Verma Shiv K, Joseph Sujith K, Verma Richa, Kushwaha Vikas, Parmar Naveen, Yadav Pawan K, Thota Jagadeshwar Reddy, Kar Susanta, Murthy P Kalpana
Division of Parasitology, CSIR-Central Drug Research Institute, New Campus, BS 10/1, Sector 10, Jankipuram Extension, Lucknow 226031, India.
Mass Spectrometry Laboratory, Sophisticated Analytical Instrument Facility, CSIR-Central Drug Research Institute, New Campus, BS 10/1, Sector 10, Jankipuram Extension, Lucknow 226031, India.
Vaccine. 2015 Jan 15;33(4):527-34. doi: 10.1016/j.vaccine.2014.11.041. Epub 2014 Nov 30.
Nitric oxide (NO) mediated mechanisms have been implicated in killing of some life-stages of Brugia malayi/Wuchereria bancrofti and protect the host through type 1 responses and IFN-γ stimulated toxic mediators' release. However, the identity of NO stimulating molecules of the parasites is not known. Three predominantly NO-stimulating SDS-PAGE resolved fractions F8 (45.24-48.64 kDa), F11 (33.44-38.44 kDa) and F12 (28.44-33.44 kDa) from B. malayi were identified and their proteins were analyzed by 2-DE and MALDI-TOF/TOF. Tropomyosin, calponin and de novo peptides were identified by 2-DE and MALDI-TOF/TOF in F8 and immunization with F8 conferred most significant protection against L3-initiated infection in Mastomys coucha. Immunized animals showed upregulated F8-induced NO, IFN-γ, TNF-α, IL-1β, IL-10, TGF-β release, cellular proliferative responses and specific IgG and IgG1. Anti-IFN-γ, anti-TNF-α, and anti-IL-1β significantly reduced F8-mediated NO generation and iNOS induction at protein levels. Anti-IFN-γ treated cells showed maximum reduction (>74%) in NO generation suggesting a predominant role of IFN-γ in iNOS induction. In conclusion, the findings suggest that F8 which contains tropomyosin, calponin and de novo peptides protects the host via IFN-γ mediated iNOS induction and may hold promise as vaccine candidate(s). This is also the first report of identification of tropomyosin and calponin in B. malayi.
一氧化氮(NO)介导的机制与马来布鲁线虫/班氏吴策线虫某些生命阶段的杀伤有关,并通过1型反应和IFN-γ刺激的毒性介质释放来保护宿主。然而,寄生虫中刺激NO产生的分子的身份尚不清楚。已鉴定出马来布鲁线虫三个主要刺激NO产生的SDS-PAGE分离组分F8(45.24 - 48.64 kDa), F11(33.44 - 38.44 kDa)和F12(28.44 - 33.44 kDa),并通过二维电泳(2-DE)和基质辅助激光解吸电离飞行时间串联质谱(MALDI-TOF/TOF)分析了它们的蛋白质。在F8中通过二维电泳和MALDI-TOF/TOF鉴定出原肌球蛋白、钙调蛋白和新生肽,用F8免疫可对库氏多乳鼠L3引发的感染提供最显著的保护。免疫动物表现出F8诱导的NO、IFN-γ、TNF-α、IL-1β、IL-10、TGF-β释放上调,细胞增殖反应以及特异性IgG和IgG1增加。抗IFN-γ、抗TNF-α和抗IL-1β在蛋白质水平上显著降低了F8介导的NO生成和诱导型一氧化氮合酶(iNOS)诱导。抗IFN-γ处理的细胞显示NO生成减少最多(>74%),表明IFN-γ在iNOS诱导中起主要作用。总之,这些发现表明,含有原肌球蛋白、钙调蛋白和新生肽的F8通过IFN-γ介导的iNOS诱导来保护宿主,有望成为候选疫苗。这也是在马来布鲁线虫中鉴定出原肌球蛋白和钙调蛋白的首次报道。