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Type 1 fimbrial phase variation in multidrug-resistant asymptomatic uropathogenic Escherichia coli clinical isolates upon adherence to HTB-4 cells
A. Ghosh, M. Mukherjee
Jazyk angličtina Země Česko
Typ dokumentu časopisecké články
Grantová podpora
EMR/2016/001670 dated 22.08.17
Science and Engineering Research Board (SERB), Department of Science and Technology, Government of India
DST/INSPIRE Fellowship/2016/ IF160069.
Department of Science &Technology, New Delhi, Government of India as she was a recipient of the INSPIRE fellowship grant (2016-2021)
- MeSH
- adheziny Escherichia coli genetika metabolismus MeSH
- bakteriální adheze * MeSH
- bakteriální fimbrie * genetika metabolismus MeSH
- bakteriurie mikrobiologie MeSH
- buněčné linie MeSH
- epitelové buňky * mikrobiologie MeSH
- infekce vyvolané Escherichia coli * mikrobiologie MeSH
- lidé MeSH
- mannosa metabolismus farmakologie MeSH
- mnohočetná bakteriální léková rezistence * genetika MeSH
- proteiny fimbrií * genetika metabolismus MeSH
- proteiny z Escherichia coli genetika metabolismus MeSH
- regulace genové exprese u bakterií MeSH
- uropatogenní Escherichia coli * genetika účinky léků izolace a purifikace MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
The adherence of bladder uroepithelial cells, subsequent expression, and regulation of type 1 fimbrial genes (key mediator of attachment) in clinical multidrug-resistant uropathogenic Escherichia coli (MDR-UPECs) isolated from individuals with asymptomatic bacteriuria (ABU) remain unexplored till date. Therefore, this study aimed to investigate the underlying molecular mechanisms associated with the adherence of clinical MDR-ABU-UPECs to human a uroepithelial cell line (HTB-4), both in the absence and presence of D-Mannose. These investigations focused on phase variation, expression, and regulation of type 1 fimbriae and were compared to a prototype ABU-strain (E. coli 83972) and symptomatic MDR-UPECs. Discordant to the ABU prototype strain, MDR-ABU-UPECs exhibited remarkable adhesive capacity that was significantly reduced after D-mannose exposure, fairly like the MDR symptomatic UPECs. The type 1 fimbrial phase variation, determined by the fim switch analysis, asserted the statistically significant incidence of "both OFF and ON" orientation among the adherent MDR-ABU-UPECs with a significant reduction in phase-ON colonies post-D-mannose exposure, akin to the symptomatic ones. This was indicative of an operative and alternating type 1 fimbrial phase switch. The q-PCR assay revealed a coordinated action of the regulatory factors; H-NS, IHF, and Lrp on the expression of FimB and FimE recombinases, which further controlled the function of fimH and fimA genes in ABU-UPECs, similar to symptomatic strains. Therefore, this study is the first of its kind to provide an insight into the regulatory crosstalk of different cellular factors guiding the adhesion of ABU-UPECs to the host. Additionally, it also advocated for the need to accurately characterize ABU-UPECs.
Citace poskytuje Crossref.org
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