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Journal of Venomous Animals and Toxins including Tropical Diseases

On-line version ISSN 1678-9199

J. Venom. Anim. Toxins incl. Trop. Dis vol.18 no.4 Botucatu  2012

http://dx.doi.org/10.1590/S1678-91992012000400009 

ORIGINAL PAPER

 

General characterization of venom from the Moroccan snakes Macrovipera mauritanica and Cerastes cerastes

 

 

Oukkache N; Lalaoui M; Ghalim N

Laboratory of Venoms and Toxins, Pasteur Institute of Morocco, Casablanca, Morocco

Correspondence to

 

 


ABSTRACT

Ophidian envenomation accidents constitute a serious public health problem in many countries around the globe. Over 5 million such accident cases occur each year causing more than 100,000 deaths. In Africa, more than 20,000 deaths per year are registered while 400,000 envenomation victims retain severe and permanent functional sequelae. In Morocco, snakebites are frequent and of greater severity in children. They occur mostly in rural areas. The incidence of these bites remains poorly understood and vastly underestimated. The epidemiological data are not well known due to the absence of a national registry, whereas a significant proportion of envenomations receive only traditional treatment methods in non-medical intensive care. This prompted us to investigate the enzymatic and biological properties of venom biochemical constituents from two of the most dangerous snake venoms in Morocco: Cerastes cerastes (Cc) and Macrovipera mauritanica (Mm). Also, we studied the immune cross-reactivity of Cc and Mm venoms in comparison to that of another important dangerous Moroccan viper, Bitis arietans (Ba), to identify the best candidates (venom or a mixture of venoms) for producing the most efficient and protective antivenom. In the present study, we report a preliminary venom characterization of Cc and Mm and the cross-reactivity that may exist between their venoms and Ba. These venoms are known to be highly toxic and contain several proteins that differ by molecular weights. Interestingly, both Cc and Mm venoms are characterized by intense hemorrhagic and phospholipase A2 activities and their ability to degrade the α and γ chains of fibrinogen. They display very low proteolysis through the casein test. After injection into mice, Cc and Mm induce myonecrosis in skeletal muscles, which most likely reflects direct action of myotoxins and indirect action of hemorrhagic molecules present in these venoms. In mice, this myonecrosis diminishes serum creatine phosphokinase (CPK) levels. As expected, Cc venom is immunogenic and induces highly protective antivenom against Mm and Ba venom antigens. This protective capacity is similar to that of the antivenom produced against the Mm venom.

Key words: Cerastes cerastes, Macrovipera mauritanica, snake venom, characterization, biological activities, cross-reaction.


 

 

INTRODUCTION

In North Africa, there are many species of front-fanged snakes but only a few are known to be dangerous. The foremost medically important species belong to the family Viperidae - Cerastes cerastes, Cc (horned viper); Macrovipera mauritanica, Mm; and Bitis arietans, Ba - which were found capable of provoking severe hemorrhagic effects and the family Elapidae - i.e. Naja haje, Nh - most notably responsible for neurotoxic effects (1, 2). In Morocco, the majority of bites (53% of venomous animal bites and 7.2% of the estimated case fatality rate) occur in rural areas during the summer season (3). They are inflicted on the feet or ankles, most frequently during the evening when there is a greater probability of accidentally treading on a snake, sometimes at night while it is sleeping or moving. In Morocco, epidemiological data remain uncertain due to the non-declaration of envenoming cases and the absence of a national registry (4).

Venom glands are highly specialized tissues that possess a high capacity for protein secretion, and are a rich source of active proteins. Snake venoms are known to contain a complex mixture of pharmacologically active molecules, including organic and mineral components, small peptides and proteins. According to their major toxic effect, snake venoms may be conveniently classified as neurotoxic (Elapidae) or hemorrhagic (Viperidae). For instance, envenomings by Macrovipera mauritanica and Cerastes cerastes are characterized by hemorrhaging and abnormalities in the blood coagulation system, while the venom of the cobra Naja haje is mainly neurotoxic and affects the nervous system (5).

