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-reviewPublication metrics
Metrics
SciVal
FWCI
0.15
SciVal
Author count
8
SciVal
Paper percentile
30
SciVal
Citations
5
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-reviewOriginal language
EnglishArticle number
104857Pages 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
0882-4010Publication IDs
- Scopus: 85103287360
Funding Details
FundersFunding numbers
PAICYT-UANL
CN885-19
NIH
P40 OD010440
NIH
-MRC
MR/P022480/1
MRC
-CONACYT
-