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Enzymatic activity and brine shrimp lethality of venom from the large brown spitting cobra (Naja ashei) and its neutralization by antivenom



Naja ashei is a snake of medical importance in Kenya, Ethiopia, Somalia, Uganda, and Tanzania. Little is known about the enzymatic (snake venom phospholipases A2; svPLA2’s) and toxic (lethal) activities of N. ashei venom and crucially, the safety and capacity of available antivenom to neutralize these effects. This study aimed to determine the enzymatic and toxic activities of N. ashei venom and the capacity of Indian and Mexican manufactured antivenoms to neutralize these effects. The protein content of the venom and the test antivenoms were also evaluated. A 12-point log concentration–response curve (0.5–22.5 µg/mL) was generated on an agarose-egg yolk model to predict the svPLA2 activity of the venom. The toxicity profiles of the venom and antivenoms were evaluated in the brine shrimp lethality assay. Lowry’s method was used for protein estimation.


Low and intermediate concentrations of the venom exhibited similar svPLA2 activities. The same was true for concentrations > 15 µg/mL. Intermediate and high doses of the venom exhibited similar mortalities in brine shrimp and test antivenoms were generally non-toxic but poorly neutralized svPLA2 activity. Mexican manufactured antivenom had lower protein content but neutralized venom-induced brine shrimp lethality much more effectively than Indian manufactured antivenom.


Snakebite may be the World’s biggest hidden health crisis [1, 2]. Estimates from the World Health Organization suggest that up to 2.7 million people are envenomed by snakes yearly and close to 140,000 die [3]. Non-fatal envenoming may also result in permanent disabilities including blindness, extensive scarring, contractures, restricted mobility, and amputations [4].

Naja ashei is a category 1 snake in Kenya, Ethiopia, Somalia, and Uganda and a category 2 snake in Tanzania [5] (Fig. 1). Category 1 snakes are highly venomous and result in high levels of morbidity, disability, or mortality [5]. Category 2 snakes are highly venomous, may cause morbidity, mortality, disability, or death but lack data to implicate them in snakebite [5].

Fig. 1

(Source: Image of Naja ashei adapted from Wikimedia Commons (Lika Ivanova:

Distribution of Naja ashei in Africa

Over the last decade, there has been a lot of interest in N. ashei [6,7,8,9,10,11]. The skull structure [9], mitochondrial DNA [10], composition, antiproliferative, and antibacterial properties of N. ashei venom have been reported [6,7,8, 11]. However, there has been little focus on the enzymatic, and lethal effects of this venom and the capacity of antivenoms to neutralize them. This study aimed to fill this gap by determining the enzymatic and toxic activities of N. ashei venom and the capacity of antivenoms to neutralize them.

Main text

Materials and methods

Snake venom and antivenom

Venom was extracted from specimens of wild-caught N. ashei maintained at the Bioken Snake Farm in Kenya (Table S1); Collected venom was snap-frozen and stored at − 20 °C. Reconstitution was done in phosphate-buffered saline (PBS) at the time of use. Antivenoms were sourced from hospitals in Kisumu County, Kenya. See (Table S2);

Animals (brine shrimp)

Brine shrimp eggs were commercially sourced from yourfishstuff (Borough of Lebanon, New Jersey, USA; Batch number; X001M8M5IZ). They were hatched at the Department of Public Health, Pharmacology, and Toxicology, University of Nairobi, and brine shrimp larvae were used for experiments.

Protein content determination of the venom and antivenoms

Lowry’s method was used [12]. An eight-point calibration curve (0.05–2 mg/mL) was developed using bovine serum albumin (BSA) as standard. Absorbance was recorded at 660 nm and the protein content of samples was inferred from the standard curve. See

svPLA2 activity of venom

The methods of Haberman and Hardt and Felix Silva et al. were used [13, 14]. Wells were made on sterile petri dishes containing agarose egg-yolk media (1:3 v/v egg yolk: PBS+ 125 µL of 0.1 mM CaCl2) prepared in a laminar flow cabinet. 10 µL of previously incubated (37 °C, 1 h) and serially diluted venom was discharged into the wells and incubated for 24 h at 50 °C. Carbol Fuchsin was used to visualize the halos which were measured by Vernier calipers. PBS was used as a negative control. Triplicate determinations were made and the least amount of venom required to elicit a 50% svPLA2 response (MPC50) was determined by regression analysis.

