Misawa Kazuhisa, Tarumoto Norihito, Tamura Shinsuke, Osa Morichika, Hamamoto Takaaki, Yuki Atsushi, Kouzaki Yuji, Imai Kazuo, Ronald Runtuwene Lucky, Yamaguchi Toshiyuki, Murakami Takashi, Maesaki Shigefumi, Suzuki Yutaka, Kawana Akihiko, Maeda Takuya
Department of Infectious Diseases and Pulmonary Medicine, National Defense Medical College, Saitama, Japan.
Department of Infectious Disease and Infection Control, Saitama Medical University, Saitama, Japan.
BMC Res Notes. 2018 Jan 20;11(1):53. doi: 10.1186/s13104-018-3169-0.
β-Lactamase-negative ampicillin-resistant Haemophilus influenzae is a common opportunistic pathogen of hospital- and community-acquired infections, harboring multiple single nucleotide polymorphisms in the ftsI gene, which codes for penicillin-binding protein-3. The objectives of this study were to perform comprehensive genetic analyses of whole regions of the penicillin-binding proteins in H. influenzae and to identify additional single nucleotide polymorphisms related to antibiotic resistance, especially to ampicillin and other cephalosporins.
In this genome analysis of the ftsI gene in 27 strains of H. influenzae, 10 of 23 (43.5%) specimens of group III genotype β-lactamase-negative ampicillin-resistant H. influenzae were paradoxically classified as ampicillin-sensitive phenotypes. Unfortunately, we could not identify any novel mutations that were significantly associated with ampicillin minimum inhibitory concentrations in other regions of the penicillin-binding proteins, and we reconfirmed that susceptibility to β-lactam antibiotics was mainly defined by previously reported SNPs in the ftsI gene. We should also consider detailed changes in expression that lead to antibiotic resistance in the future because the acquisition of resistance to antimicrobials can be predicted by the expression levels of a small number of genes.
β-内酰胺酶阴性的氨苄西林耐药流感嗜血杆菌是医院获得性感染和社区获得性感染常见的机会致病菌,其ftsI基因存在多个单核苷酸多态性,该基因编码青霉素结合蛋白-3。本研究的目的是对流感嗜血杆菌青霉素结合蛋白的整个区域进行全面的遗传分析,并鉴定与抗生素耐药性相关的其他单核苷酸多态性,尤其是对氨苄西林和其他头孢菌素的耐药性。
在对27株流感嗜血杆菌ftsI基因的基因组分析中,III型基因型β-内酰胺酶阴性的氨苄西林耐药流感嗜血杆菌的23份标本中有10份(43.5%)被反常地分类为氨苄西林敏感表型。遗憾的是,我们未能在青霉素结合蛋白的其他区域鉴定出与氨苄西林最低抑菌浓度显著相关的任何新突变,并且我们再次证实,对β-内酰胺类抗生素的敏感性主要由ftsI基因中先前报道的单核苷酸多态性决定。由于可以通过少数基因的表达水平预测对抗微生物药物的耐药性获得情况,因此我们未来还应考虑导致抗生素耐药性的表达方面的详细变化。