ABSTRACT
Abstract The aim of this study was to identify Plasmodium spp. in blood samples from nonhuman primates (NHPs) in the state of Maranhão, using classical and alternative techniques for examination of human malaria. A total of 161 blood samples from NHPs were analyzed: 141 from captive animals at a Wildlife Screening Center (CETAS) and 20 from free-living animals in a private reserve. The techniques used were microscopy, rapid diagnostic test (RDT), Indirect fluorescent antibody test (IFAT) and molecular techniques (semi-nested PCR, quantitative real-time PCR and LAMP). Two serological methods (dot-ELISA and indirect ELISA) were also standardized with rhoptry protein-soluble antigen of P. falciparum and P. berghei. Trophozoite forms of Plasmodium sp. were identified on slides from five different animals. No samples were positive through RDT and LAMP. Four samples were seropositive for P. malariae through IFAT. The samples showed low reactivity to ELISA. Plasmodium sp. was detected in 34.16% (55/161) of the samples using qPCR based on the 18S rRNA gene. After sequencing, two samples showed 100% identityl to P. malariae, one showed 97% identity to Plasmodium sp. ZOOBH and one showed 99% identity to P. falciparum . PCR was shown to be the most sensitive technique for diagnosing Plasmodium in NHP samples.
Resumo Neste estudo objetivamos identificar Plasmodium spp. em amostras sangue de primatas não humanos (PNH) do estado do Maranhão, utilizando técnicas clássicas e alternativas para o exame da malária humana. Foram analisadas 161 amostras de sangue de PNH, sendo 141 de CETAS (cativeiro) e 20 de reserva particular (vida livre), utilizando microscopia, teste de diagnóstico rápido (RDT), imunofluorescência indireta (IFI) e técnicas moleculares (semi-nested PCR, PCR em tempo real quantitativo e LAMP). Dois métodos sorológicos (dot-ELISA e ELISA indireto) também foram padronizados com antígenos solúveis de roptrias de P. falciparum e P. berghei. Formas trofozoíticas de Plasmodium sp. foram identificadas em lâminas de cinco animais diferentes. Nenhuma amostra foi positiva em TDR e LAMP. Quatro amostras foram soropositivas para P. malariae na IFI. Os soros de PNH mostraram baixa reatividade pelo ELISA indireto. Plasmodium sp. foi detectado em 34,16% (55/161) das amostras utilizando a qPCR baseada no gene 18S rRNA. No sequenciamento, duas amostras mostraram identidade com P. malariae (100%), uma com Plasmodium sp. ZOOBH (97%) e uma com P. falciparum (99%). A PCR mostrou ser a técnica mais sensível para diagnósticos de Plasmodium em amostras de PNH.
Subject(s)
Animals , Male , Plasmodium/genetics , Plasmodium/immunology , Platyrrhini/parasitology , Malaria/veterinary , Antibodies, Protozoan/blood , RNA, Ribosomal, 18S/blood , DNA, Protozoan/blood , Fluorescent Antibody Technique, Indirect , Real-Time Polymerase Chain Reaction , Malaria/diagnosis , Malaria/parasitologyABSTRACT
Parasites have been investigated for some New World primates; however, very little is known about ectoparasites and specifically fur mites. In this study, Alouatta palliata, Cebus capucinus, Saimiri oerstedii, and Ateles geoffroyi monkeys from different areas of Costa Rica were searched for fur mites. A total of 276 monkeys were evaluated, and 51 of them were positive for mites of the family Atopomelidae. Listrocarpus alouattae was identified on 22.3% of A. palliata; Listrocarpus capucinus on 12.8% of C. capucinus; and Listrocarpus costaricensis on 36.8% of S. oerstedii; No fur mites were found on A. geoffroyi. Sex was not considered a determinant of mite infestation, but prevalence was significantly higher in the Central Volcanic Mountain Range Conservation Area for L. alouattae (p=0.01) and in the Central Pacific Conservation Area for L. capucinus (p=0.002). These primate fur mites are highly host-specific. Differences in the geographical distribution may be due to monkey behavior and history, as well as to environmental conditions. Rev. Biol. Trop. 57 (1-2): 353-360. Epub 2009 June 30.
Muy poco se conoce sobre los ectoparásitos, específicamente de los ácaros del pelo, de primates del Nuevo Mundo. En este estudio se buscaron ácaros del pelo en monos Alouatta palliata, Cebus capucinus, Saimiri oerstedii y Ateles geoffroyi provenientes de diferentes áreas de Costa Rica. Se evaluaron 276 monos en total y 51 de ellos se encontraron positivos por ácaros de la familia Atopomelidae. Se identificó Listrocarpus alouattae en el 22.3% de los A. palliata, Listrocarpus capucinus en el 12.8% de los C. capucinus y Listrocarpus costaricensis en el 36.8% de los S. oerstedii. El sexo no fue un determinante de la infestación por ácaros, pero la prevalencia de L. alouattae fue significativamente mayor en el Área de Conservación Cordillera Volcánica Central (p=0.01) y la de L. capucinus fue mayor en el Área de Conservación Pacífico Central (p=0.002). Estos ácaros del pelo de primates son altamente específicos en relación con su hospedero. Las diferencias en la distribución geográfica podrían deberse al comportamiento e historia de los monos, así como a las condiciones ambientales.