Neutralization of the svPLA2 activity of venom by antivenom

The method of Iwanaga and Suzuki 1979 was used [15]. 10 µL of a 2MPC50 dose of venom was mixed with 20 µL of various doses of test antivenoms (25–400 µg/mL) in 96-well plates for 5 min on a microplate shaker. The plate was incubated at 37 °C for 20 min, 200 µL of the substrate (1.1% egg yolk suspension in 0.1 M PBS adjusted to pH 8.1 and 125 µL 0.2 mM CaCl2) was added to all wells, incubated at 37 °C and the change in absorbance of the substrate (0 to 30 min) was determined spectrophotometrically at 620 nm [15]. Triplicate determinations were made and the least amount of antivenom required to reduce svPLA2 activity by 50% (EC50) was determined by regression analysis.

Determination of the brine shrimp lethality of venom, antivenom, and controls

The method of Meyer et al. was used [16]. Ten, 48-h old brine shrimp larvae were transferred from a hatching trough to 5 mL sample vials. Aliquots (5, 50 and 500 µL) of 5 mg/mL stock solutions of the samples (venom/antivenom) were pipetted into the vials and made up to the mark using 38.5% w/v marine salt solution to make 10, 100, and 1000 µg/mL sample concentrations respectively. PBS and vincristine sulphate were used as negative and positive controls respectively. Quintuple determinations were made and surviving larvae were counted after 24, 48, and 72 h. LC50s of samples were calculated by probit analysis. LC50 was defined as the least concentration of samples which resulted in 50% mortality of brine shrimp [17].

Neutralization of venom-induced lethality

The WHO (World Health Organization) protocol on venom neutralization by antivenoms was used with modifications [5]. Varying doses of the antivenoms (25–400 µL of 100 mg/mL) were mixed with a 2LC50 dose of venom. The venom/antivenom mixtures were incubated at 37 °C for 30 min, added to vials containing brine shrimp larvae and surviving larvae were counted after 24, 48, and 72 h. The median effective concentration (EC50) of the antivenoms was determined by regression analysis and was defined as the minimum amount of antivenom (in µL) that was required to neutralize 1 mg of venom [5].

Statistical analysis

Venom concentrations were converted to log10 (x-axis) and mean responses were converted to percentages (y-axis). The concentration of venom responsible for 50% svPLA2 activity (MPC50) was predicted by regression analysis (SPSS v20). Mortalities were converted to probits and regressed against the log concentration of venom (MS Excel 2013) [18, 19]. Analysis of variance and Tukey’s post hoc test (p < 0.05) was used to evaluate dose-dependent differences in svPLA2 activity and brine shrimp lethality. Meyer’s and Clarkson’s criteria were used to infer the toxicity of substances tested in the brine shrimp lethality assay [16, 20].


There was no significant difference (p > 0.05) in the svPLA2 activity of venom doses ranging from 0.5 to 8 µg/mL (Table 1). See The same was true for doses > 15 µg/mL (Table 1). There was a positive linear relationship between the log concentration of venom and the  %svPLA2 activity (Figure S1); The correlation was significant; r(65) = 0.804, p < 0.05, regression equation was ŷ = 26.339x + 51.906, and r2 = 0.646; that is, 64.6% of the variance in the  %svPLA2 activity was predictable from the log concentration of venom. Based on this regression model, the MPC50 was found to be 0.847 µg/mL.

Table 1 The dose–response relationship of svPLA2 in Naja ashei venom

There was a negative linear relationship between the log concentration of the venom + antivenom I mixture and %svPLA2 activity (Figure S2); The correlation was significant r(14) = 0.669, p = 0.006 and regression equation was ŷ = − 44.792x + 154.164. Based on this regression model, 1 mL of antivenom I neutralized 0.08 µg of svPLA2.

There was a negative linear relationship between the log concentration of the venom + antivenom II mixture and %svPLA2 activity (Figure S3); The correlation was significant r(14) = 0.772, p = 0.001 and regression equation was ŷ = − 44.706x + 162.226. Based on this regression model 1 ml of antivenom II neutralized 0.05 µg of svPLA2.

Test antivenoms were generally non-toxic (Table 2), N. ashei venom was more toxic than vincristine sulphate (positive control) after 24 h but vincristine sulphate was more toxic than venom after 48 and 72-h (Table 2). See also,, and There was no significant difference (p > 0.05) in the % mortality of brine shrimps exposed to 100 µg/mL or 1000 µg/mL of venom after 24, 48, and 72 h. See

Table 2 The brine shrimp cytotoxicity profile of Naja ashei venom, two commercial antivenoms, and vincristine sulphate (standard cytotoxic agent)

One milliliter of antivenom II neutralized 0.207 mg of venom in the brine shrimp lethality assay but antivenom I was ineffective. See The mean protein content of the venoms and antivenoms was significantly different from each other. See


Naja ashei venom is yet to be included in immunizing mixtures of commercially available antivenom. In this study, we have demonstrated that Mexican and Indian manufactured antivenoms poorly neutralized the svPLA2 activity of this venom. We have also established that only the Mexican manufactured antivenom was effective in neutralizing the toxic effects of this venom. These observations highlight the limited efficacy of imported antivenoms in neutralizing key toxins in the venom of a snake associated with many bites in East Africa [5]. The clamor for locally manufactured antivenoms seems justified [21].

