gln Thr Leu Arg Ile Lys Ser Asp
245 250 255
Gly Asn Leu Ile Ala Pro Trp Tyr Gly His Ile Leu Ser Gly Glu Ser
260 265 270
His Gly Arg Ile Leu Lys Thr Asp Leu Lys Met Gly Ser Cys Thr Val
275 280 285
Gln Cys Gln Thr Glu Lys Gly Gly Leu Asn Thr Thr Leu Pro Phe Gln
290 295 300
Asn Val Ser Lys Tyr Ala Phe Gly Asn Cys Ser Lys Tyr Ile Gly Val
305 310 315 320
Lys Ser Leu Lys Leu Ala Val Gly Leu Arg Asn Val Pro Ser Arg Ser
325 330 335
Ser Arg Gly Leu Phe Gly Ala Ile Ala Gly Phe Ile Glu Gly Gly Trp
340 345 350
Ser Gly Leu Val Ala Gly Trp Tyr Gly Phe Gln His Ser Asn Asp Gln
355 360 365
Gly Val Gly Met Ala Ala Asp Arg Asp Ser Thr Gln Lys Ala Val Asp
370 375 380
Lys Ile Thr Ser Lys Val Asn Asn Ile Val Asp Lys Met Asn Lys Gln
385 390 395 400
Tyr Glu Ile Ile Asp His Glu Phe Ser Glu Val Glu Thr Arg Leu Asn
405 410 415
Met Ile Asn Asp Lys Val Asp Asp Gln Ile Gln Asp Ile Trp Ala Tyr
420 425 430
Asn Ala Glu Leu Leu Val Leu Leu Glu Asn Gln Lys Thr Leu Asp Glu
435 440 445
His Asp Ala Asn Val Asn Asn Leu Tyr Asn Lys Val Lys Arg Ala Leu
450 455 460
Gly Ser Asn Ala Val Glu Asp Gly Arg Gly Cys Phe Glu Leu Tyr His
465 470 475 480
Lys Cys Asp Asn His Cys Met Glu Thr Ile Arg Asn Gly Thr Tyr Asn
485 490 495
Arg Arg Lys Tyr Gln Glu Glu Ser Arg Leu Glu Arg Gln Lys Ile Glu
500 505 510
Gly Val Lys Leu Glu Ser Glu Glu Thr Tyr Lys Ile Leu Thr Ile Tyr
515 520 525
Ser Thr Val Ala Ser Ser Leu Val Ile Ala Met Gly Phe Ala Ala Phe
530 535 540
Leu Phe Trp Ala Met Ser Asn Gly Ser Cys Arg Cys Asn Ile Cys Ile
545 550 555 560
<210> 4
<211> 560
<212> PRT
<213> Artificial Sequence
<220>
<223> HA mutant L226Q
<400> 4
Met Glu Thr Val Ser Leu Ile Thr Ile Leu Val Val Ala Thr Val Ser
1 5 10 15
Ser Ala Asp Lys Ile Cys Ile Gly Tyr Gln Ser Thr Asn Ser Thr Glu
20 25 30
Thr Val Asp Thr Leu Thr Glu Asn Asn Val Pro Val Thr His Ala Lys
35 40 45
Glu Leu Leu His Thr Glu His Asn Gly Met Leu Cys Ala Thr Ser Leu
50 55 60
Gly His Pro Leu Ile Leu Asp Thr Cys Thr Ile Glu Gly Leu Ile Tyr
65 70 75 80
Gly Asn Pro Ser Cys Asp Pro Leu Leu Gly Gly Arg Glu Trp Ser Tyr
85 90 95
Ile Val Glu Arg Pro Ser Ala Val Asn Gly Leu Cys Tyr Pro Gly Asn
100 105 110
Val Glu Asn Leu Glu Glu Leu Arg Ser Leu Phe Ser Ser Ser Arg Ser
115 120 125
Tyr Gln Arg Ile Gln Ile Phe Pro Asp Thr Ile Trp Asn Val Ser Tyr
130 135 140
Ser Gly Thr Ser Lys Ala Cys Ser Asp Ser Phe Tyr Arg Ser Met Arg
145 150 155 160
Trp Leu Thr Gln Lys Asn Asn Ala Tyr Pro Thr Gln Asp Ala Gln Tyr
165 170 175
Thr Asn Asn Gln Gly Lys Asn Ile Leu Leu Met Trp Gly Ile Asn His
180 185 190
Pro Pro Thr Asp Asp Val Gln Thr Asn Leu Tyr Thr Arg Thr Asp Thr
195 200 205
Thr Thr Ser Val Ala Thr Glu Glu Met Asn Arg Val Phe Lys Pro Leu
210 215 220
Ile Gly Pro Arg Pro Leu Val Asn Gly Gln Met Gly Arg Ile Asp Tyr
225 230 235 240
Tyr Trp Ser Val Leu Lys Pro Gly Gln Thr Leu Arg Ile Lys Ser Asp
245 250 255
Gly Asn Leu Ile Ala Pro Trp Tyr Gly His Ile Leu Ser Gly Glu Ser
260 265 270
His Gly Arg Ile Leu Lys Thr Asp Leu Lys Met Gly Ser Cys Thr Val
275 280 285
Gln Cys Gln Thr Glu Lys Gly Gly Leu Asn Thr Thr Leu Pro Phe Gln
290 295 300
Asn Val Ser Lys Tyr Ala Phe Gly Asn Cys Ser Lys Tyr Ile Gly Val
305 310 315 320
Lys Ser Leu Lys Leu Ala Val Gly Leu Arg Asn Val Pro Ser Arg Ser
325 330 335
Ser Arg Gly Leu Phe Gly Ala Ile Ala Gly Phe Ile Glu Gly Gly Trp
340 345 350
Ser Gly Leu Val Ala Gly Trp Tyr Gly Phe Gln His Ser Asn Asp Gln
355 360 365
Gly Val Gly Met Ala Ala Asp Arg Asp Ser Thr Gln Lys Ala Val Asp
370 375 380
Lys Ile Thr Ser Lys Val Asn Asn Ile Val Asp Lys Met Asn Lys Gln
385 390 395 400
Tyr Glu Ile Ile Asp His Glu Phe Ser Glu Val Glu Thr Arg Leu Asn
405 410 415
Met Ile Asn Asp Lys Val Asp Asp Gln Ile Gln Asp Ile Trp Ala Tyr
420 425 430
Asn Ala Glu Leu Leu Val Leu Leu Glu Asn Gln Lys Thr Leu Asp Glu
435 440 445
His Asp Ala Asn Val Asn Asn Leu Tyr Asn Lys Val Lys Arg Ala Leu
450 455 460
Gly Ser Asn Ala Val Glu Asp Gly Arg Gly Cys Phe Glu Leu Tyr His
465 470 475 480
Lys Cys Asp Asn His Cys Met Glu Thr Ile Arg Asn Gly Thr Tyr Asn
485 490 495
Arg Arg Lys Tyr Gln Glu Glu Ser Arg Leu Glu Arg Gln Lys Ile Glu
500 505 510
Gly Val Lys Leu Glu Ser Glu Glu Thr Tyr Lys Ile Leu Thr Ile Tyr
515 520 525
Ser Thr Val Ala Ser Ser Leu Val Ile Ala Met Gly Phe Ala Ala Phe
530 535 540
Leu Phe Trp Ala Met Ser Asn Gly Ser Cys Arg Cys Asn Ile Cys Ile
545 550 555 560
<210> 5
<211> 466
<212> PRT
<213> Artificial Sequence
<220>
<223> NA wild of Y280
<400> 5
Met Asn Pro Asn Gln Lys Ile Thr Ala Ile Gly Ser Val Ser Leu Ile
1 5 10 15
Ile Ala Ile Ile Cys Leu Leu Met Gln Ile Ala Ile Leu Thr Thr Thr
20 25 30
Met Thr Phe His Phe Gly Gln Lys Glu Cys Ser Asn Pro Ser Asn Asn
35 40 45
Gln Val Val Pro Cys Glu Pro Ile Ile Ile Glu Arg Asn Thr Val His
50 55 60
Leu Thr Ser Thr Thr Ile Glu Arg Glu Ile Cys Pro Lys Val Ala Glu
65 70 75 80
Tyr Lys Asn Trp Leu Lys Pro Gln Cys Leu Ile Thr Gly Phe Ala Pro
85 90 95
Phe Ser Lys Asp Asn Ser Ile Arg Leu Ser Ala Ser Gly Asp Val Trp
100 105 110
Val Thr Arg Glu Pro Tyr Val Ser Cys Ser Pro Asp Lys Cys Tyr Gln
115 120 125
Phe Ala Leu Gly Gln Gly Thr Thr Leu Lys Asn Lys His Ser Asn Gly
130 135 140
Thr Thr Arg Asp Arg Thr Pro Tyr Arg Thr Leu Leu Met Asn Glu Leu
145 150 155 160
Gly Val Pro Phe His Leu Gly Thr Lys Gln Val Cys Ile Ala Trp Ser
165 170 175
Ser Ser Ser Cys Tyr Asp Gly Lys Ala Trp Leu His Val Cys Val Thr
180 185 190
Gly Asp Asp Gln Asn Ala Thr Ala Ser Ile Ile Tyr Asp Gly Met Leu
195 200 205
Val Asp Ser Ile Gly Ser Trp Ser Lys Asn Ile Leu Arg Thr Gln Glu
210 215 220
Ser Glu Cys Val Cys Ile Asn Gly Thr Cys Ala Val Val Met Thr Asp
225 230 235 240
Gly Ser Ala Ser Gly Val Ala Asp Thr Arg Val Leu Phe Ile Arg Glu
245 250 255
Gly Lys Ile Val Asn Ile Arg Pro Leu Ser Gly Ser Ala Gln His Val
260 265 270
Glu Glu Cys Ser Cys Tyr Pro Arg Tyr Pro Glu Ile Arg Cys Val Cys
275 280 285
Arg Asp Asn Trp Lys Gly Ser Asn Arg Pro Ile Val Tyr Ile Asn Met
290 295 300
Ala Asp Tyr Ser Ile Glu Ser Ser Tyr Val Cys Ser Gly Leu Val Gly
305 310 315 320
Asp Thr Pro Arg Asn Asp Asp Ser Ser Ser Ser Ser Asn Cys Arg Asp
325 330 335
Pro Asn Asn Glu Arg Gly Ala Pro Gly Val Lys Gly Trp Ala Phe Asp
340 345 350
Asp Gly Asn Asp Val Trp Met Gly Arg Thr Ile Lys Asn Gly Ser Arg
355 360 365
