Molecular Epidemiology of Erythromycin Resistance in Streptococcus pneumoniae Isolates from Blood and Noninvasive Sites
Open Access
- 1 September 2002
- journal article
- Published by American Society for Microbiology in Journal of Clinical Microbiology
- Vol. 40 (9) , 3313-3318
- https://doi.org/10.1128/jcm.40.9.3313-3318.2002
Abstract
Erythromycin-resistant isolates of Streptococcus pneumoniae from blood cultures and noninvasive sites were studied over a 3-year period. The prevalence of erythromycin resistance was 11.9% (19 of 160) in blood culture isolates but 4.2% (60 of 1,435) in noninvasive-site isolates. Sixty-two of the 79 resistant isolates were available for study. The M phenotype was responsible for 76% (47 of 62) of resistance, largely due to a serotype 14 clone, characterized by multilocus sequence typing as ST9, which accounted for 79% (37 of 47) of M phenotype resistance. The ST9 clone was 4.8 times more common in blood than in noninvasive sites. All M phenotype isolates were PCR positive for mef (A), but sequencing revealed that the ST9 clone possessed the mef (A) sequence commonly associated with Streptococcus pyogenes . All M phenotype isolates with this mef (A) sequence also had sequences consistent with the presence of the Tn 1207.1 genetic element inserted in the celB gene. In contrast, isolates with the mef (E) sequence normally associated with S. pneumoniae contained sequences consistent with the presence of the mega insertion element. All MLS B isolates carried erm (B), and two isolates carried both erm (B) and mef (E). Fourteen of the 15 MLS B isolates were tetracycline resistant and contained tet (M). However, six M phenotype isolates of serotypes 19 (two isolates) and 23 (four isolates) were also tetracycline resistant and contained tet (M). MICs for isolates with the mef (A) sequence were significantly higher than MICs for isolates with the mef (E) sequence ( P < 0.001). Thus, the ST9 clone of S. pneumoniae is a significant cause of invasive pneumococcal disease in northeast Scotland and is the single most important contributor to M phenotype erythromycin resistance.Keywords
This publication has 36 references indexed in Scilit:
- Structure and Dissemination of a Chromosomal Insertion Element Encoding Macrolide Efflux inStreptococcus pneumoniaeThe Journal of Infectious Diseases, 2001
- Serotype 19F Multiresistant Pneumococcal Clone Harboring Two Erythromycin Resistance Determinants [ erm (B) and mef (A)] in South AfricaAntimicrobial Agents and Chemotherapy, 2001
- The Emergence ofStreptococcus pneumoniaeResistant to Macrolide Antimicrobial Agents: A 6‐Year Population‐Based AssessmentThe Journal of Infectious Diseases, 2000
- A multilocus sequence typing scheme for Streptococcus pneumoniae: identification of clones associated with serious invasive diseaseMicrobiology, 1998
- The plasmin-binding protein Plr of group A streptococci is identified as glyceraldehyde-3-phosphate dehydrogenaseMicrobiology, 1996
- Pneumococcal meningitis in the North East Thames Region UK: epidemiology and molecular analysis of isolatesEpidemiology and Infection, 1996
- A major surface protein on group A streptococci is a glyceraldehyde-3-phosphate-dehydrogenase with multiple binding activity.The Journal of Experimental Medicine, 1992
- The integration‐excision system of the conjugative transposon Tn 1545 is structurally and functionally related to those of lambdoid phagesMolecular Microbiology, 1990
- Rapid extraction of bacterial genomic DNA with guanidium thiocyanateLetters in Applied Microbiology, 1989
- Serotyping of Streptococcus pneumoniae strains by coagglutination.Journal of Clinical Pathology, 1986