Development of Equine IgG Antivenoms against Major Snake Groups in Mozambique

Background Snake envenoming is a significant public health problem in underdeveloped and developing countries. In sub-Saharan Africa, it is estimated that 90,000–400,000 envenomations occur each year, resulting in 3,500–32,000 deaths. Envenomings are caused by snakes from the Viperidae (Bitis spp. and Echis spp.) and Elapidae (Naja spp. and Dendroaspis spp.) families. The African continent has been suffering from a severe antivenom crisis and current antivenom production is only sufficient to treat 25% of snakebite cases. Our aim is to develop high-quality antivenoms against the main snake species found in Mozambique. Methods Adult horses primed with the indicated venoms were divided into 5 groups (B. arietans; B. nasicornis + B. rhinoceros; N. melanoleuca; N. mossambica; N. annulifera + D. polylepis + D. angusticeps) and reimmunized two times for antivenom production. Blood was collected, and plasma was separated and subjected to antibody purification using caprylic acid. Plasmas and antivenoms were subject to titration, affinity determination, cross-recognition assays and in vivo venom lethality neutralization. A commercial anti-Crotalic antivenom was used for comparison. Results The purified antivenoms exhibited high titers against B. arietans, B. nasicornis and B. rhinoceros (5.18 x 106, 3.60 x 106 and 3.50 x 106 U-E/mL, respectively) and N. melanoleuca, N. mossambica and N. annulifera (7.41 x 106, 3.07 x 106 and 2.60 x 106 U-E/mL, respectively), but lower titers against the D. angusticeps and D. polylepis (1.87 x 106 and 1.67 x 106 U-E/mL). All the groups, except anti-N. melanoleuca, showed significant differences from the anti-Crotalic antivenom (7.55 x 106 U-E/mL). The affinity index of all the groups was high, ranging from 31% to 45%. Cross-recognition assays showed the recognition of proteins with similar molecular weight in the venoms and may indicate the possibility of paraspecific neutralization. The three monospecific antivenoms were able to provide in vivo protection. Conclusion Our results indicate that the anti-Bitis and anti-Naja antivenoms developed would be useful for treating snakebite envenomations in Mozambique, although their effectiveness should to be increased. We propose instead the development of monospecific antivenoms, which would serve as the basis for two polyvalent antivenoms, the anti-Bitis and anti-Elapidae. Polyvalent antivenoms represent an increase in treatment quality, as they have a wider range of application and are easier to distribute and administer to snake envenoming victims.


Introduction
Snake envenoming prevention and treatment has been a worldwide effort in underdeveloped and developing countries in Africa, Asia and South America. In sub-Saharan Africa, it is estimated that 90,000-400,000 envenomations occur per year, resulting in 3,500-32,000 fatalities [1]. Amputations and complications caused by snake envenoming affect 3% and 5.5% of envenomation victims, respectively [2]. As accidents with snake occur mostly with young men in rural areas, they can result in the removal of these men from the workforce, causing great personal and economic financial losses. Snake envenoming is caused mainly by snakes from the Viperidae (Echis spp. and Bitis spp.) and Elapidae (Naja spp. and Dendroaspis spp.) families. Viperidae snakes have a venom rich in metalloproteinases (SVMP) that can cause hemorrhagic effects and coagulatory-inducing disturbances [3]. Echis occelatus is responsible for most accidents [4], while Bitis arietans has the widest territorial distribution [5]. Elapidae snake venoms have a more pronounced neurotoxic action, targeting neuromuscular junctions, and accidents can evolve to respiratory failure [6]. Spitting cobra bites (Naja spp.) are regarded as the most medically important due to their lethality [7]. The most effective treatment against snakebite envenoming is the administration of specific antivenom. Antivenom was introduced in Africa in 1950; there were three major producers-Behringwerke A.G. (Germany), Sanofi-Pasteur (France) and the indigenous South African Institute for Medical Research (SAIMR) [8]. After the 1980's, the European companies ceased or greatly reduced their production due to the high cost of antibody production, and SAIMR struggled financially. The present production of antivenom (200,000 ampules/year) meets less than 25% of the African continent's demand for snakebite treatment [9]. In an effort to solve the problem, African authorities began importing antivenoms from India and Asia. These antivenoms are not specific against African snakes and this treatment has little efficacy, causing the population to be distrustful and look for alternatives, such as traditional healing routes [10]. Even with a new wave of antivenoms being researched [11,12,13], there is still much to be done towards fighting snakebite envenomation in sub-Saharan Africa. In this study, we concentrate on the development of antivenoms against eight snake species found in Mozambique: Bitis arietans, B. nasicornis, B. rhinoceros, Naja melanoleuca, N. mossambica, N. annulifera, Dendroaspis angusticeps and D. polylepis. Our results are promising, and provide the basis for polyvalent antivenoms that could prove viable for widespread use.

