JPWO2021067100A5 - - Google Patents

Download PDF

Info

Publication number
JPWO2021067100A5
JPWO2021067100A5 JP2022520294A JP2022520294A JPWO2021067100A5 JP WO2021067100 A5 JPWO2021067100 A5 JP WO2021067100A5 JP 2022520294 A JP2022520294 A JP 2022520294A JP 2022520294 A JP2022520294 A JP 2022520294A JP WO2021067100 A5 JPWO2021067100 A5 JP WO2021067100A5
Authority
JP
Japan
Prior art keywords
elegans
genus
composition
bacterial strain
subject
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.)
Pending
Application number
JP2022520294A
Other languages
Japanese (ja)
Other versions
JP2022551584A (en
Publication date
Application filed filed Critical
Priority claimed from PCT/US2020/052251 external-priority patent/WO2021067100A1/en
Publication of JP2022551584A publication Critical patent/JP2022551584A/en
Publication of JPWO2021067100A5 publication Critical patent/JPWO2021067100A5/ja
Pending legal-status Critical Current

Links

Description

本発明の実施形態を以下の項にさらに記載する:
[項1]
(a)少なくとも1つの細菌株またはその抽出物もしくはその成分であって、前記少なくとも1つの細菌株が、Gluconobacter属、Acetobacter属、Gluconoacaetobacter属、Acidomonas属、Ameyamaea属、Asaia属、Granulibacter属、Kozakia属、Neoasaia属、Neokomagataea属、Saccharibacter属、Swaminathania属、Tanticharoenia属、またはそれらの組み合わせを含む、前記少なくとも1つの細菌株またはその抽出物もしくはその成分と、
(b)賦形剤と、を含む、組成物。
[項2]
前記少なくとも1つの細菌株が、Gluconacetobacter hansenii、Gluconobacter oxydans、Acetobacter aceti、またはそれらの組み合わせを含む、上記項1に記載の組成物。
[項3]
前記少なくとも1つの細菌株が、Gluconacetobacter hanseniiを含む、上記項1または2に記載の組成物。
[項4]
前記少なくとも1つの細菌株またはその抽出物もしくはその成分が、C.elegans動物を含むC.elegans培養物に投与されるとき、前記C.elegans培養物中の前記C.elegans動物の平均寿命は、前記少なくとも1つの細菌株またはその抽出物もしくはその成分の投与なしで、同等のC.elegans培養物中のC.elegans動物のものと比較して、少なくとも20%延長されるという点を特徴とする、上記項1~3のいずれか1項に記載の組成物。
[項5]
前記少なくとも1つの細菌株またはその抽出物もしくはその成分が、C.elegans動物を含むC.elegans培養物に投与されるとき、前記C.elegans培養物中の前記C.elegans動物の平均咽頭ポンピング活性は、前記少なくとも1つの細菌株またはその抽出物もしくはその成分の投与なしで、同等のC.elegans培養物中のC.elegans動物のものと比較して、少なくとも20%増加するという点を特徴とする、上記項1~4のいずれか1項に記載の組成物。
[項6]
前記少なくとも1つの細菌株またはその抽出物もしくはその成分が、C.elegans動物を含むC.elegans培養物に投与されるとき、前記C.elegans培養物中の前記C.elegans動物の平均運動速度は、前記少なくとも1つの細菌株またはその抽出物もしくはその成分の投与なしで、同等のC.elegans培養物中のC.elegans動物のものと比較して、少なくとも20%増加するという点を特徴とする、上記項1~5のいずれか1項に記載の組成物。
[項7]
前記少なくとも1つの細菌株またはその抽出物もしくはその成分が、C.elegans動物を含むC.elegans培養物に投与されるとき、前記C.elegans培養物中の前記C.elegans動物の生殖能力は、前記少なくとも1つの細菌株またはその抽出物もしくはその成分の投与なしで、同等のC.elegans培養物中のC.elegans動物のものと比較して、少なくとも20%低下するという点を特徴とする、上記項1~6のいずれか1項に記載の組成物。
[項8]
前記少なくとも1つの細菌株またはその抽出物もしくはその成分が、C.elegans動物を含むC.elegans培養物が紫外線照射にさらされるとき、前記少なくとも1つの細菌株またはその抽出物もしくはその成分が投与された前記C.elegans培養物中の前記C.elegans動物の平均生存時間が、前記少なくとも1つの細菌株またはその抽出物もしくはその成分の投与なしで、同等のC.elegans培養物中のC.elegans動物のものと比較して、少なくとも20%増加するという点を特徴とする、上記項1~7のいずれか1項に記載の組成物。
[項9]
前記少なくとも1つの細菌株またはその抽出物もしくはその成分が、C.elegans動物を含むC.elegans培養物が高温にさらされるとき、前記少なくとも1つの細菌株またはその抽出物もしくはその成分が投与された前記C.elegans培養物中のC.elegans動物の平均生存時間が、前記少なくとも1つの細菌株またはその抽出物もしくはその成分の投与なしで、同等のC.elegans培養物中のC.elegans動物のものと比較して、少なくとも20%増加するという点を特徴とする、上記項1~8のいずれか1項に記載の組成物。
[項10]
前記高温が、少なくとも37℃である、上記項9に記載の組成物。
[項11]
前記少なくとも1つの細菌株またはその抽出物もしくはその成分が、C.elegans動物を含むC.elegans培養物に投与されるとき、前記C.elegans培養物中の前記C.elegan動物において観察される腸脂肪の平均量が、前記少なくとも1つの細菌株またはその抽出物もしくはその成分の投与なしで、同等のC.elegans培養物中のC.elegans動物のものと比較して、少なくとも20%低下するという点を特徴とする、上記項1~10のいずれか1項に記載の組成物。