In the context of African spitting cobras, Indian manufactured antivenom is indicated for Naja nigricollis and Naja haje envenomation while the Mexican manufactured antivenom is indicated for Naja nigricollis, Naja haje, Naja pallida, Naja nubiae and Naja katiensis [22]. Therefore, it may be inferred that the cross-neutralization of toxic proteins in N. ashei venom by Mexican manufactured antivenom was because the toxicity profile of N. ashei venom may be similar to the profile in Naja pallida, Naja nubiae, and Naja katiensis venoms but dissimilar to Naja nigricollis and Naja haje venoms.

How can the pharmacological findings in this study be explained by what is known about the composition of N. ashei venom? Hus and colleagues indicated that the most abundant proteins in N. ashei venom were cytotoxins (3FTxs; three-finger toxins) and svPLA2’s [8]. Other venom proteins include 5′N-Snake venom 5′-nucleotidase; SVMPs—snake venom metalloproteinases; CRISPs—cysteine-rich venom proteins; CVF—cobra venom factor; and VNGF—venom nerve growth factor [8]. svPLA2’s may be acidic or basic and are divided into groups IA, IIA, and IIB [23]. The fact that this study used a pH of 8.1 to run the agarose-egg yolk assay strongly suggests that the observed svPLA2 activity was basic. This corroborates the findings of a previous study which reported that a majority of N. ashei venom proteins were of low molecular weight and basic [8]. Group IA svPLA2’s are primarily found in elapids, although some have been reported in colubrids [23]. Group IIA and IIB svPLA2’s are exclusively found in viperids [23]. Since N. ashei is an elapid, the svPLA2 activity observed was most likely of the Group IA variety.

Naja ashei venom exhibited strong cytotoxic action in the brine shrimp lethality assay relative to vincristine sulphate (a standard cytotoxic). It is important to note that the brine shrimp lethality assay is a good predictor of cytotoxicity and has been widely used to reliably detect this phenomenon in the venom of the sea snake; Enhydrina schistosa [24], and in several venomous fish [25,26,27,28], snails [29,30,31], toads [32] and bees [33]. The dose and time-dependent brine-shrimp lethality observed may be a direct consequence of the non-enzymatic effects of cytotoxins i.e. paralysis, Ca2+ toxicity, and cell death [34]. However, it is unlikely that this observation was not supported by the enzymatic action of the basic Group IA svPLA2’s which have been known to cause organelle toxicity, hydrolysis of the lipid environments of cell membranes, and mitochondrial membrane disruption of the respiratory muscle [34,35,36]. An important finding in this study was that the concentration of N. ashei venom was not the only predictor of svPLA2 activity. This raises a pertinent question: what other factors may be involved in predicting this activity? It was also observed that low and intermediate doses of N. ashei venom produced similar svPLA2 activities and there was no difference in the brine shrimp mortalities caused by intermediate and high doses of the venom. This may suggest that the activities of these toxins remain fairly constant within a narrow range of venom doses.

It was established that both antivenoms were safe in brine shrimp. The evaluation of the safety profile of the test antivenoms was important because (i) snake antivenoms may cause both acute (anaphylactic/pyrogenic) and delayed (serum sickness) toxic manifestations in human envenomation [37], and (ii) the safety profile was key in informing the selection of antivenom aliquots to be used in the neutralization assay.

Based on protein estimation by Lowry’s method, it was established that Indian manufactured antivenom had a higher protein content than Mexican manufactured antivenom but was ineffective in neutralizing the toxic effects of N. ashei venom. Because both antivenoms are made up of immunoglobulin-binding fragments; F(ab)’s [22] and given the fact that Lowry’s method largely reports the aromatic acid (tyrosine and tryptophan) composition of proteins [38], it may be argued that these amino acids may not be involved in the recognition and neutralization of toxic venom proteins in N. ashei venom.


