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Kalita, B.;  Utkin, Y.N.;  Mukherjee, A.K. Cobra Venom. Encyclopedia. Available online: https://encyclopedia.pub/entry/38483 (accessed on 18 November 2024).
Kalita B,  Utkin YN,  Mukherjee AK. Cobra Venom. Encyclopedia. Available at: https://encyclopedia.pub/entry/38483. Accessed November 18, 2024.
Kalita, Bhargab, Yuri N. Utkin, Ashis K. Mukherjee. "Cobra Venom" Encyclopedia, https://encyclopedia.pub/entry/38483 (accessed November 18, 2024).
Kalita, B.,  Utkin, Y.N., & Mukherjee, A.K. (2022, December 10). Cobra Venom. In Encyclopedia. https://encyclopedia.pub/entry/38483
Kalita, Bhargab, et al. "Cobra Venom." Encyclopedia. Web. 10 December, 2022.
Cobra Venom
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This entry is adapted from the peer-reviewed paper 10.3390/toxins14120839

Cobras (genus Naja) are widely distributed over Asia and Africa, and cobra envenomation is responsible for a large number of mortality and morbidity on these continents. Like other elapid venoms, cobra venoms are neurotoxic in nature; however, they also exhibit local cytotoxic effects at the envenomed site, and the extent of cytotoxicity may vary from species to species. Cobra venoms are predominated by the non-enzymatic three-finger toxin family which constitutes about 60-75% of the total venom. Cytotoxins (CTXs), an essential class of the non-enzymatic three-finger toxin family, are ubiquitously present in cobra venoms. These low-molecular-mass toxins, contributing to about 40 to 60% of the cobra venom proteome, play a significant role in cobra venom-induced toxicity, more prominently in dermonecrosis (local effects).

membrane perturbations necrosis cobra venom antivenom neutralization

1. Epidemiology of Cobra Bites in the World

Snake envenoming is a devastating health issue that affects millions of individuals across the globe, particularly in the developing countries of tropical and subtropical regions. Global epidemiological data suggest 81,000–138,000 snakebite-associated deaths from 1.8–2.7 million cases of envenoming yearly, thereby highlighting the urgency of research into this neglected public health concern [1][2]. Moreover, region-wise distribution of snakebite data suggests most of the cases of snake envenoming are concentrated in the rural areas of South Asia, Southeast Asia, and East Sub-Saharan African countries [3].
The majority of the medically critical venomous species of snakes belong to the Viperidae (340 species), Elapidae (360 species), and Atractaspidae (69 species) families [4]. Accordingly, the World Health Organization (WHO) has recognized venomous snakes under categories 1 and 2 depending upon their distribution, venom lethality, and incidences of envenoming and deaths. Category 1 medically essential species are of the highest medical importance, and the WHO has recognized at least 109 species under this category. Furthermore, it has been observed that most medically relevant species are represented by only a few genera. For instance, about 25 Category 1 medically important snake species in Africa belong to only five genera—Naja, Dendroaspis, Echis, Bitis, and Cerastes [5].
Cobras, represented by the genus Naja (nāgá, meaning ‘snake’ in Sanskrit), belong to the Elapidae family of snakes, and most of their species are classified under Category 1 by the WHO. There are nearly 30 species of cobra (Naja) (Table 1) that are widely distributed in Africa and Asia [6][7], and they are responsible for a considerable number of snake envenoming cases on these continents. For various reasons, most global epidemiological studies have not discretely recorded the exact estimates of cobra envenoming in Africa and Asia. While neurotoxicity is one of the vital clinical manifestations to distinguish cobra envenomation, other elapid snakes, for example, mambas (Dendroaspis sp.), kraits (Bungarus sp.), or even some viperids, for example, berg adders (Bitis atropos) [8], and Russell’s vipers (Daboia russelii) from southern India and Sri Lanka [9][10][11] have also been reported to inflict neurological disorders in patients. Therefore, identifying the inflicting species based solely on clinical manifestations might not always be accurate.
Table 1. Geographical distribution of different Naja species and their WHO medical importance category. Data presented in this table were retrieved from snakebite information and the data platform maintained by the World Health Organization (https://www.who.int/teams/control-of-neglected-tropical-diseases/snakebite-envenoming/snakebite-information-and-data-platform/overview#tab=tab_1). The data were accessed on 5 October 2022.
Snake Species Common Name Medical Importance/
Category		 Region of Distribution Number of Countries Human Population (2020) in This Species’ Range
N. anchietae Anchieta’s cobra Highest, Secondary Africa 6 19,008,230
N. annulata Banded water cobra Highest, Secondary Africa 10 114,642,902
N. annulifera Snouted cobra Highest Africa 8 70,731,878
N. ashei Ashe’s spitting cobra Highest Africa 6 32,513,269
N. atra Chinese cobra Highest Asia and Australasia 5 570,266,425
N. christyi Christy’s water cobra Secondary Africa 3 15,111,896
N. guineensis Black forest cobra Highest, Secondary Africa 7 55,106,930
N. haje Egyptian cobra Highest, Secondary Africa 21 443,884,351
N. kaouthia Monocled cobra, Thai cobra Highest, Secondary Asia 11 976,884,863
N. katiensis Mali cobra, West Africa brown spitting cobra Highest, Secondary Africa 12 123,542,818
N. mandalayensis Mandalay spitting cobra Highest Asia and Australasia 1 14,774,047
N. melanoleuca Black and white cobra, Forest cobra Highest, Secondary Africa 11 244,375,176
N. mossambica Mozambique spitting cobra Highest, Secondary Africa 10 130,049,980
N. naja Indian cobra, Spectacled cobra Highest, Secondary Asia and Australasia 5 1,656,817,409
N. nigricincta Western barred spitting cobra, Zebra cobra Highest, Secondary Africa 4 11,381,021
N. nigricollis Black-necked spitting cobra Highest, Secondary Africa 33 727,256,279
N. nivea Cape cobra Highest Africa 4 17,651,152
N. nubiae Nubian spitting cobra Secondary Africa 5 39,843,095
N. oxiana Central Asian cobra, Transcaspian cobra Highest, Secondary Asia and Australasia, Middle East 8 242,127,307
N. pallida Red spitting cobra Secondary Africa 6 59,847,176
N. peroescobari Sao Tome cobra Highest Africa 1 189,185
N. philippinesis Northern Philippine cobra Highest Asia and Australasia 1 592,982,107
N. sagittifera Andaman cobra Secondary Asia and Australasia 1 373,959
N. samarensis Southern Philippine cobra, Visayan cobra Highest Asia and Australasia 1 30,350,207
N. savannula West African banded cobra Highest, Secondary Africa 16 151,894,138
N. senegalensis Senegalese cobra Highest, Secondary Africa 13 84,781,768
N. siamensis Indochinese spitting cobra, Siamese spitting cobra Highest, Secondary Asia and Australasia 5 119,240,121
N. sputatrix Southern Indonesian spitting cobra Highest, Secondary Asia and Australasia 2 167,089,984
N. subfulva Brown forest cobra Highest, Secondary Africa 22 377,545,129
N. sumatrana Equatorial spitting cobra Highest, Secondary Asia and Australasia 6 124,654,470
Moreover, except for Australia, no other countries currently employ snake venom detection kits to identify the encountered snake species [12]. Therefore, keeping track of exact numbers of envenomation by a particular snake species becomes quite challenging to identify the inflicting species taxonomically. In addition, discrepancies in epidemiological data on snake envenomation, either due to the absence of a cohesive and systematic analysis of snakebite cases or because many envenomation cases, are not reported to hospitals, may not be ruled out [13]. Nevertheless, given the wide distribution of cobras and their lethal venoms, it is reasonable to believe that these elapids contribute significantly to the morbidity and mortality associated with snake envenomation in Africa and Asia. Furthermore, evidence from a few isolated studies from some Asian and African countries indicates that the frequency of cobra (genus Naja) envenomation largely varies between 8–30% of the total envenoming cases [14][15][16][17][18].
Compositionally, cobra venoms are predominated by low-molecular-mass (<20 kDa) enzymatic and non-enzymatic toxins. In addition, among the non-enzymatic class, the three-finger toxin (3FTX) is the prominent protein (toxin) family that significantly contributes to cobra venom-induced pathophysiology and toxicity [10][19][20][21][22][23][24][25][26]. Notably, among the various sub-classes of 3FTXs, the proportion of cytotoxins (CTX) and post-synaptic neurotoxins (NTX) dictates the lethality of cobra venoms [24][27].
 

