JPS5910791B2 - Saikindo Teiyousouchi - Google Patents

Saikindo Teiyousouchi

Info

Publication number
JPS5910791B2
JPS5910791B2 JP50148081A JP14808175A JPS5910791B2 JP S5910791 B2 JPS5910791 B2 JP S5910791B2 JP 50148081 A JP50148081 A JP 50148081A JP 14808175 A JP14808175 A JP 14808175A JP S5910791 B2 JPS5910791 B2 JP S5910791B2
Authority
JP
Japan
Prior art keywords
tube
identification
bacteria
medium
present
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
JP50148081A
Other languages
Japanese (ja)
Other versions
JPS5272877A (en
Inventor
啓之介 磯野
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Terumo Corp
Original Assignee
Terumo Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Terumo Corp filed Critical Terumo Corp
Priority to JP50148081A priority Critical patent/JPS5910791B2/en
Publication of JPS5272877A publication Critical patent/JPS5272877A/en
Publication of JPS5910791B2 publication Critical patent/JPS5910791B2/en
Expired legal-status Critical Current

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  • Apparatus Associated With Microorganisms And Enzymes (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)

Description

【発明の詳細な説明】 本発明は細菌同定用装置に関し、更に詳しくは本発明は
同定用培地を含む密封式の細菌同定用チューブに関する
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a bacterial identification device, and more particularly, the present invention relates to a sealed bacterial identification tube containing an identification medium.

細菌の同定は感染症の臨床検査などに使用され、特に腸
内細菌の同定は重要度が増大している。
Identification of bacteria is used in clinical tests for infectious diseases, and the identification of intestinal bacteria in particular is becoming increasingly important.

一般に細菌の同定は生化学的性状によって行なわれ、内
外に多数の文献があるが、その最も基礎となるものはI
Bergeys Mamual J (米国)であろう
Bacteria are generally identified by their biochemical properties, and there are many documents both domestically and internationally, but the most basic one is I
Bergeys Mamual J (USA).

これらの文献に記載された基礎的同定反応に基づいて近
年腸内細菌の同定を目的とする装置が幾つか開発されて
いる。
Several devices aimed at identifying intestinal bacteria have been developed in recent years based on the basic identification reactions described in these documents.

例えば、API(APIProducts,米国)、E
nterotube ( Hoffman −LaRo
che,米国)及びlViinitek ( B B
L ,米国)などが代表的なものである。
For example, API (API Products, USA), E
nterotube (Hoffman-LaRo
che, USA) and lViinitek (B B
L, USA) are representative examples.

しかし、これら従来の細菌同定用装置は開放式若し《は
半開放式であった為乾燥培地若しくは寒天培地を使用し
℃いた。
However, these conventional bacteria identification devices were of an open or semi-open type, and therefore used a dry medium or an agar medium.

従って、コロニーカ小サい場合などには24時間培養後
も十分な反応がみもれないことが多く、必然的に同定の
誤りが生じやすかった。
Therefore, in cases where the colony size is small, a sufficient reaction is often not observed even after 24 hours of culture, and errors in identification are inevitably likely to occur.

逆に十分な反応を得るには相当長時間(例えば48時間
)を必要とする欠点があった。
On the other hand, there was a drawback that a considerably long time (for example, 48 hours) was required to obtain a sufficient reaction.

また、従来の開放式又は半開放式の細菌同定用装置では
嫌気性菌の同定が不可能であるか、若し《は別の付属的
装置を用いるという繁雑さがあった。
Furthermore, with conventional open-type or semi-open-type bacteria identification devices, it has been impossible to identify anaerobic bacteria, or it has been complicated to use other auxiliary devices.

更に、従来の開放式又は半開放式の装置ではたとえ液体
培地を使用するものであつ又も細菌汚染の問題が起り、
必然的に操作が繁雑なものが多かった。
Furthermore, conventional open or semi-open devices, even those using liquid media, pose problems of bacterial contamination;
Inevitably, many operations were complicated.

本発明はかかる従来の細菌同定用チューブの欠点を無く
した密封式の細菌同定用チーブを提供することを目的と
する。
An object of the present invention is to provide a sealed tube for bacteria identification that eliminates the drawbacks of the conventional tubes for bacteria identification.

