首页> 外文期刊>Annals of Clinical Microbiology and Antimicrobials >Superantigen profiles of emm and emm-like typeable and nontypeable pharyngeal streptococcal isolates of South India
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Superantigen profiles of emm and emm-like typeable and nontypeable pharyngeal streptococcal isolates of South India

机译:南印度的emmm和类似emmm的可分型和不可分型咽链球菌分离物的超抗原谱

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Background The major virulence factors determining the pathogenicity of streptococcal strains include M protein encoded by emm and emm-like (emmL) genes and superantigens. In this study, the distribution of emm, emmL and superantigen genes was analyzed among the streptococcal strains isolated from the patients of acute pharyngitis. Methods The streptococcal strains were isolated from the throat swabs of 1040 patients of acute pharyngitis. The emm and emmL genes were PCR amplified from each strain and sequenced to determine the emm types. The dot-blot hybridization was performed to confirm the pathogens as true emm nontypeable strains. The presence of eleven currently known superantigens was determined in all the strains by multiplex PCR. Results Totally, 124 beta-hemolytic streptococcal strains were isolated and they were classified as group A streptococcus (GAS) [15.3% (19/124)], group C streptococcus (GCS) [59.7% (74/124)] and group G streptococcus (GGS) [25.0% (31/124)]. Among 124 strains, only 35 strains were emm typeable and the remaining 89 strains were emm nontypeable. All GAS isolates were typeable, whereas most of the GCS and GGS strains were nontypeable. These nontypeable strains belong to S. anginosus [75.3% (67/89)] and S. dysgalactiae subsp. equisimilis [24.7% (22/89)]. The emm and emmL types identified in this study include emm12.0 (28.6%), stG643.0 (28.6%), stC46.0 (17.0%), emm30.11 (8.5%), emm3.0 (2.9%), emm48.0 (5.7%), st3343.0 (2.9%), emm107.0 (2.9%) and stS104.2 (2.9%). Various superantigen profiles were observed in typeable as well as nontypeable strains. Conclusions Multiplex PCR analysis revealed the presence of superantigens in all the typeable strains irrespective of their emm types. However, the presence of superantigen genes in emm and emmL nontypeable strains has not been previously reported. In this study, presence of at least one or a combination of superantigen coding genes was identified in all the emm and emmL nontypeable strains. Thus, the superantigens may inevitably play an important role in the pathogenesis of these nontypeable strains in the absence of the primary virulence factor, M protein.
机译:背景技术确定链球菌菌株致病性的主要毒力因子包括由emm和emm-like(emmL)基因和超抗原编码的M蛋白。在这项研究中,分析了从急性咽炎患者中分离出的链球菌菌株中emm,emmL和超抗原基因的分布。方法从1040例急性咽炎患者的咽拭子中分离出链球菌菌株。从每个菌株中PCR扩增emm和emmL基因,并测序以确定emm类型。进行斑点印迹杂交以确认病原体为真正的mme不可分型的菌株。通过多重PCR在所有菌株中确定了十一种目前已知的超抗原的存在。结果共分离出124株溶血性β-溶血性链球菌,分别为A组链球菌(GAS)[15.3%(19/124)],C组链球菌(GCS)[59.7%(74/124)]和G组。链球菌(GGS)[25.0%(31/124)]。在124个菌株中,只有35个菌株是埃姆氏型的,其余的89个菌株是埃姆氏型的。所有GAS分离株都是可分型的,而大多数GCS和GGS菌株是不可分型的。这些不可分型的菌株属于链球菌(S. anginosus)[75.3%(67/89)]和反乳链球菌。相当[24.7%(22/89)]。在这项研究中确定的emm和emmL类型包括emm12.0(28.6%),stG643.0(28.6%),stC46.0(17.0%),emm30.11(8.5%),emm3.0(2.9%), emm48.0(5.7%),st3343.0(2.9%),emm107.0(2.9%)和stS104.2(2.9%)。在可分型和不可分型的菌株中观察到各种超抗原概况。结论多重PCR分析表明,所有超级分型菌株均存在超抗原,而与它们的mmm类型无关。但是,以前尚未报道过emm和emmL非分型菌株中超抗原基因的存在。在这项研究中,在所有emm和emmL非分型菌株中鉴定出至少一种或多种超抗原编码基因的组合。因此,在没有主要毒力因子M蛋白的情况下,超抗原可能不可避免地在这些不可分型菌株的发病机理中发挥重要作用。

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