Monitoring Leishmania infantum infections in female lutzomyia longipalpis by using dna extraction on cation exchange paper and pcr pool testing
Tiago Leonetti Coutinho, Fernando Augusto Lima Marson, Osias Rangel, Selma Giorgio, Kamila Cristina Silva, Carlos Emilio Levy
ARTIGO
Inglês
Agradecimentos: Lauro Tatsuo Kubota of the Unicamp Chemistry Institute for the guidance and membrane supply. Kamila Cristina Silva Krywacz, biologist for the Parasitology Laboratory; and Tania Regina Zaccariotto, biologist for the Microbiology Laboratory, for technical support. T.L.C., Coordenação...
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Agradecimentos: Lauro Tatsuo Kubota of the Unicamp Chemistry Institute for the guidance and membrane supply. Kamila Cristina Silva Krywacz, biologist for the Parasitology Laboratory; and Tania Regina Zaccariotto, biologist for the Microbiology Laboratory, for technical support. T.L.C., Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (Coordination for the Improvement of Higher Education Personnel; #1650411)
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Abstract: Visceral leishmaniasis remains a serious public health issue, and Brazil was among the seven countries with the highest prevalence of this disease worldwide. The measures to control this disease are not easily developed, and the improvement of its diagnosis, surveillance, and control is...
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Abstract: Visceral leishmaniasis remains a serious public health issue, and Brazil was among the seven countries with the highest prevalence of this disease worldwide. The measures to control this disease are not easily developed, and the improvement of its diagnosis, surveillance, and control is still needed. This study aimed to carry out the polymerase chain reaction (PCR) diagnosis of Leishmania infantum in vector samples in some municipalities of the State of São Paulo, which included two municipalities with human disease transmission and two with dog transmission only. Vectors were collected in traps with luminous bait. Next, they were killed at -4 °C and kept in 70% alcohol. Groups of ten female insects (pools) were mashed on cation exchange paper (fine cellulose phosphate with 18 µEq/cm² ionic exchange capacity) for DNA extraction. The PCR was carried out to identify the natural infection of the Leishmania genus in female Lutzomyia longipalpis (Lu. Longipalpis). Out of the 3,880 Lu. longipalpis phlebotomines, 1060 were female and 2820 were male (3:1). The method used to extract the DNA in pools of ten phlebotomines and the PCR resulted in sensitivity, specificity, practicality, and faster analyses when compared to the individual analysis method. The procedure described can be used on a large scale in the leishmaniasis epidemiological surveillance, enabling a higher number of analyses and the optimization of human resources because the traditional diagnostic method is carried out via desiccation of the insect digestive system and microscopic examination, which is time-demanding and there is the need of manual skills
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COORDENAÇÃO DE APERFEIÇOAMENTO DE PESSOAL DE NÍVEL SUPERIOR - CAPES
1650411
Aberto
DOI: https://doi.org/10.3390/diagnostics12112653
Texto completo: https://www.mdpi.com/2075-4418/12/11/2653
Monitoring Leishmania infantum infections in female lutzomyia longipalpis by using dna extraction on cation exchange paper and pcr pool testing
Tiago Leonetti Coutinho, Fernando Augusto Lima Marson, Osias Rangel, Selma Giorgio, Kamila Cristina Silva, Carlos Emilio Levy
Monitoring Leishmania infantum infections in female lutzomyia longipalpis by using dna extraction on cation exchange paper and pcr pool testing
Tiago Leonetti Coutinho, Fernando Augusto Lima Marson, Osias Rangel, Selma Giorgio, Kamila Cristina Silva, Carlos Emilio Levy
Fontes
Diagnostics (Fonte avulsa) |