Multilevel Comparison of Indian Naja Venoms and Their Cross-Reactivity with Indian Polyvalent Antivenoms

Author:

Deka Archana1ORCID,Bhatia Siddharth2,Santra Vishal345,Bharti Omesh K.6ORCID,Lalremsanga Hmar Tlawmte7,Martin Gerard8ORCID,Wüster Wolfgang9ORCID,Owens John B.49,Graham Stuart9,Doley Robin1,Malhotra Anita9ORCID

Affiliation:

1. Molecular Toxinology Laboratory, Department of Molecular Biology and Biotechnology, Tezpur University, Tezpur 784028, Assam, India

2. CSIR-Centre for Cellular and Molecular Biology, Laboratory for Conservation of Endangered Species, Hyderabad 500048, Telangana, India

3. Society for Nature Conservation, Research and Community Engagement (CONCERN), Nalikul, Hooghly 712407, West Bengal, India

4. Captive and Field Herpetology, Anglesey LL65 1YU, UK

5. Snake Research Institute, Gujarat Forest Department, Government of Gujarat, Valsad 396050, Gujarat, India

6. State Institute of Health and Family Welfare, Shimla 171009, Himachal Pradesh, India

7. Department of Zoology, Mizoram University, Aizawl 796004, Mizoram, India

8. The Liana Trust, Hunsur 571189, Karnataka, India

9. Molecular Ecology and Evolution @ Bangor (MEEB), School of Natural Sciences, Bangor University, Gwynedd LL57 2UW, UK

Abstract

Snake envenoming is caused by many biological species, rather than a single infectious agent, each with a multiplicity of toxins in their venom. Hence, developing effective treatments is challenging, especially in biodiverse and biogeographically complex countries such as India. The present study represents the first genus-wide proteomics analysis of venom composition across Naja species (N. naja, N. oxiana, and N. kaouthia) found in mainland India. Venom proteomes were consistent between individuals from the same localities in terms of the toxin families present, but not in the relative abundance of those in the venom. There appears to be more compositional variation among N. naja from different locations than among N. kaouthia. Immunoblotting and in vitro neutralization assays indicated cross-reactivity with Indian polyvalent antivenom, in which antibodies raised against N. naja are present. However, we observed ineffective neutralization of PLA2 activities of N. naja venoms from locations distant from the source of immunizing venoms. Antivenom immunoprofiling by antivenomics revealed differential antigenicity of venoms from N. kaouthia and N. oxiana, and poor reactivity towards 3FTxs and PLA2s. Moreover, there was considerable variation between antivenoms from different manufacturers. These data indicate that improvements to antivenom manufacturing in India are highly desirable.

Funder

European Union

Rufford Foundation

Defence Research and Development Organisation

Department of Science and Technology

Department of Biotechnology

Indian Council of Medical Research

Publisher

MDPI AG

Subject

Health, Toxicology and Mutagenesis,Toxicology

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