Journal article
Pathogen invasion-dependent tissue reservoirs and plasmid-encoded antibiotic degradation boost plasmid spread in the gut
- Abstract:
- Many plasmids encode antibiotic resistance genes. Through conjugation, plasmids can be rapidly disseminated. Previous work identified gut luminal donor/recipient blooms and tissue-lodged plasmid-bearing persister cells of the enteric pathogen; Salmonella enterica; serovar Typhimurium (; S; .Tm) that survive antibiotic therapy in host tissues, as factors promoting plasmid dissemination among Enterobacteriaceae. However, the buildup of tissue reservoirs and their contribution to plasmid spread await experimental demonstration. Here, we asked if re-seeding-plasmid acquisition-invasion cycles by; S; .Tm could serve to diversify tissue-lodged plasmid reservoirs, and thereby promote plasmid spread. Starting with intraperitoneal mouse infections, we demonstrate that; S; .Tm cells re-seeding the gut lumen initiate clonal expansion. Extended spectrum beta-lactamase (ESBL) plasmid-encoded gut luminal antibiotic degradation by donors can foster recipient survival under beta-lactam antibiotic treatment, enhancing transconjugant formation upon re-seeding.; S; .Tm transconjugants can subsequently re-enter host tissues introducing the new plasmid into the tissue-lodged reservoir. Population dynamics analyses pinpoint recipient migration into the gut lumen as rate-limiting for plasmid transfer dynamics in our model. Priority effects may be a limiting factor for reservoir formation in host tissues. Overall, our proof-of-principle data indicates that luminal antibiotic degradation and shuttling between the gut lumen and tissue-resident reservoirs can promote the accumulation and spread of plasmids within a host over time
- Publication status:
- Published
- Peer review status:
- Peer reviewed
Actions
Access Document
- Files:
-
-
(Version of record, plain, 2.5KB, Terms of use)
-
- Publisher copy:
- 10.7554/elife.69744
- Publication website:
- https://edoc.unibas.ch/87045/1/20220119125504_61e7fc1876ae4.pdf
Authors
+ Gebert Rüf Stiftung
More from this funder
- Funder identifier:
- 10.13039/501100003357
- Grant:
- GRS-060/18
+ Boehringer Ingelheim Fonds
More from this funder
- Funder identifier:
- 10.13039/501100001645
- Grant:
- PhD Fellowship
+ Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
More from this funder
- Funder identifier:
- 10.13039/501100001711
- Grant:
- 407240_167121
- Publisher:
- eLife Sciences Publications
- Journal:
- eLife More from this journal
- Volume:
- 10
- Pages:
- e69744
- Article number:
- e69744
- Publication date:
- 2021-11-11
- Acceptance date:
- 2021-11-10
- DOI:
- EISSN:
-
2050-084X
- ISSN:
-
2050-084X
- Language:
-
English
- Keywords:
- Pubs id:
-
1339589
- Local pid:
-
pubs:1339589
- Source identifiers:
-
W4226112836
- Deposit date:
-
2026-05-07
- ARK identifier:
This ORA record was generated from metadata provided by an external service. It has not been edited by the ORA Team.
Terms of use
- Copyright date:
- 2021
- Licence:
- CC Attribution (CC BY)
If you are the owner of this record, you can report an update to it here: Report update to this record