Microbial evolution in the long-lived gut

Bibliographic Details
Main Author: Melo-Miranda, Rita
Publication Date: 2023
Other Authors: Pinto, Ana, Sousa, Ana
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: http://hdl.handle.net/10773/41259
Summary: Aging, one of the biggest health challenges of our time, is associated with several occurrences, including an increase in inflammation and gut microbial dysbiosis. These events contribute to aging by rising intestinal permeability and inflammation, but how they influence microbiota evolution and pathobiont selection remains poorly understood. Previous work described the adaptation of an E. coli commensal strain to the gut of young animals (6-9 weeks old) and showed that it acquires metabolism-related mutations, whereas, in old mice (19 months old), the pattern is shifted towards stress-related mutations, and metabolic adaptations arise slower. Here, to further understand features associated with longevity, we compared the microbial evolution in the guts of these two age groups with very old animals (25 months old). Remarkably, while very old mice were the frailest, they did not show higher intestinal inflammation than any of the two. Also, when compared with the other age groups, very old mice showed an increase in health-associated bacteria, e.g., Akkermansia muciniphila and Oscillospira sp. Interestingly, E. coli evolution in the gut of very old mice resembled the pattern found in young animals, as it displayed more metabolic than stress-related mutations. Also, it shared certain mutational targets with young mice that are absent in the old, and conversely, it shared mutations with the old that are absent in young animals. Additionally, E. coli’s evolutionary signature potentially targeted different phenotypes, such as motility and biofilm formation, according to the parallel gene-inactivating mutations observed in fimE. These findings suggest that the microbial evolution signature in the guts of long-lived mice shares similarities with both young and old mice, while also bearing unique features that may be associated with longevity.
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spelling Microbial evolution in the long-lived gutAgingMicrobial evolutionLongevityAging, one of the biggest health challenges of our time, is associated with several occurrences, including an increase in inflammation and gut microbial dysbiosis. These events contribute to aging by rising intestinal permeability and inflammation, but how they influence microbiota evolution and pathobiont selection remains poorly understood. Previous work described the adaptation of an E. coli commensal strain to the gut of young animals (6-9 weeks old) and showed that it acquires metabolism-related mutations, whereas, in old mice (19 months old), the pattern is shifted towards stress-related mutations, and metabolic adaptations arise slower. Here, to further understand features associated with longevity, we compared the microbial evolution in the guts of these two age groups with very old animals (25 months old). Remarkably, while very old mice were the frailest, they did not show higher intestinal inflammation than any of the two. Also, when compared with the other age groups, very old mice showed an increase in health-associated bacteria, e.g., Akkermansia muciniphila and Oscillospira sp. Interestingly, E. coli evolution in the gut of very old mice resembled the pattern found in young animals, as it displayed more metabolic than stress-related mutations. Also, it shared certain mutational targets with young mice that are absent in the old, and conversely, it shared mutations with the old that are absent in young animals. Additionally, E. coli’s evolutionary signature potentially targeted different phenotypes, such as motility and biofilm formation, according to the parallel gene-inactivating mutations observed in fimE. These findings suggest that the microbial evolution signature in the guts of long-lived mice shares similarities with both young and old mice, while also bearing unique features that may be associated with longevity.2024-03-27T10:14:00Z2023-10-01T00:00:00Z2023-10conference objectinfo:eu-repo/semantics/publishedVersionapplication/pdfhttp://hdl.handle.net/10773/41259engMelo-Miranda, RitaPinto, AnaSousa, Anainfo:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2024-05-06T04:54:32Zoai:ria.ua.pt:10773/41259Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T14:24:00.348123Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv Microbial evolution in the long-lived gut
title Microbial evolution in the long-lived gut
spellingShingle Microbial evolution in the long-lived gut
Melo-Miranda, Rita
Aging
Microbial evolution
Longevity
title_short Microbial evolution in the long-lived gut
title_full Microbial evolution in the long-lived gut
title_fullStr Microbial evolution in the long-lived gut
title_full_unstemmed Microbial evolution in the long-lived gut
title_sort Microbial evolution in the long-lived gut
author Melo-Miranda, Rita
author_facet Melo-Miranda, Rita
Pinto, Ana
Sousa, Ana
author_role author
author2 Pinto, Ana
Sousa, Ana
author2_role author
author
dc.contributor.author.fl_str_mv Melo-Miranda, Rita
Pinto, Ana
Sousa, Ana
dc.subject.por.fl_str_mv Aging
Microbial evolution
Longevity
topic Aging
Microbial evolution
Longevity
description Aging, one of the biggest health challenges of our time, is associated with several occurrences, including an increase in inflammation and gut microbial dysbiosis. These events contribute to aging by rising intestinal permeability and inflammation, but how they influence microbiota evolution and pathobiont selection remains poorly understood. Previous work described the adaptation of an E. coli commensal strain to the gut of young animals (6-9 weeks old) and showed that it acquires metabolism-related mutations, whereas, in old mice (19 months old), the pattern is shifted towards stress-related mutations, and metabolic adaptations arise slower. Here, to further understand features associated with longevity, we compared the microbial evolution in the guts of these two age groups with very old animals (25 months old). Remarkably, while very old mice were the frailest, they did not show higher intestinal inflammation than any of the two. Also, when compared with the other age groups, very old mice showed an increase in health-associated bacteria, e.g., Akkermansia muciniphila and Oscillospira sp. Interestingly, E. coli evolution in the gut of very old mice resembled the pattern found in young animals, as it displayed more metabolic than stress-related mutations. Also, it shared certain mutational targets with young mice that are absent in the old, and conversely, it shared mutations with the old that are absent in young animals. Additionally, E. coli’s evolutionary signature potentially targeted different phenotypes, such as motility and biofilm formation, according to the parallel gene-inactivating mutations observed in fimE. These findings suggest that the microbial evolution signature in the guts of long-lived mice shares similarities with both young and old mice, while also bearing unique features that may be associated with longevity.
publishDate 2023
dc.date.none.fl_str_mv 2023-10-01T00:00:00Z
2023-10
2024-03-27T10:14:00Z
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