中国寄生虫学与寄生虫病杂志 ›› 2017, Vol. 35 ›› Issue (1): 63-67.

• 论著 • 上一篇    下一篇

福建省部分地区鼠类巴贝虫感染调查与基因鉴定

肖方震1, 彭秀卿2, 徐国英1, 陈阳1, 林代华1, 邓艳琴1,2,*()   

  1. 1 福建省疾病预防控制中心,福建省人兽共患病研究重点实验室,福州350001
    2 福建医科大学,福州350004
  • 收稿日期:2016-06-08 出版日期:2017-02-28 发布日期:2017-03-06
  • 通讯作者: 邓艳琴
  • 基金资助:
    福建省医学创新课题(No. 2012-CXB-12)

Investigation and genetic identification on Babesia infection in rodents in some areas of Fujian Province

Fang-zhen XIAO1, Xiu-qing Peng2, Guo-ying XU1, Yang CHEN1, Dai-hua LIN1, Yan-qin DENG1,2,*()   

  1. 1 Fujian Key Laboratory for Zoonoses, Fujian Center for Disease Control and Prevention;Fuzhou 350001, China
    2 Fujian Medical University, Fuzhou 350004, China
  • Received:2016-06-08 Online:2017-02-28 Published:2017-03-06
  • Contact: Yan-qin DENG
  • Supported by:
    Supported by the Subject of Medical Innovation of Fujian Province(No. 2012?CXB?12)

摘要:

目的 了解福建省部分地区鼠类巴贝虫(Babesia)的感染状况以及基因特征。方法 2014-2015年采用笼日法在福建省邵武、清流、顺昌、永安、长乐和尤溪等6地捕鼠,现场鉴定鼠种,记录鼠类釆集时间、地点、鼠种、性别等资料。采集各鼠心脏血,采用PCR扩增巴贝虫18S rRNA片段,取阳性PCR产物送测序并进行序列比对分析,构建系统进化树分析同源性。PCR检测阳性率间的比较采用χ2检验或Fisher精确检验法。结果 共捕获209只鼠,其中家鼠71只,野鼠138只。PCR检测结果显示,巴贝虫阳性率为9.6%(20/209)。家鼠的阳性率为2.8%(2/71),其中褐家鼠(Rattus norvebicus)和黄胸鼠(R. flavipectus)各有1只阳性;野鼠的阳性率为13.0%(18/138),其中大板齿鼠(Bandicota indica)、黄毛鼠(R. losea)、社鼠(R. confucianus)和针毛鼠(R. fulvescens)等4个鼠种的阳性数分别为13、1、2和2只;野鼠的阳性率高于家鼠(P < 0.05)。6地中,尤溪的鼠类阳性率最高,为14.9%(13/87),其次为永安,阳性率为13.6%(3/22),清流的鼠类未检出巴贝虫感染阳性。雄鼠的阳性率为7.9%(9/114),雌鼠为11.6%(11/95)。成年鼠的阳性率最高,为10.4%(18/173),其次为幼年鼠,阳性率为6.3%(2/32),捕获的4只老年鼠均未检出巴贝虫感染阳性。不同地区、不同性别和不同鼠龄的巴贝虫阳性率差异无统计学意义(P > 0.05)。PCR阳性产物测序和同源性分析结果显示,样品序列相似性达100%。BLAST结果显示,血样感染的为田鼠巴贝虫(Babesia microti)。系统进化树结果显示,样品序列与源自浙江的田鼠巴贝虫的序列同源性(GenBank登录号:JQ609305)最高。结论 福建省部分地区鼠类存在田鼠巴贝虫感染,野鼠的阳性率高于家鼠。

关键词: 田鼠巴贝虫, 鼠类, 基因特征, 福建

Abstract:

Objective To explore the status of Babesia infection in rodents and the genetic characteristics of Babesia spp. in Fujian Province. Methods Rodents were captured by the night trapping method in Shaowu, Qingliu, Shunchang, Yong’an, Changle and Youxi during 2014-2015. The rodent species was identified, and information on the time and place of capture, species and sex of rodents was recorded. Blood samples was collected, in which the fragment of 18S rRNA gene of Babesia spp. was amplified by PCR. The PCR products were sequenced and the phylogenetic tree was constructed for homology analysis. Data on positive rate were analyzed with Chi-square or Fisher exact test. Results Two hundred and nine rats were captured, comprising of 71 domestic and 138 wild rats. The overall positive rate was 9.6% (20/209). The positive rate in domestic rats was 2.8% (2/71), including one Rattus norvebicus and one Rattus flavipectus. The positive rate in wild rats was 13.0% (18/138), including 13 Bandicota indica, one Rattus losea, 2 Rattus confucianus and 2 Rattus fulvescens. The positive rate was significantly higher in wild rats than in domestic rats (P < 0.05). The Youxi region had the highest positive rate(14.9%, 13/87), followed by Yong’an(13.6%, 3/22), and no positive rat was found in Qingliu. The positive rate in the male rats was 7.9% (9/114), and that in the females was 11.6% (11/95). The positive rate was highest in adult rats (10.4%, 18/173), followed by young ones (6.3%, 2/32). No positive rat was found in old rats. There was no significant difference in positive rate among different regions, between male and female rats, or among different ages (P > 0.05). The sequences of PCR products had a 100% homology. The BLAST results revealed the species to be Babesia microti. The phylogenetic tree showed that the sample sequence was the most homologous with Babesia microti from Zhejiang Province(GenBank Accession No: JQ609305). Conclusion There occurs Babesia microti infection in rats in part areas of Fujian Province. The positive rate was higher in wild rats than in domestic rats.

Key words: Babesia microti, Rodent, Genetic identification, Fujian

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