Erythromycin-resistant Streptococcus pneumoniae: phenotypes, genotypes, transposons and pneumococcal vaccine coverage rates
To assess the antibiotic resistance, transposon profiles, serotype distribution and vaccine coverage rates in 110 erythromycin-resistant S. pneumoniae clinical isolates. Erythromycin, clindamycin, tetracycline, chloramphenicol and kanamycin susceptibilities were assessed using the E-test/disc diffus...
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Veröffentlicht in: | Journal of medical microbiology 2019-06, Vol.68 (6), p.874-881 |
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description | To assess the antibiotic resistance, transposon profiles, serotype distribution and vaccine coverage rates in 110 erythromycin-resistant S. pneumoniae clinical isolates.
Erythromycin, clindamycin, tetracycline, chloramphenicol and kanamycin susceptibilities were assessed using the E-test/disc diffusion method. Inducible macrolide resistance was tested using the erythromycin-clindamycin double disc diffusion test. Serogrouping and serotyping were performed using latex particle agglutination and the Quellung reaction, respectively. Drug resistance genes and transposon-specific genes were investigated by PCR.
Of the isolates, 93 % were resistant to clindamycin; 81 % were resistant to tetracycline; 76 % were multi-drug-resistant, having resistance to both clindamycin and tetracycline; and 12 % had extended-drug resistance, being resistant to clindamycin, tetracycline, chloramphenicol and kanamycin. The majority of isolates (88.2 %) exhibited the cMLSB phenotype. The association between the cMLSB phenotype and tetracycline resistance was related to transposons Tn2010 (38.2 %), Tn6002 (21.8 %) and Tn3872 (18.2 %). M and iMLSB phenotypes were observed in 7 and 5 % of the isolates, respectively. The most frequent serotype was 19 F (40 %). Among the erythromycin-resistant pneumococci, vaccine coverage rates for the 13-valent pneumococcal conjugate vaccine (PCV-13) and the 23-valent pneumococcal polysaccharide vaccine (PPSV-23) were 76.4 and 79.1 %, respectively, compared to 82.2 and 85.1 % transposon-carrying isolates.
Multi-drug resistance among erythromycin-resistant S. pneumoniae isolates mainly occurs due to the horizontal spread of the Tn916 family of transposons. The majority of the transposon-carrying isolates are covered by 13- and 23-valent pneumococcal vaccines. Since serotype distribution and transposons in S. pneumoniae isolates may change over time, close monitoring is essential. |
doi_str_mv | 10.1099/jmm.0.000995 |
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Erythromycin, clindamycin, tetracycline, chloramphenicol and kanamycin susceptibilities were assessed using the E-test/disc diffusion method. Inducible macrolide resistance was tested using the erythromycin-clindamycin double disc diffusion test. Serogrouping and serotyping were performed using latex particle agglutination and the Quellung reaction, respectively. Drug resistance genes and transposon-specific genes were investigated by PCR.
Of the isolates, 93 % were resistant to clindamycin; 81 % were resistant to tetracycline; 76 % were multi-drug-resistant, having resistance to both clindamycin and tetracycline; and 12 % had extended-drug resistance, being resistant to clindamycin, tetracycline, chloramphenicol and kanamycin. The majority of isolates (88.2 %) exhibited the cMLSB phenotype. The association between the cMLSB phenotype and tetracycline resistance was related to transposons Tn2010 (38.2 %), Tn6002 (21.8 %) and Tn3872 (18.2 %). M and iMLSB phenotypes were observed in 7 and 5 % of the isolates, respectively. The most frequent serotype was 19 F (40 %). Among the erythromycin-resistant pneumococci, vaccine coverage rates for the 13-valent pneumococcal conjugate vaccine (PCV-13) and the 23-valent pneumococcal polysaccharide vaccine (PPSV-23) were 76.4 and 79.1 %, respectively, compared to 82.2 and 85.1 % transposon-carrying isolates.
