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1.
Acta Trop ; 137: 130-9, 2014 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-24820180

RESUMO

Anopheles annularis is one of the major vectors of malaria in Odisha, India. The present study was undertaken to determine the vectorial capacity and assess the genetic diversity of An. annularis collected from different endemic regions of Odisha. Mosquitoes were collected from thirteen endemic districts using standard entomological collection methods from 2009 to 2011. Sibling species of An. annularis were identified by PCR-RFLP and sequencing of D3 region of 28S ribosomal DNA (rDNA) region. Plasmodium falciparum (Pf) sporozoite rate and human blood fed percentage (HBF) were estimated by multiplex PCR using Pf and human specific primers. Genetic diversity of An. annularis was estimated by ISSR markers. Out of 1647 An. annularis collected, 1353 (82.15%) were collected by mechanical aspirators and 294 (17.85%) by light trap. 49 (2.97%) were positive for human blood and 18 (1.09%) were positive for Pf sporozoite. PCR-RFLP and sequencing analyses detected only An annularis A in the study areas. Overall genetic differentiation among An. annularis populations was moderate (FST=0.048) and showed significant correlation between genetic distance and geographic distance (r=0.882; P<0.05). Angul population proved to be genetically unique and was highly divergent FST>0.110) from other populations, suggesting low gene flow between them. The study indicated that only An. annularis A was found in Odisha with potential vectorial capacity that can play a major role in malaria transmission. ISSR markers proved to be useful molecular tools to evaluate genetic variability in An. annularis populations.


Assuntos
Anopheles/classificação , Anopheles/parasitologia , Variação Genética , Insetos Vetores , Plasmodium falciparum/isolamento & purificação , Animais , Anopheles/genética , Anopheles/fisiologia , Sangue , Análise por Conglomerados , DNA Ribossômico/química , DNA Ribossômico/genética , Entomologia , Comportamento Alimentar , Técnicas de Genotipagem , Humanos , Índia , Filogenia , Reação em Cadeia da Polimerase , Polimorfismo de Fragmento de Restrição , RNA Ribossômico 28S/genética , Análise de Sequência de DNA
2.
Trop Med Int Health ; 18(7): 810-21, 2013 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-23621708

RESUMO

OBJECTIVE: To identify the Anopheles culicifacies sibling species complex and study their vectorial role in malaria endemic regions of Odisha. METHODS: Mosquitoes were collected from 6 malaria endemic districts using standard entomological collection methods. An. culicifacies sibling species were identified by multiplex polymerase chain reaction (PCR) using cytochrome oxidase subunit II (COII) region of mitochondrial DNA. Plasmodium falciparum (Pf) sporozoite rate and human blood fed percentage (HBF) were estimated by PCR using Pf- and human-specific primers. Sequencing and phylogenetic analysis were performed to confirm the type of sibling species of An. culicifacies found in Odisha. RESULTS: Multiplex PCR detected An. culicifacies sibling species A, B, C, D and E in the malaria endemic regions of Odisha. An. culicifacies E was detected for the first time in Odisha, which was further confirmed by molecular phylogenetics. Highest sporozoite rate and HBF percentage were observed in An. culicifacies E in comparison with other sibling species. An. culicifacies E collected from Nawarangapur, Nuapara and Keonjhar district showed high HBF percentage and sporozoite rates. CONCLUSION: An. culicifacies B was the most abundant species, followed by An. culicifacies C and E. High sporozoite rate and HBF of An. culicifacies E indicated that it plays an important role in malaria transmission in Odisha. Appropriate control measures against An. culicifacies E at an early stage are needed to prevent further malaria transmission in Odisha.


Assuntos
Anopheles/genética , DNA Mitocondrial , Insetos Vetores/genética , Malária Falciparum/transmissão , Filogenia , Plasmodium falciparum , Esporozoítos , Animais , Sangue , Doenças Endêmicas , Humanos , Índia , Análise de Sequência de DNA , Especificidade da Espécie
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