Viperidae snake venoms contain a number of different proteins (i.e. proteases, fibrinolytic enzymes) that induce alterations in the blood coagulation cascade and interfere with the normal hemostatic system and tissue repair, usually resulting in persistent bleeding. Studies on patients envenomed by various Viperidae species revealed a fascinating variation in clinical manifestations, ranging from neurological perturbations to increased capillary permeability and edema. These pathological outcomes may be due to the additive or synergistic effects of various enzymes and toxins present in the venom (6).

When taking measures against envenoming and concomitantly treating symptoms, specific therapy consisting of immunotherapy, using polyvalent antivenom, is still of great importance. When administered at the correct time, antivenom is considered to be the only efficient treatment of snake-envenomed patients. Experimental data and clinical observations have confirmed the rapid venom-neutralizing effect of potent antivenom (1, 7). However, producing an antivenom that is both effective and safe requires a more precise biological and biochemical characterization of the venom composition and analysis of its neutralization capacity. This prompts us to look for the venom biochemical constituents and to investigate the enzymatic and biological properties of two of the most dangerous snake venoms in Morocco: Cerastes cerastes and Macrovipera mauritanica. In this paper, we also studied the immune cross-reactivity between Cc and Mm venoms in comparison with Ba venom (another dangerous viper in Morocco) with the main objective of identifying the best candidates (venom or a mixture of venoms) and methodology for producing the most efficient and protective antivenom.

 

MATERIAL AND METHODS

Venoms

Venoms of Cerastes cerastes, Macrovipera mauritanica, Bitis arietans and Naja haje were extracted by manual stimulation, centrifuged, lyophilized and kept at -20ºC at the experimental center of the Pasteur Institute of Morocco.

Protein Content

The protein content of venoms samples was determined by the colorimetric method of Markwell et al. (8). Bovine serum albumin (BSA, Sigma) was used for standard assay.

SDS-Polyacrylamide Gel Electrophoresis

SDS-PAGE was carried out according to a previously described method (9). Samples were pretreated in reducing conditions (using β-mercaptoethanol).

Determination of Lethal Dose (LD50)

Swiss strain male mice aged 2 months and weighing 18-20 g were used. All the procedures involving animals were in accordance with the ethical principles in animal research adopted by the World Health Organization (10).

Lethal potency of venom (in µg per Swiss mice) was assessed intravenously (IV) as recommended by the World Health Organization (10). Increasing amounts were injected into Swiss strain male mice (groups of five mice), in final volumes of 500 µL. The mortality percentage was recorded 24 hours after injections. The lethal dose LD50 was determined according to the method described by the software package Prism 45 (GraphPad, Inc.).

Proteolytic Activity

Proteolytic activity was estimated using casein as substrate, according to the previously described method (11). Venoms were used at doses of 50, 100 and 200 µg. A negative control was made without the venom sample. The caseinolytic activity was expressed as U/mg, i.e. by the following formula: AU/mg = (ΔA280/mg of venom) × 100.

Procoagulant Activity

Coagulant activity was determined in human plasma (12). Citrated blood samples (1 volume of 129 mM trisodium citrate and nine parts blood) were centrifuged at 1700 g for 15 minutes at 4ºC and plasma was recovered. The coagulation activity was estimated after addition of venom serial dilutions. The minimum coagulant dose (MCD) was defined as the lowest amount of venom resulting in clot formation of human plasma through 1 minute at 37ºC.

Phospholipase A2 Activity

The phospholipase A2 activity was determined according to the method of Holzer and Mackessy (13). Specific activity was expressed as follows: produced substrate nM/min/mg of venom.

Hemorrhagic Activity

Hemorrhagic activity was assessed as described by Kondo et al. (14) and modified by Theakston and Reid (12). Increasing venom doses (15 to 31 µg) in 50 µL of saline solution were injected by intradermal route (ID) in mice. Hemorrhagic measurements were recorded after two hours, according to the kinetics assay (after this time interval, the hemorrhagic areas are reabsorbed) (15). Diameters were measured and the minimum hemorrhagic dose (MHD) was defined as the venom dose that induced a lesion of 10 mm in diameter. All procedures involving the use of animals were approved by the Committee for the Ethical Use of Animals (10).