Quantification of proteins
The protein concentrations of the venoms and plasma/antivenoms were assessed by the bicinchoninic acid method [14] using a Pierce BCA Protein Assay Kit (Rockford, IL).

Ethical clearance
All animals used in this study were maintained and treated under strict ethical conditions in accordance with the "International Animal Welfare recommendations" [15] and the "Committee Members, International Society on Toxinology" [16]. This project was approved by the Ethics Committee of Animal Usage in Research (Protocol No: 1137/13) of the Instituto Butantan.

Antigen preparation, immunization schedule and antivenoms
The horses received the following mixtures: anti-B. arietans (n = 12), 3.5 mg/animal of crude B. arietans venom; anti-B. nasicornis + B. rhinoceros (n = 12), 3.5 mg/animal of crude B. nasicornis and B. rhinoceros venom mixture (1:1); anti-N. melanoleuca (n = 12), 3.5 mg/animal of crude N. melanoleuca venom; anti-N. mossambica (n = 6), 3.5 mg/animal of crude N. mossambica venom; anti-D. angusticeps + D. polylepis + N. annulifera (n = 9), 3.5 mg/animal of crude D. angusticeps, D. polylepis and N. annulifera venom mixture (1:1:1). The subcutaneous injections were performed 15 days apart at four different points in the dorsal region of each animal. The animals were primed (4 inoculations in 6 mL of complete or incomplete MMT80 adjuvant), and later re-immunized for this experiment (2 inoculations in 6 mL of PBS). Fifteen days after each inoculation post-priming, blood was collected (8 mL/animal) in vials with anticoagulant solution (heparin by venipuncture of the jugular vein). The plasma was separated by centrifugation (1,500 rpm for 15 min at 4°C) and stored at -20°C. Horse blood was collected and the plasma was separated as described above. Four equine plasma samples (Batch No: #143, #158, #223 and #356) from horses immunized with C. d. terrificus venom, according to WHO guidelines [17], were used to produce anti-Crotalic serum. These samples were provided by "Divisão de Desenvolvimento Tecnológico e Produção-Seção de Processamento de Plasmas Hiperimunes, Instituto Butantan", and they were used as a standard for comparison. The obtained plasma samples were pooled within their respective groups and immunoglobulins were purified using caprylic acid.

Antibody purification with caprylic acid
Equine antibodies were purified from plasma (2 nd immunization samples) following the procedure described by Dos Santos et al. [18]. The plasma samples were pooled within their respective groups, heated at 56°C for 15 min to achieve complement inactivation and centrifuged at 900 g for 10 min. The pH of the samples was adjusted to 5.0 through the addition of 0.1 N acetic acid. Caprylic acid was added slowly with vigorous shaking to a final concentration of 8.7%, and then the samples were left to shake for 30 min at room-temperature. After a second centrifugation step (11,000 g for 15 min), the supernatants were collected, and their pH were adjusted to between 7.0 and 7.5 through the addition of 0.1 N NaOH. The samples were filtered through a Sterile Millex 0.45 μm (Milliford Corporation, Billeric, MA). Dialysis was performed against PBS buffer using a Centricon 50 kDa Centrifugal Device (Milliford Corporation, Billeric, MA) 4,000 g for 10 min, three times. The samples were then diluted to 30 mg/mL and stored at -20°C.