[項12]
前記C.elegans動物が、成体C.elegans動物である、上記項4~11のいずれか1項に記載の組成物。
[項13]
前記C.elegans動物が、少なくとも5日齢である、上記項4~12のいずれか1項に記載の組成物。
[項14]
前記組成物が、経口投与用に配合される、上記項1~13のいずれか1項に記載の組成物。
[項15]
前記組成物が、食品、飲料、飼料組成物、または栄養補助食品である、上記項1~14のいずれか1項に記載の組成物。
[項16]
前記組成物が、液体、シロップ、錠剤、トローチ、グミ、カプセル、粉末、ゲル、またはフィルムである、上記項1~15のいずれか1項に記載の組成物。
[項17]
前記組成物が、医薬組成物である、上記項1~16のいずれか1項に記載の組成物。
[項18]
前記組成物が、腸溶コーティングされた製剤である、上記項1~17のいずれか1項に記載の組成物。
[項19]
対象に、上記項1~18のいずれか1項に記載の組成物を投与することを含む、方法。
[項20]
前記方法が、対象の寿命を延長する方法である、上記項19に記載の方法。
[項21]
前記対象の前記寿命が、前記組成物の投与なしで、同等の対象のものと比較して、少なくとも20%延長される、上記項20に記載の方法。
[項22]
前記方法が、対象の少なくとも1つの年齢関連の症状または状態の発症を低減または遅延させる方法である、上記項19に記載の方法。
[項23]
前記少なくとも1つの年齢関連の症状または状態が、前記組成物の投与なしで、同等の対象のものと比較して、前記対象において少なくとも20%低減または遅延される、上記項22に記載の方法。
[項24]
前記少なくとも1つの年齢関連の症状または状態が、前記対象の筋肉及び/または神経筋機能の低下であるか、またはそれを含む、上記項22または23に記載の方法。
[項25]
前記少なくとも1つの年齢関連の症状または状態が、脂質代謝の調節不全であるか、またはそれを含む、上記項22~24のいずれか1項に記載の方法。
[項26]
前記対象が、少なくとも30歳である、上記項19~25のいずれか1項に記載の方法。
[項27]
前記対象が、高齢対象である、上記項19~26のいずれか1項に記載の方法。
[項28]
前記対象が、哺乳動物である、上記項19~27のいずれか1項に記載の方法。
[項29]
前記対象が、ヒトである、上記項19~28のいずれか1項に記載の方法。
[項30]
前記対象の微生物叢にコロニーを形成するのに十分な量の微生物を投与することを含む、上記項19~29のいずれか1項に記載の方法。
[項31]
対象の寿命を延長するための少なくとも1つの細菌株またはその抽出物もしくはその成分の使用であって、少なくとも1つの細菌株が、Gluconobacter属、Acetobacter属、Gluconoacaetobacter属、Acidomonas属、Ameyamaea属、Asaia属、Granulibacter属、Kozakia属、Neoasaia属、Neokomagataea属、Saccharibacter属、Swaminathania属、Tanticharoenia属、またはそれらの組み合わせを含む、前記使用。
[項32]
前記少なくとも1つの細菌株が、Gluconacetobacter hansenii、Gluconobacter oxydans、Acetobacter aceti、またはそれらの組み合わせを含む、上記項31に記載の使用。
[項33]
前記少なくとも1つの細菌株が、Gluconacetobacter hanseniiを含む、上記項31または32に記載の使用。
[項34]
対象における少なくとも1つの年齢関連の症状もしくは状態の発症を低減または遅延させる少なくとも1つの細菌株またはその抽出物もしくは成分の使用であって、前記少なくとも1つの細菌株が、Gluconobacter属、Acetobacter属、Gluconoacaetobacter属、Acidomonas属、Ameyamaea属、Asaia属、Granulibacter属、Kozakia属、Neoasaia属、Neokomagataea属、Saccharibacter属、Swaminathania属、Tanticharoenia属、またはそれらの組み合わせを含む、前記使用。
[項35]
前記少なくとも1つの細菌株が、Gluconacetobacter hansenii、Gluconobacter oxydans、Acetobacter aceti、またはそれらの組み合わせを含む、上記項34に記載の使用。
[項36]
前記少なくとも1つの細菌株が、Gluconacetobacter hanseniiを含む、上記項34または35に記載の使用。
[項37]
前記少なくとも1つの年齢関連の症状または状態が、組成物の投与なしで、同等の対象のものと比較して、前記対象において少なくとも20%低減または遅延される、上記項34に記載の使用。
[項38]
前記少なくとも1つの年齢関連の症状または状態が、前記対象の筋肉及び/または神経筋機能の低下であるか、またはそれを含む、上記項34~37のいずれか1項に記載の使用。
[項39]
前記少なくとも1つの年齢関連の症状または状態が、脂質代謝の調節不全であるか、またはそれを含む、上記項34~38のいずれか1項に記載の使用。
[項40]
前記対象が、少なくとも30歳である、上記項34~39のいずれか1項に記載の使用。
[項41]
前記対象が、高齢対象である、上記項34~40のいずれか1項に記載の使用。
[項42]
前記対象が、哺乳動物である、上記項34~41のいずれか1項に記載の使用。
[項43]
前記対象が、ヒトである、上記項34~42のいずれか1項に記載の使用。
[項44]
対象の寿命、年齢関連の症状、及び/または年齢関連の状態を修正する1つ以上の微生物株の能力を特徴付ける方法であって、
(a)哺乳動物微生物叢の複数の微生物株を複数のC.elegans培養物に添加することであって、異なる微生物株を各C.elegans培養物に添加し、各培養物が、同じC.elegans株のC.elegans動物を含む、前記添加することと、
(b)前記複数の微生物株の各微生物株が、各培養物の前記C.elegans動物の1つ以上のパラメータに影響を及ぼすかどうかを決定することであって、前記1つ以上のパラメータが、老化、年齢関連の症状、及び/または年齢関連の状態に関連する、前記決定することと、を含む、前記方法。
[項45]
対象の寿命、年齢関連の症状、及び/または年齢関連の状態を修正する1つ以上の1つ以上の微生物株の能力を特徴付けるための、C.elegans動物の、使用。
[項46]
少なくとも1つの細菌株またはその抽出物もしくはその成分、及び前記賦形剤を組み合わせることを含む、上記項1~18のいずれか1項に記載の組成物の作製方法。
本発明の実施形態は、その詳細な説明と併せて説明されてきたが、前述の説明は、添付の特許請求の範囲によって定義される本発明の範囲を説明することを意図し、限定しないことを理解されたい。その他の側面、利点、及び変更は、以下の特許請求の範囲内にある。

