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Alterations of the penicillin-binding proteins and murM alleles of clinical Streptococcus pneumoniae isolates with high-level resistance to amoxicillin in Spain

dc.contributor.authorCafini, Fabio
dc.contributor.authorDel Campo, Rosa
dc.contributor.authorAlou Cervera, Luis
dc.contributor.authorSevillano Fernández, David
dc.contributor.authorMorosini, María Isabel
dc.contributor.authorBaquero, Fernando
dc.contributor.authorPrieto Prieto, José
dc.date.accessioned2024-07-29T10:42:48Z
dc.date.available2024-07-29T10:42:48Z
dc.date.issued2005-12-20
dc.description.abstractAims: The aim of this study was to analyse the nucleotide sequences of regions encoding the penicillin-binding domains of pbp1A, pbp2B and pbp2X genes and murM alleles from 14 selected amoxicillin-resistant Streptococcus pneumoniae isolates (MICs 8-16 mg/L) obtained in Spain. Methods: PFGE and dideoxynucleotide chain termination sequencing were used. Results: Analysis of PFGE profiles showed that the amoxicillin-resistant S. pneumoniae strains belonged to six different PFGE patterns including the Spain23F-1, Spain6B-2, Spain9V-3 and Spain(14)-5 international clones; however, 8 of the 14 strains belonged to the Spain9V-3 clone. These strains showed the typical changes in penicillin-binding proteins (PBPs) 1A and 2X and had 10 unique changes in the 590-641 region of PBP2B as described previously. Transformation experiments tried to incorporate the transpeptidase domain of PBP2B including the 590-641 region associated with amoxicillin-resistant pneumococci. Sequencing of the pbp2B genes revealed that part of the 3' region of the pbp2B sequence encoding a region of the domain (around amino acid 514-538 to the C terminus of PBP2B) did not recombine with the R6 pbp2B gene. The murM sequence analysis showed that 6, 6 and 2 amoxicillin-resistant S. pneumoniae strains had murMA, murMB5 and murMB6 alleles, respectively. However, strains with murMB5 or murMB6 alleles showed a single mutation (N537D) in the 537-581 region of PBP2B, while strains with the murMA allele had 12 unique changes. Conclusions: Ten unique changes in the 590-641 region of PBP2B and no specific murM alleles were found in S. pneumoniae strains isolated in Spain with an amoxicillin MIC>or=8 mg/L (MICs from 6 to 12 mg/L by 1 mg/L step dilution). In addition, the presence of specific mutations in PBP2B seems to play a key role in the presence of different murM alleles in these amoxicillin-resistant pneumococcal strains.
dc.description.departmentDepto. de Medicina
dc.description.facultyFac. de Medicina
dc.description.refereedTRUE
dc.description.statuspub
dc.identifier.citationCafini F, del Campo R, Alou L, Sevillano D, Morosini MI, Baquero F, Prieto J; Spanish Pneumococcal Network (G03/103). Alterations of the penicillin-binding proteins and murM alleles of clinical Streptococcus pneumoniae isolates with high-level resistance to amoxicillin in Spain. J Antimicrob Chemother. 2006 Feb;57(2):224-9.
dc.identifier.doi10.1093/jac/dki442
dc.identifier.essn1460-2091
dc.identifier.issn0305-7453
dc.identifier.officialurlhttps://doi.org/10.1093/jac/dki442
dc.identifier.relatedurlhttps://academic.oup.com/jac/article/57/2/224/804622
dc.identifier.urihttps://hdl.handle.net/20.500.14352/107169
dc.issue.number2
dc.journal.titleJournal of Antimicrobial Chemotherapy
dc.language.isoeng
dc.page.final229
dc.page.initial224
dc.publisherOxford University Press
dc.rights.accessRightsrestricted access
dc.subject.cdu611.02
dc.subject.keywordMurM
dc.subject.keywordPBPs
dc.subject.keywordS.pneumoniae
dc.subject.keywordhigh-level amoxicillin resistance
dc.subject.ucmMicrobiología médica
dc.subject.unesco2414 Microbiología
dc.titleAlterations of the penicillin-binding proteins and murM alleles of clinical Streptococcus pneumoniae isolates with high-level resistance to amoxicillin in Spain
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number57
dspace.entity.typePublication
relation.isAuthorOfPublication889e4dc3-c630-429e-be0f-7f0df2cff492
relation.isAuthorOfPublication518c916a-df78-48cc-9bf7-6a2aaca7d6a2
relation.isAuthorOfPublication84cd82de-c5ea-4fed-a347-4ed15fb3bcc8
relation.isAuthorOfPublication.latestForDiscovery889e4dc3-c630-429e-be0f-7f0df2cff492

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