Quantification of the antivenom antibodies
Polystyrene, high-affinity ELISA plates (96 wells) were coated with 1.0 μg/well of crude B. arietans, B. nasicornis, B. rhinoceros, N. melanoleuca, N. mossambica, D. angusticeps, D. polylepis or N. annulifera venoms in 100 μL of PBS buffer and kept overnight at 4°C. In some assays, the plates were coated with 1.0 μg/well of crude C. d. terrificus venom for standard antivenom quantification. The plates were blocked for 2 h at 37°C with 200 μL/well of PBS plus 5% BSA. The plates were washed with 200 μL/well of PBS. Serial dilutions of horse plasma (1:4,000 to 1:512,000) or IgG antivenoms (1:2,000 to 1,024,000) in PBS plus 0.1% BSA were prepared, and 100 μL/well of each dilution was added to their respective antigens. The plates were then incubated at 37°C for 1 h, and washed three times with the wash buffer (PBS plus 0.1% BSA and 0.05% Tween-20, 200 μL/well). Rabbit peroxidase-conjugated anti-horse IgG (whole molecule) (Sigma Aldrich, St. Louis, MO) diluted (1:20,000) in PBS plus 0.1% BSA (100 μL/well) was added to the plates. The plates were incubated for 1 h at 37°C. After three washes with the wash buffer, 50 μL/well of the substrate buffer was added, and the plates were incubated at room temperature for 15 min. The reaction was terminated by the addition of 50 μL/well of 4 N sulfuric acid. The absorbance at 492 nm was recorded using an ELISA plate reader (Labsystems Multiskan Ex, Thermo Fisher Scientific Inc., Walthan, MA). IgG from horses collected before immunization was used as a negative control (fixed dilution of 1:2,000). The antivenom dilution with an optical density of 0.2 was used to calculate the U-ELISA per milliliter of the undiluted antivenom solution. One U-ELISA was defined as the smallest dilution of antibody that presented an OD of 0.2 under the conditions used in the ELISA assay, as described previously [19]. The value was then multiplied by 10 to convert it to milliliters.

Antivenom affinity measurements
The affinities of the horse plasmas (2 nd immunization samples) or IgG antivenoms were measured using ELISA, following the methodology described above, with the inclusion of a potassium thiocyanate (KSCN) elution step [20,21,22]. After the serum incubation step, dilutions of KSCN (0.0 to 5.0 M, in intervals of 1.00 M) in distilled H 2 O were added to the wells and incubated for 30 min at room temperature. The remaining bound antibodies were detected with rabbit peroxidase-conjugated anti-horse IgG (whole molecule) (Sigma Aldrich, St. Louis, MO) diluted (1:20,000) in PBS plus 0.1% BSA (100 μL/well). After three washes with the wash buffer, 50 μL/well of substrate buffer was added, and the plates were incubated at room temperature for 15 min. The reaction was terminated with 50 μL/well of 4 N sulfuric acid. The absorbance at 492 nm was recorded using an ELISA plate reader (Labsystems Multiskan Ex, Thermo Fisher Scientific Inc., Waltham, MA). The results are expressed as follows: affinity index (AI) = % bound antibodies at KSCN 5 M.

SDS-PAGE and western blot cross-recognition essay
Western blot analysis was carried out according to the method previously described by Towbin et al. [23]. Crude B. arietans, B. nasicornis, B. rhinoceros, N. melanoleuca, N. mossambica, D. angusticeps, D. polylepis and N. annulifera venoms (10 μg) were treated with non-reducing SDS-PAGE sample buffer and resolved in 12.5% polyacrylamide gel. Gels were either submitted to silver staining or electroblotted onto nitrocellulose membranes, according the method described by Laemmli [24]. These membranes were blocked with PBS buffer containing 5% BSA at 37°C for 2 h, washed with PBS, and treated with the antivenom diluted to 1:20,000 in PBS plus 0.1% BSA for 1 h at room temperature on a horizontal shaker. Each membrane was treated with only one antivenom. After being washed three times with PBS plus 0.05% Tween-20, the membranes were incubated with rabbit anti-horse IgG conjugated to alkaline phosphatase (whole molecule) diluted to 1:7,500 in PBS plus 0.1% BSA. Then, the membranes were incubated for 1 h at room temperature on a horizontal shaker. The membranes were washed three times with PBS plus 0.05% Tween-20 and placed in developing solution for Western blotting. The reaction was terminated by washing with distilled water.

