共同感染的血孢子虫(血孢子虫属,Apicomplexa)在流苏(Fringillidae)的外红细胞发育过程中表现出不同的宿主组织滋养性。

IF 3.7 2区 医学 Q1 PARASITOLOGY International journal for parasitology Pub Date : 2024-01-01 DOI:10.1016/j.ijpara.2023.07.004
Tanja Himmel , Josef Harl , Julia Matt , Nora Nedorost , Madeleine Lunardi , Mikas Ilgūnas , Tatjana Iezhova , Gediminas Valkiūnas , Herbert Weissenböck
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引用次数: 0

摘要

疟原虫属、血孢子虫属和白细胞虫属的禽血孢子虫是世界各地野生鸟类常见的血液寄生虫。尽管这些寄生虫是重要的病原体,有可能损害宿主的健康,但人们对其红细胞外发育情况知之甚少,尤其是在野生动物中常见的合并感染期间。本研究旨在利用寄生于 Fringilla coelebs 的血孢子虫解决这一问题,Fringilla coelebs 是西古北常见的鸟类物种,也是多种血孢子虫寄生系的宿主。通过血片显微镜对血吸虫阳性的 20 只 F. coelebs 的血液和组织样本进行了 PCR 分析和测序,以确定寄生虫的细胞色素 b 系列。通过组织学和应用针对寄生虫 18S rRNA 的属、种和品系特异性探针进行原位杂交,检查组织切片中的外红细胞阶段。此外,还对组织阶段进行了激光显微切割,以确定寄生虫的品系。聚合酶链式反应、激光显微切割和原位杂交的综合分子检测结果显示,寄生虫的共感染率很高,其中以血吸虫系为主。首次描述了五种血包虫的外红细胞分生组织,包括大血包虫 hCCF6、流苏血包虫 hCCF3、大血包虫 hCCF5、血包虫 hROFI1 和血包虫 hCCF2。在血管系统中观察到了子囊阶段,这是以前未知的血包虫外红细胞发育模式。这些物种的子实体和巨型子实体在形态和器官分布方面各不相同,这表明子实体的发育模式具有物种特异性,对宿主组织的趋性也各不相同。报告了血液蛋白病的新病理特征。此外,对血吸虫属的外红细胞阶段进行的系统发育分析表明,非巨细胞形成种与巨细胞形成种是分开的,因此需要对血吸虫寄生虫的外红细胞发育进行进一步研究,以探索这一特征的系统发育特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Co-infecting Haemoproteus species (Haemosporida, Apicomplexa) show different host tissue tropism during exo-erythrocytic development in Fringilla coelebs (Fringillidae)

Avian haemosporidians of the genera Plasmodium, Haemoproteus, and Leucocytozoon are common blood parasites in wild birds all over the world. Despite their importance as pathogens potentially compromising host fitness and health, little is known about the exo-erythrocytic development of these parasites, particularly during co-infections which predominate in wildlife. This study aimed to address this issue using Haemoproteus parasites of Fringilla coelebs, a common bird species of the Western Palearctic and host to a variety of haemosporidian parasite lineages. Blood and tissue samples of 20 F. coelebs, positive for haemosporidians by blood film microscopy, were analysed by PCR and sequencing to determine cytochrome b lineages of the parasites. Tissue sections were examined for exo-erythrocytic stages by histology and in situ hybridization applying genus-, species-, and lineage-specific probes which target the 18S rRNA of the parasites. In addition, laser microdissection of tissue stages was performed to identify parasite lineages. Combined molecular results of PCR, laser microdissection, and in situ hybridization showed a high rate of co-infections, with Haemoproteus lineages dominating. Exo-erythrocytic meronts of five Haemoproteus spp. were described for the first known time, including Haemoproteus magnus hCCF6, Haemoproteus fringillae hCCF3, Haemoproteus majoris hCCF5, Haemoproteus sp. hROFI1, and Haemoproteus sp. hCCF2. Merogonic stages were observed in the vascular system, presenting a formerly unknown mode of exo-erythrocytic development in Haemoproteus parasites. Meronts and megalomeronts of these species were distinct regarding their morphology and organ distribution, indicating species-specific patterns of merogony and different host tissue tropism. New pathological aspects of haemoproteosis were reported. Furthermore, phylogenetic analysis of Haemoproteus spp. with regard to their exo-erythrocytic stages points towards separation of non-megalomeront-forming species from megalomeront-forming species, calling for further studies on exo-erythrocytic development of haemosporidian parasites to explore the phylogenetic character of this trait.

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来源期刊
CiteScore
8.40
自引率
2.50%
发文量
76
审稿时长
23 days
期刊介绍: International Journal for Parasitology offers authors the option to sponsor nonsubscriber access to their articles on Elsevier electronic publishing platforms. For more information please view our Sponsored Articles page. The International Journal for Parasitology publishes the results of original research in all aspects of basic and applied parasitology, including all the fields covered by its Specialist Editors, and ranging from parasites and host-parasite relationships of intrinsic biological interest to those of social and economic importance in human and veterinary medicine and agriculture.
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