Wang Jianfeng, Li Hongen, Pan Juan, Dong Jing, Zhou Xuan, Niu Xiaodi, Deng Xuming
Center of Infection and Immunity, The First Hospital, Jilin University, Changchun, China.
Key Laboratory of Zoonosis, Ministry of Education, Institute of Zoonosis, College of Veterinary Medicine, Jilin University, Changchun, China.
Front Microbiol. 2018 Feb 14;9:245. doi: 10.3389/fmicb.2018.00245. eCollection 2018.
Sortase A (SrtA)-catalyzed anchorage of surface proteins in most Gram-positive bacteria is indispensable for their virulence, suggesting that this transpeptidase is a promising target for antivirulence therapy. Here, an oligopeptide, LPRDA, was identified as an effective inhibitor of SrtA via virtual screening based on the LPXTG substrate sequence, and it was found to inhibit SrtA activity and (IC = 10.61 μM) by competitively occupying the active site of SrtA. Further, the oligopeptide treatment had no anti- activity, but it provided protection against -induced mastitis in a mouse model. These findings indicate that the oligopeptide could be used as an effective anti-infective agent for the treatment of infection caused by or other Gram-positive bacteria via the targeting of SrtA.
分选酶A(SrtA)催化大多数革兰氏阳性菌表面蛋白的锚定,这对它们的毒力至关重要,表明这种转肽酶是抗毒力治疗的一个有前景的靶点。在此,基于LPXTG底物序列通过虚拟筛选鉴定出一种寡肽LPRDA作为SrtA的有效抑制剂,发现它通过竞争性占据SrtA的活性位点来抑制SrtA活性(IC = 10.61 μM)。此外,该寡肽处理没有抗菌活性,但在小鼠模型中能预防金黄色葡萄球菌诱导的乳腺炎。这些发现表明,该寡肽可通过靶向SrtA用作治疗金黄色葡萄球菌或其他革兰氏阳性菌引起的感染的有效抗感染剂。