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Parallel evolution leading to impaired biofilm formation in invasive Salmonella strains

Abstract:
Pathogenic Salmonella strains that cause gastroenteritis are able to colonize and replicate within the intestines of multiple host species. In general, these strains have retained an ability to form the rdar morphotype, a resistant biofilm physiology hypothesized to be important for Salmonella transmission. In contrast, Salmonella strains that are host-adapted or even host-restricted like Salmonella enterica serovar Typhi, tend to cause systemic infections and have lost the ability to form the rdar morphotype. Here, we investigated the rdar morphotype and CsgD-regulated biofilm formation in two non-typhoidal Salmonella (NTS) strains that caused invasive disease in Malawian children, S. Typhimurium D23580 and S. Enteritidis D7795, and compared them to a panel of NTS strains associated with gastroenteritis, as well as S. Typhi strains. Sequence comparisons combined with luciferase reporter technology identified key SNPs in the promoter region of csgD that either shut off biofilm formation completely (D7795) or reduced transcription of this key biofilm regulator (D23580). Phylogenetic analysis showed that these SNPs are conserved throughout the African clades of invasive isolates, dating as far back as 80 years ago. S. Typhi isolates were negative for the rdar morphotype due to truncation of eight amino acids from the C-terminus of CsgD. We present new evidence in support of parallel evolution between lineages of nontyphoidal Salmonella associated with invasive disease in Africa and the archetypal host-restricted invasive serovar; S. Typhi. We hypothesize that the African invasive isolates are becoming human-adapted and 'niche specialized' with less reliance on environmental survival, as compared to gastroenteritis-causing isolates.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1371/journal.pgen.1008233

Authors

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Role:
Author
ORCID:
0000-0003-2568-6005
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Institution:
University of Oxford
Division:
MSD
Department:
NDM
Sub department:
Tropical Medicine
Role:
Author
ORCID:
0000-0001-7780-2173
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Role:
Author
ORCID:
0000-0003-1133-8093
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Role:
Author
ORCID:
0000-0001-8401-0860


Publisher:
Public Library of Science
Journal:
PLoS Genetics More from this journal
Volume:
15
Issue:
6
Article number:
e1008233
Publication date:
2019-06-24
Acceptance date:
2019-06-07
DOI:
EISSN:
1553-7404
ISSN:
1553-7390
Pmid:
31233504


Language:
English
Keywords:
Pubs id:
pubs:1023089
UUID:
uuid:6239a0bf-9b21-4e79-bbe0-4cee8dbec3fe
Local pid:
pubs:1023089
Source identifiers:
1023089
Deposit date:
2019-07-03
ARK identifier:

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