2022
DOI: 10.1128/msystems.00893-22
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Persistence and In Vivo Evolution of Vaginal Bacterial Strains over a Multiyear Time Period

Abstract: The stability of strains within the vaginal microbiota is largely uncharacterized. Should these strains be capable of persisting for extended periods of time, they could evolve within their host in response to selective pressures exerted by the host or by other members of the community.

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Cited by 8 publications
(11 citation statements)
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“…Future studies could analyse sub-CSTs, but this would greatly increase the number of possible transitions, thereby raising an acute statistical challenge (here we already had to collapse CSTs I, II, and V to introduce covariates into the model). In the same vein, analysing metagenomics data could provide additional valuable insights on vaginal microbiota long-term dynamics [21]. For example, for women who appear to have stable CSTs, we could identify the proportion of lineage replacements.…”
Section: Discussionmentioning
confidence: 99%
“…Future studies could analyse sub-CSTs, but this would greatly increase the number of possible transitions, thereby raising an acute statistical challenge (here we already had to collapse CSTs I, II, and V to introduce covariates into the model). In the same vein, analysing metagenomics data could provide additional valuable insights on vaginal microbiota long-term dynamics [21]. For example, for women who appear to have stable CSTs, we could identify the proportion of lineage replacements.…”
Section: Discussionmentioning
confidence: 99%
“…may require persistence at low levels for many years. A recent study provides evidence of persistence of several vaginal bacterial strains in reproductive age women for more than a year (France et al, 2022b).…”
Section: Discussionmentioning
confidence: 99%
“…For each lawn isolate, optical density of mid exponential phase cells was measured. Roughly 2.5 x 10 7 cells (adjusted to 0.5 x 10 7 for S. aureus to offset higher growth of this species) were added to 50 mL conical tubes along with 35 mL of molten soft TSA. Tubes were mixed by inverting 4 times, then poured into Nunc OmniTrays (Thermo Scientific 242811).…”
Section: Methodsmentioning
confidence: 99%
“…Tubes were mixed by inverting 4 times, then poured into Nunc OmniTrays (Thermo Scientific 242811). Plates were allowed to cool for up to 2 h. While plates cooled, spot cultures were prepared by normalizing the OD of late log-phase sub-cultures to OD 0.1 (roughly 6 x 10 7 CFU/mL) in fresh TSB. A 96-well pipettor (Avidien MicroPro300) was used to dispense 2 µL of spot culture onto each plate.…”
Section: Methodsmentioning
confidence: 99%