Combinations of PBPs and MurM protein variants in early and contemporary high-level penicillin-resistant Streptococcus pneumoniae isolates in Spain

Objectives: High-level penicillin resistance in Streptococcus pneumoniae requires extensive re-modulation of the penicillin-binding proteins (PBPs), and murM gene function is also required for the expression of resistance. In this work, we determined whether specific changes in PBPs were associated...

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Veröffentlicht in:Journal of antimicrobial chemotherapy 2006-05, Vol.57 (5), p.983-986
Hauptverfasser: del Campo, Rosa, Cafini, Fabio, Morosini, María Isabel, Fenoll, Asunción, Liñares, Josefina, Alou, Luis, Sevillano, David, Cantón, Rafael, Prieto, José, Baquero, Fernando
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container_end_page 986
container_issue 5
container_start_page 983
container_title Journal of antimicrobial chemotherapy
container_volume 57
creator del Campo, Rosa
Cafini, Fabio
Morosini, María Isabel
Fenoll, Asunción
Liñares, Josefina
Alou, Luis
Sevillano, David
Cantón, Rafael
Prieto, José
Baquero, Fernando
description Objectives: High-level penicillin resistance in Streptococcus pneumoniae requires extensive re-modulation of the penicillin-binding proteins (PBPs), and murM gene function is also required for the expression of resistance. In this work, we determined whether specific changes in PBPs were associated with specific MurM variants. Methods: Two collections of highly penicillin-resistant (MIC 2–8 mg/L) isolates, including 10 early (1997–1998) and 23 contemporary (2002–2004) isolates, were studied. Results: Most of the isolates belonged to clones Spain6B-2 (13 strains), Spain23F-1 (10 isolates) and Spain14-5 (20 isolates). Different protein variants of MurM (MA, MB5, MB6, MB9 and MB10), PBP1A (A–C), PBP2B (A–D) and PBP2X (A–C) were recognized, including two murM alleles not previously described. Particular [MurM-PBP1A-2B-2X] allelic combinations were predominant among the different clones, including [MA-B-B-B] for old (MIC 2 mg/L) and [MB10-C-A-B] for recent (MIC 4–8 mg/L) Spain6B-2 isolates, [MA-A-C-A] for Spain23F-1 and [MB5-A-A-A] in Spain14-5 isolates. Conclusions: Although S. pneumoniae has a basic recombinational population structure, our results indicate remarkable conservation of PBPs and MurM protein types within each clone. This suggests that particular PBPs–MurM combinations tend to be preserved and may have an independent evolutionary history in particular clones.
doi_str_mv 10.1093/jac/dkl083
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In this work, we determined whether specific changes in PBPs were associated with specific MurM variants. Methods: Two collections of highly penicillin-resistant (MIC 2–8 mg/L) isolates, including 10 early (1997–1998) and 23 contemporary (2002–2004) isolates, were studied. Results: Most of the isolates belonged to clones Spain6B-2 (13 strains), Spain23F-1 (10 isolates) and Spain14-5 (20 isolates). Different protein variants of MurM (MA, MB5, MB6, MB9 and MB10), PBP1A (A–C), PBP2B (A–D) and PBP2X (A–C) were recognized, including two murM alleles not previously described. Particular [MurM-PBP1A-2B-2X] allelic combinations were predominant among the different clones, including [MA-B-B-B] for old (MIC 2 mg/L) and [MB10-C-A-B] for recent (MIC 4–8 mg/L) Spain6B-2 isolates, [MA-A-C-A] for Spain23F-1 and [MB5-A-A-A] in Spain14-5 isolates. Conclusions: Although S. pneumoniae has a basic recombinational population structure, our results indicate remarkable conservation of PBPs and MurM protein types within each clone. This suggests that particular PBPs–MurM combinations tend to be preserved and may have an independent evolutionary history in particular clones.</description><identifier>ISSN: 0305-7453</identifier><identifier>EISSN: 1460-2091</identifier><identifier>DOI: 10.1093/jac/dkl083</identifier><identifier>PMID: 16533824</identifier><identifier>CODEN: JACHDX</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Alleles ; Anti-Bacterial Agents - pharmacology ; Antibiotics. Antiinfectious agents. Antiparasitic agents ; Bacterial Proteins - genetics ; Biological and medical sciences ; clones ; Genetic Variation ; Humans ; Medical sciences ; Microbial Sensitivity Tests ; mutations ; Penicillin Resistance - genetics ; penicillin-binding proteins ; Penicillin-Binding Proteins - genetics ; Penicillins - pharmacology ; Peptide Synthases - genetics ; Pharmacology. 