Escherichia coli type-1 fimbriae are critical to overcome initial bottlenecks of infection upon low-dose inoculation in a porcine model of cystitis

Author:

Stærk Kristian1ORCID,Grønnemose Rasmus Birkholm1ORCID,Nielsen Thomas Kastberg2,Petersen Nicky Anúel2ORCID,Palarasah Yaseelan3ORCID,Torres-Puig Sergi4ORCID,Møller-Jensen Jakob4ORCID,Kolmos Hans Jørn1ORCID,Lund Lars52ORCID,Andersen Thomas Emil61ORCID

Affiliation:

1. Research Unit of Clinical Microbiology, Department of Clinical Research, University of Southern Denmark, Odense, Denmark

2. Research Unit of Urology, Department of Clinical Research, University of Southern Denmark, Odense, Denmark

3. Department of Cancer and Inflammation Research, Department of Molecular Medicine, University of Southern Denmark, Odense, Denmark

4. Department of Biochemistry and Molecular Biology, University of Southern Denmark, Odense, Denmark

5. Department of Urology, Odense University Hospital, Odense, Denmark

6. Department of Clinical Microbiology, Odense University Hospital, Odense, Denmark

Abstract

Most uropathogenic Escherichia coli (UPEC) express type-1 fimbriae (T1F), a key virulence factor for urinary tract infection (UTI) in mice. Evidence that conclusively associates this pilus with uropathogenesis in humans has, however, been difficult to obtain. We used an experimental porcine model of cystitis to assess the role of T1F in larger mammals more closely related to humans. Thirty-one pigs were infected with UPEC strain UTI89 or its T1F deficient mutant, UTI89ΔfimH, at inoculum titres of 102 to 108 colony forming units per millilitre. Urine and blood samples were collected and analysed 7 and 14 days post-inoculation, and whole bladders were removed at day 14 and analysed for uroepithelium-associated UPEC. All animals were consistently infected and reached high urine titres independent of inoculum titre. UTI89ΔfimH successfully colonized the bladders of 1/6 pigs compared to 6/6 for the wild-type strain. Intracellular UPEC were detectable in low numbers in whole bladder explants. In conclusion, low doses of UPEC are able to establish robust infections in pigs, similar to what is presumed in humans. T1F are critical for UPEC to surpass initial bottlenecks during infection but may be dispensable once infection is established. While supporting the conclusions from mice studies regarding a general importance of T1F in successfully infecting the host, the porcine UTI models’ natural high, more human-like, susceptibility to infection, allowed us to demonstrate a pivotal role of T1F in initial establishment of infection upon a realistic low-inoculum introduction of UPEC in the bladder.

Funder

Region of Southern Denmark

Beckett-Fonden

Coloplast

Publisher

Microbiology Society

Subject

Microbiology

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