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1.
Biomed Res Int ; 2020: 7135268, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-32724808

RESUMO

Toxoplasmosis is a zoonotic infection caused by the protozoan parasite, Toxoplasma gondii. It was discovered over 100 years ago and is credited as the most successful parasitic organism worldwide, able to infect and multiply in all warm blooded animals including an estimated 2.3 billion people. Toxoplasmosis is asymptomatic in immunocompetent individuals. Infection in the developing fetus and immunocompromised individuals can cause severe clinical disease. Toxoplasmosis is also a major cause of reproductive failure in livestock. The economic impact of toxoplasmosis is believed to be substantial. Factors associated with toxoplasmosis infection have been defined. Eastern Africa region is a high-risk area mainly due to the close association of humans and livestock as well as sociocultural practices, poor environmental hygiene, and poverty. The present paper provides a narrative review of published data on toxoplasmosis in Eastern Africa.


Assuntos
Toxoplasmose/epidemiologia , África Oriental/epidemiologia , Animais , Humanos , Hospedeiro Imunocomprometido/imunologia , Gado/parasitologia , Toxoplasma/patogenicidade , Zoonoses/epidemiologia
2.
Biomed Res Int ; 2016: 7589278, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-27981052

RESUMO

The detection of Toxoplasma gondii in free-range chickens is a good indicator of possible risk to human beings. The aim of this study was to investigate the occurrence of T. gondii in free-range chicken using polymerase chain reaction (PCR). Brain samples from 105 free-range chickens from three administrative areas in Thika region, Kenya, were collected, DNA-extracted, and analyzed using PCR to detect presence of T. gondii. The overall prevalence of T. gondii in all the three areas was 79.0% (95% CI: 70.0-86.4%) and the prevalence across the three areas was not significantly different (P = 0.5088; χ2 = 1.354). Female chickens had higher (79.4%) prevalence than males (78.6%), although the difference was not significant (P = 0.922, χ2 = 0.01). However, chickens that were more than 2 years old had significantly (P = 0.003; χ2 = 11.87) higher prevalence compared to younger ones. The study indicates that there was a high occurrence of T. gondii infection in free-range chickens from Thika region and that the infection rate is age dependent. Further studies should be carried out to determine the possible role of roaming chickens in the epidemiology of the disease among humans in the area.


Assuntos
Galinhas , DNA de Protozoário , Reação em Cadeia da Polimerase/métodos , Doenças das Aves Domésticas , Toxoplasma/genética , Toxoplasmose Animal , Animais , Galinhas/sangue , Galinhas/parasitologia , DNA de Protozoário/sangue , DNA de Protozoário/genética , Feminino , Humanos , Quênia , Masculino , Doenças das Aves Domésticas/sangue , Doenças das Aves Domésticas/genética , Doenças das Aves Domésticas/parasitologia , Fatores Sexuais , Toxoplasmose Animal/sangue , Toxoplasmose Animal/genética
3.
Biomed Res Int ; 2015: 867846, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-26504841

RESUMO

Human African trypanosomiasis (HAT) is a vector-borne parasitic zoonotic disease. The disease caused by Trypanosoma brucei gambiense is the most prevalent in Africa. Early diagnosis is hampered by lack of sensitive diagnostic techniques. This study explored the potential of loop mediated isothermal amplification (LAMP) and polymerase chain reaction (PCR) in the detection of T. b. gambiense infection in a vervet monkey HAT model. Six vervet monkeys were experimentally infected with T. b. gambiense IL3253 and monitored for 180 days after infection. Parasitaemia was scored daily. Blood, cerebrospinal fluid (CSF), saliva, and urine samples were collected weekly. PCR and LAMP were performed on serum, CSF, saliva, and urine samples. The detection by LAMP was significantly higher than that of parasitological methods and PCR in all the samples. The performance of LAMP varied between the samples and was better in serum followed by saliva and then urine samples. In the saliva samples, LAMP had 100% detection between 21 and 77 dpi, whereas in urine the detection it was slightly lower, but there was over 80% detection between 28 and 91 dpi. However, LAMP could not detect trypanosomes in either saliva or urine after 140 and 126 dpi, respectively. The findings of this study emphasize the importance of LAMP in diagnosis of HAT using saliva and urine samples.


Assuntos
DNA de Protozoário/análise , DNA de Protozoário/urina , Técnicas de Amplificação de Ácido Nucleico/métodos , Saliva/parasitologia , Trypanosoma brucei gambiense/genética , Tripanossomíase Africana/diagnóstico , Animais , Chlorocebus aethiops , DNA de Protozoário/isolamento & purificação , Modelos Animais de Doenças , Parasitologia , Reação em Cadeia da Polimerase/métodos , Reprodutibilidade dos Testes , Trypanosoma brucei gambiense/isolamento & purificação , Tripanossomíase Africana/parasitologia
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