そして、本発明の目的を達成するものは、凍結乾燥した
同定用培地を含み、ゴム質のストッパーで被冠密封され
た実質的に無色透明な有底チューブからなり、その内部
が陰圧に保持され、上記ゴム質のストッパーは、シリン
ジ等の針を刺通でき、かつ、その抜去後も前記チューブ
内の密封機能を保持し5る程度の柔軟性および弾性を有
することを特徴とする細菌同定用チューブである。
A device that achieves the object of the present invention consists of a substantially colorless and transparent bottomed tube containing a freeze-dried identification medium, capped and sealed with a rubber stopper, and the inside of which is maintained under negative pressure. and the rubber stopper has flexibility and elasticity to the extent that it can be penetrated by a needle such as a syringe and maintains a sealing function within the tube even after its removal. This is a tube for use.

次に、本発明の細菌同定用チューブの一具体例を図面に
基づいて詳しく説明する。
Next, a specific example of the bacteria identification tube of the present invention will be described in detail based on the drawings.

本発明はかかる従来の細菌同定用チューブの欠点を無く
した密封式の細菌同定用チューブを提供することを目的
とする。
An object of the present invention is to provide a sealed tube for bacteria identification that eliminates the drawbacks of the conventional tubes for bacteria identification.

本発明は、凍結乾燥した同定用培地を含み、ゴ?質のス
トッパーで被冠密封された実質的に無色透明な有底チュ
ーブからなり、その内部が陰圧に保持され、上記ゴム質
のストッパーにシリンジ等の針を刺通し℃同定されるべ
き純粋培養された細菌を内部に導入することができる密
封式の細菌同定用チューブである。
The present invention includes a lyophilized identification medium, It consists of a substantially colorless and transparent bottomed tube sealed with a rubber stopper, and the inside of the tube is kept under negative pressure, and a needle such as a syringe is inserted through the rubber stopper to obtain a pure culture to be identified at °C. This is a sealed tube for bacteria identification into which bacteria can be introduced.

次に本発明の細菌同定用チューブの一具体例を図面に基
づい℃詳しく説明する。
Next, a specific example of the bacteria identification tube of the present invention will be described in detail based on the drawings.

第1図は本発明の細菌同定用チューブの断面図である。FIG. 1 is a sectional view of the tube for bacterial identification of the present invention.

チューブ本体1は実質的に無色透明のガラス又は合成樹
脂等で作られている。
The tube body 1 is made of substantially colorless and transparent glass, synthetic resin, or the like.

テユーブ本体1の中には同定用培地2が充填され、チュ
ーブの開口部はゴム質のストッパー3で密封されている
The tube body 1 is filled with an identification medium 2, and the opening of the tube is sealed with a rubber stopper 3.

同定用培地2は基本的にはグルコースのような炭水化物
、ペプトンのような蛋白質及び無機塩類を含む液体培地
が好ましく、各試験方法に応じて組成を変化させる必要
がある。
The identification medium 2 is preferably a liquid medium basically containing carbohydrates such as glucose, proteins such as peptone, and inorganic salts, and the composition needs to be changed depending on each test method.

また、培地中に特に液体状態で分解しやすい糖類を使用
する場合などには培地を凍結乾燥し、使用直前に滅菌蒸
留水等をストッパーを通してシリンジ等で添加してもよ
い。
Furthermore, when using a saccharide that is particularly easily decomposed in a liquid state in the culture medium, the culture medium may be freeze-dried, and sterile distilled water or the like may be added with a syringe or the like through a stopper immediately before use.

ストッパー3は、シリンジの針又はそれに類するもので
、刺通し5るが、針等を抜いた後もチューブの陰圧度を
一定に保持しうるものであること、言い替えれば、シリ
ンジ等の針を刺通でき、かつ、その抜去後も前記チュー
ブ内の密封機能を保持しうる程度の柔軟性および弾性を
有することが必要であり、ゴム質の材料、例えばブチル
ゴム、が好ましい。
The stopper 3 is a syringe needle or similar material that can be pierced through it, but it must be able to maintain a constant level of negative pressure in the tube even after the needle is removed. It is necessary to have flexibility and elasticity to the extent that the tube can be passed through and maintain the sealing function within the tube even after its removal, and a rubber material such as butyl rubber is preferable.

