Selection and Counterselection of Hia Expression Reveals a Key Role for Phase-Variable Expression of Hia in Infection Caused by Nontypeable Haemophilus influenzae
Hia is a major adhesin of nontypeable Haemophilus influenzae (NTHi) and has long been investigated as a vaccine candidate. Here we show that Hia phase variation is controlled by changes in the length of a polythymidine tract located in the hia promoter. Studies of an invasive clinical isolate (strai...
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Veröffentlicht in: | The Journal of infectious diseases 2015-08, Vol.212 (4), p.645-653 |
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creator | Atack, John M. Winter, Linda E. Jurcisek, Joseph A. Bakaletz, Lauren O. Barenkamp, Stephen J. Jennings, Michael P. |
description | Hia is a major adhesin of nontypeable Haemophilus influenzae (NTHi) and has long been investigated as a vaccine candidate. Here we show that Hia phase variation is controlled by changes in the length of a polythymidine tract located in the hia promoter. Studies of an invasive clinical isolate (strain R2866) show that strains expressing high Hia levels are more efficiently killed by opsonophagocytosis. An opsonophagocytic assay was used to select for a subpopulation of variants that expressed a low level of Hia, which facilitated their escape from killing by anti-Hia antisera. Conversely, a subpopulation of variants expressing a high level of Hia was selected for during passaging through Chang cells. In both cases, phase variation of Hia expression corresponded directly with discrete modal changes in polythymidine tract length. In the chinchilla model of NTHi infection, we observed consistent selection for high Hia expression upon nasopharyngeal colonization, confirming the key role of phase-variable expression of Hia within a specific niche in vivo. |
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Here we show that Hia phase variation is controlled by changes in the length of a polythymidine tract located in the hia promoter. Studies of an invasive clinical isolate (strain R2866) show that strains expressing high Hia levels are more efficiently killed by opsonophagocytosis. An opsonophagocytic assay was used to select for a subpopulation of variants that expressed a low level of Hia, which facilitated their escape from killing by anti-Hia antisera. Conversely, a subpopulation of variants expressing a high level of Hia was selected for during passaging through Chang cells. In both cases, phase variation of Hia expression corresponded directly with discrete modal changes in polythymidine tract length. In the chinchilla model of NTHi infection, we observed consistent selection for high Hia expression upon nasopharyngeal colonization, confirming the key role of phase-variable expression of Hia within a specific niche in vivo.</description><identifier>ISSN: 0022-1899</identifier><identifier>EISSN: 1537-6613</identifier><identifier>DOI: 10.1093/infdis/jiv103</identifier><identifier>PMID: 25712964</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>Adhesins, Bacterial - genetics ; Adhesins, Bacterial - metabolism ; Animals ; BACTERIA ; Carrier State ; Cell Line ; Chinchilla ; Fluorescence ; Gene Expression Regulation, Bacterial - physiology ; Haemophilus Infections - microbiology ; Haemophilus influenzae ; Haemophilus influenzae - classification ; Humans ; Major and Brief Reports ; Nasopharynx - microbiology ; Otitis Media - microbiology ; Otitis Media - pathology ; Polymerase Chain Reaction - methods ; Rodentia</subject><ispartof>The Journal of infectious diseases, 2015-08, Vol.212 (4), p.645-653</ispartof><rights>Copyright © 2015 Oxford University Press on behalf of the Infectious Diseases Society of America</rights><rights>The Author 2015. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.</rights><rights>The Author 2015. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. All rights reserved. For Permissions, please e-mail: . 