,
Brazil Bite symptoms are very different from those of
Nearctic species due to the presence of
neurotoxins (PLA2s like crotoxin and
myotoxins like
crotamine) that cause progressive paralysis. The mortality rate of cases without specific serum treatment is 72%, and 11% in cases with specific treatment. According to Consroe et al. (1992), the
LD50 value of the whole venom from
C. durissus terrificus and
C. durissus durissus is 0.13 mg/kg
IV and 1.79 mg/kg IV respectively, using standardized methods with ICR/CD-1 female mice (outbred stock). Glenn and Straight also report LD50 values of 0.19 mg/kg IV, 0.25 mg/kg
IP, and 1.4 mg/kg
SC for
C. durissus terrificus, and 1.43 mg/kg IV and 0.71 IP for
C. durissus durissus . Sanchez et al. (1992) report LD50 of male CF2 mice (outbred stock) of 0.093 mg/kg IV and 0.0485 mg/kg IP in
C. durissus collilineatus, and 0.0965-0.27 mg/kg IV and 0.092-0.141 mg/kg IP in various populations of
C. durissus terrificus (
C. d. collilineatus now synonymous with
C. d. terrificus)
. Lima et al. (1991) reported on
SC median lethal dose for whole venom of
C. d. terrificus on inbred mouse strains: 0.193 and 0.171 mg/kg for Balb/c and C57BI/6 mice respectively, and 0.078 and 0.074 mg/kg for A/J and DBA/J mice respectively. The LD50 of purified crotoxin is variously reported at 0.047 and 0.061 mg/kg IV in male and female CDC mice (outbred stock) respectively, and 0.09 mg/kg IP. The lethal dose for 60 kg humans is possibly 18 mg, while the venom yield is 20-100 mg. Sanchez et al also reported venom yield of 76 mg average (28-127 mg range) for
C. durissus collilineatus, and 50 mg average (28-67 mg range) for ''C. durissus terrificus. Crotoxin makes up anywhere from 48.5-89.4% of
C. durissus terrificus venoms total proteome, though is typically 60-70% depending on locality.
Crotalus durissus collilineatus and
C. durissus cascavella (both synonymous with
C. durissus terrificus) crotoxin abundance is also reported at 67.4% (72% PLA2 total) and 72.5% (90.6% PLA2 total) respectively. The myotoxin crotamine is also usually absent or present at various levels in
C. durissus terrificus and
C. durissus collilineatus; crotamine appears to be absent in
C. durissus cascavella.
Crotalus durissus cumanensis has lower levels of neurotoxicity than the previously discussed subspecies, with PLA2s representing 32-44% of venom proteome across various populations. Some populations can also have very high abundance of crotamine, up to 55%, whereas others might have no crotamine.
Crotalus durissus ruruima are highly dichotomous, showcasing Type I (hemorrhagic with 33% SVMP (snake venom metalloproteinases) and 10% PLA2), and Type II (neurotoxic with 21% PLA2 and 11% SVMP). Historically, yellow colored venom was associated with hemorrhagic Type I while white colored venom was associated with neurotoxic Type II. But the color of the venom is determined by the abundance of LAAO and cofactor pigments, which don't determine whether a venom is Type I or Type II. ==References==