REVIEWS

Progress in the identification of Paragonimus species by DNA technology

  • Kun-min HU ,
  • Bin ZHENG ,
  • Shao-hong CHEN ,
  • Ling AI
Expand
  • National Institute of Parasitic Diseases, Chinese Center for Disease Control and Prevention;Chinese Center for Tropical Diseases Research;WHO Collaborating Centre for Tropical Diseases;National Center for International Research on Tropical Diseases, Ministry of Science and Technology;Key Laboratory of Parasite and Vector Biology, Ministry of Health, Shanghai 200025, China

Received date: 2019-07-05

  Online published: 2019-11-07

Supported by

Supported by the National Science and Technology Major Program of China(No. 2018ZX10734-404)

Abstract

Paragonimiasis is an important food-borne parasitic disease caused by the infection of Paragonimus spp. through ingestion of the intermediate host crabs, crayfishes contaminated with Paragonimus larvae. The tremotode parasitizes in different tissues and organs of human and other mammals and cause paragonimiasis. China is the country with the most widespread of the disease and diverse species of Paragonimus. Paragonimus infections have been reported in 27 provinces or regions in China. In recent years, the development of molecular biology technology including DNA detection technique has played an important role in the identification of Paragonimus species and strains. However, different DNA detection assays own different detection sensitivity, specificity, detection time and cost. The appropriate DNA detection method should be selected according to the different needs. In this paper, the research progress in the identification of Paragonimus species and strains by the DNA detection assays developed by domestic and international scientists is reviewed in order to provide reference for accelerating the identification Paragonimus species and the diagnosis of paragonimiasis.

Cite this article

Kun-min HU , Bin ZHENG , Shao-hong CHEN , Ling AI . Progress in the identification of Paragonimus species by DNA technology[J]. CHINESE JOURNAL OF PARASITOLOGY AND PARASITIC DISEASES, 2019 , 37(5) : 598 -602 . DOI: 10.12140/j.issn.1000-7423.2019.05.016

