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Population-based analysis of invasive nontypeable pneumococci reveals that most have defective capsule synthesis genes
Since nasopharyngeal carriage of pneumococcus precedes invasive pneumococcal disease, characteristics of carriage isolates could be incorrectly assumed to reflect those of invasive isolates. While most pneumococci express a capsular polysaccharide, nontypeable pneumococci are sometimes isolated. Car...
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Published in: | PloS one 2014-05, Vol.9 (5), p.e97825-e97825 |
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description | Since nasopharyngeal carriage of pneumococcus precedes invasive pneumococcal disease, characteristics of carriage isolates could be incorrectly assumed to reflect those of invasive isolates. While most pneumococci express a capsular polysaccharide, nontypeable pneumococci are sometimes isolated. Carriage nontypeables tend to encode novel surface proteins in place of a capsular polysaccharide synthetic locus, the cps locus. In contrast, capsular polysaccharide is believed to be indispensable for invasive pneumococcal disease, and nontypeables from population-based invasive pneumococcal disease surveillance have not been extensively characterized. We received 14,328 invasive pneumococcal isolates through the Active Bacterial Core surveillance program during 2006-2009. Isolates that were nontypeable by Quellung serotyping were characterized by PCR serotyping, sequence analyses of the cps locus, and multilocus sequence typing. Eighty-eight isolates were Quellung-nontypeable (0.61%). Of these, 79 (89.8%) contained cps loci. Twenty-two nontypeables exhibited serotype 8 cps loci with defects, primarily within wchA. Six of the remaining nine isolates contained previously-described aliB homologs in place of cps loci. Multilocus sequence typing revealed that most nontypeables that lacked capsular biosynthetic genes were related to established non-encapsulated lineages. Thus, invasive pneumococcal disease caused by nontypeable pneumococcus remains rare in the United States, and while carriage nontypeables lacking cps loci are frequently isolated, such nontypeable are extremely rare in invasive pneumococcal disease. Most invasive nontypeable pneumococci possess defective cps locus genes, with an over-representation of defective serotype 8 cps variants. |
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While most pneumococci express a capsular polysaccharide, nontypeable pneumococci are sometimes isolated. Carriage nontypeables tend to encode novel surface proteins in place of a capsular polysaccharide synthetic locus, the cps locus. In contrast, capsular polysaccharide is believed to be indispensable for invasive pneumococcal disease, and nontypeables from population-based invasive pneumococcal disease surveillance have not been extensively characterized. We received 14,328 invasive pneumococcal isolates through the Active Bacterial Core surveillance program during 2006-2009. Isolates that were nontypeable by Quellung serotyping were characterized by PCR serotyping, sequence analyses of the cps locus, and multilocus sequence typing. Eighty-eight isolates were Quellung-nontypeable (0.61%). Of these, 79 (89.8%) contained cps loci. Twenty-two nontypeables exhibited serotype 8 cps loci with defects, primarily within wchA. Six of the remaining nine isolates contained previously-described aliB homologs in place of cps loci. Multilocus sequence typing revealed that most nontypeables that lacked capsular biosynthetic genes were related to established non-encapsulated lineages. Thus, invasive pneumococcal disease caused by nontypeable pneumococcus remains rare in the United States, and while carriage nontypeables lacking cps loci are frequently isolated, such nontypeable are extremely rare in invasive pneumococcal disease. Most invasive nontypeable pneumococci possess defective cps locus genes, with an over-representation of defective serotype 8 cps variants.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0097825</identifier><identifier>PMID: 24831650</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Analysis ; Bacteria ; Biology and Life Sciences ; Biosynthetic Pathways - genetics ; Carrier State - microbiology ; Defects ; Disease control ; Disease prevention ; Genes ; Genes, Bacterial ; Genomics ; Homology ; Humans ; Loci ; Medicine and Health Sciences ; Multilocus Sequence Typing ; Mutation ; Nose - microbiology ; Pathology ; Pneumococcal Infections - microbiology ; Polysaccharides ; Polysaccharides, Bacterial - biosynthesis ; Proteins ; Respiratory diseases ; Serotyping ; Streptococcus infections ; Streptococcus pneumoniae ; Streptococcus pneumoniae - genetics ; Streptococcus pneumoniae - isolation & purification ; Surveillance ; Vaccines</subject><ispartof>PloS one, 2014-05, Vol.9 (5), p.e97825-e97825</ispartof><rights>COPYRIGHT 2014 Public Library of Science</rights><rights>2014 Park et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2014 Park et al 2014 Park et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-397ce038469ffead4739e8af3257b179632c420eaacb395466b2eb8c7420377e3</citedby><cites>FETCH-LOGICAL-c692t-397ce038469ffead4739e8af3257b179632c420eaacb395466b2eb8c7420377e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1524876173/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1524876173?