Puzari Upasana, Khan Mojibur R, Mukherjee Ashis K
Microbial Biotechnology and Protein Research Laboratory, Department of Molecular Biology and Biotechnology, School of Sciences, Tezpur University, Tezpur, Assam, India.
Division of Life Sciences, Institute of Advanced Study in Science and Technology, Vigyan Path Garchuk, Paschim Boragaon, Guwahati, Assam, India.
PLoS Negl Trop Dis. 2025 Mar 14;19(3):e0012913. doi: 10.1371/journal.pntd.0012913. eCollection 2025 Mar.
Venomous or dry bites can result from snake envenomation. Therefore, developing a detection test for venomous snakebites in envenomed patients can prevent from unnecessary antivenom therapy for dry bites, thereby, saving them from adverse effects and cost of antivenom therapy.
This study demonstrates a method for the diagnosis of medically significant 'Big Four' Indian snake venoms (Naja naja, Bungarus caeruleus, Daboia russelii, Echis carinatus) in the plasma of experimentally envenomed animals (envenomed under laboratory conditions). Rabbit polyclonal antibodies (PAbs) were produced by generating modified bespoke peptides identified by computational analysis from the antigenic sites of the main toxins found in the proteome of India's 'Big Four' venomous snakes. The polyclonal antibody formulation (FPAb) prepared by mixing the five representative PAbs in the ratio of 1:1:1:1:1 demonstrated synergistic immune recognition of the 'Big Four' snakes and Naja kaouthia venoms. The recognition for these venoms under in vitro and in vivo conditions by FPAb was significantly higher (p<0.05) than commercial polyvalent antivenom produced against native venom toxins. The FPAb was tested to detect the venoms in subcutaneously envenomed rat plasmas until 240 minutes post-injection. Fourier-transform infrared spectroscopy, zeta potential, transmission electron microscopy, and atomic force microscopy characterised gold nanoparticles (AuNP) conjugated with FPAb. The FPAb-conjugated AuNP demonstrated aggregation upon interaction with venom toxins, changing the colour from red through burgundy to blue, monitored using a smartphone. From the digital image colourimetry analysis of the images, calibration curves for venoms were obtained, and each venom in the envenomed plasma at different time intervals was quantified using these curves.
A method for detection of venomous snakebites has been reported. The formulation of polyclonal antibodies generated against toxins of 'Big Four' venomous snakes of India immune-recognise venoms of 'Big Four' venomous snakes of India and N. kaouthia venoms under both in vitro and in vivo conditions. The antibody formulation conjugated to AuNP detected the venoms in envenomed plasma. This method of detection has potential to be useful for snakebite management in clinical settings.
蛇咬伤可能导致中毒或无毒咬伤。因此,开发一种针对中毒患者的毒蛇咬伤检测试验可以避免对无毒咬伤进行不必要的抗蛇毒血清治疗,从而使患者免受抗蛇毒血清治疗的不良反应和费用。
本研究展示了一种在实验性中毒动物(在实验室条件下中毒)血浆中诊断具有医学意义的印度“四大”毒蛇毒液(眼镜蛇、金环蛇、罗素蝰蛇、锯鳞蝰蛇)的方法。通过对印度“四大”毒蛇蛋白质组中主要毒素抗原位点进行计算分析,生成修饰的定制肽,从而制备兔多克隆抗体(PAbs)。以1:1:1:1:1的比例混合五种代表性PAbs制备的多克隆抗体制剂(FPAb)对“四大”毒蛇和眼镜王蛇毒液表现出协同免疫识别。在体外和体内条件下,FPAb对这些毒液的识别能力显著高于针对天然毒液毒素生产的商业多价抗蛇毒血清(p<0.05)。对FPAb进行测试,以检测皮下注射中毒大鼠血浆中的毒液,直至注射后240分钟。傅里叶变换红外光谱、zeta电位、透射电子显微镜和原子力显微镜对与FPAb偶联的金纳米颗粒(AuNP)进行了表征。与FPAb偶联的AuNP与毒液毒素相互作用时会发生聚集,颜色从红色变为紫红色再变为蓝色,可使用智能手机进行监测。通过对图像的数字图像比色法分析,获得毒液的校准曲线,并使用这些曲线对不同时间间隔中毒血浆中的每种毒液进行定量。
已报道一种检测毒蛇咬伤的方法。针对印度“四大”毒蛇毒素产生的多克隆抗体制剂在体外和体内条件下均能免疫识别印度“四大”毒蛇和眼镜王蛇的毒液。与AuNP偶联的抗体制剂可检测中毒血浆中的毒液。这种检测方法在临床环境中对蛇咬伤管理可能有用。