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Antimicrob. Chemother</addtitle><description>Objectives: High-level penicillin resistance in Streptococcus pneumoniae requires extensive re-modulation of the penicillin-binding proteins (PBPs), and murM gene function is also required for the expression of resistance. In this work, we determined whether specific changes in PBPs were associated with specific MurM variants. Methods: Two collections of highly penicillin-resistant (MIC 2–8 mg/L) isolates, including 10 early (1997–1998) and 23 contemporary (2002–2004) isolates, were studied. Results: Most of the isolates belonged to clones Spain6B-2 (13 strains), Spain23F-1 (10 isolates) and Spain14-5 (20 isolates). Different protein variants of MurM (MA, MB5, MB6, MB9 and MB10), PBP1A (A–C), PBP2B (A–D) and PBP2X (A–C) were recognized, including two murM alleles not previously described. Particular [MurM-PBP1A-2B-2X] allelic combinations were predominant among the different clones, including [MA-B-B-B] for old (MIC 2 mg/L) and [MB10-C-A-B] for recent (MIC 4–8 mg/L) Spain6B-2 isolates, [MA-A-C-A] for Spain23F-1 and [MB5-A-A-A] in Spain14-5 isolates. Conclusions: Although S. pneumoniae has a basic recombinational population structure, our results indicate remarkable conservation of PBPs and MurM protein types within each clone. This suggests that particular PBPs–MurM combinations tend to be preserved and may have an independent evolutionary history in particular clones.</description><subject>Alleles</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Antibiotics. Antiinfectious agents. 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Drug treatments</topic><topic>resistance</topic><topic>Serotyping</topic><topic>Spain</topic><topic>Species Specificity</topic><topic>Streptococcus pneumoniae</topic><topic>Streptococcus pneumoniae - genetics</topic><topic>Streptococcus pneumoniae - isolation &amp; purification</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>del Campo, Rosa</creatorcontrib><creatorcontrib>Cafini, Fabio</creatorcontrib><creatorcontrib>Morosini, María Isabel</creatorcontrib><creatorcontrib>Fenoll, Asunción</creatorcontrib><creatorcontrib>Liñares, Josefina</creatorcontrib><creatorcontrib>Alou, Luis</creatorcontrib><creatorcontrib>Sevillano, David</creatorcontrib><creatorcontrib>Cantón, Rafael</creatorcontrib><creatorcontrib>Prieto, José</creatorcontrib><creatorcontrib>Baquero, Fernando</creatorcontrib><creatorcontrib>Spanish Pneumococcal Network (G3/103)</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of antimicrobial chemotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>del Campo, Rosa</au><au>Cafini, Fabio</au><au>Morosini, María Isabel</au><au>Fenoll, Asunción</au><au>Liñares, Josefina</au><au>Alou, Luis</au><au>Sevillano, David</au><au>Cantón, Rafael</au><au>Prieto, José</au><au>Baquero, Fernando</au><aucorp>Spanish Pneumococcal Network (G3/103)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Combinations of PBPs and MurM protein variants in early and contemporary high-level penicillin-resistant Streptococcus pneumoniae isolates in Spain</atitle><jtitle>Journal of antimicrobial chemotherapy</jtitle><addtitle>J. Antimicrob. Chemother</addtitle><date>2006-05-01</date><risdate>2006</risdate><volume>57</volume><issue>5</issue><spage>983</spage><epage>986</epage><pages>983-986</pages><issn>0305-7453</issn><eissn>1460-2091</eissn><coden>JACHDX</coden><abstract>Objectives: High-level penicillin resistance in Streptococcus pneumoniae requires extensive re-modulation of the penicillin-binding proteins (PBPs), and murM gene function is also required for the expression of resistance. In this work, we determined whether specific changes in PBPs were associated with specific MurM variants. Methods: Two collections of highly penicillin-resistant (MIC 2–8 mg/L) isolates, including 10 early (1997–1998) and 23 contemporary (2002–2004) isolates, were studied. Results: Most of the isolates belonged to clones Spain6B-2 (13 strains), Spain23F-1 (10 isolates) and Spain14-5 (20 isolates). Different protein variants of MurM (MA, MB5, MB6, MB9 and MB10), PBP1A (A–C), PBP2B (A–D) and PBP2X (A–C) were recognized, including two murM alleles not previously described. Particular [MurM-PBP1A-2B-2X] allelic combinations were predominant among the different clones, including [MA-B-B-B] for old (MIC 2 mg/L) and [MB10-C-A-B] for recent (MIC 4–8 mg/L) Spain6B-2 isolates, [MA-A-C-A] for Spain23F-1 and [MB5-A-A-A] in Spain14-5 isolates. Conclusions: Although S. pneumoniae has a basic recombinational population structure, our results indicate remarkable conservation of PBPs and MurM protein types within each clone. This suggests that particular PBPs–MurM combinations tend to be preserved and may have an independent evolutionary history in particular clones.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>16533824</pmid><doi>10.1093/jac/dkl083</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record>
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subjects Alleles
Anti-Bacterial Agents - pharmacology
Antibiotics. Antiinfectious agents. Antiparasitic agents
Bacterial Proteins - genetics
Biological and medical sciences
clones
Genetic Variation
Humans
Medical sciences
Microbial Sensitivity Tests
mutations
Penicillin Resistance - genetics
penicillin-binding proteins
Penicillin-Binding Proteins - genetics
Penicillins - pharmacology
Peptide Synthases - genetics
Pharmacology. Drug treatments
resistance
Serotyping
Spain
Species Specificity
Streptococcus pneumoniae
Streptococcus pneumoniae - genetics
Streptococcus pneumoniae - isolation & purification
title Combinations of PBPs and MurM protein variants in early and contemporary high-level penicillin-resistant Streptococcus pneumoniae isolates in Spain
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