Musser James M, Beres Stephen B, Zhu Luchang, Olsen Randall J, Vuopio Jaana, Hyyryläinen Hanne-Leena, Gröndahl-Yli-Hannuksela Kirsi, Kristinsson Karl G, Darenberg Jessica, Henriques-Normark Birgitta, Hoffmann Steen, Caugant Dominque A, Smith Andrew J, Lindsay Diane S J, Boragine David M, Palzkill Timothy
Center for Molecular and Translational Human Infectious Diseases Research, Houston Methodist Research Institute and Houston Methodist Hospital, Houston, Texas, USA
Clinical Microbiology Laboratory, Department of Pathology and Genomic Medicine, Houston Methodist Research Institute and Houston Methodist Hospital, Houston, Texas, USA.
J Clin Microbiol. 2020 Mar 25;58(4). doi: 10.1128/JCM.01993-19.
Recently, two related strains with reduced susceptibility to ampicillin, amoxicillin, and cefotaxime, antibiotics commonly used to treat infections, were reported. The two strains had the same nonsynonymous (amino acid-substituting) mutation in the gene, encoding penicillin-binding protein 2X (PBP2X). This concerning report led us to investigate our library of 7,025 genome sequences of type , , and clinical strains recovered from intercontinental sources for mutations in We identified 137 strains that, combined, had 37 nonsynonymous mutations in 36 codons in Although to a lesser magnitude than the two previously published isolates, many of our strains had decreased susceptibility to multiple beta-lactam antibiotics. Many mutations were found only in single strains, but 16 groups of two or more isolates of the same type had an identical amino acid replacement. Phylogenetic analysis showed that, with one exception, strains of the same type with the same amino acid replacement were clonally related by descent. This finding indicates that strains with some amino acid changes in PBP2X can successfully spread to new human hosts and cause invasive infections. Mapping of the amino acid changes onto a three-dimensional structure of the related PBP2X suggests that some substitutions are located in regions functionally important in related pathogenic bacterial species. Decreased beta-lactam susceptibility is geographically widespread in strains of numerically common gene subtypes. Enhanced surveillance and further epidemiological and molecular genetic study of this potential emergent antimicrobial problem are warranted.
最近,有报告称发现了两种对氨苄西林、阿莫西林和头孢噻肟敏感性降低的相关菌株,这些抗生素常用于治疗感染。这两种菌株在编码青霉素结合蛋白2X(PBP2X)的基因中具有相同的非同义(氨基酸替换)突变。这一令人担忧的报告促使我们对从洲际来源收集的7025株A、B和C型临床菌株的基因组序列库进行调查,以寻找该基因中的突变。我们鉴定出137株菌株,这些菌株总共在该基因的36个密码子中有37个非同义突变。尽管我们的许多菌株对多种β-内酰胺类抗生素的敏感性降低程度低于之前公布的两株分离株,但仍存在这种情况。许多突变仅在单个菌株中发现,但有16组相同类型的两个或更多分离株具有相同的氨基酸替换。系统发育分析表明,除了一个例外,具有相同氨基酸替换的相同类型菌株通过谱系克隆相关。这一发现表明,PBP2X中发生某些氨基酸变化的菌株可以成功传播到新的人类宿主并引起侵袭性感染。将氨基酸变化映射到相关PBP2X的三维结构上表明,一些替换位于相关致病细菌物种中功能重要的区域。β-内酰胺敏感性降低在数量上常见的该基因亚型菌株中在地理上广泛存在。有必要加强对这一潜在的新出现抗菌问题的监测以及进一步的流行病学和分子遗传学研究。