Molecular detection of genes responsible for macrolide resistance among Streptococcus pneumoniae isolated in North Lebanon. Issue 6 (November 2017)

• Record Type: Journal Article
• Authors: El Ashkar, Salam; Osman, Marwan; Rafei, Rayane; Mallat, Hassan; Achkar, Marcel; Dabboussi, Fouad; Hamze, Monzer
• Is Part Of: Journal of infection and public health. Volume 10:Issue 6(2017)
• Page Start: 745
• Page End: 748
• Publication Date: 2017-11
• Subjects: Streptococcus pneumoniae -- Macrolide -- erm(B) -- mef(A/E) -- lin(A) -- Lebanon; Communicable diseases -- Periodicals; Public health -- Periodicals; Epidemiology -- Periodicals; Nosocomial infections -- Prevention -- Periodicals; Medical microbiology -- Periodicals; 614.4
• DOI: 10.1016/j.jiph.2016.11.014
• Languages: English
• ISSNs: 1876-0341

Abstract

Abstract: In recent years, the increased use of macrolides was linked with the emergence of resistance Streptococcus pneumoniae worldwide. The main aim of this study was to determine the prevalence of S. pneumoniae resistant to macrolides and to identify the macrolide resistance genotypes among clinical isolates collected in North Lebanon. Disk diffusion susceptibility method was performed for 132 strains of S. pneumoniae isolated over a period of 5 years in North Lebanon. Polymerase Chain Reaction followed by pyrosequencing was carried out for confirmation of phenotypic diagnosis. The macrolide resistance genotypes were also identified by using PCR amplification of genes implicated in this resistance: erm (A), erm (B), erm (C), msr (A), lin (A) and mef (A/E). Macrolide resistance was found in 34.1% of S. pneumoniae isolates. We observed that the cMLSB phenotype (31/45, 68.9%) was the most common in these pneumococci and erm (B) was the most common resistance gene (32/45, 71.1%). This study shows that macrolide resistance in S. pneumoniae in North Lebanon is mainly related to target site modification with predominance of cMLSb phenotype but is also mediated by efflux pumps. lin (A) gene was reported for the first time in one S. pneumoniae strain in combination with erm (B) and mef (A/E) genes.