Ser Gly Tyr Glu Thr Phe Arg Val Ile Asn Gly Trp Thr Val Ala Asn
370 375 380
Ser Lys Ser Gln Ile Asn Arg Gln Val Ile Val Asp Ser Asp Asp Trp
385 390 395 400
Ser Gly Tyr Ser Gly Ile Phe Ser Val Glu Gly Arg Glu Cys Ile Asn
405 410 415
Arg Cys Phe Tyr Val Glu Leu Ile Arg Gly Arg Pro Gln Glu Pro Arg
420 425 430
Val Trp Trp Thr Ser Asn Ser Ile Ile Val Phe Cys Gly Thr Ser Gly
435 440 445
Thr Tyr Gly Thr Gly Ser Trp Pro Asp Gly Ala Asn Ile Asn Phe Met
450 455 460
Pro Ile
465
<210> 6
<211> 758
<212> PRT
<213> Artificial Sequence
<220>
<223> PB1 of PR8
<400> 6
Met Asp Val Asn Pro Thr Leu Leu Phe Leu Lys Val Pro Ala Gln Asn
1 5 10 15
Ala Ile Ser Thr Thr Phe Pro Tyr Thr Gly Asp Pro Pro Tyr Ser His
20 25 30
Gly Thr Gly Thr Gly Tyr Thr Met Asp Thr Val Asn Arg Thr His Gln
35 40 45
Tyr Ser Glu Lys Gly Arg Trp Thr Thr Asn Thr Glu Thr Gly Ala Pro
50 55 60
Gln Leu Asn Pro Ile Asp Gly Pro Leu Pro Glu Asp Asn Glu Pro Ser
65 70 75 80
Gly Tyr Ala Gln Thr Asp Cys Val Leu Glu Ala Met Ala Phe Leu Glu
85 90 95
Glu Ser His Pro Gly Ile Phe Glu Asn Ser Cys Ile Glu Thr Met Glu
100 105 110
Val Val Gln Gln Thr Arg Val Asp Lys Leu Thr Gln Gly Arg Gln Thr
115 120 125
Tyr Asp Trp Thr Leu Asn Arg Asn Gln Pro Ala Ala Thr Ala Leu Ala
130 135 140
Asn Thr Ile Glu Val Phe Arg Ser Asn Gly Leu Thr Ala Asn Glu Ser
145 150 155 160
Gly Arg Leu Ile Asp Phe Leu Lys Asp Val Met Glu Ser Met Asn Lys
165 170 175
Glu Glu Met Gly Ile Thr Thr His Phe Gln Arg Lys Arg Arg Val Arg
180 185 190
Asp Asn Met Thr Lys Lys Met Ile Thr Gln Arg Thr Met Gly Lys Lys
195 200 205
Lys Gln Arg Leu Asn Lys Arg Ser Tyr Leu Ile Arg Ala Leu Thr Leu
210 215 220
Asn Thr Met Thr Lys Asp Ala Glu Arg Gly Lys Leu Lys Arg Arg Ala
225 230 235 240
Ile Ala Thr Pro Gly Met Gln Ile Arg Gly Phe Val Tyr Phe Val Glu
245 250 255
Thr Leu Ala Arg Ser Ile Cys Glu Lys Leu Glu Gln Ser Gly Leu Pro
260 265 270
Val Gly Gly Asn Glu Lys Lys Ala Lys Leu Ala Asn Val Val Arg Lys
275 280 285
Met Met Thr Asn Ser Gln Asp Thr Glu Leu Ser Phe Thr Ile Thr Gly
290 295 300
Asp Asn Thr Lys Trp Asn Glu Asn Gln Asn Pro Arg Met Phe Leu Ala
305 310 315 320
Met Ile Thr Tyr Met Thr Arg Asn Gln Pro Glu Trp Phe Arg Asn Val
325 330 335
Leu Ser Ile Ala Pro Ile Met Phe Ser Asn Lys Met Ala Arg Leu Gly
340 345 350
Lys Gly Tyr Met Phe Glu Ser Lys Ser Met Lys Leu Arg Thr Gln Ile
355 360 365
Pro Ala Glu Met Leu Ala Ser Ile Asp Leu Lys Tyr Phe Asn Asp Ser
370 375 380
Thr Arg Lys Lys Ile Glu Lys Ile Arg Pro Leu Leu Ile Glu Gly Thr
385 390 395 400
Ala Ser Leu Ser Pro Gly Met Met Met Gly Met Phe Asn Met Leu Ser
405 410 415
Thr Val Leu Gly Val Ser Ile Leu Asn Leu Gly Gln Lys Arg Tyr Thr
420 425 430
Lys Thr Thr Tyr Trp Trp Asp Gly Leu Gln Ser Ser Asp Asp Phe Ala
435 440 445
Leu Ile Val Asn Ala Pro Asn His Glu Gly Ile Gln Ala Gly Val Asp
450 455 460
Arg Phe Tyr Arg Thr Cys Lys Leu Leu Gly Ile Asn Met Ser Lys Lys
465 470 475 480
Lys Ser Tyr Ile Asn Arg Thr Gly Thr Phe Glu Phe Thr Ser Phe Phe
485 490 495
Tyr Arg Tyr Gly Phe Val Ala Asn Phe Ser Met Glu Leu Pro Ser Phe
500 505 510
Gly Val Ser Gly Ile Asn Glu Ser Ala Asp Met Ser Ile Gly Val Thr
515 520 525
Val Ile Lys Asn Asn Met Ile Asn Asn Asp Leu Gly Pro Ala Thr Ala
530 535 540
Gln Met Ala Leu Gln Leu Phe Ile Lys Asp Tyr Arg Tyr Thr Tyr Arg
545 550 555 560
Cys His Ile Gly Asp Thr Gln Ile Gln Thr Arg Arg Ser Phe Glu Ile
565 570 575
Lys Lys Leu Trp Glu Gln Thr Arg Ser Lys Ala Gly Leu Leu Val Ser
580 585 590
Asp Gly Gly Pro Asn Leu Tyr Asn Ile Arg Asn Leu His Ile Pro Glu
595 600 605
Val Cys Leu Lys Trp Glu Leu Met Asp Glu Asp Tyr Gln Gly Arg Leu
610 615 620
Cys Asn Pro Leu Asn Pro Phe Val Ser His Lys Glu Ile Glu Ser Met
625 630 635 640
Asn Asn Ala Val Met Met Pro Ala His Gly Pro Ala Lys Asn Met Glu
645 650 655
Tyr Asp Ala Val Ala Thr Thr His Ser Trp Ile Pro Lys Arg Asn Arg
660 665 670
Ser Ile Leu Asn Thr Ser Gln Arg Gly Val Leu Glu Asp Glu Gln Met
675 680 685
Tyr Gln Arg Cys Cys Asn Leu Phe Glu Lys Phe Phe Pro Ser Ser Ser
690 695 700
Tyr Arg Arg Pro Val Gly Ile Ser Ser Met Val Glu Ala Met Val Ser
705 710 715 720
Arg Ala Arg Ile Asp Ala Arg Ile Asp Phe Glu Ser Gly Arg Ile Lys
725 730 735
Lys Glu Glu Phe Thr Glu Ile Met Lys Ile Cys Ser Thr Ile Glu Glu
740 745 750
Leu Arg Arg Gln Lys ***
755
<210> 7
<211> 717
<212> PRT
<213> Artificial Sequence
<220>
<223> PA of PR8
<400> 7
Met Glu Asp Phe Val Arg Gln Cys Phe Asn Pro Met Ile Val Glu Leu
1 5 10 15
Ala Glu Lys Thr Met Lys Glu Tyr Gly Glu Asp Leu Lys Ile Glu Thr
20 25 30
Asn Lys Phe Ala Ala Ile Cys Thr His Leu Glu Val Cys Phe Met Tyr
35 40 45
Ser Asp Phe His Phe Ile Asn Glu Gln Gly Glu Ser Ile Ile Val Glu
50 55 60
Leu Gly Asp Pro Asn Ala Leu Leu Lys His Arg Phe Glu Ile Ile Glu
65 70 75 80
Gly Arg Asp Arg Thr Met Ala Trp Thr Val Val Asn Ser Ile Cys Asn
85 90 95
Thr Thr Gly Ala Glu Lys Pro Lys Phe Leu Pro Asp Leu Tyr Asp Tyr
100 105 110
Lys Glu Asn Arg Phe Ile Glu Ile Gly Val Thr Arg Arg Glu Val His
115 120 125
Ile Tyr Tyr Leu Glu Lys Ala Asn Lys Ile Lys Ser Glu Lys Thr His
130 135 140
Ile His Ile Phe Ser Phe Thr Gly Glu Glu Met Ala Thr Lys Ala Asp
145 150 155 160
Tyr Thr Leu Asp Glu Glu Ser Arg Ala Arg Ile Lys Thr Arg Leu Phe
165 170 175
Thr Ile Arg Gln Glu Met Ala Ser Arg Gly Leu Trp Asp Ser Phe Arg
180 185 190
Gln Ser Glu Arg Gly Glu Glu Thr Ile Glu Glu Arg Phe Glu Ile Thr
195 200 205
Gly Thr Met Arg Lys Leu Ala Asp Gln Ser Leu Pro Pro Asn Phe Ser
210 215 220
Ser Leu Glu Asn Phe Arg Ala Tyr Val Asp Gly Phe Glu Pro Asn Gly
225 230 235 240
Tyr Ile Glu Gly Lys Leu Ser Gln Met Ser Lys Glu Val Asn Ala Arg
245 250 255
Ile Glu Pro Phe Leu Lys Thr Thr Pro Arg Pro Leu Arg Leu Pro Asn
260 265 270
Gly Pro Pro Cys Ser Gln Arg Ser Lys Phe Leu Leu Met Asp Ala Leu
275 280 285
Lys Leu Ser Ile Glu Asp Pro Ser His Glu Gly Glu Gly Ile Pro Leu
290 295 300
Tyr Asp Ala Ile Lys Cys Met Arg Thr Phe Phe Gly Trp Lys Glu Pro
305 310 315 320
Asn Val Val Lys Pro His Glu Lys Gly Ile Asn Pro Asn Tyr Leu Leu
325 330 335
Ser Trp Lys Gln Val Leu Ala Glu Leu Gln Asp Ile Glu Asn Glu Glu
340 345 350
Lys Ile Pro Lys Thr Lys Asn Met Lys Lys Thr Ser Gln Leu Lys Trp
355 360 365
Ala Leu Gly Glu Asn Met Ala Pro Glu Lys Val Asp Phe Asp Asp Cys
370 375 380
Lys Asp Val Gly Asp Leu Lys Gln Tyr Asp Ser Asp Glu Pro Glu Leu