Multi-drug resistance among erythromycin-resistant S. pneumoniae isolates mainly occurs due to the horizontal spread of the Tn916 family of transposons. The majority of the transposon-carrying isolates are covered by 13- and 23-valent pneumococcal vaccines. Since serotype distribution and transposons in S. pneumoniae isolates may change over time, close monitoring is essential.</description><identifier>ISSN: 0022-2615</identifier><identifier>EISSN: 1473-5644</identifier><identifier>DOI: 10.1099/jmm.0.000995</identifier><identifier>PMID: 31116101</identifier><language>eng</language><publisher>England</publisher><ispartof>Journal of medical microbiology, 2019-06, Vol.68 (6), p.874-881</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c329t-14c6e3e82f6f3e54b1ca1da7d5a85a0daf307b86cefc7c45da68fb8ad1953cb73</citedby><cites>FETCH-LOGICAL-c329t-14c6e3e82f6f3e54b1ca1da7d5a85a0daf307b86cefc7c45da68fb8ad1953cb73</cites><orcidid>0000-0003-1498-5368 ; 0000-0003-2150-5553</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,3744,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31116101$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Akdoğan Kittana, Fatma Nur</creatorcontrib><creatorcontrib>Mustak, Inci Basak</creatorcontrib><creatorcontrib>Hascelik, Gulsen</creatorcontrib><creatorcontrib>Saricam, Seyyide</creatorcontrib><creatorcontrib>Gurler, Nezahat</creatorcontrib><creatorcontrib>Diker, Kadir Serdar</creatorcontrib><title>Erythromycin-resistant Streptococcus pneumoniae: phenotypes, genotypes, transposons and pneumococcal vaccine coverage rates</title><title>Journal of medical microbiology</title><addtitle>J Med Microbiol</addtitle><description>To assess the antibiotic resistance, transposon profiles, serotype distribution and vaccine coverage rates in 110 erythromycin-resistant S. pneumoniae clinical isolates.
Erythromycin, clindamycin, tetracycline, chloramphenicol and kanamycin susceptibilities were assessed using the E-test/disc diffusion method. Inducible macrolide resistance was tested using the erythromycin-clindamycin double disc diffusion test. Serogrouping and serotyping were performed using latex particle agglutination and the Quellung reaction, respectively. Drug resistance genes and transposon-specific genes were investigated by PCR.
Of the isolates, 93 % were resistant to clindamycin; 81 % were resistant to tetracycline; 76 % were multi-drug-resistant, having resistance to both clindamycin and tetracycline; and 12 % had extended-drug resistance, being resistant to clindamycin, tetracycline, chloramphenicol and kanamycin. The majority of isolates (88.2 %) exhibited the cMLSB phenotype. The association between the cMLSB phenotype and tetracycline resistance was related to transposons Tn2010 (38.2 %), Tn6002 (21.8 %) and Tn3872 (18.2 %). M and iMLSB phenotypes were observed in 7 and 5 % of the isolates, respectively. The most frequent serotype was 19 F (40 %). Among the erythromycin-resistant pneumococci, vaccine coverage rates for the 13-valent pneumococcal conjugate vaccine (PCV-13) and the 23-valent pneumococcal polysaccharide vaccine (PPSV-23) were 76.4 and 79.1 %, respectively, compared to 82.2 and 85.1 % transposon-carrying isolates.
Multi-drug resistance among erythromycin-resistant S. pneumoniae isolates mainly occurs due to the horizontal spread of the Tn916 family of transposons. The majority of the transposon-carrying isolates are covered by 13- and 23-valent pneumococcal vaccines. Since serotype distribution and transposons in S. pneumoniae isolates may change over time, close monitoring is essential.</description><issn>0022-2615</issn><issn>1473-5644</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNpFkDtPwzAUhS0EglLYmFFGhqbYcZwHG6rKQ6rEAMzWjXPTpkrsYDuVIv48qVpgOmf4zhk-Qm4YnTOa5_fbtp3TOaVjFydkwuKUhyKJ41MyoTSKwihh4oJcOrellKWc5-fkgjPGEkbZhHwv7eA31rSDqnVo0dXOg_bBu7fYeaOMUr0LOo19a3QN-BB0G9TGDx26WbD-r96Cdp1xRrsAdHmc7PfQBDtQ4z0GyuzQwhoDCx7dFTmroHF4fcwp-XxafixewtXb8-vicRUqHuU-ZLFKkGMWVUnFUcQFU8BKSEsBmQBaQsVpWmSJwkqlKhYlJFlVZFCyXHBVpHxK7g6_nTVfPTov29opbBrQaHono4hHNE14zEd0dkCVNc5ZrGRn6xbsIBmVe91y1C2pPOge8dvjc1-0WP7Bv375D1pZgCY</recordid><startdate>201906</startdate><enddate>201906</enddate><creator>Akdoğan Kittana, Fatma