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, 2015, 836496

Resistance Determinants and Their Association With Different Transposons in the Antibiotic-Resistant Streptococcus Pneumoniae


Resistance Determinants and Their Association With Different Transposons in the Antibiotic-Resistant Streptococcus Pneumoniae

Izabela Korona-Glowniak et al. Biomed Res Int.


Multiple resistance of Streptococcus pneumoniae is generally associated with their unique recombination-mediated genetic plasticity and possessing the mobile genetic elements. The aim of our study was to detect antibiotic resistance determinants and conjugative transposons in 138 antibiotic-resistant pneumococcal strains isolated from nasopharynx of healthy young children from Lublin, Poland. These strains resistant to tetracycline and/or to chloramphenicol/erythromycin/clindamycin were tested by PCR using the specific genes as markers. The presence of Tn916 family transposons, carrying tet(M) and int/xisTn916, was observed in all of the tested strains. Tn916 was detected in 16 strains resistant only to tetracycline. Tn6002 and Tn3872-related element were found among 99 erm(B)-carrying strains (83.8% and 3.0%, resp.). Eight strains harbouring mef(E) and erm(B) genes were detected, suggesting the presence of Tn2010 and Tn2017 transposons. Among 101 chloramphenicol-resistant strains, two variants of Tn5252-related transposon were distinguished depending on the presence of int/xis5252 genes specific for cat gene-containing Tn5252 (75.2% of strains) or int Sp23FST81 gene, specific for cat-containing ICESp23FST81 element (24.8% of strains). In 6 strains Tn916-like and Tn5252-like elements formed a Tn5253-like structure. Besides clonal dissemination of resistant strains of pneumococci in the population, horizontal transfer of conjugative transposons is an important factor of the high prevalence of antibiotic resistance.


Figure 1
Figure 1
Transposon distribution among pneumococcal serotype of 138 S. pneumoniae nasopharyngeal isolates from healthy young children.

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    1. Bogaert D., de Groot R., Hermans P. W. M. Streptococcus pneumoniae colonisation: the key to pneumococcal disease. Lancet Infectious Diseases. 2004;4(3):144–154. doi: 10.1016/s1473-3099(04)00938-7. - DOI - PubMed
    1. Givon-Lavi N., Fraser D., Porat N., Dagan R. Spread of Streptococcus pneumoniae and antibiotic-resistant S. pneumoniae from day-care center attendees to their younger siblings. Journal of Infectious Diseases. 2002;186(11):1608–1614. doi: 10.1086/345556. - DOI - PubMed
    1. Roberts A. P., Mullany P. Tn916-like genetic elements: a diverse group of modular mobile elements conferring antibiotic resistance. FEMS Microbiology Reviews. 2011;35(5):856–871. doi: 10.1111/j.1574-6976.2011.00283.x. - DOI - PubMed
    1. Shiojima T., Fujiki Y., Sagai H., Iyobe S., Morikawa A. Prevalence of Streptococcus pneumoniae isolates bearing macrolide resistance genes in association with integrase genes of conjugative transposons in Japan. Clinical Microbiology and Infection. 2005;11(10):808–813. doi: 10.1111/j.1469-0691.2005.01232.x. - DOI - PubMed
    1. Montanari M. P., Mingoia M., Giovanetti E., Varaldo P. E. Differentiation of resistance phenotypes among erythromycin-resistant pneumococci. Journal of Clinical Microbiology. 2001;39(4):1311–1315. doi: 10.1128/JCM.39.4.1311-1315.2001. - DOI - PMC - PubMed

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