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CONTENT - International Society of Zoological Sciences

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S14 ICZ2008 - Abstracts<br />

Evolutionary and ecological relationships <strong>of</strong> the venoms <strong>of</strong><br />

the related coral snakes Micrurus dissoleucus and Micrurus<br />

mipartitus<br />

Camila Renjifo 1 , Alain Riveros 2 , Armando Sanchez 2 , Juan Manuel<br />

Renjifo 3 , Henry Aceros 2 , Darío Riascos 2 , Jairo Maldonado and<br />

Gabriel Pascual<br />

1 Pontificia Universidad Javeriana, Bogotá-Colombia Facultad de<br />

Ciencias Básicas, Departamento de Biología, Colombia<br />

2 Pontificia Universidad Javeriana, Bogotá-Colombia, Facultad de<br />

Medicina, Departamento de ciencias fisiológicas, Colombia<br />

3 Universidad del Magdalena, Santa Marta-Colombia, Facultad de<br />

Ciencias, Departamento de Biología, Colombia<br />

The venoms <strong>of</strong> coral snakes (genus Micrurus) clinically produce<br />

flaccid paralysis; the high-rate <strong>of</strong> mortality results from respiratory<br />

failure. While studies have investigated potential human effects,<br />

the neurotoxic effects have been poorly investigated in terms <strong>of</strong><br />

venom evolutionary relationships. The purpose <strong>of</strong> this study was to<br />

investigate the physiological effects on neuromuscular junction <strong>of</strong><br />

the venom <strong>of</strong> the closely related species Micrurus dissoleucus and<br />

Micrurus mipartitus to be able to compare their venoms in terms <strong>of</strong><br />

ecology. While both species are likely to be specialist-feeders on<br />

reptiles, they occupy very different habitats. M. dissoleucus lives<br />

mainly in xeric to semiarid or seasonal dry regions while M.<br />

mipartitus is found in a wide range <strong>of</strong> habitats including lower<br />

montane wet forest and cloud forest. We examined the<br />

neurotoxicity <strong>of</strong> M. dissoleucus and M. mipartitus venoms in chick<br />

biventer cervicis muscle preparations and the venoms were also<br />

compared by mass spectrometry. M. dissoleucus and M. mipartitus<br />

venom produced a progressive decrease in the amplitude <strong>of</strong><br />

miniature end-plate potentials, with the indirect stimuli, until these<br />

were abolished, both venoms significantly inhibited contractile<br />

responses to the exogenous nicotinic agonists (i.e. ACh and CCh)<br />

but not KCl, showing mainly a post synaptic effect with different<br />

doses and times <strong>of</strong> blocking. These results allow for a relation <strong>of</strong><br />

toxicity to ecology and shed additional light on the forces driving<br />

venom evolution.<br />

Evolution <strong>of</strong> venomous reptiles<br />

Nicolas Vidal<br />

UMR 7138, Systématique, Evolution, Adaptation, Département<br />

Systématique et Evolution, C.P. 26, Muséum National d’Histoire<br />

Naturelle, 43 Rue Cuvier, Paris 75005, France<br />

The evolution <strong>of</strong> the venomous function is considered to be a key<br />

innovation driving ecological diversification in advanced snakes.<br />

Recent phylogenetic, toxicological, and histological results<br />

demonstrate a single early origin <strong>of</strong> venom in squamate reptiles in<br />

the Jurassic that may also have been a key factor in the adaptive<br />

radiation and subsequent ecological success <strong>of</strong> several lizard<br />

lineages. The well-supported anguimorph/iguanian/snake clade,<br />

named Toxic<strong>of</strong>era, represent ~4600 out <strong>of</strong> ~7900 extant squamate<br />

species, or 58 % <strong>of</strong> the total squamate species diversity. These<br />

results provide new insights into the evolution <strong>of</strong> the venom system<br />

in squamate reptiles and open additional new avenues for<br />

biomedical research and drug design using hitherto unexplored<br />

venom proteins. Among snakes, the caenophidian venom<br />

apparatus has experienced extensive evolutionary tinkering<br />

throughout its history. All traits, ranging from biochemical<br />

(specialization <strong>of</strong> the venoms) to dentition and glandular<br />

morphology, have changed independently, resulting in many kinds<br />

<strong>of</strong> toxins and diverse delivery systems. Rear-fanged—or more<br />

correctly defined, non front-fanged—caenophidians possess<br />

complex venoms containing multiple toxin types, while the frontfanged<br />

venom system appeared three times independently: once<br />

early in caenophidian evolution with viperids, once within<br />

atractaspidines, and once with elapids. Further a reduction <strong>of</strong> the<br />

venom system is observed in species in which constriction has<br />

been secondarily evolved as the preferred method <strong>of</strong> prey capture<br />

or dietary preference has switched from live prey to eggs or to<br />

slugs and snails.<br />

- 48 -<br />

Variation in snake venom composition; evidence for natural<br />

selection and adaptation to diet<br />

Wolfgang Wüster, Axel Barlow, Catharine E. Pook and Nicholas R.<br />

Casewell<br />

Bangor University, School <strong>of</strong> Biological <strong>Sciences</strong>, Bangor LL57<br />

2UW, UK<br />

Variation in venom composition in snakes is a ubiquitous<br />

phenomenon at all taxonomic levels. The causes <strong>of</strong> this variation<br />

have been subject to considerable debates, especially at low<br />

taxonomic levels (within species and between closely related<br />

species). Some authors have argued for the importance <strong>of</strong> natural<br />

selection for different prey items, whereas others suggest that the<br />

high lethal potential <strong>of</strong> most snakes makes natural selection for<br />

different prey types unlikely.<br />

This lecture will summarise the available evidence on causes <strong>of</strong><br />

venom variation in snakes. There is ample evidence for the likely<br />

role <strong>of</strong> natural selection from correlation between variation in<br />

venom composition and diet, examples <strong>of</strong> high levels <strong>of</strong> resistance<br />

to venom in some prey animals, the reduction in venomous<br />

function in snakes feeding on undefended prey, and apparent<br />

specific action <strong>of</strong> venom against the main prey <strong>of</strong> the snakes.<br />

This information is complemented with novel data on variation in<br />

venom composition, gene expression and diet in saw-scaled vipers<br />

(Echis): the four main species groups in the genus differ<br />

pr<strong>of</strong>oundly in the proportion <strong>of</strong> arthropods in the diet. Venom<br />

toxicity to scorpions reflects the importance <strong>of</strong> arthropods in the<br />

diet <strong>of</strong> the species groups, and gene expression patterns reflect<br />

adaptation <strong>of</strong> venom composition to physiologically highly<br />

divergent prey types.

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