OprF and OprL Conjugate as Vaccine Candidates against Pseudomonas aeruginosa; an in Silico Study

  • سال انتشار: 1396
  • محل انتشار: مجله میکروبیولوژی پزشکی و بیماریهای عفونی، دوره: 6، شماره: 1
  • کد COI اختصاصی: JR_JMMI-6-1_001
  • زبان مقاله: انگلیسی
  • تعداد مشاهده: 94
دانلود فایل این مقاله

نویسندگان

Zahra Payandeh

Department of Biotecnology, Faculty of Medicine, Zanjan University of Medical Science, Zanjan, Iran

Bahman Khalesi

Department of Research and Production of Poultry Viral Vaccine, Razi Vaccine and Serum Research Institute, Agricultural Research Education and Extention Organization (AREEO), Karaj, Iran

Maysam Mard-Soltani

Department of Clinical Biochemistry, Faculty of Medical Sciences, Dezful University of Medical Sciences, Dezful, Iran

Fateme Sefid

Department of Biology, Shahed University, Tehran, Iran

چکیده

Introduction: Vaccine studies against Pseudomonas aeruginosa have often focused on outer membrane proteins (OPRs) due to their potent stimulation of the immune response. Using major outer membrane proteins of cell walls (mOMPs) of P. aeruginosa and other Gram-negative bacteria actively stimulate the immune system without any toxic side effects. Moreover, these antigens show immunological cross-reactivity with mOMPs of other serotypes belonging to the same species. The main OPRs of P. aeruginosa, OprF, and OprL, have received much attention from biologists as the potential OPR-based vaccine candidates. Methods: Homology modeling of OprF and OprL was done based on the template structures obtained from the BLAST search. The quality of OprF and OprL molecules was assessed using GMQE and QMEAN۴ quality assessment tools. The secondary structure of the proteins was predicted as well as the structural topology, subcellular localization, functional analyses, signal peptide and B cell epitopes of proteins. Results: The structures of OprF and OprL proteins were successfully modeled and assessed using ۴RLC-A and ۴G۴V-A as template structures. The regions of the proteins with a high B cell epitope density were identified as candidates for vaccine design. These regions contain functional and exposed amino acids. In these regions, the majority of amino acids were hydrophilic, flexible and accessible. Conclusion: It should be noted that in silico approaches are appealing alternatives for empirical methods. These approaches could pave the way for precise vaccine design efforts with lower cost and time.

کلیدواژه ها

Pseudomonas aeruginosa, Vaccine candidate, OprF, OprL, Bioinformatic

اطلاعات بیشتر در مورد COI

COI مخفف عبارت CIVILICA Object Identifier به معنی شناسه سیویلیکا برای اسناد است. COI کدی است که مطابق محل انتشار، به مقالات کنفرانسها و ژورنالهای داخل کشور به هنگام نمایه سازی بر روی پایگاه استنادی سیویلیکا اختصاص می یابد.

کد COI به مفهوم کد ملی اسناد نمایه شده در سیویلیکا است و کدی یکتا و ثابت است و به همین دلیل همواره قابلیت استناد و پیگیری دارد.