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c403t-6fd27130abf80cd0fde009387cfd04fcb333bda37eaa9301b18adc5e21fe9c043</citedby><cites>FETCH-LOGICAL-c403t-6fd27130abf80cd0fde009387cfd04fcb333bda37eaa9301b18adc5e21fe9c043</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/43709636$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/43709636$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,776,780,799,881,27903,27904,57995,58228</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25712964$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Atack, John M.</creatorcontrib><creatorcontrib>Winter, Linda E.</creatorcontrib><creatorcontrib>Jurcisek, Joseph A.</creatorcontrib><creatorcontrib>Bakaletz, Lauren O.</creatorcontrib><creatorcontrib>Barenkamp, Stephen J.</creatorcontrib><creatorcontrib>Jennings, Michael P.</creatorcontrib><title>Selection and Counterselection of Hia Expression Reveals a Key Role for Phase-Variable Expression of Hia in Infection Caused by Nontypeable Haemophilus influenzae</title><title>The Journal of infectious diseases</title><addtitle>J Infect Dis</addtitle><description>Hia is a major adhesin of nontypeable Haemophilus influenzae (NTHi) and has long been investigated as a vaccine candidate. Here we show that Hia phase variation is controlled by changes in the length of a polythymidine tract located in the hia promoter. Studies of an invasive clinical isolate (strain R2866) show that strains expressing high Hia levels are more efficiently killed by opsonophagocytosis. An opsonophagocytic assay was used to select for a subpopulation of variants that expressed a low level of Hia, which facilitated their escape from killing by anti-Hia antisera. Conversely, a subpopulation of variants expressing a high level of Hia was selected for during passaging through Chang cells. In both cases, phase variation of Hia expression corresponded directly with discrete modal changes in polythymidine tract length. In the chinchilla model of NTHi infection, we observed consistent selection for high Hia expression upon nasopharyngeal colonization, confirming the key role of phase-variable expression of Hia within a specific niche in vivo.</description><subject>Adhesins, Bacterial - genetics</subject><subject>Adhesins, Bacterial - metabolism</subject><subject>Animals</subject><subject>BACTERIA</subject><subject>Carrier State</subject><subject>Cell Line</subject><subject>Chinchilla</subject><subject>Fluorescence</subject><subject>Gene Expression Regulation, Bacterial - physiology</subject><subject>Haemophilus Infections - microbiology</subject><subject>Haemophilus influenzae</subject><subject>Haemophilus influenzae - classification</subject><subject>Humans</subject><subject>Major and Brief Reports</subject><subject>Nasopharynx - microbiology</subject><subject>Otitis Media - microbiology</subject><subject>Otitis Media - pathology</subject><subject>Polymerase Chain Reaction - methods</subject><subject>Rodentia</subject><issn>0022-1899</issn><issn>1537-6613</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkk-PFCEQxYnRuOPq0aOGo5d2oemB5mJiJquzcaNm_XMlNBQOkx5ooXvi-HH8pLL2OFlPnkhe_epRFA-hp5S8pESyCx-c9fli6_eUsHtoQZdMVJxTdh8tCKnrirZSnqFHOW8JIQ3j4iE6q5eC1pI3C_TrE_RgRh8D1sHiVZzCCCmfxOjw2mt8-WNIkPOtcgN70H3GGr-DA76JPWAXE_640Rmqrzp53RXpTsPRwgd8FdzRdqWnDBZ3B_w-hvEwwJ-mtYZdHDa-n3LBXT9B-KnhMXrgyoXw5Hieoy9vLj-v1tX1h7dXq9fXlWkIGyvubC0oI7pzLTGWOAukLKgVxlnSONMxxjqrmQCtJSO0o622Zgk1dSBN2cw5ejX7DlO3A2sgjEn3akh-p9NBRe3Vv5XgN-pb3KtmyWQrRTF4cTRI8fsEeVQ7nw30vQ4Qp6yoEKytW07q_6O8OHIqaVvQakZNijkncKeJKFG3EVBzBNQcgcI_v_uME_33zwvwbAa2eYzpVG-YIJIzzn4DMHC9YA</recordid><startdate>20150815</startdate><enddate>20150815</enddate><creator>Atack, John M.</creator><creator>Winter, Linda E.</creator><creator>Jurcisek, Joseph A.</creator><creator>Bakaletz, Lauren O.</creator><creator>Barenkamp, Stephen J.</creator><creator>Jennings, Michael P.