Molecular characterization of pneumococci with efflux-mediated erythromycin resistance and identification of a novel mef gene subclass, mef(I)

被引:41
作者
Cochetti, I
Vecchi, M
Mingoia, M
Tili, E
Catania, MR
Manzin, A
Varaldo, PE
Montanari, MP
机构
[1] Polytech Univ Marche, Sch Med, Inst Microbiol & Biomed Sci, I-60131 Ancona, Italy
[2] Univ Naples Federico II, Dept Cellular & Mol Biol & Pathol, I-80131 Naples, Italy
关键词
D O I
10.1128/AAC.49.12.4999-5006.2005
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The molecular genetics of macrolide resistance were analyzed in 49 clinical pneumococci (including an "atypical" bile-insoluble strain currently assigned to the new species Streptococcus pseudopneumoniae) with efflux-mediated erythromycin resistance (M phenotype). All test strains bad the mef gene, identified as mef(A) in 30 isolates and mef(E) in 19 isolates (including the S. pseudopneumoniae strain) on the basis of PCR-restriction fragment length polymorphism analysis. Twenty-eight of the 30 mef(A) isolates shared a pulsed-field gel electrophoresis (PFGE) type corresponding to the England(14)-9 clone. Of those isolates, 27 (20 belonging to serotype 14) yielded multilocus sequence type ST9, and one isolate yielded a new sequence type. The remaining two mef(A) isolates had different PFGE types and yielded an ST9 type and a new sequence type. Far greater heterogeneity was displayed by the 19 mef(E) isolates, which fell into 11 PFGE types, 12 serotypes (though not serotype 14), and 12 sequence types (including two new ones and an undetermined type for the S. pseudopneumoniae strain). In all mef(A) pneumococci, the mef element was a regular Tn1207.1 transposon, whereas of the mef(E) isolates, 17 carried the mega element and 2 exhibited a previously unreported organization, with no PCR evidence of the other open reading frames of mega. The mef gene of these two isolates, which did not match with the mef(E) gene of the mega element (93.6% homology) and which exhibited comparable homology (91.4%) to the mef(A) gene of the Tn1207.1 transposon, was identified as a novel mef gene variant and was designated mef(I). While penicillin-nonsusceptible isolates (three resistant isolates and one intermediate isolate) were all mef(E) strains, tetracycline resistance was also detected in three mef(A) isolates, due to the tet(M) gene carried bv a Ta916-like transposon. A similar mechanism accounted for resistance in four of the five tetracycline-resistant isolates carrying mef(E), in three of which mega was inserted in the Tn916-like transposon, giving rise to the composite element Tn2009. In the fifth mef(E)-positive tetracycline-resistant isolate (the S. pseudopneumoniae strain), tetracycline resistance was due to the presence of the tet(O) gene, apparently unlinked to mef(E).
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页码:4999 / 5006
页数:8
相关论文
共 46 条
[1]   Molecular epidemiology of erythromycin resistance in Streptococcus pneumoniae isolates from blood and noninvasive sites [J].
Amezaga, MR ;
Carter, PE ;
Cash, P ;
McKenzie, H .
JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (09) :3313-3318
[2]   Accuracy of phenotypic and genotypic testing for identification of Streptococcus pneumoniae and description of Streptococcus pseudopneumoniae sp nov. [J].
Arbique, JC ;
Poyart, C ;
Trieu-Cuot, P ;
Quesne, G ;
Carvalho, MDS ;
Steigerwalt, AG ;
Morey, RE ;
Jackson, D ;
Davidson, RJ ;
Facklam, RR .
JOURNAL OF CLINICAL MICROBIOLOGY, 2004, 42 (10) :4686-4696
[3]   Distribution of subclasses mefA and mefE of the mefA gene among clinical isolates of macrolide-resistant (M-Phenotype) Streptococcus pneumoniae, viridans group Streptococci, and Streptococcus pyogenes [J].
Ardanuy, C ;
Tubau, F ;
Liñares, J ;
Domínguez, MA ;
Pallarés, R ;
Martín, R .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2005, 49 (02) :827-829
[4]   Distribution and molecular analysis of mef(A)-containing elements in tetracycline-susceptible and -resistant Streptococcus pyogenes clinical isolates with efflux-mediated erythromycin resistance [J].
Brenciani, A ;
Ojo, KK ;
Monachetti, A ;
Menzo, S ;
Roberts, MC ;
Varaldo, PE ;
Giovanetti, E .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2004, 54 (06) :991-998
[5]   Molecular cloning and functional analysis of a novel macrolide-resistance determinant, mefA, from Streptococcus pyogenes [J].
Clancy, J ;
Petitpas, J ;
DibHajj, F ;
Yuan, W ;
Cronan, M ;
Kamath, AV ;
Bergeron, J ;
Retsema, JA .
MOLECULAR MICROBIOLOGY, 1996, 22 (05) :867-879
[6]   UNCONSTRAINED BACTERIAL PROMISCUITY - THE TN916-TN1545 FAMILY OF CONJUGATIVE TRANSPOSONS [J].
CLEWELL, DB ;
FLANNAGAN, SE ;
JAWORSKI, DD .
TRENDS IN MICROBIOLOGY, 1995, 3 (06) :229-236
[7]   Acquired macrolide resistance genes in pathogenic Neisseria spp. isolated between 1940 and 1987 [J].
Cousin, S ;
Whittington, WLH ;
Roberts, MC .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2003, 47 (12) :3877-3880
[8]   Characterization and prevalence of MefA, MefE, and the associated msr(D) gene in Streptococcus pneumoniae clinical isolates [J].
Daly, MM ;
Doktor, S ;
Flamm, R ;
Shortridge, D .
JOURNAL OF CLINICAL MICROBIOLOGY, 2004, 42 (08) :3570-3574
[9]   Tn2009, a Tn916-like element containing mef(E) in Streptococcus pneumoniae [J].
Del Grosso, M ;
d'Abusco, AS ;
Iannelli, F ;
Pozzi, G ;
Pantosti, A .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2004, 48 (06) :2037-2042
[10]   Macrolide efflux genes mef(A) and mef(E) are carried by different genetic elements in Streptococcus pneumoniae [J].
Del Grosso, M ;
Iannelli, F ;
Messina, C ;
Santagati, M ;
Petrosillo, N ;
Stefani, S ;
Pozzi, G ;
Pantosti, A .
JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (03) :774-778