Embodiments of the invention are further described in the following sections:
[Section 1]
(a) at least one bacterial strain or an extract or component thereof, wherein the at least one bacterial strain is a member of the genus Gluconobacter, genus Acetobacter, genus Gluconoacaetobacter, genus Acidomonas, genus Ameyamaea, genus Asaia, genus Granulibacter, Ko genus zakia , the genus Neoasaia, the genus Neokomagataea, the genus Saccharibacter, the genus Swaminathania, the genus Tanticharoenia, or a combination thereof;
(b) an excipient.
[Section 2]
2. The composition of paragraph 1, wherein the at least one bacterial strain comprises Gluconacetobacter hansenii, Gluconobacter oxydans, Acetobacter aceti, or a combination thereof.
[Section 3]
3. The composition according to item 1 or 2, wherein the at least one bacterial strain comprises Gluconacetobacter hansenii.
[Section 4]
The at least one bacterial strain or extract or component thereof is C. C. elegans, including C. elegans animals. When administered to C. elegans cultures, the C. elegans culture. The C. elegans culture. The average lifespan of C. elegans animals is the same as that of an equivalent C. elegans animal without administration of said at least one bacterial strain or extract or component thereof. C. elegans culture. Composition according to any one of the above clauses 1 to 3, characterized in that it is prolonged by at least 20% compared to that of P. elegans animals.
[Section 5]
The at least one bacterial strain or extract or component thereof is C. C. elegans, including C. elegans animals. When administered to C. elegans cultures, the C. elegans culture. The C. elegans culture. The average pharyngeal pumping activity of C. elegans animals was greater than that of an equivalent C. elegans animal without administration of said at least one bacterial strain or extract or component thereof. C. elegans culture. Composition according to any one of the above clauses 1 to 4, characterized in that it is increased by at least 20% compared to that of P. elegans animals.
[Section 6]
The at least one bacterial strain or extract or component thereof is C. C. elegans, including C. elegans animals. When administered to C. elegans cultures, the C. elegans culture. The C. elegans culture. The average locomotor speed of C. elegans animals was higher than that of an equivalent C. elegans animal without administration of said at least one bacterial strain or extract or component thereof. C. elegans culture. Composition according to any one of the above clauses 1 to 5, characterized in that it is increased by at least 20% compared to that of P. elegans animals.
[Section 7]
The at least one bacterial strain or extract or component thereof is C. C. elegans, including C. elegans animals. When administered to C. elegans cultures, the C. elegans culture. The C. elegans culture. The reproductive performance of C. elegans animals is determined by the same level of C. elegans without administration of said at least one bacterial strain or extracts or components thereof. C. elegans culture. Composition according to any one of the above clauses 1 to 6, characterized in that the composition is reduced by at least 20% compared to that of P. elegans animals.
[Section 8]
The at least one bacterial strain or extract or component thereof is C. C. elegans, including C. elegans animals. When the C. elegans culture is exposed to ultraviolet radiation, said at least one bacterial strain or extract or component thereof has been administered. The C. elegans culture. The average survival time of C. elegans animals is longer than that of equivalent C. elegans animals without administration of said at least one bacterial strain or extract or component thereof. C. elegans culture. Composition according to any one of the above clauses 1 to 7, characterized in that it is increased by at least 20% compared to that of P. elegans animals.
[Section 9]
The at least one bacterial strain or extract or component thereof is C. C. elegans, including C. elegans animals. When the C. elegans culture is exposed to high temperatures, the at least one bacterial strain or extract or component thereof has been administered. C. elegans culture. The average survival time of C. elegans animals is longer than that of equivalent C. elegans animals without administration of said at least one bacterial strain or extract or component thereof. C. elegans culture. Composition according to any one of the above clauses 1 to 8, characterized in that it is increased by at least 20% compared to that of P. elegans animals.
[Section 10]
10. The composition according to item 9 above, wherein the high temperature is at least 37°C.
[Section 11]
The at least one bacterial strain or extract or component thereof is C. C. elegans, including C. elegans animals. When administered to C. elegans cultures, the C. elegans culture. The C. elegans culture. The average amount of intestinal fat observed in C. elegan animals is lower than that observed in C. elegan animals without administration of said at least one bacterial strain or extract or component thereof. C. elegans culture. 11. Composition according to any one of the above clauses 1 to 10, characterized in that the composition is reduced by at least 20% compared to that of P. elegans animals.
[Section 12]
Said C. elegans animals are infected with adult C. elegans animals. The composition according to any one of items 4 to 11 above, which is a P. elegans animal.
[Section 13]
Said C. 13. The composition according to any one of paragraphs 4 to 12 above, wherein the P. elegans animal is at least 5 days old.
[Section 14]
14. The composition according to any one of items 1 to 13 above, wherein the composition is formulated for oral administration.
[Section 15]
The composition according to any one of items 1 to 14 above, wherein the composition is a food, a beverage, a feed composition, or a nutritional supplement.
[Section 16]
16. The composition according to any one of items 1 to 15 above, wherein the composition is a liquid, syrup, tablet, troche, gummy, capsule, powder, gel, or film.
[Section 17]
The composition according to any one of items 1 to 16 above, wherein the composition is a pharmaceutical composition.
