畜牧与饲料科学 ›› 2025, Vol. 46 ›› Issue (6): 95-100.doi: 10.12160/j.issn.1672-5190.2025.06.013

• 动物疾病防控 • 上一篇    下一篇

塔城地区3个藏猪引种场隐孢子虫感染情况的分子检测

徐俊飞1, 朱婷婷1,2, 赫永强1, 徐佳宁1, 王圆梦1, 张振杰1, 齐萌1   

  1. 1.塔里木大学动物科学与技术学院,新疆 阿拉尔 843300;
    2.新疆生产建设兵团第九师农业科学研究所(畜牧科学研究所),新疆 额敏 834601
  • 收稿日期:2025-10-27 出版日期:2025-11-30 发布日期:2026-01-26
  • 通讯作者: 齐萌(1985—),男,教授,博士,博士生导师,主要研究方向为人兽共患病病原生物学。
  • 作者简介:徐俊飞(1995—),男,硕士研究生,主要研究方向为动物群发病防控。
  • 基金资助:
    新疆生产建设兵团第九师科技计划项目(2022JS004)

Molecular Detection of Cryptosporidium Infection in Three Tibetan Pig Introduction Farms in Tacheng Area

XU Junfei1, ZHU Tingting1, 2, HE Yongqiang1, XU Jianing1, WANG Yuanmeng1, ZHANG Zhenjie1, QI Meng1   

  1. 1. College of Animal Science and Technology, Tarim University, Alaer 843300, China;
    2. Agricultural Science Research Institute(Animal Husbandry Science Research Institute)of the Ninth Division of the Xinjiang Production and Construction Corps, Emin 834601, China
  • Received:2025-10-27 Online:2025-11-30 Published:2026-01-26

摘要: [目的] 了解塔城地区引进藏猪感染的隐孢子虫种类和分布情况。[方法] 采集塔城地区3个引种场藏猪粪便样本506份,其中断奶前仔猪(<30日龄)、断奶后仔猪(31~90日龄)、育肥猪(91~180日龄)和成年猪(>240日龄)的粪便样本分别为126份、126份、130份和124份,使用巢氏PCR法进行检测和序列分析,鉴定隐孢子虫种类,通过构建进化树分析其遗传特征。[结果] 基于隐孢子虫SSU rRNA基因位点,发现3个引种场藏猪隐孢子虫感染的总阳性率为11.26%(57/506),其中引种A场、B场和C场的隐孢子虫阳性率分别为8.00%(16/200)、10.00%(20/200)和19.81%(21/106),统计学差异极显著(P<0.01);断奶前和断奶后藏猪隐孢子虫阳性率分别为8.73%(11/126)和36.51%(46/126),育肥猪和成年猪未发现隐孢子虫感染,统计学差异极显著(P<0.01)。经序列比对,鉴定出2种隐孢子虫,分别为种母猪隐孢子虫(n=36)和猪隐孢子虫(n=21);2种隐孢子虫与不同宿主源猪隐孢子虫和种母猪隐孢子虫各自聚类形成同一进化支,与其他隐孢子虫种类形成不同进化支和亚群。[结论] 塔城地区3个引种场藏猪感染隐孢子虫较为普遍,以断奶前后幼龄猪易感,感染的虫种为猪隐孢子虫和种母猪隐孢子虫,提示应加强引种场的环境控制和隐孢子虫预防工作。

关键词: 藏猪, 隐孢子虫, 种类, 鉴定, 检测

Abstract: [Objective] To clarify the species and distribution of Cryptosporidium in introduced Tibetan pigs in Tacheng Area. [Methods] A total of 506 fecal samples were collected from Tibetan pigs in three introduction farms in Tacheng Area, including 126 samples from pre-weaning piglets (<30 days old), 126 from post-weaning piglets (31-90 days old), 130 from fattening pigs (91-180 days old), and 124 from adult pigs (>240 days old). Detection and sequence analysis were performed using nested PCR to identify Cryptosporidium species, and phylogenetic analysis was conducted to examine their genetic characteristics. [Results] Based on the Cryptosporidium SSU rRNA gene locus, the overall positive rate of Cryptosporidium infection in Tibetan pigs across the three farms was 11.26% (57/506). The positive rates in Farm A, Farm B and Farm C were 8.00% (16/200), 10.00% (20/200) and 19.81% (21/106), respectively, showing an extremely significant statistical difference (P<0.01). The positive rates in pre-weaning and post-weaning piglets were 8.73% (11/126) and 36.51% (46/126), respectively, while no Cryptosporidium infection was detected in fattening pigs and adult pigs, with an extremely significant statistical difference (P<0.01). Sequence alignment identified two Cryptosporidium species, namely C. suisn=36) and C. scrofarumn=21). These two species clustered in the same clades as C. suis and C. scrofarum isolates from different hosts, respectively, and formed distinct clades and subclusters from other Cryptosporidium species. [Conclusion] Cryptosporidium infection is prevalent in Tibetan pigs from the three introduction farms in Tacheng Area, with pre-weaning and post-weaning piglets being highly susceptible. The infecting species are C. suis and C. scrofarum, suggesting that enhanced environmental control and Cryptosporidium prevention measures should be implemented in introduction farms.

Key words: Tibetan pig, Cryptosporidium, species, identification, detection

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