In vivo lethality neutralization essay
Male Swiss mice, 18-20 g, were used in protocols to determine the lethality (LD 50 ) of the venoms and the neutralizing potency (ED 50 ) of the antivenoms. For LD 50 determination, different venom quantities were prepared in 0.85% NaCl solution and intraperitoneally injected (500 μL) in the mice. Four mice were used per venom dose. Deaths were recorded after 48 h, and LD 50 was estimated by probits analysis [25]. For ED 50 determination, a fixed amount of 3 LD 50 of snake venom and various dilutions of the respective purified antivenoms (1:5, 1:10, 1:20, and 1:40) were incubated for 30 min at 37°C. Venom samples incubated only with 0.85% NaCl solution were used as controls. After incubation, 500 μL aliquots of the mixtures were intraperitoneally injected in the mice. Four mice were used per dilution. The death/survival ratio was recorded at 3 h, 24 h and 48 h after the injection. ED 50 was estimated by probits analysis. Data is expressed as Specific Activity (μg of venom neutralized by 1mg of antibodies).

Statistical analysis
The data was analyzed using one-way ANOVA, followed by the Dunnett's Multiple Comparison Test (standard antivenom as comparison), or two-way ANOVA, followed by the Bonferroni Post-Test (standard antivenom as comparison). Differences were considered to be significant if P < 0.05. Analysis was performed using GraphPad Prism 5 for Windows (Graph-Pad Software, San Diego, USA).

Hyperimmune plasma titration
The titration of the plasmas against the respective venoms was performed using ELISA. The plates were sensitized with 1 μg/well of antigen, and the plasma dilutions ranged from 1:4,000 to 1:512,000. Titration curves from different immunizations and groups showed similar kinetics ( Fig 1A). When titers were compared, differences between different immunizations were not found (Fig 1B). The groups anti-B arietans and anti-B. nasicornis + B. rhinoceros showed similar results, with titers ranging from 3.47 x 10 6 to 4.62 x 10 6 U-ELISA/mL. The anti-N. mossambica and anti-N. melanoleuca groups displayed the highest titers, 4.55 x 10 6 to 5.12 x 10 6 U-ELISA/ mL. Significant differences were not found between those groups and the standard anti-Crotalic antivenom (4.21 x 10 6 U-ELISA/mL). The group anti-D. angusticeps + D. polylepis + N. annulifera showed higher titers against N. annulifera venom (from 2.67 x 10 6 up to 3.93 x 10 6 U-ELISA/mL), and lower titers against the Dendroaspis venoms, between 1.46 x 10 6 and 2.23 x 10 6 U-ELISA/mL. This group was also the only one to show a statistically significant difference when compared to the standard anti-Crotalic antivenom.

Hyperimmune plasma affinity determination
Affinity determination was performed by ELISA with the inclusion of an elution step with KSCN, a chaotropic agent, in concentrations ranging from 0 M to 5 M. Only plasma samples from the 2 nd immunization were used, and the dilution was fixed at 1:20,000. The affinity curves obtained for all groups presented similar kinetic behaviors (Fig 2A). The affinity index determination showed a similar percentage of bound antibodies between the experimental groups with the affinity index ranging from 40% to 49% against most of the venoms tested ( Fig  2B). The highest affinity was obtained with the anti-N. melanoleuca plasma (60%). No statistical significant difference was found between the experimental groups and the standard anti-Crotalic antivenom (44%).

Antibody preparation titration
Plasmas samples (2 nd immunization) were used for the IgG antibody purification with caprylic acid. The titration of the resulting IgG antivenoms was performed with ELISA, as described previously, with antibody dilutions ranging from 1:2,000 to 1:1,024,000. The titration curves again displayed similar kinetics, with a more pronounced decline towards greater antibody dilutions (Fig 3A). We observed a small increase in titers after purification in the anti-B. arietans (5.18 x 10 6 U-ELISA/mL), anti-B. nasicornis + B. rhinoceros (3.50 x 10 6 and 3.60 x 10 6 U-ELISA/mL, respectively) and an small decrease in titers in anti-D. angusticeps + D. polylepis + N. annulifera (1.87 x 10 6 , 1.67 x 10 6 and 2.60 x 10 6 U-ELISA/mL, respectively) groups. The anti-N. mossambica group had a high decrease in titers (3.07 x 10 6 U-ELISA/ mL), while the anti-N. melanoleuca group showed a big increase; it had the highest titers (7.41 x 10 6 U-ELISA/mL). We found statistically significant differences between all the groups, with the exception of anti-N. melanoleuca, when compared to the purified standard anti-Crotalic antivenom (7.55 x 10 6 U-ELISA/mL) (Fig 3B).