385 390 395 400
Arg Ser Leu Ala Ser Trp Ile Gln Asn Glu Phe Asn Lys Ala Cys Glu
405 410 415
Leu Thr Asp Ser Ser Trp Ile Glu Leu Asp Glu Ile Gly Glu Asp Val
420 425 430
Ala Pro Ile Glu His Ile Ala Ser Met Arg Arg Asn Tyr Phe Thr Ser
435 440 445
Glu Val Ser His Cys Arg Ala Thr Glu Tyr Ile Met Lys Gly Val Tyr
450 455 460
Ile Asn Thr Ala Leu Leu Asn Ala Ser Cys Ala Ala Met Asp Asp Phe
465 470 475 480
Gln Leu Ile Pro Met Ile Ser Lys Cys Arg Thr Lys Glu Gly Arg Arg
485 490 495
Lys Thr Asn Leu Tyr Gly Phe Ile Ile Lys Gly Arg Ser His Leu Arg
500 505 510
Asn Asp Thr Asp Val Val Asn Phe Val Ser Met Glu Phe Ser Leu Thr
515 520 525
Asp Pro Arg Leu Glu Pro His Lys Trp Glu Lys Tyr Cys Val Leu Glu
530 535 540
Ile Gly Asp Met Leu Ile Arg Ser Ala Ile Gly Gln Val Ser Arg Pro
545 550 555 560
Met Phe Leu Tyr Val Arg Thr Asn Gly Thr Ser Lys Ile Lys Met Lys
565 570 575
Trp Gly Met Glu Met Arg Arg Cys Leu Leu Gln Ser Leu Gln Gln Ile
580 585 590
Glu Ser Met Ile Glu Ala Glu Ser Ser Val Lys Glu Lys Asp Met Thr
595 600 605
Lys Glu Phe Phe Glu Asn Lys Ser Glu Thr Trp Pro Ile Gly Glu Ser
610 615 620
Pro Lys Gly Val Glu Glu Ser Ser Ile Gly Lys Val Cys Arg Thr Leu
625 630 635 640
Leu Ala Lys Ser Val Phe Asn Ser Leu Tyr Ala Ser Pro Gln Leu Glu
645 650 655
Gly Phe Ser Ala Glu Ser Arg Lys Leu Leu Leu Ile Val Gln Ala Leu
660 665 670
Arg Asp Asn Leu Glu Pro Gly Thr Phe Asp Leu Gly Gly Leu Tyr Glu
675 680 685
Ala Ile Glu Glu Cys Leu Ile Asn Asp Pro Trp Val Leu Leu Asn Ala
690 695 700
Ser Trp Phe Asn Ser Phe Leu Thr His Ala Leu Ser ***
705 710 715
<210> 8
<211> 498
<212> PRT
<213> Artificial Sequence
<220>
<223> NP of PR8
<400> 8
Met Ala Ser Gln Gly Thr Lys Arg Ser Tyr Glu Gln Met Glu Thr Asp
1 5 10 15
Gly Glu Arg Gln Asn Ala Thr Glu Ile Arg Ala Ser Val Gly Lys Met
20 25 30
Ile Gly Gly Ile Gly Arg Phe Tyr Ile Gln Met Cys Thr Glu Leu Lys
35 40 45
Leu Ser Asp Tyr Glu Gly Arg Leu Ile Gln Asn Ser Leu Thr Ile Glu
50 55 60
Arg Met Val Leu Ser Ala Phe Asp Glu Arg Arg Asn Lys Tyr Leu Glu
65 70 75 80
Glu His Pro Ser Ala Gly Lys Asp Pro Lys Lys Thr Gly Gly Pro Ile
85 90 95
Tyr Arg Arg Val Asn Gly Lys Trp Met Arg Glu Leu Ile Leu Tyr Asp
100 105 110
Lys Glu Glu Ile Arg Arg Ile Trp Arg Gln Ala Asn Asn Gly Asp Asp
115 120 125
Ala Thr Ala Gly Leu Thr His Met Met Ile Trp His Ser Asn Leu Asn
130 135 140
Asp Ala Thr Tyr Gln Arg Thr Arg Ala Leu Val Arg Thr Gly Met Asp
145 150 155 160
Pro Arg Met Cys Ser Leu Met Gln Gly Ser Thr Leu Pro Arg Arg Ser
165 170 175
Gly Ala Ala Gly Ala Ala Val Lys Gly Val Gly Thr Met Val Met Glu
180 185 190
Leu Val Arg Met Ile Lys Arg Gly Ile Asn Asp Arg Asn Phe Trp Arg
195 200 205
Gly Glu Asn Gly Arg Lys Thr Arg Ile Ala Tyr Glu Arg Met Cys Asn
210 215 220
Ile Leu Lys Gly Lys Phe Gln Thr Ala Ala Gln Lys Ala Met Met Asp
225 230 235 240
Gln Val Arg Glu Ser Arg Asn Pro Gly Asn Ala Glu Phe Glu Asp Leu
245 250 255
Thr Phe Leu Ala Arg Ser Ala Leu Ile Leu Arg Gly Ser Val Ala His
260 265 270
Lys Ser Cys Leu Pro Ala Cys Val Tyr Gly Pro Ala Val Ala Ser Gly
275 280 285
Tyr Asp Phe Glu Arg Glu Gly Tyr Ser Leu Val Gly Ile Asp Pro Phe
290 295 300
Arg Leu Leu Gln Asn Ser Gln Val Tyr Ser Leu Ile Arg Pro Asn Glu
305 310 315 320
Asn Pro Ala His Lys Ser Gln Leu Val Trp Met Ala Cys His Ser Ala
325 330 335
Ala Phe Glu Asp Leu Arg Val Leu Ser Phe Ile Lys Gly Thr Lys Val
340 345 350
Leu Pro Arg Gly Lys Leu Ser Thr Arg Gly Val Gln Ile Ala Ser Asn
355 360 365
Glu Asn Met Glu Thr Met Glu Ser Ser Thr Leu Glu Leu Arg Ser Arg
370 375 380
Tyr Trp Ala Ile Arg Thr Arg Ser Gly Gly Asn Thr Asn Gln Gln Arg
385 390 395 400
Ala Ser Ala Gly Gln Ile Ser Ile Gln Pro Thr Phe Ser Val Gln Arg
405 410 415
Asn Leu Pro Phe Asp Arg Thr Thr Ile Met Ala Ala Phe Asn Gly Asn
420 425 430
Thr Glu Gly Arg Thr Ser Asp Met Arg Thr Glu Ile Ile Arg Met Met
435 440 445
Glu Ser Ala Arg Pro Glu Asp Val Ser Phe Gln Gly Arg Gly Val Phe
450 455 460
Glu Leu Ser Asp Glu Lys Ala Ala Ser Pro Ile Val Pro Ser Phe Asp
465 470 475 480
Met Ser Asn Glu Gly Ser Tyr Phe Phe Gly Asp Asn Ala Glu Glu Tyr
485 490 495
Asp Asn
<210> 9
<211> 252
<212> PRT
<213> Artificial Sequence
<220>
<223> M of PR8
<400> 9
Met Ser Leu Leu Thr Glu Val Glu Thr Tyr Val Leu Ser Ile Ile Pro
1 5 10 15
Ser Gly Pro Leu Lys Ala Glu Ile Ala Gln Arg Leu Glu Asp Val Phe
20 25 30
Ala Gly Lys Asn Thr Asp Leu Glu Val Leu Met Glu Trp Leu Lys Thr
35 40 45
Arg Pro Ile Leu Ser Pro Leu Thr Lys Gly Ile Leu Gly Phe Val Phe
50 55 60
Thr Leu Thr Val Pro Ser Glu Arg Gly Leu Gln Arg Arg Arg Phe Val
65 70 75 80
Gln Thr Ala Leu Asn Gly Asn Gly Asp Pro Asn Asn Met Asp Lys Ala
85 90 95
Val Lys Leu Tyr Arg Lys Leu Lys Arg Glu Ile Thr Phe His Gly Ala
100 105 110
Lys Glu Ile Ser Leu Ser Tyr Ser Ala Gly Ala Leu Ala Ser Cys Met
115 120 125
Gly Leu Ile Tyr Asn Arg Met Gly Ala Val Thr Thr Glu Val Ala Phe
130 135 140
Gly Leu Val Cys Ala Thr Cys Glu Gln Ile Ala Asp Ser Gln His Arg
145 150 155 160
Ser His Arg Gln Met Val Thr Thr Thr Asn Pro Leu Ile Arg His Glu
165 170 175
Asn Arg Met Val Leu Ala Ser Thr Thr Ala Lys Ala Met Glu Gln Met
180 185 190
Ala Gly Ser Ser Glu Gln Ala Ala Glu Ala Met Glu Val Ala Ser Gln
195 200 205
Ala Arg Gln Met Val Gln Ala Met Arg Thr Ile Gly Thr His Pro Ser
210 215 220
Ser Ser Ala Gly Leu Lys Asn Asp Leu Leu Glu Asn Leu Gln Ala Tyr
225 230 235 240
Gln Lys Arg Met Gly Val Gln Met Gln Arg Phe Lys
245 250
<210> 10
<211> 231
<212> PRT
<213> Artificial Sequence
<220>
<223> NS of PR8
<400> 10
Met Asp Pro Asn Thr Val Ser Ser Phe Gln Val Asp Cys Phe Leu Trp
1 5 10 15
His Val Arg Lys Arg Val Ala Asp Gln Glu Leu Gly Asp Ala Pro Phe
20 25 30
Leu Asp Arg Leu Arg Arg Asp Gln Lys Ser Leu Arg Gly Arg Gly Ser
35 40 45
Thr Leu Gly Leu Asp Ile Lys Thr Ala Thr Arg Ala Gly Lys Gln Ile
50 55 60
Val Glu Arg Ile Leu Lys Glu Glu Ser Asp Glu Ala Leu Lys Met Thr
65 70 75 80
Met Ala Ser Val Pro Ala Ser Arg Tyr Leu Thr Asp Met Thr Leu Glu
85 90 95
Glu Met Ser Arg Asp Trp Ser Met Leu Ile Pro Lys Gln Lys Val Ala
100 105 110
Gly Pro Leu Cys Ile Arg Met Asp Gln Ala Ile Met Asp Lys Asn Ile
115 120 125
Ile Leu Lys Ala Asn Phe Ser Val Ile Phe Asp Arg Leu Glu Thr Leu
130 135 140
Ile Leu Leu Arg Ala Phe Thr Glu Glu Gly Ala Ile Val Gly Glu Ile
145 150 155 160