2. Composition of Cobra Venom: A Summary

Biochemical and pharmacological analyses of crude Naja venom and their purified toxins are crucial in highlighting the variation in venom composition owing to the different geographical locations of these species [28][29]. However, these conventional methods are not apt for the characterization of non-enzymatic proteins, and with cobra venoms being primarily dominated by non-enzymatic toxins, a comprehensive cobra venom composition has yet to be unraveled. Recent developments in mass spectrometry-based snake venom toxin profiling have enabled thorough analysis of cobra venom composition. Proteomic findings have suggested that cobra venoms are predominated by enzymatic phospholipase A2 (PLA2) (~13–15 kDa) and non-enzymatic 3FTXs (~6–9 kDa); together, they constitute about 90% of the total cobra venom. Other enzymatic proteins in cobra venoms include L-amino acid oxidase, serine proteases, metalloproteases, phosphodiesterases, 5′-nucleotidases, cholinesterases, phospholipase B, hyaluronidases, and aminopeptidases. In addition, the minor non-enzymatic classes of toxins in cobra venoms include Cobra venom factors, Kunitz-type serine protease inhibitors, nerve growth factors, cystatin, natriuretic peptides, cysteine-rich secretory proteins, ohanin-like proteins or vespryns, vascular endothelial growth factors, and C-type lectins or snaclecs (reviewed by [4][30][31]).
Notably, the proportion of cobra venom CTXs was found to vary dramatically across different Naja species; it was ~13% in Taiwanese N. kaouthia venom, while it constitutes ~73% of N. nigricollis venom (Figure 1). In general, venoms from African spitting cobras have a higher proportion of CTXs than the Asiatic cobra ones, indicating geographical variation in snake venom composition. Interestingly, while the abundance of neurotoxins corresponds well to the severity of neurotoxicity in envenomed patients, the extent of local tissue-damaging effects of cobra venom do not correlate well with the proportions of CTXs, thereby suggesting variable cytotoxicity of the toxin isoforms as well as a contribution by other cobra venom toxins that can inflict local effects on their own or in complex with CTXs [32].
Figure 1. Proteomics analyses determined the relative abundance of CTXs in cobra venoms from diverse geographical locations (Source Kalita et al [33]). The mean relative abundance of CTX in African cobra venoms (61.1 ± 12.6%) is significantly higher as compared to Asian cobra venoms (38.8 ± 17.2%); p-value = 0.001.

References

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