[Section 18]
The composition according to any one of items 1 to 17 above, wherein the composition is an enteric-coated formulation.
[Section 19]
A method comprising administering to a subject the composition according to any one of items 1 to 18 above.
[Section 20]
20. The method according to item 19, wherein the method is a method of extending the lifespan of a subject.
[Section 21]
21. The method of claim 20, wherein the lifespan of the subject is increased by at least 20% compared to that of an equivalent subject without administration of the composition.
[Section 22]
20. The method of clause 19, wherein the method is a method of reducing or delaying the onset of at least one age-related symptom or condition in a subject.
[Section 23]
23. The method of clause 22, wherein the at least one age-related symptom or condition is reduced or delayed in the subject by at least 20% as compared to an equivalent subject without administration of the composition.
[Section 24]
24. The method of paragraph 22 or 23, wherein said at least one age-related symptom or condition is or comprises a decline in muscle and/or neuromuscular function of said subject.
[Section 25]
25. The method of any one of paragraphs 22 to 24 above, wherein said at least one age-related symptom or condition is or comprises dysregulation of lipid metabolism.
[Section 26]
26. The method according to any one of paragraphs 19 to 25 above, wherein the subject is at least 30 years old.
[Section 27]
27. The method according to any one of items 19 to 26 above, wherein the subject is an elderly subject.
[Section 28]
28. The method according to any one of items 19 to 27 above, wherein the subject is a mammal.
[Section 29]
29. The method according to any one of items 19 to 28 above, wherein the subject is a human.
[Section 30]
30. The method according to any one of items 19 to 29 above, comprising administering an amount of microorganisms sufficient to colonize the microbial flora of the subject.
[Section 31]
Use of at least one bacterial strain or extract or component thereof for extending the lifespan of a subject, wherein the at least one bacterial strain is a member of the genus Gluconobacter, the genus Acetobacter, the genus Gluconoacaetobacter, the genus Acidomonas, the genus Ameyamaea, the genus Asaia. , Granulibacter, Kozakia, Neoasaia, Neokomagataea, Saccharibacter, Swaminathania, Tanticharoenia, or combinations thereof.
[Section 32]
32. The use according to clause 31, wherein the at least one bacterial strain comprises Gluconacetobacter hansenii, Gluconobacter oxydans, Acetobacter aceti, or a combination thereof.
[Section 33]
The use according to paragraph 31 or 32 above, wherein the at least one bacterial strain comprises Gluconacetobacter hansenii.
[Section 34]
Use of at least one bacterial strain or extract or component thereof to reduce or delay the onset of at least one age-related symptom or condition in a subject, wherein said at least one bacterial strain is a member of the genus Gluconobacter, genus Acetobacter, Gluconoacaetobacter Genus, Acidomonas, Ameyamaea, Asaia, Granulibacter, Kozakia, Neoasaia, Neokomagataea, Saccharibacter, Swaminathania, Tantich Said use comprising the genus aroenia, or a combination thereof.
[Section 35]
35. The use according to paragraph 34, wherein the at least one bacterial strain comprises Gluconacetobacter hansenii, Gluconobacter oxydans, Acetobacter aceti, or a combination thereof.
[Section 36]
36. The use according to paragraph 34 or 35 above, wherein the at least one bacterial strain comprises Gluconacetobacter hansenii.
[Section 37]
35. The use according to clause 34, wherein said at least one age-related symptom or condition is reduced or delayed in said subject by at least 20% compared to that of an equivalent subject without administration of the composition.
[Section 38]
Use according to any one of the above clauses 34 to 37, wherein said at least one age-related symptom or condition is or comprises a decline in muscle and/or neuromuscular function of said subject.
[Section 39]
The use according to any one of paragraphs 34 to 38 above, wherein said at least one age-related symptom or condition is or comprises dysregulation of lipid metabolism.
[Section 40]
The use according to any one of clauses 34 to 39 above, wherein the subject is at least 30 years old.
[Section 41]
The use according to any one of the above items 34 to 40, wherein the subject is an elderly subject.
[Section 42]
The use according to any one of the above items 34 to 41, wherein the subject is a mammal.
[Section 43]
The use according to any one of the above items 34 to 42, wherein the subject is a human.
[Section 44]
A method of characterizing the ability of one or more microbial strains to modify lifespan, age-related symptoms, and/or age-related conditions in a subject, the method comprising:
(a) Multiple microbial strains of the mammalian microbiome are combined with multiple C. elegans culture, by adding different microbial strains to each C. elegans culture. C. elegans cultures, each culture containing the same C. elegans culture. C. elegans strain. elegans animal;
(b) Each of the microbial strains of the plurality of microbial strains has the C. elegans animal, wherein the one or more parameters are associated with aging, an age-related symptom, and/or an age-related condition. The method comprises:
[Section 45]
C. for characterizing the ability of one or more microbial strains to modify lifespan, age-related symptoms, and/or age-related conditions in a subject. elegans animals, use.
[Section 46]
19. A method for making a composition according to any one of paragraphs 1 to 18 above, comprising combining at least one bacterial strain or an extract thereof or a component thereof and the excipient.
While embodiments of the invention have been described in conjunction with the detailed description thereof, the foregoing description is intended to illustrate and not limit the scope of the invention, which is defined by the appended claims. I want you to understand. Other aspects, advantages, and modifications are within the scope of the following claims.