</creator><general>Oxford University Press</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>7QL</scope><scope>7T2</scope><scope>7U2</scope><scope>7U9</scope><scope>C1K</scope><scope>H94</scope><scope>5PM</scope></search><sort><creationdate>20150815</creationdate><title>Selection and Counterselection of Hia Expression Reveals a Key Role for Phase-Variable Expression of Hia in Infection Caused by Nontypeable Haemophilus influenzae</title><author>Atack, John M. ; Winter, Linda E. ; Jurcisek, Joseph A. ; Bakaletz, Lauren O. ; Barenkamp, Stephen J. ; Jennings, Michael P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c403t-6fd27130abf80cd0fde009387cfd04fcb333bda37eaa9301b18adc5e21fe9c043</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adhesins, Bacterial - genetics</topic><topic>Adhesins, Bacterial - metabolism</topic><topic>Animals</topic><topic>BACTERIA</topic><topic>Carrier State</topic><topic>Cell Line</topic><topic>Chinchilla</topic><topic>Fluorescence</topic><topic>Gene Expression Regulation, Bacterial - physiology</topic><topic>Haemophilus Infections - microbiology</topic><topic>Haemophilus influenzae</topic><topic>Haemophilus influenzae - classification</topic><topic>Humans</topic><topic>Major and Brief Reports</topic><topic>Nasopharynx - microbiology</topic><topic>Otitis Media - microbiology</topic><topic>Otitis Media - pathology</topic><topic>Polymerase Chain Reaction - methods</topic><topic>Rodentia</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Atack, John M.</creatorcontrib><creatorcontrib>Winter, Linda E.</creatorcontrib><creatorcontrib>Jurcisek, Joseph A.</creatorcontrib><creatorcontrib>Bakaletz, Lauren O.</creatorcontrib><creatorcontrib>Barenkamp, Stephen J.</creatorcontrib><creatorcontrib>Jennings, Michael P.</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>Bacteriology Abstracts (Microbiology B)</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Safety Science and Risk</collection><collection>Virology and AIDS Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Atack, John M.</au><au>Winter, Linda E.</au><au>Jurcisek, Joseph A.</au><au>Bakaletz, Lauren O.</au><au>Barenkamp, Stephen J.</au><au>Jennings, Michael P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Selection and Counterselection of Hia Expression Reveals a Key Role for Phase-Variable Expression of Hia in Infection Caused by Nontypeable Haemophilus influenzae</atitle><jtitle>The Journal of infectious diseases</jtitle><addtitle>J Infect Dis</addtitle><date>2015-08-15</date><risdate>2015</risdate><volume>212</volume><issue>4</issue><spage>645</spage><epage>653</epage><pages>645-653</pages><issn>0022-1899</issn><eissn>1537-6613</eissn><abstract>Hia is a major adhesin of nontypeable Haemophilus influenzae (NTHi) and has long been investigated as a vaccine candidate. Here we show that Hia phase variation is controlled by changes in the length of a polythymidine tract located in the hia promoter. Studies of an invasive clinical isolate (strain R2866) show that strains expressing high Hia levels are more efficiently killed by opsonophagocytosis. An opsonophagocytic assay was used to select for a subpopulation of variants that expressed a low level of Hia, which facilitated their escape from killing by anti-Hia antisera. Conversely, a subpopulation of variants expressing a high level of Hia was selected for during passaging through Chang cells. In both cases, phase variation of Hia expression corresponded directly with discrete modal changes in polythymidine tract length. 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subjects | Adhesins, Bacterial - genetics Adhesins, Bacterial - metabolism Animals BACTERIA Carrier State Cell Line Chinchilla Fluorescence Gene Expression Regulation, Bacterial - physiology Haemophilus Infections - microbiology Haemophilus influenzae Haemophilus influenzae - classification Humans Major and Brief Reports Nasopharynx - microbiology Otitis Media - microbiology Otitis Media - pathology Polymerase Chain Reaction - methods Rodentia |
title | Selection and Counterselection of Hia Expression Reveals a Key Role for Phase-Variable Expression of Hia in Infection Caused by Nontypeable Haemophilus influenzae |
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