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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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 |
format | Article |
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(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.</description><identifier>ISSN: 1350-0872</identifier><identifier>EISSN: 1465-2080</identifier><identifier>DOI: 10.1099/mic.0.001101</identifier><identifier>PMID: 34623231</identifier><language>eng</language><publisher>England: Microbiology Society</publisher><subject>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</subject><ispartof>Microbiology (Society for General Microbiology), 2021-10, Vol.167 (10)</ispartof><rights>2021 The Authors 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c384t-a6921fe952e3868d30b7dcbecbde3b8282cbfb0d65fd6df26a007293b26828c73</citedby><cites>FETCH-LOGICAL-c384t-a6921fe952e3868d30b7dcbecbde3b8282cbfb0d65fd6df26a007293b26828c73</cites><orcidid>0000-0001-9453-1141 ; 0000-0002-6008-3771 ; 0000-0001-7558-6817 ; 0000-0002-8976-6488 ; 0000-0002-9337-0232 ; 0000-0001-6411-9981 ; 0000-0002-5640-953X ; 0000-0003-2410-0375 ; 0000-0003-0391-9568</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8698211/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8698211/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34623231$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><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><title>Escherichia coli type-1 fimbriae are critical to overcome initial bottlenecks of infection upon low-dose inoculation in a porcine model of cystitis</title><title>Microbiology (Society for General Microbiology)</title><addtitle>Microbiology (Reading)</addtitle><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.</description><subject>Animals</subject><subject>Antibodies, Bacterial - blood</subject><subject>Bacterial Load</subject><subject>Colony Count, Microbial</subject><subject>Cystitis - microbiology</subject><subject>Disease Models, Animal</subject><subject>Escherichia coli Infections - microbiology</subject><subject>Fimbriae, Bacterial - genetics</subject><subject>Fimbriae, Bacterial - immunology</subject><subject>Fimbriae, Bacterial - metabolism</subject><subject>Gentamicins - pharmacology</subject><subject>Microbial Viability - drug effects</subject><subject>Microbial Virulence and Pathogenesis</subject><subject>Mutation</subject><subject>Swine</subject><subject>Urinary Bladder - microbiology</subject><subject>Urinary Tract Infections - microbiology</subject><subject>Uropathogenic Escherichia coli - drug effects</subject><subject>Uropathogenic Escherichia coli - genetics</subject><subject>Uropathogenic Escherichia coli - immunology</subject><subject>Uropathogenic Escherichia coli - pathogenicity</subject><subject>Virulence Factors - genetics</subject><subject>Virulence Factors - metabolism</subject><issn>1350-0872</issn><issn>1465-2080</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkc1u1DAUhSMEoqVlxxp5yaIZ_DNxnA0SqtqCVIkNXVv2zTVjcOJgO0XzHLwwnk6pYGNb53z3XEunad4wumF0GN5PHjZ0QyljlD1rTtlWdi2nij6vb9HRlqqenzSvcv5ema2k7GVzIraSCy7YafP7KsMOk4edNwRi8KTsF2wZcX6yyRskJiGB5IsHE0iJJN5jgjgh8XMVq2ZjKQFnhB-ZRFdlh1B8nMm61CPEX-0Y8wGPsAbz4PiZGLLEBH5GMsURw2ES9rnUyHzevHAmZHz9eJ81d9dXXy8_tbdfbj5ffrxtQahtaY0cOHM4dByFkmoU1PYjWAQ7orCKKw7WWTrKzo1ydFwaSns-CMtlNaEXZ82HY-6y2glHwLkkE_SS_GTSXkfj9f_O7Hf6W7zXSg6KM1YD3j0GpPhzxVz05DNgCGbGuGbNO0XlIHqpKnpxRCHFnBO6pzWM6kOPdRQ01cceK_723689wX-LE38A-HydpQ</recordid><startdate>20211001</startdate><enddate>20211001</enddate><creator>Stærk, Kristian</creator><creator>Grønnemose, Rasmus Birkholm</creator><creator>Nielsen, Thomas Kastberg</creator><creator>Petersen, Nicky Anúel</creator><creator>Palarasah, Yaseelan</creator><creator>Torres-Puig, Sergi</creator><creator>Møller-Jensen, Jakob</creator><creator>Kolmos, Hans Jørn</creator><creator>Lund, Lars</creator><creator>Andersen, Thomas Emil</creator><general>Microbiology Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><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></search><sort><creationdate>20211001</creationdate><title>Escherichia coli type-1 fimbriae are critical to overcome initial bottlenecks of infection upon low-dose inoculation in a porcine model of cystitis</title><author>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</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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