References

[1] 诸欣平, 苏川. 人体寄生虫学[M]. 9版. 北京: 人民卫生出版社, 2018: 102-105.
[2] World Health Organization.Control of foodborne trematode infections[R]. Geneva: WHO, 1995: 1-157.
[3] Paiboon S, Banchob S, Sasithorn K, et al. Food-borne trematodes[M]//Farrar J, Hotez P, Junghanss T, et al. Manson’s Tropical Infectious Diseases. 23rd ed. Amsterdam: Elsevier, 2013: 726-736.
[4] 陈心陶, 安耕九, 李桂林, 等. 中国动物志扁形动物们吸虫纲复殖目并殖吸虫科[M]. 北京: 科学出版社, 1985: 19-107.
[5] 赵慰先. 人体寄生虫学 [M]. 2版. 北京: 人民卫生出版社, 1983: 472-520.
[6] 吴观陵. 人体寄生虫学 [M]. 3版. 北京: 人民卫生出版社, 2005: 427-428.
[7] 李娟, 周本江. 并殖吸虫的分类研究进展[J]. 国际医学寄生虫病杂志, 2008, 35(3): 149-152.
[8] 吴观陵. 人体寄生虫学 [M]. 3版. 北京: 人民卫生出版社, 2005: 421-422.
[9] 章子豪, 张耀娟, 陆志刚. 卫氏并殖吸虫囊蚴和成虫抗原的分析及单克隆抗体识别[J]. 中国寄生虫病防治杂志, 1994, 7(4): 266-269.
[10] 李晓娟, 杨毅梅. PCR技术应用于寄生虫分类鉴定的研究进展[J]. 中国病原生物学杂志, 2009, 4(1): 69-70, 35.
[11] Le TH, Blair D, McManus DP. Mitochondrial DNA sequences of human schistosomes: the current status[J]. Int J Parasitol, 2000, 30(3): 283-290.
[12] Devi KR, Narain K, Agatsuma T, et al. Morphological and molecular characterization of Paragonimus westermani in northeastern India[J]. Acta Trop, 2010, 116(1): 31-38.
[13] Blair D, Wu B, Chang ZS, et al. A molecular perspective on the genera Paragonimus braun, Euparagonimus chen and Pagumogonimus chen[J]. J Helminthol, 1999, 73(4): 295-299.
[14] 陈少华, 陆予云, 朱福祺, 等. 广东省主要并殖吸虫DNA序列分析[J]. 热带医学杂志, 2017, 17(3): 337-342, 413.
[15] Lenis C, Galiano A, Vélez I, et al. Morphological and molecular characterization of Paragonimus caliensis little, 1968 (trematoda: Paragonimidae) from medellin and pichinde, Colombia[J]. Acta Trop, 2018, 183: 95-102.
[16] Doanh PN, Tu LA, Van Hien H, et al. First intermediate hosts of Paragonimus spp. in Vietnam and identification of intramolluscan stages of different Paragonimus species[J]. Parasit Vectors, 2018, 11(1): 328.
[17] Ryu JS, Hwang UW, Min DY, et al. Molecular identification of Paragonimus ohirai and P. westermani from Anhui Province, China[J]. Parasite, 2000, 7(4): 305-309.
[18] 李娜, 张敏, 崔彬, 等. PCR-RFLP技术在兽医寄生虫学上的应用[J]. 动物医学进展, 2007, 28(1): 92-95.
[19] 张晨昊, 杨毅梅. 分子标记技术在寄生虫分类鉴定中的应用[J]. 中国寄生虫学与寄生虫病杂志, 2009, 27(3): 261-266.
[20] 王恩荣, 郑韧坚, Cain GD.二倍体型及三倍体型卫氏并殖吸虫的DNA重复顺序的比较研究[J]. 中国寄生虫学与寄生虫病杂志, 1991, 9(1): 46-49.
[21] 张克新, 王恩荣, 王继春. 两类型卫氏并殖吸虫DNA重复顺序的进一步比较观察[J]. 中国寄生虫病防治杂志, 1994, 7(3): 186-189.
[22] 肖建华, 陈翠娥, 张悟澄, 等. 六地卫氏并殖吸虫及斯氏狸殖吸虫种间和种内虫体重复DNA序列的比较[J]. 中国寄生虫学与寄生虫病杂志, 1993, 11(4): 279-281.
[23] 钱宝珍, Sugiyama H, Waikagu J, 等. 哈氏并殖吸虫ITS2基因和CO1基因序列分析[J]. 中国寄生虫学与寄生虫病杂志, 2006, 24(2): 119-121.
[24] Sugiyama H, Morishima Y, Kameoka Y, et al. Polymerase chain reaction (PCR)-based molecular discrimination between Paragonimus westermani and P. miyazakii at the metacercarial stage[J]. Mol Cell Probes, 2002, 16(3): 231-236.
[25] Ota M, Seki T, Nomura N, et al. Modified PCR-RFLP method for HLA-DPB1 and -DQA1 genotyping[J]. Tissue Antigens, 1991, 38(2): 60-71.
[26] Williams JG, Kubelik AR, Livak KJ, et al. DNA polymorphisms amplified by arbitrary primers are useful as genetic markers[J]. Nucleic Acids Res, 1990, 18(22): 6531-6535.
[27] 钱宝珍, 沈琦. 卫氏并殖吸虫致病品系PCR-RAPD分子标记的初步研究[J]. 中国人兽共患病学报, 2006, 22(3): 249-251.
[28] Intapan PM, Kosuwan T, Wongkham C, et al. Genomic characterization of lung flukes, Paragonimus heterotremus, P. siamensis, P. Harinasutai, P. westermani and P. bangkokensis by RAPD markers[J]. Vet Parasitol, 2004, 124(1/2): 55-64.
[29] 刘超群, 关飞, 陈彦, 等. 应用RAPD技术对我国11个地域株并殖吸虫遗传变异的初步探讨[J]. 中国人兽共患病学报, 2008, 24(11): 1041-1044.
[30] 单小云, 楼宏强, 胡野, 等. SSR-PCR和常规PCR检测不同地区并殖吸虫遗传变异的比较研究[J]. 中国人兽共患病学报, 2011, 27(11): 1001-1004.
[31] van Herwerden L, Blair D, Agatsuma T. Genetic diversity in parthenogenetic triploid Paragonimus westermani[J]. Int J Parasitol, 1999, 29(9): 1477-1482.
[32] Rakoczy-Trojanowska M, Bolibok H.Characteristics and a comparison of three classes of microsatellite-based markers and their application in plants[J]. Cell Mol Biol Lett, 2004, 9(2): 221-238.
[33] 陈彦, 牛安欧, 刘超群, 等. 应用ISSR-PCR技术对我国11株并殖吸虫遗传变异的研究[J]. 中国病原生物学杂志, 2008, 3(11): 828-831, 837.
[34] 陈凤华, 孙建华, 马盈盈, 等. 实时荧光定量PCR技术在病原体快检中的研究进展与应用[J]. 中华临床医师杂志(电子版), 2013, 7(23): 11004-11006.
[35] 杨丽娟, 冉丹丹. 实时荧光定量PCR在动物疫病中的应用[J]. 农技服务, 2013, 30(2): 170-171.
[36] 王本敬. Real-time PCR检测水体日本血吸虫尾蚴和小鼠感染早期检测的研究[D]. 苏州: 苏州大学, 2011.
[37] 张媛. 肉(鱼)源性寄生虫检测方法的研究[D]. 大连: 辽宁师范大学, 2008.
[38] 宋蓓, 康熙雄, 牛靖萱, 等. qRT-PCR检测斯氏并殖吸虫不同虫期PsMt01基因表达研究[J]. 寄生虫与医学昆虫学报, 2014, 21(1): 1-5.
[39] 赵昕, 郑秋月, 曹际娟, 等. 卫氏并殖吸虫PCR和实时荧光PCR快速检测方法的建立[J]. 生物技术通报, 2008(S1): 358-361.
[40] Tantrawatpan C, Saijuntha W, Manochantr S, et al. A singleplex real-time fluorescence resonance energy transfer PCR with melting curve analysis for the differential detection of Paragonimus heterotremus, Echinostoma malayanum and Fasciola gigantica eggs in faeces[J]. Trans R Soc Trop Med Hyg, 2016, 110(1): 74-83.
[41] Mori Y, Nagamine K, Tomita N, et al. Detection of loop-mediated isothermal amplification reaction by turbidity derived from magnesium pyrophosphate formation[J]. Biochem Biophys Res Commun, 2001, 289(1): 150-154.
[42] 莫金余, 李健. 寄生虫病环介导等温扩增技术研究进展[J]. 湖北医药学院学报, 2014, 33(5): 506-510.
[43] 陈家旭, 艾琳, 陈木新, 等. 一种快速检测卫氏并殖吸虫的试剂盒和方法: 中国, CN101956013A. 2011-01-26.
[44] Chen MX, Ai L, Zhang RL, et al. Sensitive and rapid detection of Paragonimus westermani infection in humans and animals by loop-mediated isothermal amplification (LAMP)[J]. Parasitol Res, 2011, 108(5): 1193-1198.
[45] Tantrawatpan C, Intapan PM, Janwan P, et al. Molecular identification of Paragonimus species by DNA pyrosequencing technology[J]. Parasitol Int, 2013, 62(3): 341-345.
Outlines

/

〈 〉