研究简报

单一性别日本血吸虫尾蚴的获得

  • 魏梦甜 ,
  • 王阳 ,
  • 张璧辉 ,
  • 孙军
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  • 同济大学医学院,传染病与疫苗研究所,上海200092

作者简介:魏梦甜(1998-),女,本科生,从事寄生虫病研究。E-mail:2643343998@qq.com

收稿日期: 2018-08-02

  网络出版日期: 2019-03-18

基金资助

国家自然科学基金(No. 81071383)

Isolation of single-sex cercaria of Schistosoma japonicum

  • Meng-tian WEI ,
  • Yang WANG ,
  • Bi-hui ZHANG ,
  • Jun SUN
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  • School of Medicine, Tongji University Shanghai 200092, China

Received date: 2018-08-02

  Online published: 2019-03-18

Supported by

Supported by the National Natural Science Foundation of China (No. 81071383)

摘要

阐明人工制备阳性钉螺释放日本血吸虫尾蚴性别类型的规律和特点,为需要获取单一性别尾蚴的研究提供理论依据。通过毛蚴对钉螺“一对一”(1只毛蚴感染1只钉螺)和“多对一”(约10只毛蚴感染1只钉螺)感染方式分别制备阳性钉螺。分别用单只钉螺释放的尾蚴感染单只小鼠,3周后收集小鼠体内的日本血吸虫童虫,通过显微镜观察鉴定童虫的性别,提取童虫DNA,用RRPS、M5A、MPA、2AAA、MF1、J5N等6对微卫星引物进行PCR扩增,扫板分析短串联重复(STR)位点的多态性,比较每一个钉螺所释放全部尾蚴所发育成的童虫基因型差异。镜检结果表明,“一对一”感染的4只小鼠所收集的血吸虫童虫,1只为全雌虫,3只为全雄虫;“多对一”感染的43只小鼠所收集的血吸虫童虫,19只为全雌虫(44.2%),7只为全雄虫(16.3%),17只为雌雄虫共存(39.5%)。各虫体DNA样品,PCR产物琼脂糖电泳的结果和STR扫板分析结果基本一致,但是PCR产物直接电泳分析结果不能精确显示扩增对象的多态性。STR扫板分析结果显示,“一对一”感染的虫体,STR的峰型相似,提示基因型相似,但是同一钉螺来源的不同虫体间仍存在细微差异;“多对一”感染的虫体,STR样品峰型有较大差异,提示样品具有不同的基因型,其中单一钉螺释放的所有尾蚴发育成的童虫有如下特点:雌雄共存,但可分为雌多雄少、雌少雄多和雌雄对等3种情况;全雄虫,基因型相同或不同;全雌虫,基因型相同或不同。总之,毛蚴“一对一”感染钉螺,可以获得基因型一致的、单一性别的尾蚴;混合感染的“多对一”感染方式也可得到单一性别尾蚴,但单性尾蚴基因型不一致。

本文引用格式

魏梦甜 , 王阳 , 张璧辉 , 孙军 . 单一性别日本血吸虫尾蚴的获得[J]. 中国寄生虫学与寄生虫病杂志, 2019 , 37(1) : 111 -114 . DOI: 10.12140/j.issn.1000-7423.2019.01.022

Abstract

To obtain the single-sex cercaria for relevant research of schistosomiasis a single miracidium or multiple miracidia were used to infect one snail (one-to-one or multiple-to-one models). The released cercaria from each infected snail were used to infect a mouse. Immature adult worms or schistosomula were collected from each infected mouse 3 weeks after infection and the sex of the worms was identified under microscope. The genotype variation was determined by PCR with 6 short tandem repeats (STRs) primers (RRPS, M5A, MPA, 2AAA, MF1 and J5N). Among 4 mice infected with "one-to-one"cercaria, single-sex worms were obtained in all mice, one mouse with female and three mice with male worms. However, among 43 mice infected with cercaria from "multiple-to-one"snails, 19 contained female worms (44.2%), 7 contained male worms (16.3%) and 17 contained mixed-sex worms (39.5%). STR analysis with 6 pairs of microsatellite primers, better than electrophoresis analysis of PCR products, showed the nearly identical genotype for worms collected from "one-to-one" groups and different genotypes for worms collected from "multiple-to-one" groups. Minor genetic variation was detected between single-sex worms collected from "one-to-one" groups possibly due to the mutation(s) occurred during self-reproduction and development in snail. Worms from "multiple-to-one" groups showed significant genetic polymorphism in terms of different STR patterns, even for the single-sex worms compared to those collected from "one-to-one" groups. In conclusion, single-sex cercaria can be obtained by infecting a snail with single miracidium ("one-to-one" model) with nearly identical genotype. Even though the single-sex cercaria are possibly obtained by the multiple-to-one infection model, the genotype is mixed and complicated.

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