Histological Study

To analyze histopathological effects of venom, two groups of six mice were used. Each mouse received a sub-lethal dose of venom by intraperitoneal route (IP). The animal was sacrificed 60 minutes after venom injection. Organ tissues, 5 microns in thickness, were investigated through microscopic examination.

Assay of Creatine Phosphokinase (CPK) in Blood

Assay of creatine phosphokinase concentration (CPK) in blood was performed at three hours after venom injection. Serum was recovered immediately from blood by centrifugation. CPK measurement was performed according to the recommendations of the Chemistry Kodak Vitros System (USA).

Fibrinogenolytic Activity

Proteolytic activity upon fibrinogen was measured as described by Naves de Souza et al. (16) with some modifications. Fibrinogen solution (2 mg/mL) in 20 µL (PBS) was incubated with venom dilution at 37ºC for two hours. Fibrinogenic activity was stopped using 20 µL of a solution containing 10% (v/v) glycerol, 10% (v/v) β-mercaptoethanol, 2% (v/v) SDS and 0.05% (w/v) bromophenol blue. Fibrinogen hydrolysis was demonstrated using SDS-PAGE.

Production of Antivenoms

Monospecific antivenom was produced as follows. Horses were hyper-immunized subcutaneously with increasing doses of Cc or Mm venoms, at multiple sites around the neck. Complete Freund Adjuvant was used for primary immunization and incomplete Freund adjuvant for secondary immunization. Boosters were made using a saline solution (NaCl 0.85%). Hyper-immunization program was assessed by injection of the same dose, at two-week intervals, until the antibody titer reached a high level. At the end of the immunization program, horses were bled, plasma proteins fractionated by precipitation with ammonium sulfate and immunoglobulins enzymatically digested to produce F(ab')2 fragments. The fractions containing the F(ab')2 fragments were extensively dialyzed against saline solution (17).

Double Immunodiffusion to Control Specificity of the Antivenoms

Double immunodiffusion assay was performed using slides containing 5 mL of 1% agarose (Sigma) in PBS pH 7.4. Wells were punched and filled with 20 µL of 20 mg/mL of venom proteins or with 100 µL of antivenom solution. After 48 hours of incubation at 37ºC, the slides were washed with 0.15 M NaCl for 72 hours, with the solution being changed every 12 hours, before drying at 37ºC and staining with Coomasie Brilliant Blue R (Bio-Rad).

Determination of Effective Doses (ED50)

A fixed amount (3 LD50) of venom was incubated with increasing volumes (0 to 300 µL) of antivenom, 30 minutes at 37ºC. Each mixture (0.5 mL) was injected by IP and IV routes into five mice. Deaths were recorded up to 48 hours. As a control, another group of mice received 3 LD50 of venom without antiserum treatment. Data were analyzed using the method of the software package Prism 45 (GraphPad, Inc.) and effective neutralization was expressed as effective dose 50% (ED50). ED50 was defined as the volume (µL) needed to prevent death in 50% of the injected mice for the 3 LD50 venom dose.

 

RESULTS

Protein Content and Lethal Dose 50% (LD50) of Snake Venoms

Swiss mice were used throughout this procedure to evaluate the toxicity of tested venoms. First, we estimated the protein concentrations, using BSA as the standard. Our results showed that 1mg of lyophilized venom contains 1000 µg of Mm proteins and about 987 µg of Cc proteins. Thus, we estimated that 1 mg of venom has an average of 1 mg of proteins. Herein, proteins correspond to the total dry weight of venom used to study biological effects.

Toxicity was assessed by IV injection of increasing venom amounts. The toxicity assessment was repeated three times. The Cc venom is the most toxic with an LD50 of 5.75 µg/mouse; Mm venom displays an LD50 that average 5.97 µg/mouse. However, Ba venom is approximately 10 fold less toxic (LD50 of 52.54 µg/mouse).

Biochemical Characterization of Cerastes cerastes and Macrovipera mauritanica Venoms

The SDS-PAGE protein profiles were analyzed following Coomassie blue staining. Figure 1 shows that all venoms differ in composition. Each of the venoms from Cerastes cerastes and Macrovipera mauritanica contains a pool of proteins with different molecular weights. The Naja haje venom profile reveals protein bands of lower molecular weights.