Claims (46)

(a)少なくとも1つの細菌株またはその抽出物もしくはその成分であって、前記少なくとも1つの細菌株が、Gluconobacter属、Acetobacter属、Gluconoacaetobacter属、Acidomonas属、Ameyamaea属、Asaia属、Granulibacter属、Kozakia属、Neoasaia属、Neokomagataea属、Saccharibacter属、Swaminathania属、Tanticharoenia属、またはそれらの組み合わせを含む、前記少なくとも1つの細菌株またはその抽出物もしくはその成分と、
(b)賦形剤と、を含む、組成物。
(a) at least one bacterial strain or an extract or component thereof, wherein the at least one bacterial strain is a member of the genus Gluconobacter, genus Acetobacter, genus Gluconoacaetobacter, genus Acidomonas, genus Ameyamaea, genus Asaia, genus Granulibacter, Ko genus zakia , the genus Neoasaia, the genus Neokomagataea, the genus Saccharibacter, the genus Swaminathania, the genus Tanticharoenia, or a combination thereof;
(b) an excipient.
前記少なくとも1つの細菌株が、Gluconacetobacter hansenii、Gluconobacter oxydans、Acetobacter aceti、またはそれらの組み合わせを含む、請求項1に記載の組成物。 2. The composition of claim 1, wherein the at least one bacterial strain comprises Gluconacetobacter hansenii, Gluconobacter oxydans, Acetobacter aceti, or a combination thereof. 前記少なくとも1つの細菌株が、Gluconacetobacter hanseniiを含む、請求項1または2に記載の組成物。 3. The composition of claim 1 or 2, wherein the at least one bacterial strain comprises Gluconacetobacter hansenii. 前記少なくとも1つの細菌株またはその抽出物もしくはその成分が、C.elegans動物を含むC.elegans培養物に投与されるとき、前記C.elegans培養物中の前記C.elegans動物の平均寿命は、前記少なくとも1つの細菌株またはその抽出物もしくはその成分の投与なし同等のC.elegans培養物中のC.elegans動物のものと比較して、少なくとも20%延長されるという点を特徴とする、請求項1~3のいずれか1項に記載の組成物。 The at least one bacterial strain or extract or component thereof is C. C. elegans, including C. elegans animals. When administered to C. elegans cultures, the C. elegans culture. The C. elegans culture. The average lifespan of C. elegans animals is the same as that of C. elegans animals without administration of said at least one bacterial strain or extracts or components thereof. C. elegans culture. Composition according to any one of claims 1 to 3, characterized in that it is prolonged by at least 20% compared to that of P. elegans animals. 前記少なくとも1つの細菌株またはその抽出物もしくはその成分が、C.elegans動物を含むC.elegans培養物に投与されるとき、前記C.elegans培養物中の前記C.elegans動物の平均咽頭ポンピング活性は、前記少なくとも1つの細菌株またはその抽出物もしくはその成分の投与なし同等のC.elegans培養物中のC.elegans動物のものと比較して、少なくとも20%増加するという点を特徴とする、請求項1~4のいずれか1項に記載の組成物。 The at least one bacterial strain or extract or component thereof is C. C. elegans, including C. elegans animals. When administered to C. elegans cultures, the C. elegans culture. The C. elegans culture. The average pharyngeal pumping activity of C. elegans animals was greater than that of equivalent C. elegans animals without administration of said at least one bacterial strain or extract or component thereof. C. elegans culture. Composition according to any one of claims 1 to 4, characterized in that it is increased by at least 20% compared to that of P. elegans animals. 前記少なくとも1つの細菌株またはその抽出物もしくはその成分が、C.elegans動物を含むC.elegans培養物に投与されるとき、前記C.elegans培養物中の前記C.elegans動物の平均運動速度は、前記少なくとも1つの細菌株またはその抽出物もしくはその成分の投与なし同等のC.elegans培養物中のC.elegans動物のものと比較して、少なくとも20%増加するという点を特徴とする、請求項1~5のいずれか1項に記載の組成物。 The at least one bacterial strain or extract or component thereof is C. C. elegans, including C. elegans animals. When administered to C. elegans cultures, the C. elegans culture. The C. elegans culture. The average locomotor speed of C. elegans animals was higher than that of the equivalent C. elegans animals without administration of said at least one bacterial strain or extract or component thereof. C. elegans culture. Composition according to any one of claims 1 to 5, characterized in that it is increased by at least 20% compared to that of P. elegans animals. 前記少なくとも1つの細菌株またはその抽出物もしくはその成分が、C.elegans動物を含むC.elegans培養物に投与されるとき、前記C.elegans培養物中の前記C.elegans動物の生殖能力は、前記少なくとも1つの細菌株またはその抽出物もしくはその成分の投与なし同等のC.elegans培養物中のC.elegans動物のものと比較して、少なくとも20%低下するという点を特徴とする、請求項1~6のいずれか1項に記載の組成物。 The at least one bacterial strain or extract or component thereof is C. C. elegans, including C. elegans animals. When administered to C. elegans cultures, the C. elegans culture. The C. elegans culture. The reproductive capacity of C. elegans animals is affected by the equivalent C. elegans without administration of said at least one bacterial strain or extracts thereof or components thereof. C. elegans culture. Composition according to any one of claims 1 to 6, characterized in that it is reduced by at least 20% compared to that of P. elegans animals. 前記少なくとも1つの細菌株またはその抽出物もしくはその成分が、C.elegans動物を含むC.elegans培養物が紫外線照射にさらされるとき、前記少なくとも1つの細菌株またはその抽出物もしくはその成分が投与された前記C.elegans培養物中の前記C.elegans動物の平均生存時間が、前記少なくとも1つの細菌株またはその抽出物もしくはその成分の投与なし同等のC.elegans培養物中のC.elegans動物のものと比較して、少なくとも20%増加するという点を特徴とする、請求項1~7のいずれか1項に記載の組成物。 The at least one bacterial strain or extract or component thereof is C. C. elegans, including C. elegans animals. When the C. elegans culture is exposed to ultraviolet radiation, said at least one bacterial strain or extract or component thereof has been administered. The C. elegans culture. The mean survival time of C. elegans animals is the same as that of C. elegans animals without administration of said at least one bacterial strain or extract or component thereof. C. elegans culture. Composition according to any one of claims 1 to 7, characterized in that it is increased by at least 20% compared to that of P. elegans animals. 前記少なくとも1つの細菌株またはその抽出物もしくはその成分が、C.elegans動物を含むC.elegans培養物が高温にさらされるとき、前記少なくとも1つの細菌株またはその抽出物もしくはその成分が投与された前記C.elegans培養物中のC.elegans動物の平均生存時間が、前記少なくとも1つの細菌株またはその抽出物もしくはその成分の投与なし同等のC.elegans培養物中のC.elegans動物のものと比較して、少なくとも20%増加するという点を特徴とする、請求項1~8のいずれか1項に記載の組成物。 