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从受 Tetratrichomonas gallinarum 和 Blastocystis spp. 污染的体内感染中建立单胞原生动物组织滴虫培养物。

Establishing mono-eukaryotic Histomonas meleagridis cultures from in vivo infection contaminated with Tetratrichomonas gallinarum and Blastocystis spp.

机构信息

Laboratory of Livestock Physiology, Immunology and Genetics, KULeuven, Kasteelpark Arenberg 30, 3001 Heverlee, Belgium.

Electron Microscopy Unit, Veterinary and Agrochemical Research Centre, CODA-CERVA, Groeselenberg 99, 1180 Ukkel, Belgium.

出版信息

Parasitology. 2013 Sep;140(10):1266-74. doi: 10.1017/S0031182013000723. Epub 2013 Jun 21.

DOI:10.1017/S0031182013000723
PMID:23790160
Abstract

SUMMARY The necessity to easily establish Histomonas meleagridis cultures has been underlined extensively by many researchers in order to gain more insights in the biology of H. meleagridis. In addition the occurrence of different protozoa in the caeca of birds impedes, however, the isolation and propagation of H. meleagridis from field outbreaks. Therefore, in a kinetic study using transmission electron microscopy the deleterious effects of adventitious protozoa including Tetratrichomonas gallinarum and Blastocystis spp. on cultured H. meleagridis were examined. To overcome this issue, an easy and successful approach to establish the mono-eukaryotic H. meleagridis culture free of other host's protozoa is proposed. At 10 days post infection, liver lesions of H. meleagridis-infected birds were isolated and inoculated into culture media pre-incubated with caecal bacteria. After 48 h of incubation, presence of H. meleagridis in the cultures was confirmed through morphological evaluation. Additionally, TEM examination and analysis by PCR amplification of the small subunit rRNA gene could exclude the co-cultivation of T. gallinarum and Blastocystis spp. Furthermore, after successful propagation and maintenance of the cultured H. meleagridis, its pathogenicity was affirmed in an infection experiment in turkeys.

摘要

摘要

许多研究人员强调了轻松建立火鸡组织滴虫培养物的必要性,以便更深入地了解火鸡组织滴虫的生物学特性。此外,鸟类盲肠中存在不同的原生动物,这阻碍了火鸡组织滴虫从野外爆发中分离和繁殖。因此,本研究采用透射电子显微镜的方法对偶然原生动物(包括鸡六鞭毛虫和蓝氏贾第鞭毛虫)对培养的火鸡组织滴虫的有害影响进行了动力学研究。为了解决这个问题,提出了一种简单而成功的方法来建立无其他宿主原生动物的单原生动物火鸡组织滴虫培养物。在感染后 10 天,从感染火鸡组织滴虫的鸟类的肝脏病变中分离出肝脏病变,并将其接种到预先用盲肠细菌孵育的培养基中。孵育 48 小时后,通过形态学评估确认培养物中存在火鸡组织滴虫。此外,通过 TEM 检查和小亚基 rRNA 基因的 PCR 扩增分析,可以排除鸡六鞭毛虫和蓝氏贾第鞭毛虫的共同培养。此外,在成功繁殖和维持培养的火鸡组织滴虫后,在火鸡感染实验中证实了其致病性。

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