 

 

Proteolytic, Coagulant and Phospholipase A2 Activities

Casein substrate was used to determine the proteolytic activity displayed by snake venoms. According to the obtained results, proteolytic activity is estimated at 31.0 ± 1.5 U/mg and 20.2 ± 6.0 U/mg for of Mm and Cc venoms, respectively.

A procoagulant activity in human plasma was detected from both Cc and Mm venoms. Compared to the positive control value (8.0 ± 2.7 nM/min/mg, Crotalus durissus terrificus venom), Cc venom showed higher phospholipase activity (25.0 ± 3.0 nM/min/mg), when compared to Mm venom (7.0 ± 5.0 nM/min/mg) and Nh venom (6.7 ± 4.0 nM/min/mg) activities. Among all recorded phospholipase activities, we conclude that Cc venom presents the highest intensity.

Hemorrhagic Activity

Intradermal injection was used to estimate hemorrhagic potency of the venoms. Our results show that Cc and Mm venoms are endowed with a hemorrhagic feature. This activity is dose-dependent (Figure 2).

The minimal hemorrhagic dose (MHD) is used to evaluate the hemorrhagic power. Our results demonstrated that an intradermal inoculation induces a strong hemorrhage with MHD of 0.13 and 0.63 in µg/mouse for Cc and Mm venoms, respectively. Nh venom has no hemorrhagic effect, despite the clear observation of edema and symptoms of myotoxicity (Figure 3).

Effect of the Venom on Muscle Metabolism

Evaluation of enzyme activity by means of measuring the creatine phosphokinase concentration in blood is the method used for estimating pathological effects such as myonecrosis. The serum CPK concentration is recorded three hours after induction of envenomation. For both Cc and Mm venoms, we observed a threefold increase of CPK serum concentration, a variation that is dependent on the venom dose.

Change in Muscle Tissue of Mice

Intramuscular injection of the venom caused tissue changes such as intense hemorrhages, edema, myonecrosis and inflammatory infiltrates. The observed intensity of alterations is more severe in the case of Cc venom (Figure 4).

Fibrinogenolytic Activity

Macrovipera mauritanica and Cerastes cerastes venoms act on two subunits of fibrinogen (α and γ). This activity is not detected in Naja haje venom (Figure 5). Indeed, the ability of Mm and Cc venoms to degrade the α and γ chains of fibrinogen was evident. However, β chain degradation was not detectable.

 

 

Control of Antivenom Specificity

A qualitative immunodiffusion assay was used to check antivenom specificity against any particular venom. Robust specific immunoprecipitation was observed among Cc venom and monospecific anti-Cc venom groups. A similar result was produced by Mm venom and its antivenom (Figure 6). For both monospecific antivenoms, the immunoprecipitation bands demonstrated the existence of specific antibodies against different venom proteins.

Determination of Effective Doses (ED50)

In order to analyze the ability of monovalent Cc and Mm antivenoms to neutralize the lethal effect of Cc, Mm and Ba venoms, in vivo experiments were performed. Table 1 shows that both monovalent antivenoms (i.e. anti-Cc and anti-Mm, respectively) were able to neutralize the toxicity of venom molecules responsible for the lethality. Indeed, anti-Cc antivenom was more effective at neutralizing Ba venom with an ED50 of 84.3 µL/mouse when compared to the anti-Mm capacity (ED50 of 117.3 µL/mouse).

The Cc antivenom more effectively neutralized Mm venom (ED50 of 62.4 µL/mouse) than Ba venom (ED50 of 84.3 µL/mouse). Similarly, the neutralizing capacity of Mm venom was higher than the capacities of Cc and, consequently, Ba (ED50 of 78 and 117.3 µL/mouse for Cc and Ba venoms, respectively). The best protective effect is obtained from the antivenom and venom that were used in the immunization program.

 

DISCUSSION

Snakebites constitute a common cause of injury and death in several regions of the world where they are considered an important public health problem. Their epidemiology is known only in a fragmentary way such that the number of poisoning cases is underestimated at 5 million per year with a mortality rate of 2.5% (18).