The at least one bacterial strain or extract or component thereof is C. C. elegans, including C. elegans animals. When the C. elegans culture is exposed to high temperatures, the at least one bacterial strain or extract or component thereof has been administered. C. elegans culture. The mean survival time of C. elegans animals is the same as that of C. elegans animals without administration of said at least one bacterial strain or extract or component thereof. C. elegans culture. Composition according to any one of claims 1 to 8, characterized in that it is increased by at least 20% compared to that of P. elegans animals. 前記高温が、少なくとも37℃である、請求項9に記載の組成物。 10. The composition of claim 9, wherein the elevated temperature is at least 37<0>C. 前記少なくとも1つの細菌株またはその抽出物もしくはその成分が、C.elegans動物を含むC.elegans培養物に投与されるとき、前記C.elegans培養物中の前記C.elegan動物において観察される腸脂肪の平均量が、前記少なくとも1つの細菌株またはその抽出物もしくはその成分の投与なし同等のC.elegans培養物中のC.elegans動物のものと比較して、少なくとも20%低下するという点を特徴とする、請求項1~10のいずれか1項に記載の組成物。 The at least one bacterial strain or extract or component thereof is C. C. elegans, including C. elegans animals. When administered to C. elegans cultures, the C. elegans culture. The C. elegans culture. The average amount of intestinal fat observed in C. elegan animals was higher than that of the equivalent C. elegan without administration of said at least one bacterial strain or extract or component thereof. C. elegans culture. Composition according to any one of claims 1 to 10, characterized in that it is reduced by at least 20% compared to that of P. elegans animals. 前記C.elegans動物が、成体C.elegans動物である、請求項4~11のいずれか1項に記載の組成物。 Said C. elegans animals are infected with adult C. elegans animals. The composition according to any one of claims 4 to 11, which is a P. elegans animal. 前記C.elegans動物が、少なくとも5日齢である、請求項4~12のいずれか1項に記載の組成物。 Said C. Composition according to any one of claims 4 to 12, wherein the P. elegans animal is at least 5 days old. 前記組成物が、経口投与用に配合される、請求項1~13のいずれか1項に記載の組成物。 A composition according to any one of claims 1 to 13, wherein the composition is formulated for oral administration. 前記組成物が、食品、飲料、飼料組成物、または栄養補助食品である、請求項1~14のいずれか1項に記載の組成物。 A composition according to any one of claims 1 to 14, wherein the composition is a food, beverage, feed composition, or nutritional supplement. 前記組成物が、液体、シロップ、錠剤、トローチ、グミ、カプセル、粉末、ゲル、またはフィルムである、請求項1~15のいずれか1項に記載の組成物。 A composition according to any one of claims 1 to 15, wherein the composition is a liquid, syrup, tablet, troche, gummy, capsule, powder, gel, or film. 前記組成物が、医薬組成物である、請求項1~16のいずれか1項に記載の組成物。 A composition according to any one of claims 1 to 16, wherein the composition is a pharmaceutical composition. 前記組成物が、腸溶コーティングされた製剤である、請求項1~17のいずれか1項に記載の組成物。 A composition according to any one of claims 1 to 17, wherein the composition is an enteric coated formulation. 対象への投与用である、請求項1~18のいずれか1項に記載の組成物。 A composition according to any one of claims 1 to 18, which is for administration to a subject . 前記対象の寿命を延長するためのものである、請求項19に記載の組成物20. The composition of claim 19, wherein the composition is for extending the lifespan of the subject. 前記対象の前記寿命が、前記組成物の投与なし同等の対象のものと比較して、少なくとも20%延長される、請求項20に記載の組成物21. The composition of claim 20, wherein the lifespan of the subject is increased by at least 20% compared to that of an equivalent subject without administration of the composition. 前記対象の少なくとも1つの年齢関連の症状または状態の発症を低減または遅延させるためのものである、請求項19に記載の組成物20. The composition of claim 19, wherein the composition is for reducing or delaying the onset of at least one age-related symptom or condition in the subject . 前記少なくとも1つの年齢関連の症状または状態が、前記組成物の投与なし同等の対象のものと比較して、前記対象において少なくとも20%低減または遅延される、請求項22に記載の組成物23. The composition of claim 22, wherein the at least one age-related symptom or condition is reduced or delayed in the subject by at least 20% compared to that of an equivalent subject without administration of the composition. 前記少なくとも1つの年齢関連の症状または状態が、前記対象の筋肉及び/または神経筋機能の低下であるか、またはそれを含む、請求項22または23に記載の組成物24. The composition of claim 22 or 23, wherein the at least one age-related symptom or condition is or comprises a decline in muscle and/or neuromuscular function of the subject. 前記少なくとも1つの年齢関連の症状または状態が、脂質代謝の調節不全であるか、またはそれを含む、請求項22~24のいずれか1項に記載の組成物 25. A composition according to any one of claims 22 to 24, wherein the at least one age-related symptom or condition is or comprises dysregulation of lipid metabolism. 前記対象が、少なくとも30歳である、請求項19~25のいずれか1項に記載の組成物 Composition according to any one of claims 19 to 25, wherein the subject is at least 30 years old. 前記対象が、高齢対象である、請求項19~26のいずれか1項に記載の組成物 Composition according to any one of claims 19 to 26, wherein the subject is an elderly subject. 前記対象が、哺乳動物である、請求項19~27のいずれか1項に記載の組成物 The composition according to any one of claims 19 to 27, wherein the subject is a mammal. 前記対象が、ヒトである、請求項19~28のいずれか1項に記載の組成物 The composition according to any one of claims 19 to 28, wherein the subject is a human. 前記対象の微生物叢にコロニーを形成するのに十分な量投与される、請求項19~29のいずれか1項に記載の組成物 Composition according to any one of claims 19 to 29, administered in an amount sufficient to colonize the microbial flora of said subject. 対象の寿命を延長するための組成物であって、前記組成物が少なくとも1つの細菌株またはその抽出物もしくはその成分を含み、前記少なくとも1つの細菌株が、Gluconobacter属、Acetobacter属、Gluconoacaetobacter属、Acidomonas属、Ameyamaea属、Asaia属、Granulibacter属、Kozakia属、Neoasaia属、Neokomagataea属、Saccharibacter属、Swaminathania属、Tanticharoenia属、またはそれらの組み合わせを含む、前記組成物 A composition for extending the lifespan of a subject, the composition comprising at least one bacterial strain or an extract thereof or a component thereof, wherein the at least one bacterial strain is a member of the genus Gluconobacter, the genus Acetobacter, the genus Gluconoacaetobacter, Genus Acidomonas, Genus Ameyamaea, Genus Asaia, Genus Granulibacter, Genus Kozakia, Genus Neoasaia, Genus Neokomagataea, Genus Saccharibacter, Genus Swaminathania, Tantichar oenia sp., or a combination thereof. 