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dc.contributor.authorWang, S.P.es_ES
dc.contributor.authorRubio, Luis A.es_ES
dc.contributor.authorDuncan, Sylvia H.es_ES
dc.contributor.authorDonachie, G. E.es_ES
dc.contributor.authorHoltrop, Grietjees_ES
dc.contributor.authorLo, Galianaes_ES
dc.contributor.authorFarquharson, F.Mes_ES
dc.contributor.authorWagner, J.es_ES
dc.contributor.authorParkhill, Julianes_ES
dc.contributor.authorLouis, P.es_ES
dc.contributor.authorWalker, Alan W.es_ES
dc.contributor.authorFlint, Harry J.es_ES
dc.date.accessioned2020-12-16T09:20:28Z-
dc.date.available2020-12-16T09:20:28Z-
dc.date.issued2020-
dc.identifierdoi: 10.1128/MSYSTEMS.00645-20-
dc.identifierissn: 2379-5077-
dc.identifier.citationmSystems 5 (2020)es_ES
dc.identifier.urihttp://hdl.handle.net/10261/225006-
dc.description.abstractLactate can be produced by many gut bacteria, but in adults its accumulation in the colon is often an indicator of microbiota perturbation. Using continuous culture anaerobic fermentor systems, we found that lactate concentrations remained low in communities of human colonic bacteria maintained at pH 6.5, even when DL-lactate was infused at 10 or 20 mM. In contrast, lower pH (5.5) led to periodic lactate accumulation following lactate infusion in three fecal microbial communities examined. Lactate accumulation was concomitant with greatly reduced butyrate and propionate production and major shifts in microbiota composition, with Bacteroidetes and anaerobic Firmicutes being replaced by Actinobacteria, lactobacilli, and Proteobacteria. Pure-culture experiments confirmed that Bacteroides and Firmicutes isolates were susceptible to growth inhibition by relevant concentrations of lactate and acetate, whereas the lactate-producer Bifidobacterium adolescentis was resistant. To investigate system behavior further, we used a mathematical model (microPop) based on 10 microbial functional groups. By incorporating differential growth inhibition, our model reproduced the chaotic behavior of the system, including the potential for lactate infusion both to promote and to rescue the perturbed system. The modeling revealed that system behavior is critically dependent on the proportion of the community able to convert lactate into butyrate or propionate. Communities with low numbers of lactate-utilizing bacteria are inherently less stable and more prone to lactate-induced perturbations. These findings can help us to understand the consequences of interindividual microbiota variation for dietary responses and microbiota changes associated with disease states. IMPORTANCE Lactate is formed by many species of colonic bacteria, and can accumulate to high levels in the colons of inflammatory bowel disease subjects. Conversely, in healthy colons lactate is metabolized by lactate-utilizing species to the short-chain fatty acids butyrate and propionate, which are beneficial for the host. Here, we investigated the impact of continuous lactate infusions (up to 20 mM) at two pH values (6.5 and 5.5) on human colonic microbiota responsiveness and metabolic outputs. At pH 5.5 in particular, lactate tended to accumulate in tandem with decreases in butyrate and propionate and with corresponding changes in microbial composition. Moreover, microbial communities with low numbers of lactate-utilizing bacteria were inherently less stable and therefore more prone to lactate-induced perturbations. These investigations provide clear evidence of the important role these lactate utilizers may play in health maintenance. These should therefore be considered as potential new therapeutic probiotics to combat microbiota perturbations.-
dc.description.sponsorshipThe Rowett Institute and BioSS receive core financial support from the Scottish Government Rural and Environmental Sciences and Analytical Services (SG-RESAS). S.P.W. gratefully acknowledges the Rongchang campus of Southwest University, Chongqing, China, for financial support. L.A.R. acknowledges receipt of a Salvador de Madariaga scholarship (PRX16/00148) from the Spanish Ministry of Education, and MICIIN (project AGL 2017-83772R) for publication costs. J.W., J.P., and 16S rRNA gene sequencing costs were funded by the Wellcome Trust (grant WT098051).-
dc.languageeng-
dc.relationinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/AGL 2017-83772R-
dc.relation.isversionofPublisher's version-
dc.rightsopenAccess-
dc.titlePivotal roles for pH, lactate, and lactate-utilizing bacteria in the stability of a human colonic microbial ecosystemes_ES
dc.typeartículoes_ES
dc.identifier.doi10.1128/MSYSTEMS.00645-20-
dc.relation.publisherversionhttps://msystems.asm.org/content/5/5/e00645-20-
dc.date.updated2020-12-16T09:20:29Z-
dc.rights.licensehttp://creativecommons.org/licenses/by/4.0/-
dc.contributor.funderScottish Government's Rural and Environment Science and Analytical Services-
dc.contributor.funderSouthwest University-
dc.contributor.funderMinisterio de Ciencia e Innovación (España)-
dc.relation.csices_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100004837es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100006250es_ES
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextopen-
item.fulltextWith Fulltext-
item.openairetypeartículo-
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