Instituto de Biomedicina de Valencia, CSIC, Jaume Roig 11, 46010 Valencia, Spain.
J Proteome Res. 2010 Jan;9(1):528-44. doi: 10.1021/pr9008749.
We report a comparative venomic and antivenomic characterization of the venoms of newborn and adult specimens of the Central American rattlesnake, Crotalus simus, and of the subspecies cumanensis, durissus, ruruima, and terrificus of South American Crotalus durissus. Neonate and adult C. simus share about 50% of their venom proteome. The venom proteome of 6-week-old C. simus is predominantly made of the neurotoxic heterodimeric phospholipase A(2) (PLA(2) crotoxin) (55.9%) and serine proteinases (36%), whereas snake venom Zn(2+)-metalloproteinases (SVMPs), exclusively of class PIII, represent only 2% of the total venom proteins. In marked contrast, venom from adult C. simus comprises toxins from 7 protein families. A large proportion (71.7%) of these toxins are SVMPs, two-thirds of which belong to the PIII class. These toxin profiles correlate well with the overall biochemical and pharmacological features of venoms from adult (hemorrhagic) and newborn (neurotoxic) C. simus specimens. The venoms of the South American Crotalus subspecies belong to one of two distinct phenotypes. C. d. cumanensis exhibits high levels of SVMPs and low lethal potency (LD(50)), whereas C. d. subspecies terrificus, ruruima, and durissus have low SVMP activity and high neurotoxicity to mice. Their overall toxin compositions explain the outcome of envenomation by these species. Further, in all C. simus and C. durissus venoms, the concentration of neurotoxins (crotoxin and crotamine) is directly related with lethal activity, whereas lethality and metalloproteinase activity show an inverse relationship. The similar venom toxin profiles of newborn C. simus and adult C. durissus terrificus, ruruima, and durissus subspecies strongly suggests that the South American taxa have retained juvenile venom characteristics in the adult form (paedomorphism) along their North-South stepping-stone dispersal. The driving force behind paedomorphism is often competition or predation pressure. The increased concentration of the neurotoxins crotoxin and crotamine in South American rattlesnake venoms strongly argues that the gain of neurotoxicity and lethal venom activities to mammals may have represented the key axis along which overall venom toxicity has evolved during Crotalus durissus invasion of South America. The paedomorphic trend is supported by a decreasing LNC (lethal neurotoxicity coefficient, defined as the ratio between the average LD(50) of the venom and the crotoxin + crotamine concentration) along the North-South axis, coincident with the evolutionary dispersal pattern of the Neotropical rattlesnakes. The indistinguisable immunoreactivity patterns of Costa Rican and Venezuelan polyvalent antivenoms toward C. simus and C. durissus venoms strongly suggest the possibility of using these antivenoms indistinctly for the management of snakebites by adult C. simus and by certain C. d. cumanensis populations exhibiting a hemorrhagic venom phenotype. The antivenomic results also explain why the antivenoms effectively neutralize the hemorrhagic activity of adult C. simus venoms but does not protect against adult C. durissus sp. and newborn C. simus envenomations. The identification of evolutionary trends among tropical Crotalus, as reported here, may have an impact in defining the mixture of venoms for immunization to produce an effective pan-American anti-Crotalus antivenom.
我们报告了中美洲响尾蛇(Crotalus simus)的新生和成年标本以及南美的 Crotalus durissus 的 cumanaensis、durissus、ruruima 和 terrificus 亚种的毒液和抗毒液的比较特征。新生和成年的 C. simus 共享大约 50%的毒液蛋白质组。6 周龄的 C. simus 毒液蛋白质组主要由神经毒性异二聚体磷脂酶 A2(PLA2 crotoxin)(55.9%)和丝氨酸蛋白酶(36%)组成,而蛇毒 Zn2+金属蛋白酶(SVMPs),仅占总毒液蛋白的 2%。相比之下,来自成年 C. simus 的毒液包含来自 7 种毒素家族的毒素。这些毒素中的很大一部分(71.7%)是 SVMPs,其中三分之二属于 PIII 类。这些毒素谱与成年(出血性)和新生(神经毒性)C. simus 标本毒液的整体生化和药理学特征很好地相关。南美的 Crotalus 亚种毒液属于两种截然不同的表型之一。C. d. cumanaensis 表现出高水平的 SVMPs 和低致死效力(LD50),而 C. d. 亚种 terrificus、ruruima 和 durissus 的 SVMP 活性低,但对小鼠具有高神经毒性。它们的整体毒素组成解释了这些物种的毒液中毒的结果。此外,在所有 C. simus 和 C. durissus 毒液中,神经毒素(crotoxin 和 crotamine)的浓度与致死活性直接相关,而致死活性和金属蛋白酶活性呈反比关系。新生 C. simus 和成年 C. durissus terrificus、ruruima 和 durissus 亚种的毒液毒素谱非常相似,强烈表明南美分类群在其南北阶梯式扩散过程中保留了幼年毒液特征(幼态持续)。幼态持续的驱动力通常是竞争或捕食压力。南美响尾蛇毒液中神经毒素 crotoxin 和 crotamine 的浓度增加强烈表明,神经毒性和致死性毒液活性对哺乳动物的获得可能是 Crotalus durissus 入侵南美洲期间整体毒液毒性进化的关键轴线。沿南北轴的 LNC(致死神经毒性系数,定义为毒液的平均 LD50 与 crotoxin+crotamine 浓度的比值)的降低趋势支持了幼态持续的趋势,与新热带响尾蛇的进化扩散模式一致。哥斯达黎加和委内瑞拉多价抗蛇毒血清对 C. simus 和 C. durissus 毒液的免疫反应模式相同,强烈表明可以使用这些抗蛇毒血清来治疗成年 C. simus 和表现出血性毒液表型的某些 C. d. cumanaensis 人群的蛇咬伤,而不会产生任何区别。抗毒液组学结果还解释了为什么抗蛇毒血清能有效中和成年 C. simus 毒液的出血活性,但不能保护成年 C. durissus sp.和新生 C. simus 免受毒液侵害。在这里报告的热带 Crotalus 之间的进化趋势的鉴定可能会对确定用于免疫的毒液混合物产生影响,以产生有效的泛美抗 Crotalus 抗蛇毒血清。