Nur</creator><creator>Mustak, Inci Basak</creator><creator>Hascelik, Gulsen</creator><creator>Saricam, Seyyide</creator><creator>Gurler, Nezahat</creator><creator>Diker, Kadir Serdar</creator><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-1498-5368</orcidid><orcidid>https://orcid.org/0000-0003-2150-5553</orcidid></search><sort><creationdate>201906</creationdate><title>Erythromycin-resistant Streptococcus pneumoniae: phenotypes, genotypes, transposons and pneumococcal vaccine coverage rates</title><author>Akdoğan Kittana, Fatma Nur ; Mustak, Inci Basak ; Hascelik, Gulsen ; Saricam, Seyyide ; Gurler, Nezahat ; Diker, Kadir Serdar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c329t-14c6e3e82f6f3e54b1ca1da7d5a85a0daf307b86cefc7c45da68fb8ad1953cb73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Akdoğan Kittana, Fatma Nur</creatorcontrib><creatorcontrib>Mustak, Inci Basak</creatorcontrib><creatorcontrib>Hascelik, Gulsen</creatorcontrib><creatorcontrib>Saricam, Seyyide</creatorcontrib><creatorcontrib>Gurler, Nezahat</creatorcontrib><creatorcontrib>Diker, Kadir Serdar</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of medical microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Akdoğan Kittana, Fatma Nur</au><au>Mustak, Inci Basak</au><au>Hascelik, Gulsen</au><au>Saricam, Seyyide</au><au>Gurler, Nezahat</au><au>Diker, Kadir Serdar</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Erythromycin-resistant Streptococcus pneumoniae: phenotypes, genotypes, transposons and pneumococcal vaccine coverage rates</atitle><jtitle>Journal of medical microbiology</jtitle><addtitle>J Med Microbiol</addtitle><date>2019-06</date><risdate>2019</risdate><volume>68</volume><issue>6</issue><spage>874</spage><epage>881</epage><pages>874-881</pages><issn>0022-2615</issn><eissn>1473-5644</eissn><abstract>To assess the antibiotic resistance, transposon profiles, serotype distribution and vaccine coverage rates in 110 erythromycin-resistant S. pneumoniae clinical isolates.
Erythromycin, clindamycin, tetracycline, chloramphenicol and kanamycin susceptibilities were assessed using the E-test/disc diffusion method. Inducible macrolide resistance was tested using the erythromycin-clindamycin double disc diffusion test. Serogrouping and serotyping were performed using latex particle agglutination and the Quellung reaction, respectively. Drug resistance genes and transposon-specific genes were investigated by PCR.
Of the isolates, 93 % were resistant to clindamycin; 81 % were resistant to tetracycline; 76 % were multi-drug-resistant, having resistance to both clindamycin and tetracycline; and 12 % had extended-drug resistance, being resistant to clindamycin, tetracycline, chloramphenicol and kanamycin. The majority of isolates (88.2 %) exhibited the cMLSB phenotype. The association between the cMLSB phenotype and tetracycline resistance was related to transposons Tn2010 (38.2 %), Tn6002 (21.8 %) and Tn3872 (18.2 %). M and iMLSB phenotypes were observed in 7 and 5 % of the isolates, respectively. The most frequent serotype was 19 F (40 %). Among the erythromycin-resistant pneumococci, vaccine coverage rates for the 13-valent pneumococcal conjugate vaccine (PCV-13) and the 23-valent pneumococcal polysaccharide vaccine (PPSV-23) were 76.4 and 79.1 %, respectively, compared to 82.2 and 85.1 % transposon-carrying isolates.
Multi-drug resistance among erythromycin-resistant S. pneumoniae isolates mainly occurs due to the horizontal spread of the Tn916 family of transposons. The majority of the transposon-carrying isolates are covered by 13- and 23-valent pneumococcal vaccines. Since serotype distribution and transposons in S. pneumoniae isolates may change over time, close monitoring is essential.</abstract><cop>England</cop><pmid>31116101</pmid><doi>10.1099/jmm.0.000995</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-1498-5368</orcidid><orcidid>https://orcid.org/0000-0003-2150-5553</orcidid><oa>free_for_read</oa></addata></record> |
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title | Erythromycin-resistant Streptococcus pneumoniae: phenotypes, genotypes, transposons and pneumococcal vaccine coverage rates |
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