In Morocco, the fact that vipers are responsible for a large number of accidents may reflect the general abundance of this species and the increased level of direct contact. The accidents inflicted by these snakes are mainly characterized by hemorrhagic damage (3, 4).

The present study aimed to evaluate the biochemical, enzymatic and biological properties of venoms of the most dangerous Moroccan snakes, namely Cerastes cerastes and Macrovipera mauritanica. To study the cross-reactivity that may exist between the venoms, specific horse antivenoms were produced with the objective of identifying the best candidate or mixture for producing a highly protective antivenom to fight snake envenomation in North Africa.

First, dried venoms were biochemically investigated. Gel electrophoresis analysis demonstrated several protein bands certainly responsible for almost all of the observed biological effects (6, 19, 20). Proteolytic activity, studied following the casein test, was low compared to other venoms reported in the literature (e.g. Philodryas venom). Phospholipase A2 activity is an important characteristic presented by Cc and Mm venoms. We estimated this activity to be four times higher in Cc venom than in Mm venom and in comparison to the positive control. Our results are in concordance with the recently reported studies (6, 21). PLA2 has been purified and characterized since 1990 from Algeria Cerastes cerastes (22).

Cerastes cerastes and Macrovipera mauritanica venoms are characterized by their ability to degrade fibrinogen subunits (i.e. α and γ chains). However, Nh (belonging to Elapidae family) venom does not display any detectable hemorrhagic activity. Nevertheless, we highlighted the presence of edema with symptoms of myotoxicity, very lower proteolytic and phospholipase activities and an absence of fibrinogenolytic activity.

Hemorrhaging is one of the most significant pathophysiological effects induced by vipers (23, 24). In this study, we have shown that injections of Cc or Mm venoms induce myonecrosis in skeletal muscles, which most likely was the result of myotoxin's direct action and hemorragin's indirect action. In muscle tissue, the myonecrosis induced a reduction of the serum CPK concentration (25).

Cc and Mm venoms were immunogenic and able to induce high levels of specific antibody titers when inoculated in horses. Indeed, monovalent anti- Cc and anti-Mm antivenoms cross-recognize several protein bands within Cc and Mm venoms and were able to cross-reactively recognize Ba venom. The data obtained from in vivo neutralization clearly indicated that both monovalent antivenoms (anti-Cc and anti-Mm) contain a high ratio of specific antibodies capable of recognizing and undoubtedly neutralizing Cc, Mm and Ba venom components. The use of Cc antivenom, which demonstrated better cross-reactivity, is of major therapeutic interest.

 

CONCLUSION

Cerastes cerastes and Macrovipera mauritanica venoms of Morocco are very toxic and contain several proteins that differ by molecular weights. Both venoms are characterized by not only high hemorrhagic and phospholipase A2 activities but also their ability to degrade the α and γ chains of fibrinogen. Our results highlight the high immunogenicity of Cc, which leads to the induction of a horse antivenom that is highly protective against Cc, Mm and Ba whole venoms. Indeed, this protective capacity is higher when compared to the Mm-specific antivenom product.

 

ACKNOWLEDGMENTS

We are grateful to Dr. J. P. Chippaux for valuable suggestions and helpfulness during the preparation of the manuscript. We are indebted to Dr. L. Boussadda (Responsible for the Animal Unit of the Pasteur Institute of Morocco) for providing ophidian venoms. We are grateful to Ms. F. Chgoury for technical assistance.

 

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Correspondence to:
Noreddine Ghalim
Pasteur Institute of Morocco, 1 Place Louis Pasteur
20360-Casablanca, Morocco
Phone: +212 6 75 84 20 68. Fax: +212 5 22 26 09 57
Email: nghalim@yahoo.fr

Received: September 25, 2012.
Accepted: November 6, 2012.
Abstract published online: November 9, 2012.
Full paper published online: November 30, 2012.
CONFLICTS OF INTEREST: The authors declare no conflicts of interest.
FINANCIAL SOURCE: This research was supported by the Pasteur Institute of Morocco which is a public institution under the Ministry of Health.
ETHICS COMMITTEE APPROVAL: All the procedures involving animals were in accordance with the ethical principles in animal research adopted by the World Health Organization (10).

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