Microbial evolution in the long-lived gut
Main Author: | |
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Publication Date: | 2023 |
Other Authors: | , |
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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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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conference object |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
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publishedVersion |
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http://hdl.handle.net/10773/41259 |
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http://hdl.handle.net/10773/41259 |
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eng |
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openAccess |
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