Brenciani Andrea, Bacciaglia Alessandro, Vecchi Manuela, Vitali Luca A, Varaldo Pietro E, Giovanetti Eleonora
Institute of Microbiology and Biomedical Sciences, Polytechnic University of Marche Medical School, Via Tronto 10/A, 60020 Ancona, Italy.
Antimicrob Agents Chemother. 2007 Apr;51(4):1209-16. doi: 10.1128/AAC.01484-06. Epub 2007 Jan 29.
This study was directed at characterizing the genetic elements carrying the methylase gene erm(B), encoding ribosome modification-mediated resistance to macrolide, lincosamide, and streptogramin B (MLS) antibiotics, in Streptococcus pyogenes. In this species, erm(B) is responsible for MLS resistance in constitutively resistant isolates (cMLS phenotype) and in a subset (iMLS-A) of inducibly resistant isolates. A total of 125 erm(B)-positive strains were investigated, 81 iMLS-A (uniformly tetracycline susceptible) and 44 cMLS (29 tetracycline resistant and 15 tetracycline susceptible). Whereas all tetracycline-resistant isolates carried the tet(M) gene, tet(M) sequences were also detected in most tetracycline-susceptible isolates (81/81 iMLS-A and 7/15 cMLS). In 2 of the 8 tet(M)-negative cMLS isolates, erm(B) was carried by a plasmid-located Tn917-like transposon. erm(B)- and tet(M)-positive isolates were tested by PCR for the presence of genes int (integrase), xis (excisase), and tndX (resolvase), associated with conjugative transposons of the Tn916 family. In mating experiments using representatives of different combinations of phenotypic and genotypic characteristics as donors, erm(B) and tet(M) were consistently cotransferred, suggesting their linkage in individual genetic elements. The linkage was confirmed by pulsed-field gel electrophoresis and hybridization studies, and different elements, variably associated with the different phenotypes/genotypes, were detected and characterized by amplification and sequencing experiments. A previously unreported genetic organization, observed in all iMLS-A and some cMLS isolates, featured an erm(B)-containing DNA insertion into the tet(M) gene of a defective Tn5397, a Tn916-related transposon. This new element was designated Tn1116. Genetic elements not previously described in S. pyogenes also included Tn6002, an unpublished transposon whose complete sequence is available in GenBank, and Tn3872, a composite element resulting from the insertion of the Tn917 transposon into Tn916 [associated with a tet(M) gene expressed in some cMLS isolates and silent in others]. The high frequency of association between a tetracycline-susceptible phenotype and tet(M) genes suggests that transposons of the Tn916 family, so far typically associated solely with a tetracycline-resistant phenotype, may be more widespread in S. pyogenes than currently believed.
本研究旨在鉴定化脓性链球菌中携带甲基化酶基因erm(B)的遗传元件,该基因编码核糖体修饰介导的对大环内酯类、林可酰胺类和链阳菌素B(MLS)抗生素的抗性。在该菌种中,erm(B)导致组成型抗性菌株(cMLS表型)和部分诱导型抗性菌株(iMLS-A)产生MLS抗性。共研究了125株erm(B)阳性菌株,其中81株为iMLS-A(均对四环素敏感),44株为cMLS(29株对四环素耐药,15株对四环素敏感)。所有四环素耐药菌株均携带tet(M)基因,在大多数四环素敏感菌株中也检测到tet(M)序列(81/81 iMLS-A和7/15 cMLS)。在8株tet(M)阴性的cMLS菌株中,有2株的erm(B)由质粒定位的Tn917样转座子携带。通过PCR检测erm(B)和tet(M)阳性菌株中与Tn916家族接合转座子相关的int(整合酶)、xis(解离酶)和tndX(解离酶)基因的存在情况。在使用具有不同表型和基因型特征组合的代表作为供体的交配实验中,erm(B)和tet(M)始终共同转移,表明它们在单个遗传元件中连锁。通过脉冲场凝胶电泳和杂交研究证实了这种连锁关系,并通过扩增和测序实验检测和鉴定了与不同表型/基因型可变相关的不同元件。在所有iMLS-A和部分cMLS菌株中观察到一种以前未报道的遗传结构,其特征是在有缺陷的Tn5397(一种Tn916相关转座子)的tet(M)基因中插入了一个含erm(B)的DNA片段。这个新元件被命名为Tn1116。化脓性链球菌中以前未描述的遗传元件还包括Tn6002(一种未发表的转座子,其完整序列可在GenBank中获得)和Tn3872(一种复合元件,由Tn917转座子插入Tn916产生[与一些cMLS菌株中表达的tet(M)基因相关,而在其他菌株中沉默])。四环素敏感表型与tet(M)基因之间的高关联频率表明,迄今为止通常仅与四环素耐药表型相关的Tn916家族转座子在化脓性链球菌中的分布可能比目前认为的更为广泛。