中国寄生虫学与寄生虫病杂志 ›› 2023, Vol. 41 ›› Issue (2): 245-248.doi: 10.12140/j.issn.1000-7423.2023.02.021

• 研究简报 • 上一篇    下一篇

福建漳州流浪犬、猫芽囊原虫感染调查及基因分型

李永霞1,2(), 李梦蕊1,2, 李诗艺1,2, 黄潇航1,2, 吴炜1,3, 黄志坚1,2, 殷光文1,2,*()   

  1. 1 福建农林大学动物科学学院(蜂学学院),福州 350002
    2 福建省动物药物工程实验室,福州 350002
    3 漳州康德宠物医院,福建漳州 363100
  • 收稿日期:2022-07-05 修回日期:2022-10-07 出版日期:2023-04-23 发布日期:2023-04-23
  • 通讯作者: 殷光文
  • 作者简介:李永霞(1998-),女,硕士研究生,从事兽医寄生虫学与分子免疫学。E-mail:liyx_000@163.com
  • 基金资助:
    横向课题-福建省犬蜱和跳蚤感染情况调查及药物治疗效果检测(CZ2020107)

Investigation of Blastocystis spp. infection in stray dogs and cats and the parasite genotyping in Zhangzhou, Fujian

LI Yongxia1,2(), LI Mengrui1,2, LI Shiyi1,2, HUANG Xiaohang1,2, WU Wei1,3, HUANG Zhijian1,2, YIN Guangwen1,2,*()   

  1. 1 College of Animal Sciences(College of Bee Science), Fujian Agriculture and Forestry University,Fuzhou 350002, China
    2 Fujian Animal Drug Engineering Laboratory, Fuzhou 350002, China
    3 Zhangzhou Kangde Pet Hospital, Zhangzhou 363100, Fujian, China
  • Received:2022-07-05 Revised:2022-10-07 Online:2023-04-23 Published:2023-04-23
  • Contact: YIN Guangwen
  • Supported by:
    Supported by Cross-sectional Project-Investigation on the Infection of Ticks and Feas in Dogs and Detection of Drug Treatment Effect in Fujian Province(CZ2020107)

摘要:

为了解福建省漳州市部分流浪动物收容中心犬、猫芽囊原虫感染情况,采集漳州地区救助犬、猫粪样并提取DNA,以芽囊原虫核糖体小亚基RNA(SSU rRNA)为引物进行PCR扩增。对阳性样品进行Sanger测序,根据GenBank公共数据库资源进行BLAST序列比对分析,采用MAGE 7.0软件构建系统进化树。共采集猫粪121份、犬粪119份。经PCR检验共7份样品阳性,其中犬芽囊原虫阳性率为5.04%(6/119),猫芽囊原虫阳性率为0.82%(1/121),犬、猫间阳性率差异具有统计学意义(χ2 = 4.153,P < 0.05)。不同月龄的犬间、猫间,以及不同性别的犬间、猫间芽囊原虫阳性率差异均无统计学意义(χ2 = 2.149、0.340、0.818、1.176,P > 0.05)。仅1份犬粪样的PCR扩增序列测序成功,为SSU rRNA基因序列YN-145株序列,通过BLAST序列比对,与人兽共患型芽囊原虫ST3亚型(GenBank登录号分别为MW404497.1、MW242639.1、MW767066.1)的一致性为95%~97%。系统进化树中YN-145序列与ST3形成同一聚类分支。

关键词: 芽囊原虫, 犬, 猫, 基因亚型, 福建漳州

Abstract:

To investigate the prevalence of Blastocystis infections among dogs and cats at stray animal shelters in Zhangzhou City, Fujian Province, fecal samples were collected from rescued dogs and cats in Zhangzhou City, and DNA was extracted. Blastocystis ribosomal small subunit RNA (SSU rRNA) was used as a primer for PCR amplification. The positive samples were sent for Sanger sequencing, followed by BLAST sequence alignment analysis using the GenBank public database resources. A phylogenetic tree was constructed using MEGA 7.0 software. A total of 121 cat fecal samples and 119 dog fecal samples were collected. PCR test showed that the Blastocystis positivity rate of 5.04% (6/119) in dogs and 0.82% (1/121) in cats. The difference between dogs and cats was statistically significant (χ2 = 4.153, P < 0.05). Only one fecal sample from a dog was successfully sequenced by PCR amplification of the SSU rRNA gene, yielding the YN-145 sequence. Sequence alignment using BLAST showed a high similarity of 95%-97% with zoonotic Blastocystis ST3 subtype sequences (GenBank accession numbers MW404497.1, MW242639.1, and MW767066.1). Phylogenetic analysis revealed that the YN-145 sequence formed a separate cluster within the ST3 subtype.

Key words: Blastocystis, Dog, Cat, Genotype, Zhangzhou, Fujian

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