Affiliation:
1. Department of Biomedical Sciences, Section of Microbiology, Torrette Hospital, 60126 Ancona, Italy
2. Clinical Bacteriology Laboratory, Torrette Hospital, 60126 Ancona, Italy
Abstract
ABSTRACT
Several drug resistances in
Streptococcus pneumoniae
are associated with mobile genetic elements, which are loosely subdivided into a group of smaller (18- to 27-kb) and a group of larger (>50-kb) elements. While the elements of the former group, which typically carry the tetracycline resistance determinant
tet
(M) and whose prototype is Tn
916
(18 kb), have been studied extensively, the larger elements, whose prototype is Tn
5253
(∼65.5 kb), are not as well explored. Tn
5253
is a composite structure consisting of two independent conjugative transposons, Tn
5251
(which is virtually identical to Tn
916
) and Tn
5252
(∼47.5 kb), with the former inserted into the latter. Tn
5252
, which so far has only partially been sequenced, carries an integrase gene, driving its site-specific insertion into the host cell genome, and the chloramphenicol resistance
cat
pC194
determinant. This study investigated 20 clinical isolates of
S. pneumoniae
, which were selected on the basis of
cat
pC194
-mediated chloramphenicol resistance. All 20 isolates harbored a Tn
5253
-like element. The composite elements (some of which have been completely sequenced) demonstrated considerable heterogeneity that stemmed from a dual variability: in the Tn
5252
-like element, due primarily to differences in the integrase gene but also to differences in cargo genes and in the overall genetic organization, and in the Tn
916
-like element, with the possible involvement, besides Tn
916
, of a number of Tn
916
family pneumococcal elements carrying different erythromycin resistance genes. In mating experiments, only one composite element, containing a less typical Tn
916
family element, appeared to be nonmobile. Being part of a Tn
5253
-like composite element may confer on some Tn
916
-like transposons, which are apparently nontransferable as independent genetic elements, the ability to be mobilized.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Cited by
27 articles.
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