Department of Pathobiology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
Department of Immunology, Pasteur Institute of Iran, Tehran, Iran.
Infect Genet Evol. 2023 Aug;112:105449. doi: 10.1016/j.meegid.2023.105449. Epub 2023 May 22.
Gonorrhea is an urgent antimicrobial resistance threat and its therapeutic options are continuously getting restricted. Moreover, no vaccine has been approved against it so far. Hence, the present study aimed to introduce novel immunogenic and drug targets against antibiotic-resistant Neisseria gonorrhoeae strains. In the first step, the core proteins of 79 complete genomes of N. gonorrhoeae were retrieved. Next, the surface-exposed proteins were evaluated from different aspects such as antigenicity, allergenicity, conservancy, and B-cell and T-cell epitopes to introduce promising immunogenic candidates. Then, the interactions with human Toll-like receptors (TLR-1, 2, and 4), and immunoreactivity to elicit humoral and cellular immune responses were simulated. On the other hand, to identify novel broad-spectrum drug targets, the cytoplasmic and essential proteins were detected. Then, the N. gonorrhoeae metabolome-specific proteins were compared to the drug targets of the DrugBank, and novel drug targets were retrieved. Finally, the protein data bank (PDB) file availability and prevalence among the ESKAPE group and common sexually transmitted infection (STI) agents were assessed. Our analyses resulted in the recognition of ten novel and putative immunogenic targets including murein transglycosylase A, PBP1A, Opa, NlpD, Azurin, MtrE, RmpM, LptD, NspA, and TamA. Moreover, four potential and broad-spectrum drug targets were identified including UMP kinase, GlyQ, HU family DNA-binding protein, and IF-1. Some of the shortlisted immunogenic and drug targets have confirmed roles in adhesion, immune evasion, and antibiotic resistance that can induce bactericidal antibodies. Other immunogenic and drug targets might be associated with the virulence of N. gonorrhoeae as well. Thus, further experimental studies and site-directed mutations are recommended to investigate the role of potential vaccine and drug targets in the pathogenesis of N. gonorrhoeae. It seems that the efforts for proposing novel vaccines and drug targets appear to be paving the way for a prevention-treatment strategy against this bacterium. Additionally, a combination of bactericidal monoclonal antibodies and antibiotics is a promising approach to curing N. gonorrhoeae.
淋病是一种紧急的抗微生物药物耐药性威胁,其治疗选择不断受到限制。此外,迄今为止尚未批准针对该疾病的疫苗。因此,本研究旨在针对抗生素耐药淋病奈瑟菌(Neisseria gonorrhoeae)菌株引入新的免疫原性和药物靶标。在第一步中,检索了 79 株淋病奈瑟菌完整基因组的核心蛋白。接下来,从抗原性、变应原性、保守性以及 B 细胞和 T 细胞表位等不同方面评估了表面暴露蛋白,以引入有前途的免疫原性候选物。然后,模拟了与人类 Toll 样受体(TLR-1、2 和 4)的相互作用以及引发体液和细胞免疫应答的免疫原性。另一方面,为了鉴定新的广谱药物靶标,检测了细胞质和必需蛋白。然后,将淋病奈瑟菌代谢组特异性蛋白与 DrugBank 的药物靶标进行比较,以检索新的药物靶标。最后,评估了蛋白质数据库(PDB)文件的可用性以及 ESKAPE 组和常见性传播感染(STI)病原体中的流行情况。我们的分析结果识别出了十个新的和有潜力的免疫原性靶标,包括肽聚糖转糖基酶 A、PBP1A、Opa、NlpD、天青杀素、MtrE、RmpM、LptD、NspA 和 TamA。此外,还确定了四个潜在的广谱药物靶标,包括 UMP 激酶、GlyQ、HU 家族 DNA 结合蛋白和 IF-1。一些入选的免疫原性和药物靶标已被证实可在黏附、免疫逃避和抗生素耐药性方面发挥作用,从而诱导杀菌性抗体。其他免疫原性和药物靶标可能与淋病奈瑟菌的毒力有关。因此,建议进行进一步的实验研究和定点突变,以研究潜在疫苗和药物靶标在淋病奈瑟菌发病机制中的作用。看来,提出新的疫苗和药物靶标的努力似乎为针对这种细菌的预防治疗策略铺平了道路。此外,杀菌性单克隆抗体和抗生素的联合使用是治疗淋病奈瑟菌的一种很有前途的方法。