{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,24]],"date-time":"2026-09-24T12:14:55Z","timestamp":1790252095173,"version":"4.1.0"},"reference-count":81,"publisher":"American Society for Microbiology","issue":"18","license":[{"start":{"date-parts":[[2011,9,15]],"date-time":"2011-09-15T00:00:00Z","timestamp":1316044800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.asm.org\/non-commercial-tdm-license"}],"content-domain":{"domain":["journals.asm.org"],"crossmark-restriction":true},"short-container-title":["J Bacteriol"],"published-print":{"date-parts":[[2011,9,15]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n          <jats:p>\n            \u03c6A1122 is a T7-related bacteriophage infecting most isolates of\n            <jats:named-content xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" content-type=\"genus-species\" xlink:type=\"simple\">Yersinia pestis<\/jats:named-content>\n            , the etiologic agent of plague, and used by the CDC in the identification of\n            <jats:named-content xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" content-type=\"genus-species\" xlink:type=\"simple\">Y. pestis<\/jats:named-content>\n            . \u03c6A1122 infects\n            <jats:named-content xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" content-type=\"genus-species\" xlink:type=\"simple\">Y. pestis<\/jats:named-content>\n            grown both at 20\u00b0C and at 37\u00b0C. Wild-type\n            <jats:named-content xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" content-type=\"genus-species\" xlink:type=\"simple\">Yersinia pseudotuberculosis<\/jats:named-content>\n            strains are also infected but only when grown at 37\u00b0C. Since\n            <jats:named-content xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" content-type=\"genus-species\" xlink:type=\"simple\">Y. pestis<\/jats:named-content>\n            expresses rough lipopolysaccharide (LPS) missing the O-polysaccharide (O-PS) and expression of\n            <jats:named-content xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" content-type=\"genus-species\" xlink:type=\"simple\">Y. pseudotuberculosis<\/jats:named-content>\n            O-PS is largely suppressed at temperatures above 30\u00b0C, it has been assumed that the phage receptor is rough LPS. We present here several lines of evidence to support this. First, a rough derivative of\n            <jats:named-content xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" content-type=\"genus-species\" xlink:type=\"simple\">Y. pseudotuberculosis<\/jats:named-content>\n            was also \u03c6A1122 sensitive when grown at 22\u00b0C. Second, periodate treatment of bacteria, but not proteinase K treatment, inhibited the phage binding. Third, spontaneous \u03c6A1122 receptor mutants of\n            <jats:named-content xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" content-type=\"genus-species\" xlink:type=\"simple\">Y. pestis<\/jats:named-content>\n            and rough\n            <jats:named-content xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" content-type=\"genus-species\" xlink:type=\"simple\">Y. pseudotuberculosis<\/jats:named-content>\n            could not be isolated, indicating that the receptor was essential for bacterial growth under the applied experimental conditions. Fourth, heterologous expression of the\n            <jats:named-content xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" content-type=\"genus-species\" xlink:type=\"simple\">Yersinia enterocolitica<\/jats:named-content>\n            O:3 LPS outer core hexasaccharide in both\n            <jats:named-content xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" content-type=\"genus-species\" xlink:type=\"simple\">Y. pestis<\/jats:named-content>\n            and rough\n            <jats:named-content xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" content-type=\"genus-species\" xlink:type=\"simple\">Y. pseudotuberculosis<\/jats:named-content>\n            effectively blocked the phage adsorption. Fifth, a gradual truncation of the core oligosaccharide into the Hep\/Glc (\n            <jats:sc>l<\/jats:sc>\n            -\n            <jats:italic>glycero<\/jats:italic>\n            -\n            <jats:sc>d<\/jats:sc>\n            -\n            <jats:italic>manno-<\/jats:italic>\n            heptose\/\n            <jats:sc>d<\/jats:sc>\n            -glucopyranose)-Kdo\/Ko (3-deoxy-\n            <jats:sc>d<\/jats:sc>\n            -\n            <jats:italic>manno<\/jats:italic>\n            -oct-2-ulopyranosonic acid\/\n            <jats:sc>d<\/jats:sc>\n            -\n            <jats:italic>glycero<\/jats:italic>\n            -\n            <jats:sc>d<\/jats:sc>\n            -\n            <jats:italic>talo-<\/jats:italic>\n            oct-2-ulopyranosonic acid) region in a series of LPS mutants was accompanied by a decrease in phage adsorption, and finally, a\n            <jats:italic>waaA<\/jats:italic>\n            mutant expressing only lipid A, i.e., also missing the Kdo\/Ko region, was fully \u03c6A1122 resistant. Our data thus conclusively demonstrated that the \u03c6A1122 receptor is the Hep\/Glc-Kdo\/Ko region of the LPS core, a common structure in\n            <jats:named-content xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" content-type=\"genus-species\" xlink:type=\"simple\">Y. pestis<\/jats:named-content>\n            and\n            <jats:named-content xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" content-type=\"genus-species\" xlink:type=\"simple\">Y. pseudotuberculosis<\/jats:named-content>\n            .\n          <\/jats:p>","DOI":"10.1128\/jb.00339-11","type":"journal-article","created":{"date-parts":[[2011,7,16]],"date-time":"2011-07-16T07:11:02Z","timestamp":1310800262000},"page":"4963-4972","update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":88,"title":["Identification of the Lipopolysaccharide Core of Yersinia pestis and Yersinia pseudotuberculosis as the Receptor for Bacteriophage \u03c6A1122"],"prefix":"10.1128","volume":"193","author":[{"given":"Saija","family":"Kiljunen","sequence":"first","affiliation":[{"name":"Department of Medical Biochemistry and Molecular Biology, Institute of Biomedicine, University of Turku, Turku, Finland"},{"name":"Department of Bacteriology and Immunology, Infection Biology Research Program, Haartman Institute, University of Helsinki, Helsinki, Finland"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Neeta","family":"Datta","sequence":"additional","affiliation":[{"name":"Department of Bacteriology and Immunology, Infection Biology Research Program, Haartman Institute, University of Helsinki, Helsinki, Finland"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Svetlana V.","family":"Dentovskaya","sequence":"additional","affiliation":[{"name":"State Research Center for Applied Microbiology and Biotechnology, Obolensk, Moscow Region, Russia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Andrey P.","family":"Anisimov","sequence":"additional","affiliation":[{"name":"State Research Center for Applied Microbiology and Biotechnology, Obolensk, Moscow Region, Russia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yuriy A.","family":"Knirel","sequence":"additional","affiliation":[{"name":"N.D. 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