Rapid detection and identification of four major Schistosoma species by high-resolution melt (HRM) analysis

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• 作者：Juan Li ; Guang-Hui Zhao ; RuiQing Lin ; David Blair ; Hiromu Sugiyama…
• 关键词：Schistosoma ; Schistosomiasis ; High ; resolution melt curve (HRM) ; Rapid identification ; Differentiation ; 18S rDNA
• 刊名：Parasitology Research
• 出版年：2015
• 出版时间：November 2015
• 年：2015
• 卷：114
• 期：11
• 页码：4225-4232
• 全文大小：1,005 KB
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• 作者单位：Juan Li (1) (2)
  Guang-Hui Zhao (3)
  RuiQing Lin (4)
  David Blair (5)
  Hiromu Sugiyama (6)
  Xing-Quan Zhu (1)
  
  1. State Key Laboratory of Veterinary Etiological Biology, Key Laboratory of Veterinary Parasitology of Gansu Province, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, Gansu Province, 730046, People’s Republic of China
  2. Institute of Animal Health, Guangdong Academy Agricultural Sciences, Guangzhou, Guangdong Province, 510640, People’s Republic of China
  3. College of Veterinary Medicine, Northwest A & F University, Yangling, Shaanxi Province, 712100, People’s Republic of China
  4. College of Veterinary Medicine, South China Agricultural University, Guangzhou, Guangdong Province, 510642, People’s Republic of China
  5. School of Marine and Tropical Biology, James Cook University, Townsville, Queensland, 4811, Australia
  6. Department of Parasitology, National Institute of Infectious Diseases, 113-8421, Tokyo, Japan
  
• 刊物类别：Biomedical and Life Sciences
• 刊物主题：Biomedicine
  Medical Microbiology
  Microbiology
  Immunology
  
• 出版者：Springer Berlin / Heidelberg
• ISSN：1432-1955

文摘

Schistosomiasis, caused by blood flukes belonging to several species of the genus Schistosoma, is a serious and widespread parasitic disease. Accurate and rapid differentiation of these etiological agents of animal and human schistosomiasis to species level can be difficult. We report a real-time PCR assay coupled with a high-resolution melt (HRM) assay targeting a portion of the nuclear 18S rDNA to detect, identify, and distinguish between four major blood fluke species (Schistosoma japonicum, Schistosoma mansoni, Schistosoma haematobium, and Schistosoma mekongi). Using this system, the Schistosoma spp. was accurately identified and could also be distinguished from all other trematode species with which they were compared. As little as 10? ng genomic DNA from a Schistosoma sp. could be detected. This process is inexpensive, easy, and can be completed within 3 h. Examination of 21 representative Schistosoma samples from 15 geographical localities in seven endemic countries validated the value of the HRM detection assay and proved its reliability. The melting curves were characterized by peaks of 83.65 °C for S. japonicum and S. mekongi, 85.65 °C for S. mansoni, and 85.85 °C for S. haematobium. The present study developed a real-time PCR coupled with HRM analysis assay for detection and differential identification of S. mansoni, S. haematobium, S. japonicum, and S. mekongi. This method is rapid, sensitive, and inexpensive. It has important implications for epidemiological studies of Schistosoma. Keywords Schistosoma Schistosomiasis High-resolution melt curve (HRM) Rapid identification Differentiation 18S rDNA