Antivenom affinity determination
The affinity curves displayed similar kinetics both between groups and with pre-and post-purification samples (Fig 4A). The affinity indices decreased compared to the pre-purification samples, ranging between 31% and 37% against most venoms. The anti-N. melanoleuca group showed the highest results (45% bound antibodies at KSCN 5 M). This group was also the only one to show a statistically significant difference when compared to the standard anti-Crotalic antivenom (33%) (Fig 4B).

Cross-recognition by western blot
The venoms (10 μg) were treated with non-reducing SDS-PAGE resolved in 12.5% polyacrylamide gel. Samples were either stained with silver ( Fig 5A) or electroblotted onto nitrocellulose membranes for Western blot (Fig 5B-5F) recognition with the purified antibodies (2 nd immunization), diluted 1:20,000. The venom from B. arietans, B. nasicornis and B. rhinoceros showed a similar pattern, with protein bands close to 15 kDa, related to PLA 2 , 20-60 kDa, related to SVSPs, and 60-120 kDa, related to SVMPs [26,27]. The N. mossambica, N. melanoleuca and N. annulifera venoms were also similar, with protein bands close to 20, 25 and 60 kDa, related to SVMPs. The N. melanoleuca and N. annulifera venoms also displayed protein bands close to 15 kDa, related to PLA 2 , and two high weight proteins bands, 85 kDa (related to SVMPs) and 120 kDa (CVF) [28]. The venom from D. angusticeps and D. polylepis showed a few protein bands, close to 25, 40, 60 and 85 kDa, related to SVMPs [29]. The anti-B. arietans (Fig 5B) and The plates were sensitized with 1 μg of antigen/well and the plasma dilutions ranged from 1:4,000 to 1:512,000. The dotted line represents an OD of 0.2. The titers are expressed as Units-ELISA/mL x 10 6 . The medians were compared by two-way ANOVA followed by the Bonferroni Post-Test (standard antivenom as comparison), *P < 0.05, **P < 0.01, and ***P < 0.001. The data are representative of three independent experiments. doi:10.1371/journal.pntd.0004325.g001 anti-B. nasicornis + B. rhinoceros antivenoms (Fig 5C) exhibited bands close to 20, 25, 60, 85 and 120 kDa, present with the different Bitis venoms, and bands close to 60 kDa with the other venoms. The anti-B. nasicornis + B. rhinoceros antivenom was also able to resolve bands close to 15 kDa on the Bitis venoms. The anti-N. melanoleuca (Fig 5D) and anti-N. mossambica antivenoms (Fig 5E) showed bands close to 20-25, 60 and 85 kDa on most venoms tested, a band close to 10 kDa on the N. melanoleuca and N. mossambica venoms and a band over 120 kDa on the N. melanoleuca and N. annulifera venoms. The anti-D. angusticeps + D. polylepis + N. annulifera antivenom (Fig 5F) recognized the same bands as the monospecific Naja antivenoms, plus a band between 10 and 15 kDa on the Dendroaspis venoms (BPTI-like toxins). Protein bands with 25, 60 and 85 kDa appeared on all the venoms tested and were crossrecognized by all experimental antivenoms.

In vivo venom lethality neutralization
In vivo protection (ED 50 ) was determined by the injection of 3 LD 50 of the venom, incubate with different concentrations of the respective antivenom (1:5, 1:10, 1:20, 1:40). The three monospecific antivenoms were effective in neutralizing venom lethality (Table 1). Anti-B. arietans showed the highest specific activity, with 77 μg of venom neutralized by 1 mg of antivenom, and it was followed by anti-N. mossambica (16 μg venom/mg of antivenom) and anti-N. melanoleuca (11 μg of venom/mg of antivenom). Anti-B. nasicornis + B. rhinoceros provided protection against B. nasicornis venom (54 μg of venom/mg of antivenom), however it was not able to protect against B. rhinoceros lethal activity. The polyspecific anti-D. angusticeps + D. polylepis + N. annulifera was not able to neutralize the lethality of any of the three venoms, and in vivo protection was not achieved in this group.