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24831650$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Miyaji, Eliane Namie</contributor><creatorcontrib>Park, In Ho</creatorcontrib><creatorcontrib>Geno, K Aaron</creatorcontrib><creatorcontrib>Sherwood, Logan K</creatorcontrib><creatorcontrib>Nahm, Moon H</creatorcontrib><creatorcontrib>Beall, Bernard</creatorcontrib><title>Population-based analysis of invasive nontypeable pneumococci reveals that most have defective capsule synthesis genes</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Since nasopharyngeal carriage of pneumococcus precedes invasive pneumococcal disease, characteristics of carriage isolates could be incorrectly assumed to reflect those of invasive isolates. While most pneumococci express a capsular polysaccharide, nontypeable pneumococci are sometimes isolated. Carriage nontypeables tend to encode novel surface proteins in place of a capsular polysaccharide synthetic locus, the cps locus. In contrast, capsular polysaccharide is believed to be indispensable for invasive pneumococcal disease, and nontypeables from population-based invasive pneumococcal disease surveillance have not been extensively characterized. We received 14,328 invasive pneumococcal isolates through the Active Bacterial Core surveillance program during 2006-2009. Isolates that were nontypeable by Quellung serotyping were characterized by PCR serotyping, sequence analyses of the cps locus, and multilocus sequence typing. Eighty-eight isolates were Quellung-nontypeable (0.61%). Of these, 79 (89.8%) contained cps loci. Twenty-two nontypeables exhibited serotype 8 cps loci with defects, primarily within wchA. Six of the remaining nine isolates contained previously-described aliB homologs in place of cps loci. Multilocus sequence typing revealed that most nontypeables that lacked capsular biosynthetic genes were related to established non-encapsulated lineages. Thus, invasive pneumococcal disease caused by nontypeable pneumococcus remains rare in the United States, and while carriage nontypeables lacking cps loci are frequently isolated, such nontypeable are extremely rare in invasive pneumococcal disease. Most invasive nontypeable pneumococci possess defective cps locus genes, with an over-representation of defective serotype 8 cps variants.</description><subject>Analysis</subject><subject>Bacteria</subject><subject>Biology and Life Sciences</subject><subject>Biosynthetic Pathways - genetics</subject><subject>Carrier State - microbiology</subject><subject>Defects</subject><subject>Disease control</subject><subject>Disease prevention</subject><subject>Genes</subject><subject>Genes, Bacterial</subject><subject>Genomics</subject><subject>Homology</subject><subject>Humans</subject><subject>Loci</subject><subject>Medicine and Health Sciences</subject><subject>Multilocus Sequence Typing</subject><subject>Mutation</subject><subject>Nose - microbiology</subject><subject>Pathology</subject><subject>Pneumococcal Infections - microbiology</subject><subject>Polysaccharides</subject><subject>Polysaccharides, Bacterial - biosynthesis</subject><subject>Proteins</subject><subject>Respiratory diseases</subject><subject>Serotyping</subject><subject>Streptococcus infections</subject><subject>Streptococcus pneumoniae</subject><subject>Streptococcus pneumoniae - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Park, In Ho</au><au>Geno, K Aaron</au><au>Sherwood, Logan K</au><au>Nahm, Moon H</au><au>Beall, Bernard</au><au>Miyaji, Eliane Namie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Population-based analysis of invasive nontypeable pneumococci reveals that most have defective capsule synthesis genes</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2014-05-15</date><risdate>2014</risdate><volume>9</volume><issue>5</issue><spage>e97825</spage><epage>e97825</epage><pages>e97825-e97825</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Since nasopharyngeal carriage of pneumococcus precedes invasive pneumococcal disease, characteristics of carriage isolates could be incorrectly assumed to reflect those of invasive isolates. While most pneumococci express a capsular polysaccharide, nontypeable pneumococci are sometimes isolated. Carriage nontypeables tend to encode novel surface proteins in place of a capsular polysaccharide synthetic locus, the cps locus. In contrast, capsular polysaccharide is believed to be indispensable for invasive pneumococcal disease, and nontypeables from population-based invasive pneumococcal disease surveillance have not been extensively characterized. We received 14,328 invasive pneumococcal isolates through the Active Bacterial Core surveillance program during 2006-2009. Isolates that were nontypeable by Quellung serotyping were characterized by PCR serotyping, sequence analyses of the cps locus, and multilocus sequence typing. Eighty-eight isolates were Quellung-nontypeable (0.61%). Of these, 79 (89.8%) contained cps loci. Twenty-two nontypeables exhibited serotype 8 cps loci with defects, primarily within wchA. Six of the remaining nine isolates contained previously-described aliB homologs in place of cps loci. Multilocus sequence typing revealed that most nontypeables that lacked capsular biosynthetic genes were related to established non-encapsulated lineages. Thus, invasive pneumococcal disease caused by nontypeable pneumococcus remains rare in the United States, and while carriage nontypeables lacking cps loci are frequently isolated, such nontypeable are extremely rare in invasive pneumococcal disease. Most invasive nontypeable pneumococci possess defective cps locus genes, with an over-representation of defective serotype 8 cps variants.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>24831650</pmid><doi>10.1371/journal.pone.0097825</doi><oa>free_for_read</oa></addata></record> |
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subjects | Analysis Bacteria Biology and Life Sciences Biosynthetic Pathways - genetics Carrier State - microbiology Defects Disease control Disease prevention Genes Genes, Bacterial Genomics Homology Humans Loci Medicine and Health Sciences Multilocus Sequence Typing Mutation Nose - microbiology Pathology Pneumococcal Infections - microbiology Polysaccharides Polysaccharides, Bacterial - biosynthesis Proteins Respiratory diseases Serotyping Streptococcus infections Streptococcus pneumoniae Streptococcus pneumoniae - genetics Streptococcus pneumoniae - isolation & purification Surveillance Vaccines |
title | Population-based analysis of invasive nontypeable pneumococci reveals that most have defective capsule synthesis genes |
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