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1.
Bull Soc Pathol Exot ; 108(1): 73-7, 2015 Feb.
Artigo em Francês | MEDLINE | ID: mdl-25307881

RESUMO

Toxoplasma gondii is an obligate, intracellular, parasitic protozoan within the phylum Apicomplexa that causes toxoplasmosis in mammalian hosts (including humans) and birds. We used modified direct agglutination test for the screening of the animals' sera collected in Senegal. In total, 419 animals' sera have been studied: 103 bovines, 43 sheep, 52 goats, 63 horses, 13 donkeys and 145 dogs. The collection of sera was performed in four different regions of Senegal: Dakar, Sine Saloum, Kedougou and Basse Casamance from 2011 to 2013. We have revealed antibodies in 13% of bovines, 16% of sheep, 15% of goats, 30% of horses, 23% of donkeys and 67% of dogs. Private dogs from villages were more often to have the anti-Toxoplasma antibodies compared to security society-owned dogs from Dakar. It may be explained by different meal consumed by dogs (factory-produced meal for dogs from Dakar vs. irregular sources for village dogs). Intense circulation of T. gondii in the studied zone may explain the unusually high seroprevalence among horses and donkeys. Tropical climate with high temperature and humidity is favorable for the conservation of oocysts of T. gondii. Results presented here may contribute to the evaluation of the risks of toxoplasmosis in humans in Senegal.


Assuntos
Animais Domésticos , Toxoplasmose Animal/epidemiologia , Animais , Animais Domésticos/sangue , Animais Domésticos/parasitologia , Anticorpos Antiprotozoários/sangue , Bovinos , Cães , Equidae , Cabras , Cavalos , Senegal/epidemiologia , Estudos Soroepidemiológicos , Ovinos , Toxoplasmose Animal/sangue
2.
Parasite ; 18(4): 345-8, 2011 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-22091467

RESUMO

Samples (serum or meat juice) collected from 205 animals in New Caledonia in April 2009 were tested for antibodies against Toxoplasma gondii by ELISA using the multi-species ID Screen® Toxoplasmosis Indirect kit (IDVET, Montpellier). Antibodies to T. gondii were detected in 2% (1/49) of the pigs, in 3.3% (1/30) of the cattle, in 13.8% (4/29) of Rusa deers, in 16% (4/25) of the horses, in 32.8% (21/64) of the dogs, and in 50% (4/8) of cats. Statistically, no significant difference was observed between T. gondii seroprevalence and age or sex. No survey on the prevalence of T. gondii in animals has ever been conducted in New Caledonia and this is the first serological evidence of T. gondii in Rusa deer (Cervus timorensis russa). These results indicate an important circulation of T. gondii exists in the animal populations of New Caledonia. In view of humans being exposed, it is advisable to insist on sanitary education and on respect for good hygienic and food practice.


Assuntos
Animais Domésticos/parasitologia , Animais Selvagens/parasitologia , Anticorpos Antiprotozoários/sangue , Toxoplasma/imunologia , Toxoplasmose Animal/epidemiologia , Animais , Gatos , Bovinos , Cervos , Diafragma/parasitologia , Cães , Feminino , Cavalos , Masculino , Músculo Masseter/parasitologia , Carne/parasitologia , Nova Caledônia/epidemiologia , Estudos Soroepidemiológicos , Suínos
3.
J Virol Methods ; 176(1-2): 74-7, 2011 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-21703306

RESUMO

A one-step real time quantitative RT-PCR (qRT-PCR) assay was developed to detect all published Dugbe virus (DUGV) genomes of the Nairovirus genus. Primers and probes were designed to detect specific sequences on the most conserved regions of the S segment. The limit of detection of the assay was 10 copies per reaction which is an improvement of 3 log(10)FFU/mL over the sensitivity of conventional RT-PCR. The specificity of the primers and probe was confirmed with the closely related Nairoviruses CCHFV and Hazara virus, and on the non-related viruses Coronavirus and Influenza A virus. This qRT-PCR assay was used to screen nucleic acids extracted from 498 ticks collected in the Republic of Chad. One sample was found positive suggesting that DUGV is present in this part of the world. The molecular assay developed in this study is sensitive, specific and rapid and can be used for research and epidemiological studies.


Assuntos
Bovinos/virologia , Ixodidae/virologia , Nairovirus/isolamento & purificação , RNA Viral/isolamento & purificação , Reação em Cadeia da Polimerase Via Transcriptase Reversa/métodos , Animais , Vetores Aracnídeos/virologia , Infecções por Bunyaviridae/epidemiologia , Infecções por Bunyaviridae/veterinária , Infecções por Bunyaviridae/virologia , Doenças dos Bovinos/epidemiologia , Doenças dos Bovinos/virologia , Chade/epidemiologia , Primers do DNA , Feminino , Humanos , Masculino , Nairovirus/genética , RNA Viral/análise , RNA Viral/genética , Reprodutibilidade dos Testes , Sensibilidade e Especificidade
4.
Med Trop (Mars) ; 71(5): 517-8, 2011 Oct.
Artigo em Francês | MEDLINE | ID: mdl-22235637

RESUMO

Sera obtained from 31 domestic and feral animals in Djibouti were assayed for leptospiral antibodies using the microscopic agglutination test. Antibodies were detected in 26 samples (84%), corresponding to 116 positive reactions. The most common antigen serogroups were Icterohaemorrhagiae and Australis. The highest titre was recorded for serovar Munchen (1:1280) in sera from Somalian wild asses and goats. This study shows a broad dispersion and high prevalence of the different Leptospira serogroups tested. High biodiversity has been previously reported in tropical countries and is thought to be linked to the wide range of reservoir mammals. Additional study will be needed to identify the reservoirs of the different serogroups in this part of Africa.


Assuntos
Camelus/microbiologia , Equidae/microbiologia , Cabras/microbiologia , Leptospirose/veterinária , Testes de Aglutinação , Animais , Djibuti , Leptospira interrogans/imunologia , Leptospirose/sangue
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