Ser Pro Leu Pro Ser Leu Pro Gly His Thr Ala Glu Asp Val Lys Asn
165 170 175
Ala Val Gly Val Leu Ile Gly Gly Leu Glu Trp Asn Asp Asn Thr Val
180 185 190
Arg Val Ser Glu Thr Leu Gln Arg Phe Ala Trp Arg Ser Ser Asn Glu
195 200 205
Asn Gly Arg Pro Pro Leu Thr Pro Lys Gln Lys Arg Glu Met Ala Gly
210 215 220
Thr Ile Arg Ser Glu Val ***
225 230
<210> 11
<211> 2280
<212> DNA
<213> Artificial Sequence
<220>
<223> PB2 wild gene of 01310
<400> 11
atggagagaa taaaggaact aagagatttg atgtcacagt ctcgcactcg cgagatactg 60
acaaaaacca ctgtggacca tatggccata atcaagaaat acacatcggg aagacaggag 120
aagaaccccg ctctcagaat gaaatggatg atggcaatga aatacccgat tacagctgac 180
aaaagaataa tggagataat ccctgaaaga aatgagcaag gtcaaactct ctggagcaaa 240
acgaatgatg ctggatcaga taaggtaatg gtatcacctc tggctgtgac gtggtggaat 300
agaaatggac caacaacaag cacaatccat tatcccaagg tatataaaac ttactttgag 360
aaggttgaaa ggttgaaaca cggaaccttt ggccccattc atttccgaaa tcaagtcaaa 420
atacgccgca gggttgacat aaacccgggc catgcagacc tcagtgctag agaagcacaa 480
gatgttatca tggaggtcgt tttcccgaat gaggttggag ccaggatact gacatcagaa 540
tcacaattga caataacaaa ggaaaagaaa gaagaactcc aggattgtaa gattgctcct 600
ttaatggtgg catacatgtt agaaagagaa ctggttcgca agaccagatt cctaccagtg 660
gctggcggga caagcagcgt gtatatagaa gtactacatt tgactcaagg aacctgctgg 720
gagcagatgt acacaccagg aggggaagta aggaatgatg atgttgacca gagtttgatc 780
attgctgcta gaaacattgt aaggagagca acagtatcag cagacccatt ggcctcgctc 840
ttggagatgt gtcatggtac acaaataggc ggaataagaa tggtagacat ccttagacaa 900
aacccaacag aagagcaagc cgtggatata tgcaaggcag caataggcct aagaatcagt 960
tcatctttca gctttggagg tttcactttc aaaagaacaa gtgggtcttc tgtcaagaag 1020
gaagaagaag tgcttacagg caacctccag acattgaaaa taagagtgca tgagggatat 1080
gaggaattca caatggttgg gcgaagagca acagccctcc taaggaaagc aaccagaagg 1140
ctgattcaac tgatagtaag tgggagagac gaacaatcaa tcgctgaagc gatcattgta 1200
gcaatggtat tttcacaaga ggactgcatg ataaaggcag tccgaggtga tttgaacttc 1260
gtgaacagag cgaaccagcg actgaacccc atgcaccaac ttctgaggca cttccaaaaa 1320
gatgcaaaag tgttgtttca gaactgggga attgaaccca tcgacaatgt catggggatg 1380
attggaatat tgcccgacat gactcccagc acagagatgt cactaagagg agtgagagtc 1440
agcaaaatgg gagtggacga atactctagc actgaaagag tggttgtgag tattgatcgt 1500
ttcttaaggg ttcgagatca gagggggaac atacttctat cccctgaaga agttagtgag 1560
acacaaggga cggaaaagtt aacaataaca tattcatcgt ctatgatgtg ggagattaac 1620
ggcccggaat cagtgctagt taacacatac caatggatca ttaggaattg ggagactgtg 1680
aagattcagt ggtctcaaga tcctactatg ttatacaata aggtggaatt tgaacccttt 1740
caatctctgg tacctaaagc tgccagaggc caatatagtg gatttgtgag aacgctattc 1800
caacaaatgc gtgatgtact gggaacattt gacactgttc agataataaa gctgctacca 1860
tttgccgcag ccccaccaga gcagagtagg atgcagtttt cttctctgac tgtgaatgta 1920
agaggctcag gaatgagaat ccttgtgaga ggcaactccc ctgtgtttaa ttacaacaag 1980
gcaaccaaga ggcttacagt cctcgggaag gatgcaggtg cactcacaga agacccagat 2040
gaaggaacag caggagtgga atccgcagta ttgagaggat tcctaattct aggcaaagaa 2100
gacaagagat acggaccagc attgagcatc aacgaattga gcaatcttgc gaaaggggag 2160
aaagctaatg tattgatagg gcaaggagac gtagtgttgg taatgaaacg gaaacgggac 2220
tctagcatac ttactgacag ccagacagcg accaaaagaa ttcgaatggc catcaattag 2280
2280
<210> 12
<211> 2280
<212> DNA
<213> Artificial Sequence
<220>
<223> PB2 mutant gene
<400> 12
atggagagaa taaaggaact aagagatttg atgtcacagt ctcgcactcg cgagatactg 60
acaaaaacca ctgtggacca tatggccata atcaagaaat acacatcggg aagacaggag 120
aagaaccccg ctctcagaat gaaatggatg atggcaatga aatacccgat tacagctgac 180
aaaagaataa tggagatgat ccctgaaaga aatgagcaag gtcaaactct ctggagcaaa 240
acgaatgatg ctggatcaga taaggtaatg gtatcacctc tggctgtgac gtggtggaat 300
agaaatggac caacaacaag cacagtccat tatcccaagg tatataaaac ttactttgag 360
aaggttgaaa ggttgaaaca cggaaccttt ggccccgttc atttccgaaa tcaagtcaaa 420
atacgccgca gggttgacat aaacccgggc catgcagacc tcagtgctag agaagcacaa 480
gatgttatca tggaggtcgt tttcccgaat gaggttggag ccaggatact gacatcagaa 540
tcacaattga caataacaaa ggaaaagaaa gaagaactcc aggattgtaa gattgctcct 600
ttaatggtgg catacatgtt agaaagagaa ctggttcgca agaccagatt cctaccagtg 660
gctggcggga caagcagcgt gtatatagaa gtactacatt tgactcaagg aacctgctgg 720
gagcagatgt acacaccagg aggggaagta aggaatgatg atgttgacca gagtttgatc 780
attgctgcta gaaacattgt aaggagagca acagtatcag cagacccatt ggcctcgctc 840
ttggagatgt gtcatggtac acaaataggc ggaataagaa tggtagacat ccttagacaa 900
aacccaacag aagagcaagc cgtggatata tgcaaggcag caataggcct aagaatcagt 960
tcatctttca gctttggagg tttcactttc aaaagaacaa gtgggtcttc tgtcaagaag 1020
gaagaagaag tgcttacagg caacctccag acattgaaaa taagagtgca tgagggatat 1080
gaggaattca caatggttgg gcgaagagca acagccctcc taaggaaagc aaccagaagg 1140
ctgattcaac tgatagtaag tgggagagac gaacaatcaa tcgctgaagc gatcattgta 1200
gcaatggtat tttcacaaga ggactgcatg ataaaggcag tccgaggtga tttgaacttc 1260
gtgaacagag cgaaccagcg actgaacccc atgcaccaac ttctgaggca cttccaaaaa 1320
gatgcaaaag tgttgtttca gaactgggga attgaaccca tcgacaatgt catggggatg 1380
attggaatat tgcccgacat gactcccagc acagagatgt cactaagagg agtgagagtc 1440
agcaaaatgg gagtggacga atactctagc actgaaagag tggttgtgag tattgatcgt 1500
ttcttaaggg ttcgagatca gagggggaac atacttctat cccctgaaga agttagtgag 1560
acacaaggga cggaaaagtt aacaataaca tattcatcgt ctatgatgtg ggagattaac 1620
ggcccggaat cagtgctagt taacacatac caatggatca ttaggaattg ggagactgtg 1680
aagattcagt ggtctcaaga tcctactatg ttatacaata aggtggaatt tgaacccttt 1740
caatctctgg tacctaaagc tgccagaggc caatatagtg gatttgtgag aacgctattc 1800
caacaaatgc gtgatgtact gggaacattt gacactgttc agataataaa gctgctacca 1860
tttgccgcag ccccaccaga gcagagtagg atgcagtttt cttctctgac tgtgaatgta 1920
agaggctcag gaatgagaat ccttgtgaga ggcaactccc ctgtgtttaa ttacaacaag 1980
gcaaccaaga ggcttacagt cctcgggaag gatgcaggtg cactcacaga agacccagat 2040
gaaggaacag caggagtgga atccgcagta ttgagaggat tcctaattct aggcaaagaa 2100
gacaagagat acggaccagc attgagcatc aacgaattga gcaatcttgc gaaaggggag 2160
aaagctaatg tattgatagg gcaaggagac gtagtgttgg taatgaaacg gaaacgggac 2220
tctagcatac ttactgacag ccagacagcg accaaaagaa ttcgaatggc catcaattag 2280
2280
<210> 13
<211> 1683
<212> DNA
<213> Artificial Sequence
<220>
<223> HA wild gene of Y280
<400> 13
atggagacag tatcactaat aactatacta gtagtggcaa cagtgagcag tgcagataag 60
atctgcatcg gctatcaatc aacaaactcc acggaaactg tggacacact aacagaaaac 120