Discussion
Polyvalent antivenoms often use multi-specific venom mixtures for immunization [8,11,12,30]. Snake venoms are a very complex mixture of components with different immunogenic properties. This means that a few, or even a single more immunogenic component, can skew the immune response towards themselves, while the less immunogenic antigens are ignored by the immune system. Using monospecific antigenic mixtures, we can customize the immunization protocols to obtain the optimal response against each venom. By pooling the antivenoms afterwards, we are able to more accurately calculate the quantity of each neutralizing antibody in the final mixture. By increasing the specific activity of the antivenom, lower doses are required for treatment, thus reducing the risk of emerging undesirable reactions.
The immunization process should be oriented towards the development of high-affinity antibodies and long-lived memory B cells. The inoculation of low antigen dosages, combined with multiple inoculation sites and longer immunization intervals, will lead to clonal expansion of only the high affinity lymphocytes (for a review, consult McHeyzer-Willians et al. [31]). This strategy had already been successfully tested by our group in the context of antivenom production [22]. In this study, we were able to obtain high-quality antibodies in a short time, and little to no difference was observed between our experimental antibodies and the commercial anti-Crotalic antivenom produced by Instituto Butantan. In vivo protection was achieved with the three monospecific antivenoms, but not with the two polyspecific antivenoms.
The anti-B. arietans and anti-B. nasicornis + B. rhinoceros antivenoms yielded high titers and had high affinity scores. Western blot also revealed a very similar recognition pattern for both antivenoms. Despite these venoms having a very similar composition, the antivenoms showed little paraspecific activity, demonstrated by the drop in titers in the cross-recognition quantification assay. The anti-B arietans antivenom was capable of neutralizing its respective venom lethal activity, however the anti-B. nasicornis + B. rhinoceros was only able to provide protection against B. nasicornis venom. It has been shown that antivenoms containing anti-B. arietans and anti-B. gabonica antibodies were not able to neutralize the lethal activity of B. nasicornis, although they effectively neutralized B. rhinoceros venom [12]. To ensure protection against Bitis envenomation, we suggest the development of monospecific B. arietans, B. nasicornis and B. rhinoceros antivenoms, which would be pooled afterwards in a single anti-Bitis antivenom.
The anti-N. melanoleuca and anti-N. mossambica antivenoms yielded high titers and affinity. The antivenoms were also effective in providing in vivo protection against their respective antivenoms. The protein bands as observed by Western blot revealed a very similar recognition profile from both antivenoms, and the cross-recognition titration demonstrated paraspecific activity. Although this suggests that cross-neutralization is a possibility, it has been shown that N. melanoleuca antivenom alone is unable to neutralize the lethal activity of N. mossambica [32]. N. melanoleuca venom has mostly neurotoxic components, while N. mossambica venom also possesses important cytotoxic components. Both anti-Naja antivenoms should be considered when designing polyspecific antivenoms.
The anti-D. angusticeps + D. polyleps + N. annulifera antivenom showed poor results. Although titration against N. annulifera and other Naja venoms was satisfactory, titers against the Dendroaspis venom were very low. The recognition of venom proteins by Western blot also  revealed a pattern very similar to the two monospecific anti-Naja antivenoms. Considering the profile observed in the Western blot, the difference in titers, and the presence of pro-inflammatory components in Naja venom [33], we concluded that the N. annulifera venom acted as the dominant antigen, directing the immune response to it. In vivo lethality neutralization was not determined, as the antivenom was ineffective in providing protection against any of three venoms tested. To obtain proper protection against Dendroaspis, we suggest the removal of N. annulifera and the production of monospecific anti-D. angusticeps and anti-D. polylepis antivenoms.
Our data supports the production of two antivenoms for use in Mozambique: an anti-Bitis composed of a mixture of monospecific anti-B. arietans, anti-B. nasicornis and anti-B. rhinoceros antivenoms, and an anti-Elapidae, composed of a mixture of monospecific anti-N. melanoleuca, anti-N. mossambica, anti-D. angusticeps and anti-D. polylepis antivenoms. The antivenoms proposed here could be supplied in parallel, and differential diagnosis would ensure the correct choice of treatment (Viperidae envenomation is characterized by hemorrhage and coagulatory disturbances [3], while Elapidae venom has neurotoxic properties [7]). Lyophilization of the product would be required to increase shelf life and facilitate storage and distribution.

Conclusion
The antivenoms produced in this study, specific against medically important African snakes, showed high titers, affinity, ability to cross-recognize venoms in in vitro essays and were capable of in vivo protection. The proposed polyvalent anti-Bitis and anti-Elapidae antivenoms would be effective in the treatment of snake envenoming in Mozambique and could be further developed for continental use. The availability and distribution of these antivenoms to the population in the rural areas would represent an important step in treating snake envenomation in Africa.