陰圧度はシリンジでチューブ内に加えるコロニー懸濁液
の量、培養中に発生するガスの量などを考慮して決定さ
れる。
The degree of negative pressure is determined by taking into consideration the amount of colony suspension added into the tube with a syringe, the amount of gas generated during culture, etc.

クロストリジウムテタニー( Clostridium
tetani )のような嫌気性菌ノ同定を行なうチ
ューブにはN2又はCO等のガスが空気の代りに入れら
れる。
Clostridium tetany (Clostridium tetany)
A gas such as N2 or CO is introduced in place of air in the tube used to identify anaerobic bacteria such as P. tetani.

また、好気性菌でも数係のCOが混入した方が繁殖しや
すい細菌の同定を行なう場合にも空気の一部なC02で
置換する。
Also, when identifying aerobic bacteria that are more likely to propagate when mixed with a numerical coefficient of CO, part of the air is replaced with CO2.

以上のような構成の細菌同定用チューブは全体的に滅菌
されていることは言うまでもない。
It goes without saying that the bacteria identification tube configured as described above is completely sterilized.

同定試薬は従来通り同定反応によつ又最初から同定用培
地中に混入させるか若しくは培養後にシリンジ等で添加
する。
The identification reagent is mixed into the identification medium from the beginning during the identification reaction as usual, or added with a syringe or the like after culturing.

例えば、フエニルアラニンデアミナーゼ試験では塩化第
二鉄試薬を培養後に添加すれば陽性の場合暗赤色に変化
する。
For example, in a phenylalanine deaminase test, if a ferric chloride reagent is added after incubation, the color turns dark red if positive.

また、インドール試験でも培養後にコボック試薬を添加
すると陽性の場合には赤色に変化する。
Also, in the indole test, if Kobok's reagent is added after culturing, the color turns red if positive.

一方、ブドウ糖試験(炭水化物分解試験)ではプチルチ
モールブルー又はフェノールレッドを試薬として最初か
ら同定用培地に添加しておく。
On the other hand, in a glucose test (carbohydrate decomposition test), petyl thymol blue or phenol red is added as a reagent to the identification medium from the beginning.

陽性の場合にはブテルチモールブルーは青色から黄色に
変化し、フェノールレッドは赤色から黄色に変化する。
If positive, buterthymol blue changes from blue to yellow, and phenol red changes from red to yellow.

次に、本発明の細菌同定用チューブの使用方法を説明す
る。
Next, a method of using the bacteria identification tube of the present invention will be explained.

本装置は直ちにそのまま同定操作に使用できる。This device can be used immediately for identification operations.

単一コロニーを生理食塩水若しくは適当な培地に懸濁し
たもの又は純粋培養した細菌5をシリンジ4等でストッ
パーを通し℃所定量だけ同定用培地に添加する(第3図
)。
A single colony suspended in physiological saline or an appropriate medium, or a pure culture of bacteria 5, is passed through a stopper using a syringe 4 or the like, and a predetermined amount of the bacteria is added to the identification medium (Fig. 3).

約37℃で24時間培養すれば、特に液体培地を使用し
た場合には同定に必要な十分な反応が得られる。
Incubation at about 37° C. for 24 hours provides a sufficient reaction for identification, especially when a liquid medium is used.

その結果、最初から試薬が添加してある装置ではそのま
ま、あるいはその後試薬を添加して色の変化を観察する
As a result, if a reagent is added to the device from the beginning, the change in color can be observed either as is or after the reagent is added.

本発明の細菌同定用チューブは密封式であるから、好都
合なことに液体培地を使用することができ、従って判定
までの時間が短縮されしかも同定の確実性、信頼性も向
上した。
Since the tube for bacterial identification of the present invention is of a sealed type, a liquid medium can be advantageously used, thereby shortening the time required for determination, and improving the certainty and reliability of identification.

