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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/36106
Title: Molecular detection of the avian malaria parasite Plasmodium gallinaceum in Thailand
Authors: Sittiporn Pattaradilokrat
Wisawa Tiyamanee
Phumin Simpalipan
Morakot Kaewthamasorn
Tawee Saiwichai
Jian Li
Pongchai Harnyuttanakorn
Chulalongkorn University
Mahidol University
Xiamen University
Keywords: Immunology and Microbiology;Medicine
Issue Date: 30-May-2015
Citation: Veterinary Parasitology. Vol.210, No.1-2 (2015), 1-9
Abstract: © 2015 Elsevier B.V. Avian malaria is one of the most common veterinary problems in Southeast Asia. The standard molecular method for detection of the avian malaria parasite involves the phenol-chloroform extraction of parasite genomic (g)DNA followed by the amplification of parasite gDNA using polymerase chain reaction (PCR). However, the phenol-chloroform extraction method is time-consuming and requires large amounts of samples and toxic organic solvents, thereby limiting its applications for parasite detection in the field. This study aimed to compare the performance of chelex-100 resin and phenol/chloroform extraction methods for the extraction of Plasmodium gallinaceum gDNA from whole avian blood that had been dried on filter papers (a common field sampling method). The specificity and sensitivity of PCR assays for P. gallinaceum cytochrome B (cytb) and cytochrome oxidase subunit I (coxI) gene fragments (544 and 588. bp, respectively) were determined, and found to be more sensitive with gDNA extracted by the chelex-100 resin method than with the phenol/chloroform method. These PCR assays were also performed to detect P. gallinaceum in 29 blood samples dried on filter papers from domestic chickens in a malaria endemic area, where the reliable identification of seven field isolates of P. gallinaceum was obtained with an accuracy of 100%. The analysis of cytb and coxI gene nucleotide sequences revealed the existence of at least two genetically distinct populations of P. gallinaceum in Thailand, both of which differed from the reference strain 8A of P. gallinaceum. In conclusion, the chelex-100 resin extraction method is a simple and sensitive method for isolating gDNA from whole avian blood dried on filter paper. Genomic DNA extracted by the chelex method could subsequently be applied for the PCR-based detection of P. gallinaceum and DNA sequencing. Our PCR assays provide a reliable diagnostic tool for molecular epidemiological studies of P. gallinaceum infections in domestic chickens and wild birds.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84928700063&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/36106
ISSN: 18732550
03044017
Appears in Collections:Scopus 2011-2015

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