Affiliation:
1. Institute of Microbiology and Biomedical Sciences, Polytechnic University of Marche Medical School, 60131 Ancona
2. Department of Cellular and Molecular Biology and Pathology, University of Naples “Federico II,” 80131 Naples, Italy
Abstract
ABSTRACT
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 had 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 Tn
1207.1
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 Tn
1207.1
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 by a Tn
916
-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 Tn
916
-like transposon, giving rise to the composite element Tn
2009
. 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).
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Cited by
48 articles.
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