aatgtccctg taacacatgc caaagaactg ctccacacag agcataatgg gatgctgtgt 180
gcaacaagct tgggacaccc tcttattcta gacacctgca ccattgaagg gctaatttat 240
ggcaatcctt cttgtgatcc attgctggga ggaagagaat ggtcctatat cgtcgagagg 300
ccatcagccg ttaacggatt atgttatccc gggaatgtag aaaatctaga agagctaaga 360
tcacttttta gttcttctag gtcttatcaa aggatccaga tctttccaga cacaatctgg 420
aatgtgtctt acagtgggac aagcaaagca tgctcggatt cattctacag aagcatgaga 480
tggttgactc aaaagaacaa cgcttaccct acccaagatg ctcaatacac aaataatcag 540
ggaaagaaca ttcttctcat gtggggtata aatcatccac ccactgatga tgtgcagaca 600
aatctgtaca ccagaactga cacaacaaca agtgtggcaa cagaggaaat gaatagggtc 660
tttaaaccat tgataggacc aaggcctctt gtcaacggtt tgatgggaag aattgattat 720
tattggtcgg tattgaaacc gggccaaacg ctgcggataa aatctgatgg gaatctaata 780
gctccatggt atggacacat cctttcagga gagagccacg gaagaatcct aaagactgac 840
ttaaaaatgg gtagctgcac agtgcagtgt caaacagaga aaggtggctt aaacactaca 900
ttgcccttcc aaaatgtaag taagtatgca tttggaaact gctcaaagta cattggcgta 960
aagagtctca aacttgcagt tggtctgagg aatgtgcctt ctagatctag cagaggacta 1020
ttcggggcca tagcaggatt tatagaggga ggttggtcag gactggttgc tggttggtat 1080
gggttccagc attcaaatga ccaaggggtt ggtatggcag cagatagaga ttcaacccaa 1140
aaggcagttg ataaaataac atccaaagtg aataatatag tcgacaaaat gaacaagcag 1200
tatgaaatca ttgatcatga attcagtgag gtagaaacta ggcttaacat gatcaatgat 1260
aaggttgatg atcaaatcca agatatatgg gcatataatg cagaattgct agttctgctc 1320
gaaaaccaga aaacactcga tgaacatgac gctaatgtga acaatctata taataaagtg 1380
aagagggcgt tgggttccaa tgcagtggaa gatgggagag gatgtttcga gctataccac 1440
aaatgtgata accattgcat ggagacaatt cggaatggga cctacaacag gaggaagtat 1500
caagaggaat caagattaga aagacagaaa atagaggggg tcaagctgga atctgaagaa 1560
acttacaaaa tcctcaccat ttattcgact gtcgcctcat ctcttgtgat tgcaatgggg 1620
tttgctgcct ttttgttctg ggccatgtcc aacgggtcct gcagatgcaa catttgtata 1680
taa 1683
<210> 14
<211> 1683
<212> DNA
<213> Artificial Sequence
<220>
<223> HA mutant gene
<400> 14
atggagacag tatcactaat aactatacta gtagtggcaa cagtgagcag tgcagataag 60
atctgcatcg gctatcaatc aacaaactcc acggaaactg tggacacact aacagaaaac 120
aatgtccctg taacacatgc caaagaactg ctccacacag agcataatgg gatgctgtgt 180
gcaacaagct tgggacaccc tcttattcta gacacctgca ccattgaagg gctaatttat 240
ggcaatcctt cttgtgatcc attgctggga ggaagagaat ggtcctatat cgtcgagagg 300
ccatcagccg ttaacggatt atgttatccc gggaatgtag aaaatctaga agagctaaga 360
tcacttttta gttcttctag gtcttatcaa aggatccaga tctttccaga cacaatctgg 420
aatgtgtctt acagtgggac aagcaaagca tgctcggatt cattctacag aagcatgaga 480
tggttgactc aaaagaacaa cgcttaccct acccaagatg ctcaatacac aaataatcag 540
ggaaagaaca ttcttctcat gtggggtata aatcatccac ccactgatga tgtgcagaca 600
aatctgtaca ccagaactga cacaacaaca agtgtggcaa cagaggaaat gaatagggtc 660
tttaaaccat tgataggacc aaggcctctt gtcaacggtc agatgggaag aattgattat 720
tattggtcgg tattgaaacc gggccaaacg ctgcggataa aatctgatgg gaatctaata 780
gctccatggt atggacacat cctttcagga gagagccacg gaagaatcct aaagactgac 840
ttaaaaatgg gtagctgcac agtgcagtgt caaacagaga aaggtggctt aaacactaca 900
ttgcccttcc aaaatgtaag taagtatgca tttggaaact gctcaaagta cattggcgta 960
aagagtctca aacttgcagt tggtctgagg aatgtgcctt ctagatctag cagaggacta 1020
ttcggggcca tagcaggatt tatagaggga ggttggtcag gactggttgc tggttggtat 1080
gggttccagc attcaaatga ccaaggggtt ggtatggcag cagatagaga ttcaacccaa 1140
aaggcagttg ataaaataac atccaaagtg aataatatag tcgacaaaat gaacaagcag 1200
tatgaaatca ttgatcatga attcagtgag gtagaaacta ggcttaacat gatcaatgat 1260
aaggttgatg atcaaatcca agatatatgg gcatataatg cagaattgct agttctgctc 1320
gaaaaccaga aaacactcga tgaacatgac gctaatgtga acaatctata taataaagtg 1380
aagagggcgt tgggttccaa tgcagtggaa gatgggagag gatgtttcga gctataccac 1440
aaatgtgata accattgcat ggagacaatt cggaatggga cctacaacag gaggaagtat 1500
caagaggaat caagattaga aagacagaaa atagaggggg tcaagctgga atctgaagaa 1560
acttacaaaa tcctcaccat ttattcgact gtcgcctcat ctcttgtgat tgcaatgggg 1620
tttgctgcct ttttgttctg ggccatgtcc aacgggtcct gcagatgcaa catttgtata 1680
taa 1683
<210> 15
<211> 1401
<212> DNA
<213> Artificial Sequence
<220>
<223> NA wild gene of Y280
<400> 15
atgaatccaa atcagaagat aacagcaatt ggctctgttt ctctaatcat tgcgataata 60
tgtctcctca tgcaaattgc catcttaaca acgactatga cattccattt cgggcagaaa 120
gaatgcagta acccatcgaa taatcaggtg gtgccatgtg aaccgatcat aatagagagg 180
aacacagtgc atttgactag cactaccata gagagggaaa tttgtcctaa ggtagcagaa 240
tataaaaatt ggttaaaacc acaatgccta attacagggt tcgccccttt ctcaaaggac 300
aactcaatta ggctttctgc aagtggggat gtctgggtaa caagagaacc ttatgtctca 360
tgcagtccag acaaatgtta tcaatttgca cttgggcagg gaaccaccct gaagaacaag 420
cactcaaatg gcactacacg cgatagaacc ccttacagga ctcttttaat gaatgaatta 480
ggtgtcccgt ttcatttagg aaccaaacaa gtgtgcatag catggtctag ttcaagctgt 540
tatgatggga aagcatggtt acacgtttgt gttactgggg atgatcaaaa tgctactgct 600
agtatcatct atgatgggat gctcgttgac agtattggat catggtccaa aaacatcctc 660
agaactcagg agtcagaatg tgtttgcatc aatggaactt gtgcagtggt aatgactgat 720
ggaagtgcat caggagttgc cgacactaga gtattattca taagagaagg gaaaatcgta 780
aatattagac cgttgtcagg aagtgctcag cacgttgagg aatgctcctg ttatccccga 840
tatcctgaaa ttagatgtgt ttgcagagac aattggaagg gctccaatag gcccattgta 900
tatataaata tggctgatta tagcattgaa tccagttatg tgtgctcggg acttgttggc 960
gacacaccaa gaaatgatga tagctccagc agcagcaact gcagagaccc taataacgaa 1020
agaggggccc caggagtgaa agggtgggct tttgacgacg ggaatgatgt ttggatggga 1080
cggacaatca aaaatggttc gcgttcaggt tatgagactt ttagggtcat aaatggttgg 1140
actgtggcta attcaaagtc acagataaat aggcaagtca tagttgacag tgacgactgg 1200
tctgggtatt ccggcatctt ctctgtcgag ggcagagaat gcatcaacag gtgtttttat 1260
gtggagttga taagagggag accacaggaa cccagagtgt ggtggacatc aaatagcatc 1320
attgtattct gtggaacctc aggtacatat ggaacaggct catggcctga tggagcgaat 1380
atcaacttca tgccaatata a 1401
<210> 16
<211> 2275
<212> DNA
<213> Artificial Sequence
<220>
<223> PB1 gene of PR8
<400> 16
atggatgtca atccgacctt acttttctta aaagtgccag cacaaaatgc tataagcaca 60
actttccctt atactggaga ccctccttac agccatggga caggaacagg atacaccatg 120
gatactgtca acaggacaca tcagtactca gaaaagggaa gatggacaac aaacaccgaa 180
actggagcac cgcaactcaa cccgattgat gggccactgc cagaagacaa tgaaccaagt 240
ggttatgccc aaacagattg tgtattggag gcgatggctt tccttgagga atcccatcct 300