また、他の装置類を使用せずに本装置だけで嫌気性菌の
同定を簡単におこなうことができる。
Furthermore, anaerobic bacteria can be easily identified using this device alone without using any other equipment.

更に、密封式であるから細菌汚染の問題もないばかりか
、密封式のわりには細菌接種等の操作が極めて簡単であ
るなどの利点がある。
Furthermore, since it is a sealed type, there is no problem of bacterial contamination, and it has the advantage that operations such as bacterial inoculation are extremely simple for a sealed type.

本発明の細菌同定用チューブは同定のオーダーによつ℃
試験項目を自由に選択でき、細菌の予想が立つ場合には
試験項目を容易に省略することもできるし、同定途中で
試験項目を増加させることもできるなどの便利さがある
The tube for bacterial identification of the present invention depends on the order of identification.
It is convenient because test items can be freely selected, test items can be easily omitted when the bacteria are predicted, and test items can be increased during identification.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は本発明の細菌同定用チューブの一具体例の断面
図である。 第2図は本発明の細菌同定用トレイの一具体例の断面図
である。 第3図はシリンジで細菌懸濁液を本発明の細菌同定用チ
ューブに添加している状態を示す一部断面図である。 1はチューブ、1′はトレイ、1〃はウエル、2は同定
用培地、3はストッパーを表わす。 −171−
FIG. 1 is a sectional view of a specific example of the tube for identifying bacteria of the present invention. FIG. 2 is a sectional view of a specific example of the tray for bacterial identification of the present invention. FIG. 3 is a partial cross-sectional view showing a state in which a bacterial suspension is being added to the tube for bacterial identification of the present invention using a syringe. 1 is a tube, 1' is a tray, 1 is a well, 2 is an identification medium, and 3 is a stopper. -171-

Claims (1)

【特許請求の範囲】[Claims] 1 凍結乾燥した同定用培地を含み、ゴム質のストッパ
ーで被冠密封された実質的に無色透明な有底チューブか
らなり、その内部が陰圧に保持され、上記ゴム質のスト
ッパーは、シリンジ等の針を刺通でき、かつ、その抜去
後も前記テユーブ内の密封機能を保持しうる程度の柔軟
性および弾性を有することを特徴とする細菌同定用テユ
ープ。
1 Consists of a substantially colorless and transparent bottomed tube containing a freeze-dried identification medium and sealed with a rubber stopper, the inside of which is maintained under negative pressure, and the rubber stopper is suitable for use with syringes, etc. 1. A tube for bacterial identification, characterized in that it has enough flexibility and elasticity to allow a needle to be pierced through the tube, and to maintain a sealing function within the tube even after the tube is removed.
JP50148081A 1975-12-12 1975-12-12 Saikindo Teiyousouchi Expired JPS5910791B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP50148081A JPS5910791B2 (en) 1975-12-12 1975-12-12 Saikindo Teiyousouchi

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP50148081A JPS5910791B2 (en) 1975-12-12 1975-12-12 Saikindo Teiyousouchi

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP18928282A Division JPS58134988A (en) 1982-10-29 1982-10-29 Tray for identification of bacterial strain

Publications (2)

Publication Number Publication Date
JPS5272877A JPS5272877A (en) 1977-06-17
JPS5910791B2 true JPS5910791B2 (en) 1984-03-12

Family

ID=15444792

Family Applications (1)

Application Number Title Priority Date Filing Date
JP50148081A Expired JPS5910791B2 (en) 1975-12-12 1975-12-12 Saikindo Teiyousouchi

Country Status (1)

Country Link
JP (1) JPS5910791B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6315984U (en) * 1986-07-14 1988-02-02

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS485189U (en) * 1971-06-03 1973-01-20
JPS4880775A (en) * 1972-01-06 1973-10-29

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS485189U (en) * 1971-06-03 1973-01-20
JPS4880775A (en) * 1972-01-06 1973-10-29

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6315984U (en) * 1986-07-14 1988-02-02

Also Published As

Publication number Publication date
JPS5272877A (en) 1977-06-17

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