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Defining chaperone-usher fimbriae repertoire in Serratia marcescens

  • Martin Gonzalez Montalvo
    ,
  • Faviola Tavares Carreón
    ,
  • Gloria M. González
    ,
  • Hiram Villanueva Lozano
    ,
  • Inmaculada García Romero
    ,
  • Universidad Autonoma de Nuevo Leon
    ,
  • Wellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast
Research Output:
Contribution to journal
Article
Peer-review

Publication metrics

Metrics

SciVal
FWCI
0.15
SciVal
Author count
8
SciVal
Paper percentile
30
SciVal
Citations
5
Scopus
Citations

Abstract

Chaperone-usher (CU) fimbriae are surface organelles particularly prevalent among the Enterobacteriaceae. Mainly associated to their adhesive properties, CU fimbriae play key roles in biofilm formation and host cell interactions. Little is known about the fimbriome composition of the opportunistic human pathogen Serratia marcescens. Here, by using a search based on consensus fimbrial usher protein (FUP) sequences, we identified 421 FUPs across 39 S. marcescens genomes. Further analysis of the FUP-containing loci allowed us to classify them into 20 conserved CU operons, 6 of which form the S. marcescens core CU fimbriome. A new systematic nomenclature is proposed according to FUP sequence phylogeny. We also established an in vivo transcriptional assay comparing CU promoter expression between an environmental and a clinical isolate of S. marcescens, which revealed that promoters from 3 core CU operons (referred as fgov, fpo, and fps) are predominantly expressed in the two strains and might represent key core adhesion appendages contributing to S. marcescens pathogenesis.

Publication Information

Output type

Research Output:
Contribution to journal
Article
Peer-review

Original language

English

Article number

104857

Pages from-to (Number of pages)

Pages 104857-104861 (6 pages)

Journal (Volume, Issue Number)

Microbial Pathogenesis (Volume 154, Issue 104857)

Publication milestones

  • Published - 15/05/2021

Publication status

Published - 15/05/2021

ISSN

0882-4010

Publication IDs

  • Scopus: 85103287360

Funding Details

FundersFunding numbers
PAICYT-UANL
CN885-19
NIH
P40 OD010440
NIH
-
MRC
MR/P022480/1
MRC
-
CONACYT
-