The svPLA2 activity and toxicity of N. ashei venom remain fairly constant within a narrow range of venom doses. Commercially available antivenoms are generally safe but have limited efficacy in neutralizing the svPLA2 activity of N. ashei venom. Moreover, only Mexican manufactured antivenom cross-neutralizes toxic venom proteins in N. ashei venom. We recommend studies on the activities of other toxins in this venom and their neutralization by antivenom.


Snake venom is a complex mixture of toxins. This study only evaluated the snake venom phospholipases A2 activity and brine shrimp lethality of N. ashei venom. To fully understand the capacity of antivenoms to neutralize N. ashei venom, it may be necessary to evaluate other toxins in this venom.

Availability of data and materials

All data generated or analyzed during this study are included in this published article. [And its additional information files below]. Information on the snakes whose venom was used in this study (Table S1); Details on the snake antivenom used in this study (Table S2); Raw data of the absorbance values (660 nm) of different concentrations of bovine serum albumin (protein standard), Naja ashei venom, and antivenom; The data output from the analysis of variance (+Tukey’s post hoc test) to determine dose-dependent differences in the svPLA2 activity of Naja ashei venom; The data output from the simple linear regression analysis to determine the %vPLA2 activity of different concentrations of Naja ashei venom (Figure S1); The data output from the simple linear regression to determine the capacity of antivenom I and II to neutralize the svPLA2 activity of Naja ashei venom (Figure S2), and (Figure S3);, The data output from probit regression analysis to determine the toxicity of Naja ashei venom, and vincristine and the safety of antivenom in brine shrimp;,, and The data output from analysis of variance (+Tukey’s post hoc test) to determine dose-dependent differences in Naja ashei venom-induced brine shrimp lethality; The data output from simple linear regression to determine the capacity of antivenom to neutralize Naja ashei venom-induced brine shrimp lethality The data output from analysis of variance (+Tukey’s post hoc test) to determine the differences in the mean protein content of Naja ashei venom and antivenom I and II


svPLA2 :

Snake venom phospholipase A2


Brine shrimp lethality assay

LC50 :

Lethal concentration responsible for 50% mortality

MPC50 :

The minimum phospholipase concentration responsible for 50% response

EC50 :

The least amount of antivenom (in µL) required to neutralize 1 mg of venom


Deoxyribonucleic acid


Bovine Serum Albumin






Volume by volume




Microgram per milliliter




Enzyme-linked Immunosorbent assay


Phosphate-buffered saline

CaCl2 :

Calcium chloride


World Health Organization


Milligram per milliliter

r2 :

Coefficient of determination

LD50 :

Median lethal dose


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The authors would like to acknowledge Ms. Claire Taylor and Mr. Boniface Momanyi of the Bioken Snake Farm (Watamu, Kenya) for providing the venom samples. We would also like to thank Ms. Vivian of the Department of Animal Physiology, the University of Nairobi who helped us in freeze-drying the venom samples and Dr. Nduhiu, Mr. Mainga, Mr. Maloba, Mr. Nderitu, Mr. Antony (BVM student) and Mr. Bett of the Department of Public Health, Pharmacology and Toxicology for their assistance in the phospholipase and brine shrimp lethality assays. Special gratitude to Dr. Nelson Odhiambo and Edna Opiyo of the Nyakach Sub County Hospital for providing the antivenom samples that were used in this study. We also wish to thank Dr. Joshua Onono and Mr. Duke Gekonge for their assistance in statistical analysis.


This study did not receive any external funding.

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Conceptualization: MO, FO, and JG; data curation: all authors; formal analysis: MO; investigation: all authors; methodology: MO; project administration: MO and FO, resources; all authors; software: MO; supervision; JM, JG, PM, and VO; validation: FO, JM, JG, PM, and VO; visualization: MO; writing original draft: MO: writing review and editing: all authors. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Mitchel Otieno Okumu.

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Ethics approval and consent to participate

This study was approved by the Biosafety, Animal Use, and Ethics Committee of the Faculty of Veterinary Medicine, University of Nairobi. REF BAUEC/2019/220 issued on 24th April 2019. The animals (brine shrimps; Artemia salina) used in this study were commercially sourced thus the owner’s consent was not required.

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The authors declares that they have no competing interests.

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Okumu, M.O., Mbaria, J.M., Gikunju, J.K. et al. Enzymatic activity and brine shrimp lethality of venom from the large brown spitting cobra (Naja ashei) and its neutralization by antivenom. BMC Res Notes 13, 325 (2020).

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  • Snake venom phospholipases A2
  • Brine shrimp lethality assay
  • Snake venom toxicity
  • Naja ashei
  • Brine shrimp
  • Artemia salina
  • Probit analysis
  • LC50
  • EC50
  • MPC50