Schistosomus Reflexus Syndrome in Olive Ridley Sea Turtles (Lepidochelys olivacea)

被引:11
|
作者
Barcenas-Ibarra, A. [1 ]
Rojas-Lleonart, I. [2 ]
Lozano-Guzman, R. I. [3 ]
Garcia-Gasca, A. [1 ]
机构
[1] Ctr Invest Alimentac & Desarrollo, Ave Sabalo Cerritos S-N, Mazatlan 82100, Sinaloa, Mexico
[2] Univ Cent Marta Abreu de Las Villas IRL, Santa Clara, Villa Clara, Cuba
[3] Inst Tecnol Ciudad Victoria RILG, Ciudad Victoria, Tamaulipas, Mexico
关键词
chelonian; embryogenesis; olive ridley; Lepidochelys olivacea; schistosomus reflexus syndrome; congenital malformations; sea turtles; embryos; conservation; MALFORMATION; WALL;
D O I
10.1177/0300985816651682
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The olive ridley sea turtle (Lepidochelys olivacea), considered the most abundant sea turtle species, is listed as vulnerable on the International Union for Conservation of Nature Red List. The most important nesting areas are located in the Eastern Pacific, and congenital malformations have been previously reported in this species. The present study was conducted in a single population at El Verde beach, one of the most important nesting beaches for the species in the northwestern Mexican Pacific. The study was based on embryos that had been incubated in a controlled environment. Schistosomus reflexus syndrome (SRS) was observed in 124 of 20257 olive ridley embryos (0.6%), comprising 124 of 400 (31%) cases of congenital malformations over a 7-month period. Affected embryos had malformations of the carapace, bridge, or plastron, resulting in exposure of the abdominal or thoracic viscera, as well as spinal malformation and abnormal positioning of limbs adjacent to the head with subsequent ankylosis. SRS phenotypes (although lethal) varied from mild to severe, although most cases were severe. SRS was mostly associated with congenital malformations in the neck (short neck, 80%), tail (anury, 38%), and flippers (different types of dysmelias, 53%). In most cases of severe SRS, ankyloses were present. Documenting these findings could be important to identify the cause of the developmental defects, and identification of the cause of the defects may be of significance to the population and to our efforts to manage this and other populations at risk.
引用
收藏
页码:171 / 177
页数:7
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