前記少なくとも1つの細菌株が、Gluconacetobacter hansenii、Gluconobacter oxydans、Acetobacter aceti、またはそれらの組み合わせを含む、請求項31に記載の組成物32. The composition of claim 31, wherein the at least one bacterial strain comprises Gluconacetobacter hansenii, Gluconobacter oxydans, Acetobacter aceti, or a combination thereof. 前記少なくとも1つの細菌株が、Gluconacetobacter hanseniiを含む、請求項31または32に記載の組成物33. The composition of claim 31 or 32, wherein the at least one bacterial strain comprises Gluconacetobacter hansenii. 対象における少なくとも1つの年齢関連の症状もしくは状態の発症を低減または遅延させるための組成物であって、前記組成物が少なくとも1つの細菌株またはその抽出物もしくは成分を含み、前記少なくとも1つの細菌株が、Gluconobacter属、Acetobacter属、Gluconoacaetobacter属、Acidomonas属、Ameyamaea属、Asaia属、Granulibacter属、Kozakia属、Neoasaia属、Neokomagataea属、Saccharibacter属、Swaminathania属、Tanticharoenia属、またはそれらの組み合わせを含む、前記組成物 A composition for reducing or delaying the onset of at least one age-related symptom or condition in a subject, said composition comprising at least one bacterial strain or an extract or component thereof, said at least one bacterial strain The genus Gluconobacter, the genus Acetobacter, the genus Gluconoacaetobacter, the genus Acidomonas, the genus Ameyamaea, the genus Asaia, the genus Granulibacter, the genus Kozakia, the genus Neoasaia, and the genus Neoasaia. The composition comprises the genus Omagataea, the genus Saccharibacter, the genus Swaminathania, the genus Tanticharoenia, or a combination thereof. Things . 前記少なくとも1つの細菌株が、Gluconacetobacter hansenii、Gluconobacter oxydans、Acetobacter aceti、またはそれらの組み合わせを含む、請求項34に記載の組成物35. The composition of claim 34, wherein the at least one bacterial strain comprises Gluconacetobacter hansenii, Gluconobacter oxydans, Acetobacter aceti, or a combination thereof. 前記少なくとも1つの細菌株が、Gluconacetobacter hanseniiを含む、請求項34または35に記載の組成物 36. The composition of claim 34 or 35, wherein the at least one bacterial strain comprises Gluconacetobacter hansenii. 前記少なくとも1つの年齢関連の症状または状態が、組成物の投与なし同等の対象のものと比較して、前記対象において少なくとも20%低減または遅延される、請求項34に記載の組成物35. The composition of claim 34, wherein the at least one age-related symptom or condition is reduced or delayed in the subject by at least 20% compared to that of an equivalent subject without administration of the composition. 前記少なくとも1つの年齢関連の症状または状態が、前記対象の筋肉及び/または神経筋機能の低下であるか、またはそれを含む、請求項34~37のいずれか1項に記載の組成物38. A composition according to any one of claims 34 to 37, wherein the at least one age-related symptom or condition is or comprises a decline in muscle and/or neuromuscular function of the subject. 前記少なくとも1つの年齢関連の症状または状態が、脂質代謝の調節不全であるか、またはそれを含む、請求項34~38のいずれか1項に記載の組成物 39. A composition according to any one of claims 34 to 38, wherein the at least one age-related symptom or condition is or comprises dysregulation of lipid metabolism. 前記対象が、少なくとも30歳である、請求項34~39のいずれか1項に記載の組成物 A composition according to any one of claims 34 to 39, wherein the subject is at least 30 years old. 前記対象が、高齢対象である、請求項34~40のいずれか1項に記載の組成物 Composition according to any one of claims 34 to 40, wherein the subject is an elderly subject. 前記対象が、哺乳動物である、請求項34~41のいずれか1項に記載の組成物 The composition according to any one of claims 34 to 41, wherein the subject is a mammal. 前記対象が、ヒトである、請求項34~42のいずれか1項に記載の組成物 The composition according to any one of claims 34 to 42, wherein the subject is a human. 対象の寿命、年齢関連の症状、及び/または年齢関連の状態を修正する1つ以上の微生物株の能力を特徴付ける方法であって、
(a)哺乳動物微生物叢の複数の微生物株を複数のC.elegans培養物に添加することであって、異なる微生物株を各C.elegans培養物に添加し、各培養物が、同じC.elegans株のC.elegans動物を含む、前記添加することと、
(b)前記複数の微生物株の各微生物株が、各培養物の前記C.elegans動物の1つ以上のパラメータに影響を及ぼすかどうかを決定することであって、前記1つ以上のパラメータが、老化、年齢関連の症状、及び/または年齢関連の状態に関連する、前記決定することと、を含む、前記方法。
A method of characterizing the ability of one or more microbial strains to modify lifespan, age-related symptoms, and/or age-related conditions in a subject, the method comprising:
(a) Multiple microbial strains of the mammalian microbiome are combined with multiple C. elegans culture, by adding different microbial strains to each C. elegans culture. C. elegans cultures, each culture containing the same C. elegans culture. C. elegans strain. elegans animal;
(b) Each of the microbial strains of the plurality of microbial strains is selected from the C. elegans animal, wherein the one or more parameters are associated with aging, an age-related symptom, and/or an age-related condition. The method comprises:
対象の寿命、年齢関連の症状、及び/または年齢関連の状態を修正する1つ以上の微生物株の能力を特徴付けるための、C.elegans動物の、使用。 C. for characterizing the ability of one or more microbial strains to modify the lifespan, age-related symptoms, and/or age-related conditions of a subject. elegans animals, use. 前記少なくとも1つの細菌株またはその抽出物もしくはその成分、及び前記賦形剤を組み合わせることを含む、請求項1~30のいずれか1項に記載の組成物の作製方法。 31. A method of making a composition according to any one of claims 1 to 30 , comprising combining said at least one bacterial strain or an extract thereof or a component thereof and said excipient.
JP2022520294A 2019-10-01 2020-09-23 Compositions and methods for extending life Pending JP2022551584A (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201962909186P 2019-10-01 2019-10-01
US62/909,186 2019-10-01
PCT/US2020/052251 WO2021067100A1 (en) 2019-10-01 2020-09-23 Compositions and methods for extending lifespan