ggtatttttg aaaactcgtg tattgaaacg atggaggttg ttcagcaaac acgagtagac 360
aagctgacac aaggccgaca gacctatgac tggactctaa atagaaacca acctgctgca 420
acagcattgg ccaacacaat agaagtgttc agatcaaatg gcctcacggc caatgagtct 480
ggaaggctca tagacttcct taaggatgta atggagtcaa tgaacaaaga agaaatgggg 540
atcacaactc attttcagag aaagagacgg gtgagagaca atatgactaa gaaaatgata 600
acacagagaa caatgggtaa aaagaagcag agattgaaca aaaggagtta tctaattaga 660
gcattgaccc tgaacacaat gaccaaagat gctgagagag ggaagctaaa acggagagca 720
attgcaaccc cagggatgca aataaggggg tttgtatact ttgttgagac actggcaagg 780
agtatatgtg agaaacttga acaatcaggg ttgccagttg gaggcaatga gaagaaagca 840
aagttggcaa atgttgtaag gaagatgatg accaattctc aggacaccga actttctttc 900
accatcactg gagataacac caaatggaac gaaaatcaga atcctcggat gtttttggcc 960
atgatcacat atatgaccag aaatcagccc gaatggttca gaaatgttct aagtattgct 1020
ccaataatgt tctcaaacaa aatggcgaga ctgggaaaag ggtatatgtt tgagagcaag 1080
agtatgaaac ttagaactca aatacctgca gaaatgctag caagcatcga tttgaaatat 1140
ttcaatgatt caacaagaaa gaagattgaa aaaatccgac cgctcttaat agaggggact 1200
gcatcattga gccctggaat gatgatgggc atgttcaata tgttaagcac tgtattaggc 1260
gtctccatcc tgaatcttgg acaaaagaga tacaccaaga ctacttactg gtgggatggt 1320
cttcaatcct ctgacgattt tgctctgatt gtgaatgcac ccaatcatga agggattcaa 1380
gccggagtcg acaggtttta tcgaacctgt aagctacttg gaatcaatat gagcaagaaa 1440
aagtcttaca taaacagaac aggtacattt gaattcacaa gttttttcta tcgttatggg 1500
tttgttgcca atttcagcat ggagcttccc agttttgggg tgtctgggat caacgagtca 1560
gcggacatga gtattggagt tactgtcatc aaaaacaata tgataaacaa tgatcttggt 1620
ccagcaacag ctcaaatggc ccttcagttg ttcatcaaag attacaggta cacgtaccga 1680
tgccatatag gtgacacaca aatacaaacc cgaagatcat ttgaaataaa gaaactgtgg 1740
gagcaaaccc gttccaaagc tggactgctg gtctccgacg gaggcccaaa tttatacaac 1800
attagaaatc tccacattcc tgaagtctgc ctaaaatggg aattgatgga tgaggattac 1860
caggggcgtt tatgcaaccc actgaaccca tttgtcagcc ataaagaaat tgaatcaatg 1920
aacaatgcag tgatgatgcc agcacatggt ccagccaaaa acatggagta tgatgctgtt 1980
gcaacaacac actcctggat ccccaaaaga aatcgatcca tcttgaatac aagtcaaaga 2040
ggagtacttg aggatgaaca aatgtaccaa aggtgctgca atttatttga aaaattcttc 2100
cccagcagtt catacagaag accagtcggg atatccagta tggtggaggc tatggtttcc 2160
agagcccgaa ttgatgcacg gattgatttc gaatctggaa ggataaagaa agaagagttc 2220
actgagatca tgaagatctg ttccaccatt gaagagctca gacggcaaaa atagg 2275
<210> 17
<211> 2151
<212> DNA
<213> Artificial Sequence
<220>
<223> PA gene of PR8
<400> 17
atggaagatt ttgtgcgaca atgcttcaat ccgatgattg tcgagcttgc ggaaaaaaca 60
atgaaagagt atggggagga cctgaaaatc gaaacaaaca aatttgcagc aatatgcact 120
cacttggaag tatgcttcat gtattcagat tttcacttca tcaatgagca aggcgagtca 180
ataatcgtag aacttggtga tccaaatgca cttttgaagc acagatttga aataatcgag 240
ggaagagatc gcacaatggc ctggacagta gtaaacagta tttgcaacac tacaggggct 300
gagaaaccaa agtttctacc agatttgtat gattacaagg agaatagatt catcgaaatt 360
ggagtaacaa ggagagaagt tcacatatac tatctggaaa aggccaataa aattaaatct 420
gagaaaacac acatccacat tttctcgttc actggggaag aaatggccac aaaggcagac 480
tacactctcg atgaagaaag cagggctagg atcaaaacca gactattcac cataagacaa 540
gaaatggcca gcagaggcct ctgggattcc tttcgtcagt ccgagagagg agaagagaca 600
attgaagaaa ggtttgaaat cacaggaaca atgcgtaagc ttgccgacca aagtctcccg 660
ccgaacttct ccagccttga aaattttaga gcctatgtgg atggattcga accgaacggc 720
tacattgagg gcaagctgtc tcaaatgtcc aaagaagtaa atgctagaat tgaacctttt 780
ttgaaaacaa caccacgacc acttagactt ccgaatgggc ctccctgttc tcagcggtcc 840
aaattcctgc tgatggatgc cttaaaatta agcattgagg acccaagtca tgaaggagag 900
ggaataccgc tatatgatgc aatcaaatgc atgagaacat tctttggatg gaaggaaccc 960
aatgttgtta aaccacacga aaagggaata aatccaaatt atcttctgtc atggaagcaa 1020
gtactggcag aactgcagga cattgagaat gaggagaaaa ttccaaagac taaaaatatg 1080
aagaaaacaa gtcagctaaa gtgggcactt ggtgagaaca tggcaccaga aaaggtagac 1140
tttgacgact gtaaagatgt aggtgatttg aagcaatatg atagtgatga accagaattg 1200
aggtcgcttg caagttggat tcagaatgag tttaacaagg catgcgaact gacagattca 1260
agctggatag agctcgatga gattggagaa gatgtggctc caattgaaca cattgcaagc 1320
atgagaagga attatttcac atcagaggtg tctcactgca gagccacaga atacataatg 1380
aagggagtgt acatcaatac tgccttgctt aatgcatctt gtgcagcaat ggatgatttc 1440
caattaattc caatgataag caagtgtaga actaaggagg gaaggcgaaa gaccaacttg 1500
tatggtttca tcataaaagg aagatcccac ttaaggaatg acaccgacgt ggtaaacttt 1560
gtgagcatgg agttttctct cactgaccca agacttgaac cacataaatg ggagaagtac 1620
tgtgttcttg agataggaga tatgcttata agaagtgcca taggccaggt ttcaaggccc 1680
atgttcttgt atgtgagaac aaatggaacc tcaaaaatta aaatgaaatg gggaatggag 1740
atgaggcgtt gcctcctcca gtcacttcaa caaattgaga gtatgattga agctgagtcc 1800
tctgtcaaag agaaagacat gaccaaagag ttctttgaga acaaatcaga aacatggccc 1860
attggagagt cccccaaagg agtggaggaa agttccattg ggaaggtctg caggacttta 1920
ttagcaaagt cggtattcaa cagcttgtat gcatctccac aactagaagg attttcagct 1980
gaatcaagaa aactgcttct tatcgttcag gctcttaggg acaacctgga acctgggacc 2040
tttgatcttg gggggctata tgaagcaatt gaggagtgcc tgattaatga tccctgggtt 2100
ttgcttaatg cttcttggtt caactccttc cttacacatg cattgagtta g 2151
<210> 18
<211> 1497
<212> DNA
<213> Artificial Sequence
<220>
<223> NP gene of PR8
<400> 18
atggcgtctc aaggcaccaa acgatcttac gaacagatgg agactgatgg agaacgccag 60
aatgccactg aaatcagagc atccgtcgga aaaatgattg gtggaattgg acgattctac 120
atccaaatgt gcaccgaact caaactcagt gattatgagg gacggttgat ccaaaacagc 180
ttaacaatag agagaatggt gctctctgct tttgacgaaa ggagaaataa ataccttgaa 240
gaacatccca gtgcggggaa agatcctaag aaaactggag gacctatata caggagagta 300
aacggaaagt ggatgagaga actcatcctt tatgacaaag aagaaataag gcgaatctgg 360
cgccaagcta ataatggtga cgatgcaacg gctggtctga ctcacatgat gatctggcat 420
tccaatttga atgatgcaac ttatcagagg acaagagctc ttgttcgcac cggaatggat 480
cccaggatgt gctctctgat gcaaggttca actctcccta ggaggtctgg agccgcaggt 540
gctgcagtca aaggagttgg aacaatggtg atggaattgg tcagaatgat caaacgtggg 600
atcaatgatc ggaacttctg gaggggtgag aatggacgaa aaacaagaat tgcttatgaa 660
agaatgtgca acattctcaa agggaaattt caaactgctg cacaaaaagc aatgatggat 720
caagtgagag agagccggaa cccagggaat gctgagttcg aagatctcac ttttctagca 780
cggtctgcac tcatattgag agggtcggtt gctcacaagt cctgcctgcc tgcctgtgtg 840
tatggacctg ccgtagccag tgggtacgac tttgaaaggg agggatactc tctagtcgga 900
