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Copyright of Revista Mexicana de Biodiversidad is the property of Universidad Nacional Autonoma de Mexico, Instituto de Biologia and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

A new, monotypic genus of the interstitial marine cyclopoid copepod family Cyclopinidae G.O. Sars, 1913 is described from male and female specimens collected at Laguna de Términos, a large coastal lagoon system in the southern Gulf of Mexico. Mexiclopina campechana gen. et sp. n. cannot be adequately placed in any extant genus within the family. It differs from other cyclopinid genera in having a unique combination of characters including: 1) absence of modified brush-like seta on the mandibular exopod; 2) maxillule exopod with stout setal elements and brush-like setae absent; 3) basis of mandible with one seta; 4) presence of a modified seta on endopod of fourth leg; 5) fifth leg exopod unsegmented, armed with three elements in the female and five in the male; 6) intercoxal sclerite of first swimming leg with two medial spiniform processes on distal margin. The new genus is monotypic and appears to be most closely related to Cyclopina Claus, 1863 and Heptnerina Ivanenko & Defaye, 2004; the new species was compared with species of Cyclopina and it resembles C. americana Herbst, 1982 and C. caissara Lotufo, 1994. This is the second record of a species of Cyclopinidae in Mexico and the first in the Gulf of Mexico; the number of cyclopinid species recorded from the Americas is now 13. [ABSTRACT FROM AUTHOR]

Abstract: The paper describes an introductory characterization of antigenic stimulation of excretion–secretion products (ESP) of Gnathostoma binucleatum advanced third-stage larvae cultured in vitro and proteinases present in this products. Excretory and secretory proteins were obtained after 10 larvae were maintained in 5% CO2 RPMI medium. The supernatant was collected each week for two months. The proteins were dialyzed, concentrated, and separated in 10% SDS–PAGE gels under reducing conditions and transferred to nitrocellulose paper for immunoblot analyses. G. binucleatum immunized mice serum was used to determine protein antigenicity. Four proteins of 40, 80, 120, and 208kDa persisted for two months and three proteins, 80, 120, and 208kDa were recognized for antibodies of mice. In SDS–PAGE gelatin substrate gels ESP resolved as two proteins with molecular weight of 80 and 208kDa that were sensitive to a metalloproteinase inhibitor, and thus it may be inferred that they might be used for diagnosis of gnathostomiasis. [Copyright &y& Elsevier]