Fonseca Érica L, Marin Michel A, Freitas Fernanda S, Vitório Bruna S A, de Araújo Flávio M G, Camargo Dhian R A, Coimbra Roney S, De Filippis Ivano R, Vicente Ana Carolina P
Instituto Oswaldo Cruz, FIOCRUZ, Rio de Janeiro, RJ, Brazil.
Instituto Oswaldo Cruz, FIOCRUZ, Rio de Janeiro, RJ, Brazil.
Int J Med Microbiol. 2017 Sep;307(6):287-290. doi: 10.1016/j.ijmm.2017.05.004. Epub 2017 May 25.
Penicillin is the antibiotic of choice for the treatment of meningococcal infections, and mutations in penA gene are involved with reduced susceptibility (pen) emergence to this antibiotic. This study aimed to characterize the penA allelic diversity, their association with pen phenotype and distribution among prevalent meningococci serogroups in Brazil. The entire penA from 49 invasive strains of distinct serogroups circulating in Brazil for more than two decades were obtained by PCR and sequencing. Additionally, the penA from 22 publicly available complete Neisseria meningitidis genomes from Brazil were included in the study. The allelic diversity was determined and a genetic tree was built using the penA sequence alignment. The penicillin MIC was obtained by the E-Test method. In general, the identified penA alleles correlated with the observed pen phenotype. The canonical penA1 was the most prevalent allele, however, several altered penA were also identified in strains presenting increased penicillin MICs. It was identified a new penA amino acid position (residue 480) that possibly influence the penicillin MIC in some strains. Interestingly, the altered penA14 was found in pen invasive MenC cc103 strains spread in Brazil and persisting since 2011, indicating that the biological cost imposed by pen phenotype can be ameliorated by particular features present in this lineage, which represents an additional public health threat.
青霉素是治疗脑膜炎球菌感染的首选抗生素,penA基因的突变与对该抗生素敏感性降低(青霉素耐药)的出现有关。本研究旨在表征penA等位基因多样性、它们与青霉素耐药表型的关联以及在巴西流行的脑膜炎球菌血清群中的分布情况。通过聚合酶链反应(PCR)和测序,获得了在巴西流行二十多年的49株不同血清群侵袭性菌株的完整penA基因。此外,本研究还纳入了来自巴西的22个公开可用的脑膜炎奈瑟菌完整基因组中的penA基因。通过penA序列比对确定等位基因多样性并构建遗传树。采用E-Test法测定青霉素最低抑菌浓度(MIC)。总体而言,鉴定出的penA等位基因与观察到的青霉素耐药表型相关。典型的penA1是最常见的等位基因,然而,在青霉素MIC升高的菌株中也鉴定出了几种变异的penA。在某些菌株中,发现了一个可能影响青霉素MIC的新的penA氨基酸位置(第480位残基)。有趣的是,在自2011年以来在巴西传播并持续存在的青霉素耐药C群cc103型菌株中发现了变异的penA14,这表明该谱系中存在的特定特征可以减轻青霉素耐药表型带来的生物学代价,这构成了另一种公共卫生威胁。