atagaccctt tcagactgct tcaaaacagc caagtgtaca gcctaatcag accaaatgag 960
aatccagcac acaagagtca actggtgtgg atggcatgcc attctgccgc atttgaagat 1020
ctaagagtat taagcttcat caaagggacg aaggtgctcc caagagggaa gctttccact 1080
agaggagttc aaattgcttc caatgaaaat atggagacta tggaatcaag tacacttgaa 1140
ctgagaagca ggtactgggc cataaggacc agaagtggag gaaacaccaa tcaacagagg 1200
gcatctgcgg gccaaatcag catacaacct acgttctcag tacagagaaa tctccctttt 1260
gacagaacaa ccattatggc agcattcaat gggaatacag aggggagaac atctgacatg 1320
aggaccgaaa tcataaggat gatggaaagt gcaagaccag aagatgtgtc tttccagggg 1380
cggggagtct tcgagctctc ggacgaaaag gcagcgagcc cgatcgtgcc ttcctttgac 1440
atgagtaatg aaggatctta tttcttcgga gacaatgcag aggagtacga caattaa 1497
<210> 19
<211> 1002
<212> DNA
<213> Artificial Sequence
<220>
<223> M gene of PR8
<400> 19
atgagtcttc taaccgaggt cgaaacgtac gttctctcta tcatcccgtc aggccccctc 60
aaagccgaga tagcacagag acttgaagat gtctttgcag ggaagaacac cgatcttgag 120
gttctcatgg aatggctaaa gacaagacca atcctgtcac ctctgactaa ggggatttta 180
ggatttgtgt tcacgctcac cgtgcccagt gagcgaggac tgcagcgtag acgctttgtc 240
caaactgccc ttaatgggaa cggggatcca aataacatgg acaaagcagt taaactgtat 300
aggaagctca agagggagat aacattccat ggggccaaag aaatctcact cagttattct 360
gctggtgcac ttgccagttg tatgggcctc atatacaaca ggatgggggc tgtgaccact 420
gaagtggcat ttggcctggt atgtgcaacc tgtgaacaga ttgctgactc ccagcatcgg 480
tctcataggc aaatggtgac aacaaccaat ccactaatca gacatgagaa cagaatggtt 540
ttagccagca ctacagctaa ggctatggag caaatggctg gatcgagtga gcaagcagca 600
gaggccatgg aggttgctag tcaggctagg caaatggtgc aagcgatgag aaccattggg 660
actcatccta gctccagtgc tggtctgaaa aatgatcttc ttgaaaattt gcaggcctat 720
cagaaacgaa tgggggtgca gatgcaacgg ttcaagtgat cctctcgcta ttgccgcaaa 780
tatcattggg atcttgcact tgacattgtg gattcttgat cgtctttttt tcaaatgcat 840
ttaccgtcgc tttaaatacg gactgaaagg agggccttct acggaaggag tgccaaagtc 900
tatgagggaa gaatatcgaa aggaacagca gagtgctgtg gatgctgacg atggtcattt 960
tgtcagcata gagctggagt aaaaaactac cttgtttcta ct 1002
<210> 20
<211> 693
<212> DNA
<213> Artificial Sequence
<220>
<223> NS gene of PR8
<400> 20
atggatccaa acactgtgtc aagctttcag gtagattgct ttctttggca tgtccgcaaa 60
cgagttgcag accaagaact aggcgatgcc ccattccttg atcggcttcg ccgagatcag 120
aaatccctaa gaggaagggg cagtactctc ggtctggaca tcaagacagc cacacgtgct 180
ggaaagcaga tagtggagcg gattctgaaa gaagaatccg atgaggcact taaaatgacc 240
atggcctctg tacctgcgtc gcgttaccta actgacatga ctcttgagga aatgtcaagg 300
gactggtcca tgctcatacc caagcagaaa gtggcaggcc ctctttgtat cagaatggac 360
caggcgatca tggataagaa catcatactg aaagcgaact tcagtgtgat ttttgaccgg 420
ctggagactc taatattgct aagggctttc accgaagagg gagcaattgt tggcgaaatt 480
tcaccattgc cttctcttcc aggacatact gctgaggatg tcaaaaatgc agttggagtc 540
ctcatcggag gacttgaatg gaatgataac acagttcgag tctctgaaac tctacagaga 600
ttcgcttgga gaagcagtaa tgagaatggg agacctccac tcactccaaa acagaaacga 660
gaaatggcgg gaacaattag gtcagaagtt tga 693
<210> 21
<211> 760
<212> PRT
<213> Artificial Sequence
<220>
<223> PB2 wild of PR8
<400> 21
Met Glu Arg Ile Lys Glu Leu Arg Asn Leu Met Ser Gln Ser Arg Thr
1 5 10 15
Arg Glu Ile Leu Thr Lys Thr Thr Val Asp His Met Ala Ile Ile Lys
20 25 30
Lys Tyr Thr Ser Gly Arg Gln Glu Lys Asn Pro Ala Leu Arg Met Lys
35 40 45
Trp Met Met Ala Met Lys Tyr Pro Ile Thr Ala Asp Lys Arg Ile Thr
50 55 60
Glu Met Ile Pro Glu Arg Asn Glu Gln Gly Gln Thr Leu Trp Ser Lys
65 70 75 80
Met Asn Asp Ala Gly Ser Asp Arg Val Met Val Ser Pro Leu Ala Val
85 90 95
Thr Trp Trp Asn Arg Asn Gly Pro Ile Thr Asn Thr Val His Tyr Pro
100 105 110
Lys Ile Tyr Lys Thr Tyr Phe Glu Arg Val Glu Arg Leu Lys His Gly
115 120 125
Thr Phe Gly Pro Val His Phe Arg Asn Gln Val Lys Ile Arg Arg Arg
130 135 140
Val Asp Ile Asn Pro Gly His Ala Asp Leu Ser Ala Lys Glu Ala Gln
145 150 155 160
Asp Val Ile Met Glu Val Val Phe Pro Asn Glu Val Gly Ala Arg Ile
165 170 175
Leu Thr Ser Glu Ser Gln Leu Thr Ile Thr Lys Glu Lys Lys Glu Glu
180 185 190
Leu Gln Asp Cys Lys Ile Ser Pro Leu Met Val Ala Tyr Met Leu Glu
195 200 205
Arg Glu Leu Val Arg Lys Thr Arg Phe Leu Pro Val Ala Gly Gly Thr
210 215 220
Ser Ser Val Tyr Ile Glu Val Leu His Leu Thr Gln Gly Thr Cys Trp
225 230 235 240
Glu Gln Met Tyr Thr Pro Gly Gly Glu Val Arg Asn Asp Asp Val Asp
245 250 255
Gln Ser Leu Ile Ile Ala Ala Arg Asn Ile Val Arg Arg Ala Ala Val
260 265 270
Ser Ala Asp Pro Leu Ala Ser Leu Leu Glu Met Cys His Ser Thr Gln
275 280 285
Ile Gly Gly Ile Arg Met Val Asp Ile Leu Arg Gln Asn Pro Thr Glu
290 295 300
Glu Gln Ala Val Asp Ile Cys Lys Ala Ala Met Gly Leu Arg Ile Ser
305 310 315 320
Ser Ser Phe Ser Phe Gly Gly Phe Thr Phe Lys Arg Thr Ser Gly Ser
325 330 335
Ser Val Lys Arg Glu Glu Glu Val Leu Thr Gly Asn Leu Gln Thr Leu
340 345 350
Lys Ile Arg Val His Glu Gly Tyr Glu Glu Phe Thr Met Val Gly Arg
355 360 365
Arg Ala Thr Ala Ile Leu Arg Lys Ala Thr Arg Arg Leu Ile Gln Leu
370 375 380
Ile Val Ser Gly Arg Asp Glu Gln Ser Ile Ala Glu Ala Ile Ile Val
385 390 395 400
Ala Met Val Phe Ser Gln Glu Asp Cys Met Ile Lys Ala Val Arg Gly
405 410 415
Asp Leu Asn Phe Val Asn Arg Ala Asn Gln Arg Leu Asn Pro Met His
420 425 430
Gln Leu Leu Arg His Phe Gln Lys Asp Ala Lys Val Leu Phe Gln Asn
435 440 445
Trp Gly Val Glu Pro Ile Asp Asn Val Met Gly Met Ile Gly Ile Leu
450 455 460
Pro Asp Met Thr Pro Ser Ile Glu Met Ser Met Arg Gly Val Arg Ile
465 470 475 480
Ser Lys Met Gly Val Asp Glu Tyr Ser Ser Thr Glu Arg Val Val Val
485 490 495
Ser Ile Asp Arg Phe Leu Arg Ile Arg Asp Gln Arg Gly Asn Val Leu
500 505 510
Leu Ser Pro Glu Glu Val Ser Glu Thr Gln Gly Thr Glu Lys Leu Thr
515 520 525
Ile Thr Tyr Ser Ser Ser Met Met Trp Glu Ile Asn Gly Pro Glu Ser
530 535 540
Val Leu Val Asn Thr Tyr Gln Trp Ile Ile Arg Asn Trp Glu Thr Val
545 550 555 560
Lys Ile Gln Trp Ser Gln Asn Pro Thr Met Leu Tyr Asn Lys Met Glu
565 570 575
Phe Glu Pro Phe Gln Ser Leu Val Pro Lys Ala Ile Arg Gly Gln Tyr
580 585 590
Ser Gly Phe Val Arg Thr Leu Phe Gln Gln Met Arg Asp Val Leu Gly
595 600 605
Thr Phe Asp Thr Ala Gln Ile Ile Lys Leu Leu Pro Phe Ala Ala Ala
610 615 620
Pro Pro Lys Gln Ser Arg Met Gln Phe Ser Ser Phe Thr Val Asn Val
625 630 635 640
Arg Gly Ser Gly Met Arg Ile Leu Val Arg Gly Asn Ser Pro Val Phe
645 650 655
Asn Tyr Asn Lys Ala Thr Lys Arg Leu Thr Val Leu Gly Lys Asp Ala