Publications (2)

Publication Number Publication Date
JP2022551584A JP2022551584A (en) 2022-12-12
JPWO2021067100A5 true JPWO2021067100A5 (en) 2023-09-28

Family

ID=75337328

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2022520294A Pending JP2022551584A (en) 2019-10-01 2020-09-23 Compositions and methods for extending life

Country Status (9)

Country Link
US (1) US20220330597A1 (en)
EP (1) EP4037697A4 (en)
JP (1) JP2022551584A (en)
KR (1) KR20220073796A (en)
CN (1) CN114555102A (en)
AU (1) AU2020359357A1 (en)
CA (1) CA3153779A1 (en)
IL (1) IL291798A (en)
WO (1) WO2021067100A1 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114365845B (en) * 2022-02-18 2023-03-28 吉林大学 Plant fermentation composition and preparation method and application thereof

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008214215A (en) * 2007-03-01 2008-09-18 Mitsukan Group Honsha:Kk Composition having apoptosis induction ability
US20160051596A1 (en) * 2014-08-21 2016-02-25 Food Industry Research And Development Institute Novel acetobacter and gluconacetobacter strains and their metabolites for use in inhibiting xanthine oxidase
US10722543B2 (en) * 2016-01-28 2020-07-28 Oxyrase, Inc. Methods for inhibiting tumor growth using anaerobe microorganisms
JP2018131416A (en) * 2017-02-16 2018-08-23 国立大学法人 鹿児島大学 Immunopotentiators and methods of making the same
WO2019043951A1 (en) * 2017-09-04 2019-03-07 キユーピー株式会社 Food composition containing cells of acetic acid bacterium, and method for producing same
WO2019147652A1 (en) * 2018-01-23 2019-08-01 The General Hospital Corporation Compositions and methods for improving mitochondrial function
US11284609B2 (en) * 2019-09-12 2022-03-29 MarvelBiome, Inc. Compositions and methods for characterizing a microbiome

Similar Documents

Publication Publication Date Title
US11872255B2 (en) Methods and compositions of preventing and treating dental caries
JP4455333B2 (en) Probiotic bacteria: Lactobacillus fermentum
CN109419814B (en) Application of paradisella gordonii to inhibition of fatty liver disease
EP3560506A1 (en) Pharmaceutical composition comprising indigo pulverata levis extract or fraction thereof as effective ingredient for preventing or treating inflammatory bowel disease
CN106994134B (en) Application of intestinal probiotics in prevention and/or treatment of diabetes and related diseases thereof
Hoseinifar et al. Dietary apple peel-derived pectin improved growth performance, antioxidant enzymes and immune response in common carp, Cyprinus carpio (Linnaeus, 1758)
WO2018090983A9 (en) Saponin compound for improving intestinal microflora, preparation method and use thereof
CN113925923B (en) Anti-acne and whitening compound probiotic composition and preparation method thereof
JP5945092B2 (en) Neutral fat reducing agent
JP2020516699A (en) Tumor Chemotherapy Microbial Agents to Prevent Enterotoxicity
CN109419816B (en) Application of bacteroides cellulolyticus in preventing and/or treating heart diseases
NO331751B1 (en) Use of dietary fiber or a mixture of dietary fiber for the preparation of a composition for oral administration for the treatment of systemic infections in fish.
JP2022508125A (en) Use of Lactobacillus plantarum TWK10 in the manufacture of probiotic compositions for post-exercise inflammation or body fat reduction
JP5843169B2 (en) Fructose absorption inhibitor
JP2018532380A (en) Enterobacteriaceae butyric acid intestini and uses thereof
WO2019109348A1 (en) Use of butyribacter intestini in preventing and/or treating inflammation-related diseases
JPWO2021067100A5 (en)
WO1998035664A1 (en) Athletic endurance increasing agent in food
Asok et al. Probiotics and periodontal disease
CN110869035A (en) Application of xenobacter saxifragi in preparation of composition for preventing and/or treating lipid metabolism-related diseases
KR102158598B1 (en) Composition for preventing or treating behcet&#39;s diseases or herpes simplex virus infection containing lactobacillus animalis
JP2018118915A (en) Non-alcoholic liver injury inhibitor
JP2014005225A (en) Agent for suppressing appetite improvement and body weight gain
JP2022552759A (en) Composition for prevention or treatment of obesity or obesity-induced metabolic syndrome containing Enterococcus faecalis as an active ingredient
CN106974940B (en) Application of probiotics of scleritis in treating and preventing obesity and related diseases