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

Most uropathogenic (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 asse...

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Veröffentlicht in:Microbiology (Society for General Microbiology) 2021-10, Vol.167 (10)
Hauptverfasser: Stærk, Kristian, Grønnemose, Rasmus Birkholm, Nielsen, Thomas Kastberg, Petersen, Nicky Anúel, Palarasah, Yaseelan, Torres-Puig, Sergi, Møller-Jensen, Jakob, Kolmos, Hans Jørn, Lund, Lars, Andersen, Thomas Emil
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container_title Microbiology (Society for General Microbiology)
container_volume 167
creator Stærk, Kristian
Grønnemose, Rasmus Birkholm
Nielsen, Thomas Kastberg
Petersen, Nicky Anúel
Palarasah, Yaseelan
Torres-Puig, Sergi
Møller-Jensen, Jakob
Kolmos, Hans Jørn
Lund, Lars
Andersen, Thomas Emil
description Most uropathogenic (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, UTI89Δ , at inoculum titres of 10 to 10 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. UTI89Δ 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.
doi_str_mv 10.1099/mic.0.001101
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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, UTI89Δ , at inoculum titres of 10 to 10 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. UTI89Δ 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. 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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, UTI89Δ , at inoculum titres of 10 to 10 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. UTI89Δ 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. 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Grønnemose, Rasmus Birkholm ; Nielsen, Thomas Kastberg ; Petersen, Nicky Anúel ; Palarasah, Yaseelan ; Torres-Puig, Sergi ; Møller-Jensen, Jakob ; Kolmos, Hans Jørn ; Lund, Lars ; Andersen, Thomas Emil</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c384t-a6921fe952e3868d30b7dcbecbde3b8282cbfb0d65fd6df26a007293b26828c73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Animals</topic><topic>Antibodies, Bacterial - blood</topic><topic>Bacterial Load</topic><topic>Colony Count, Microbial</topic><topic>Cystitis - microbiology</topic><topic>Disease Models, Animal</topic><topic>Escherichia coli Infections - microbiology</topic><topic>Fimbriae, Bacterial - genetics</topic><topic>Fimbriae, Bacterial - immunology</topic><topic>Fimbriae, Bacterial - metabolism</topic><topic>Gentamicins - pharmacology</topic><topic>Microbial Viability - drug effects</topic><topic>Microbial Virulence and Pathogenesis</topic><topic>Mutation</topic><topic>Swine</topic><topic>Urinary Bladder - microbiology</topic><topic>Urinary Tract Infections - microbiology</topic><topic>Uropathogenic Escherichia coli - drug effects</topic><topic>Uropathogenic Escherichia coli - genetics</topic><topic>Uropathogenic Escherichia coli - immunology</topic><topic>Uropathogenic Escherichia coli - pathogenicity</topic><topic>Virulence Factors - genetics</topic><topic>Virulence Factors - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stærk, Kristian</creatorcontrib><creatorcontrib>Grønnemose, Rasmus Birkholm</creatorcontrib><creatorcontrib>Nielsen, Thomas Kastberg</creatorcontrib><creatorcontrib>Petersen, Nicky Anúel</creatorcontrib><creatorcontrib>Palarasah, Yaseelan</creatorcontrib><creatorcontrib>Torres-Puig, Sergi</creatorcontrib><creatorcontrib>Møller-Jensen, Jakob</creatorcontrib><creatorcontrib>Kolmos, Hans Jørn</creatorcontrib><creatorcontrib>Lund, Lars</creatorcontrib><creatorcontrib>Andersen, Thomas Emil</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Microbiology (Society for General Microbiology)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stærk, Kristian</au><au>Grønnemose, Rasmus Birkholm</au><au>Nielsen, Thomas Kastberg</au><au>Petersen, Nicky Anúel</au><au>Palarasah, Yaseelan</au><au>Torres-Puig, Sergi</au><au>Møller-Jensen, Jakob</au><au>Kolmos, Hans Jørn</au><au>Lund, Lars</au><au>Andersen, Thomas Emil</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Escherichia coli type-1 fimbriae are critical to overcome initial bottlenecks of infection upon low-dose inoculation in a porcine model of cystitis</atitle><jtitle>Microbiology (Society for General Microbiology)</jtitle><addtitle>Microbiology (Reading)</addtitle><date>2021-10-01</date><risdate>2021</risdate><volume>167</volume><issue>10</issue><issn>1350-0872</issn><eissn>1465-2080</eissn><abstract>Most uropathogenic (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, UTI89Δ , at inoculum titres of 10 to 10 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. UTI89Δ 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.</abstract><cop>England</cop><pub>Microbiology Society</pub><pmid>34623231</pmid><doi>10.1099/mic.0.001101</doi><orcidid>https://orcid.org/0000-0001-9453-1141</orcidid><orcidid>https://orcid.org/0000-0002-6008-3771</orcidid><orcidid>https://orcid.org/0000-0001-7558-6817</orcidid><orcidid>https://orcid.org/0000-0002-8976-6488</orcidid><orcidid>https://orcid.org/0000-0002-9337-0232</orcidid><orcidid>https://orcid.org/0000-0001-6411-9981</orcidid><orcidid>https://orcid.org/0000-0002-5640-953X</orcidid><orcidid>https://orcid.org/0000-0003-2410-0375</orcidid><orcidid>https://orcid.org/0000-0003-0391-9568</orcidid><oa>free_for_read</oa></addata></record>
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subjects Animals
Antibodies, Bacterial - blood
Bacterial Load
Colony Count, Microbial
Cystitis - microbiology
Disease Models, Animal
Escherichia coli Infections - microbiology
Fimbriae, Bacterial - genetics
Fimbriae, Bacterial - immunology
Fimbriae, Bacterial - metabolism
Gentamicins - pharmacology
Microbial Viability - drug effects
Microbial Virulence and Pathogenesis
Mutation
Swine
Urinary Bladder - microbiology
Urinary Tract Infections - microbiology
Uropathogenic Escherichia coli - drug effects
Uropathogenic Escherichia coli - genetics
Uropathogenic Escherichia coli - immunology
Uropathogenic Escherichia coli - pathogenicity
Virulence Factors - genetics
Virulence Factors - metabolism
title Escherichia coli type-1 fimbriae are critical to overcome initial bottlenecks of infection upon low-dose inoculation in a porcine model of cystitis
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