Publication: Molecular detection of the avian malaria parasite Plasmodium gallinaceum in Thailand
Issued Date
2015-05-30
Resource Type
ISSN
18732550
03044017
03044017
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2-s2.0-84928700063
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Mahidol University
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SCOPUS
Bibliographic Citation
Veterinary Parasitology. Vol.210, No.1-2 (2015), 1-9
Suggested Citation
Sittiporn Pattaradilokrat, Wisawa Tiyamanee, Phumin Simpalipan, Morakot Kaewthamasorn, Tawee Saiwichai, Jian Li, Pongchai Harnyuttanakorn Molecular detection of the avian malaria parasite Plasmodium gallinaceum in Thailand. Veterinary Parasitology. Vol.210, No.1-2 (2015), 1-9. doi:10.1016/j.vetpar.2015.03.023 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/36106
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Title
Molecular detection of the avian malaria parasite Plasmodium gallinaceum in Thailand
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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.