660 665 670
Gly Thr Leu Thr Glu Asp Pro Asp Glu Gly Thr Ala Gly Val Glu Ser
675 680 685
Ala Val Leu Arg Gly Phe Leu Ile Leu Gly Lys Glu Asp Lys Arg Tyr
690 695 700
Gly Pro Ala Leu Ser Ile Asn Glu Leu Ser Asn Leu Ala Lys Gly Glu
705 710 715 720
Lys Ala Asn Val Leu Ile Gly Gln Gly Asp Val Val Leu Val Met Lys
725 730 735
Arg Lys Arg Asp Ser Ser Ile Leu Thr Asp Ser Gln Thr Ala Thr Lys
740 745 750
Arg Ile Arg Met Ala Ile Asn ***
755 760
<210> 22
<211> 2280
<212> DNA
<213> Artificial Sequence
<220>
<223> PB2 wild gene of PR8
<400> 22
atggagagaa taaaggaact aagagatttg atgtcacagt ctcgcactcg cgagatactg 60
acaaaaacca ctgtggacca tatggccata atcaagaaat acacatcggg aagacaggag 120
aagaaccccg ctctcagaat gaaatggatg atggcaatga aatacccgat tacagctgac 180
aaaagaataa tggagataat ccctgaaaga aatgagcaag gtcaaactct ctggagcaaa 240
acgaatgatg ctggatcaga taaggtaatg gtatcacctc tggctgtgac gtggtggaat 300
agaaatggac caacaacaag cacaatccat tatcccaagg tatataaaac ttactttgag 360
aaggttgaaa ggttgaaaca cggaaccttt ggccccattc atttccgaaa tcaagtcaaa 420
atacgccgca gggttgacat aaacccgggc catgcagacc tcagtgctag agaagcacaa 480
gatgttatca tggaggtcgt tttcccgaat gaggttggag ccaggatact gacatcagaa 540
tcacaattga caataacaaa ggaaaagaaa gaagaactcc aggattgtaa gattgctcct 600
ttaatggtgg catacatgtt agaaagagaa ctggttcgca agaccagatt cctaccagtg 660
gctggcggga caagcagcgt gtatatagaa gtactacatt tgactcaagg aacctgctgg 720
gagcagatgt acacaccagg aggggaagta aggaatgatg atgttgacca gagtttgatc 780
attgctgcta gaaacattgt aaggagagca acagtatcag cagacccatt ggcctcgctc 840
ttggagatgt gtcatggtac acaaataggc ggaataagaa tggtagacat ccttagacaa 900
aacccaacag aagagcaagc cgtggatata tgcaaggcag caataggcct aagaatcagt 960
tcatctttca gctttggagg tttcactttc aaaagaacaa gtgggtcttc tgtcaagaag 1020
gaagaagaag tgcttacagg caacctccag acattgaaaa taagagtgca tgagggatat 1080
gaggaattca caatggttgg gcgaagagca acagccctcc taaggaaagc aaccagaagg 1140
ctgattcaac tgatagtaag tgggagagac gaacaatcaa tcgctgaagc gatcattgta 1200
gcaatggtat tttcacaaga ggactgcatg ataaaggcag tccgaggtga tttgaacttc 1260
gtgaacagag cgaaccagcg actgaacccc atgcaccaac ttctgaggca cttccaaaaa 1320
gatgcaaaag tgttgtttca gaactgggga attgaaccca tcgacaatgt catggggatg 1380
attggaatat tgcccgacat gactcccagc acagagatgt cactaagagg agtgagagtc 1440
agcaaaatgg gagtggacga atactctagc actgaaagag tggttgtgag tattgatcgt 1500
ttcttaaggg ttcgagatca gagggggaac atacttctat cccctgaaga agttagtgag 1560
acacaaggga cggaaaagtt aacaataaca tattcatcgt ctatgatgtg ggagattaac 1620
ggcccggaat cagtgctagt taacacatac caatggatca ttaggaattg ggagactgtg 1680
aagattcagt ggtctcaaga tcctactatg ttatacaata aggtggaatt tgaacccttt 1740
caatctctgg tacctaaagc tgccagaggc caatatagtg gatttgtgag aacgctattc 1800
caacaaatgc gtgatgtact gggaacattt gacactgttc agataataaa gctgctacca 1860
tttgccgcag ccccaccaga gcagagtagg atgcagtttt cttctctgac tgtgaatgta 1920
agaggctcag gaatgagaat ccttgtgaga ggcaactccc ctgtgtttaa ttacaacaag 1980
gcaaccaaga ggcttacagt cctcgggaag gatgcaggtg cactcacaga agacccagat 2040
gaaggaacag caggagtgga atccgcagta ttgagaggat tcctaattct aggcaaagaa 2100
gacaagagat acggaccagc attgagcatc aacgaattga gcaatcttgc gaaaggggag 2160
aaagctaatg tattgatagg gcaaggagac gtagtgttgg taatgaaacg gaaacgggac 2220
tctagcatac ttactgacag ccagacagcg accaaaagaa ttcgaatggc catcaattag 2280
2280
Claims (22)
- 인플루엔자 바이러스 A/CHICKEN/KOREA/01310/2001(H9N2)의 중합효소 염기성 단백질 2(polymerase basic protein 2: PB2)에서 66번 아이소루신(I)을 메티오닌(M)으로, 109번 아이소루신(I)을 발린(V)으로 그리고 133번 아이소루신(I)을 발린(V)으로 변이시킨 단백질을 포함하는 재조합 인플루엔자 바이러스.
- 제1항에 있어서,
인플루엔자 바이러스의 헤마글루티닌(hemagglutinin: HA) 단백질 및 뉴라미니다제(neuraminidase: NA)를 더 포함하는, 재조합 인플루엔자 바이러스. - 제1항에 있어서,
인플루엔자 바이러스의 중합효소 염기성 단백질 1(polymerase basic protein 1: PB1), 중합효소 산성 단백질(polymerase acidic protein: PA), 핵단백질(nucleoprotein: NP), 매트릭스 단백질(matrix: M) 및 비구조 단백질(nonstructural protein: NS)로 이루어진 군으로부터 선택된 하나 이상을 더 포함하는 재조합 인플루엔자 바이러스. - 제1항에 있어서,
상기 염기성 단백질 2(polymerase basic protein 2: PB2) 단백질은 서열번호 1의 아미노산 서열을 갖는 것인, 재조합 H9N2 인플루엔자 바이러스. - 제2항에 있어서,
헤마글루티닌(hemagglutinin: HA) 단백질 및 뉴라미니다제(neuraminidase: NA)는 아형 H9N2 조류 인플루엔자 바이러스의 헤마글루티닌(hemagglutinin: HA) 단백질 및 뉴라미니다제(neuraminidase: NA)인, 재조합 인플루엔자 바이러스. - 제5항에 있어서,
상기 뉴라미니다제(neuraminidase: NA)는 인플루엔자 바이러스 Y280 lineage (A/chicken/Korea/SL20/2020)(H9N2)의 뉴라미다제(neuraminidase; NA)이고,
상기 헤마글루티닌(hemagglutinin: HA) 단백질은 인플루엔자 바이러스 Y280 lineage (A/chicken/Korea/SL20/2020)(H9N2)의 헤마글루티닌(hemagglutinin; HA) 또는 인플루엔자 바이러스 Y280 lineage (A/chicken/Korea/SL20/2020)(H9N2)의 헤마글루티닌(hemagglutinin; HA)에서 226번 류신이 글루타민으로 변이된 것인, 재조합 인플루엔자 바이러스. - 제6항에 있어서,
상기 헤마글루티닌(hemagglutinin: HA) 단백질은 서열번호 3 또는 서열번호 4의 아미노산 서열로 구성되는 것인, 재조합 인플루엔자 바이러스. - 제6항에 있어서,
상기 뉴라미니다제(neuraminidase: NA)는 서열번호 5의 아미노산 서열로 구성되는 것인, 재조합 인플루엔자 바이러스. - 제3항에 있어서,
상기 인플루엔자 바이러스의 PB1, PA, NP, M 및 NS 단백질은 인플루엔자 바이러스 A/Puerto Rico/8/34(H1N1)의 PB1, PA, NP, M 및 NS 단백질인, 재조합 인플루엔자 바이러스. - 제3항에 있어서,
상기 중합효소 염기성 단백질 1(polymerase basic protein 1: PB1)은 서열번호 6의 아미노산 서열로 구성되는 것인, H9N2 재조합 인플루엔자 바이러스. - 제2항에 있어서,
상기 중합효소 산성 단백질(polymerase acidic protein: PA)는 서열번호 7의 아미노산 서열로 구성되는 것인, H9N2 재조합 인플루엔자 바이러스. - 제2항에 있어서,
상기 핵단백질(nucleoprotein: NP)는 서열번호 8의 아미노산 서열로 구성되는 것인, H9N2 재조합 인플루엔자 바이러스. - 제2항에 있어서,
상기 매트릭스 단백질(matrix: M)은 서열번호 9의 아미노산 서열로 구성되는 것인, H9N2 재조합 인플루엔자 바이러스. - 제2항에 있어서,
상기 비구조 단백질(nonstructural protein: NS)은 서열번호 10의 아미노산 서열로 구성되는 것인, 재조합 H9N2 인플루엔자 바이러스. - 기탁번호 KCTC 14691BP의 재조합 인플루엔자 바이러스.
- 제1항 내지 제15항 중 어느 한 항의 재조합 인플루엔자 바이러스를 포함하는 인플루엔자 바이러스 백신.
- 제 16항에 있어서,
사독 백신 또는 생독 백신인, 백신. - 인플루엔자 바이러스 A/CHICKEN/KOREA/01310/2001(H9N2)의 서열번호 1로 표시되는 중합효소 염기성 단백질 2(polymerase basic protein 2: PB2)에서 66번 아이소루신(I)이 메티오닌(M)으로, 109번 아이소루신(I)이 발린(V)으로, 그리고 133번 아이소루신(I)이 발린(V)으로 변이된 PB2 단백질을 코딩하는 폴리뉴클레오타이드를 포함하는 재조합 벡터.
- 인플루엔자 바이러스 A/CHICKEN/KOREA/01310/2001(H9N2)의 서열번호 1로 표시되는 염기성 단백질 2(polymerase basic protein 2: PB2)에서 66번 아이소루신(I)이 메티오닌(M)으로, 109번 아이소루신(I)이 발린(V)으로 그리고 133번 아이소루신(I)이 발린(V)으로 변이된 PB2 단백질을 코딩하는 폴리뉴클레오타이드를 포함하는 재조합 인플루엔자 바이러스 제조용 조성물.
- 제19항에 있어서,
상기 폴리뉴클레오타이드는 벡터에 포함된 것인, 재조합 인플루엔자 바이러스 제조용 조성물. - 제18항의 재조합 벡터 또는 제19항 내지 제20항 중 어느 한 항의 조성물을 발육란에 접종하는 단계를 포함하는 재조합 인플루엔자 바이러스 제조방법.
- 제21항에 있어서,
상기 제조방법은 접종된 발육란을 배양하는 단계를 더 포함하는, 재조합 인플루엔자 바이러스 제조방법.
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