Jutzeler Kathrin S, Clec'h Winka LE, Chevalier Frédéric D, Anderson Timothy J C
Host Parasite Interaction program, Texas Biomedical Research Institute, P.O. Box 760549, 78245 San Antonio, Texas, USA.
UT Health, Microbiology, Immunology & Molecular Genetics, San Antonio, TX 78229.
bioRxiv. 2024 Jan 13:2024.01.12.574230. doi: 10.1101/2024.01.12.574230.
The role of pathogen genotype in determining disease severity and immunopathology has been studied intensively in microbial pathogens including bacteria, fungi, protozoa, and viruses, but is poorly understood in parasitic helminths. The medically important blood fluke is an excellent model system to study the impact of helminth genetic variation on immunopathology. Our laboratory has demonstrated that laboratory schistosome populations differ in sporocyst growth and cercarial production in the intermediate snail host and worm establishment and fecundity in the vertebrate host. Here, we (i) investigate the hypothesis that schistosome genotype plays a significant role in immunopathology and related parasite life history traits in the vertebrate mouse host and (ii) quantify the relative impact of parasite and host genetics on infection outcomes.
We infected BALB/c and C57BL/6 mice with four different laboratory schistosome populations from Africa and the Americas. We quantified disease progression in the vertebrate host by measuring body weight and complete blood count (CBC) with differential over an infection period of 12 weeks. On sacrifice, we assessed parasitological (egg and worm counts, fecundity), immunopathological (organ measurements and histopathology), and immunological (CBC with differential and cytokine profiles) characteristics to determine the impact of parasite and host genetics.
We found significant variation between parasite populations in worm numbers, fecundity, liver and intestine egg counts, liver and spleen weight, and fibrotic area, but not in granuloma size. Variation in organ weight was explained by egg burden and by intrinsic parasite factors independent of egg burden. We found significant variation between infected mouse lines in cytokines (IFN-γ, TNF-α), eosinophil, lymphocyte, and monocyte counts.
This study showed that both parasite and host genotype impact the outcome of infection. While host genotype explains most of the variation in immunological traits, parasite genotype explains most of the variation in parasitological traits, and both host and parasite genotype impact immunopathology outcomes.
病原体基因型在决定疾病严重程度和免疫病理学方面的作用,在包括细菌、真菌、原生动物和病毒在内的微生物病原体中已得到深入研究,但在寄生蠕虫中却知之甚少。具有医学重要性的血吸虫是研究蠕虫遗传变异对免疫病理学影响的极佳模型系统。我们实验室已证明,实验室血吸虫种群在中间螺宿主中的孢蚴生长和尾蚴产生,以及在脊椎动物宿主中的成虫建立和繁殖力方面存在差异。在此,我们(i)研究血吸虫基因型在脊椎动物小鼠宿主的免疫病理学及相关寄生虫生活史特征中起重要作用这一假设,(ii)量化寄生虫和宿主基因对感染结果的相对影响。
我们用来自非洲和美洲的四个不同实验室血吸虫种群感染BALB/c和C57BL/6小鼠。在12周的感染期内,通过测量体重和进行全血细胞计数(CBC)及分类来量化脊椎动物宿主中的疾病进展。在处死时,我们评估了寄生虫学(虫卵和虫体计数、繁殖力)、免疫病理学(器官测量和组织病理学)以及免疫学(CBC及分类和细胞因子谱)特征,以确定寄生虫和宿主基因的影响。
我们发现不同寄生虫种群在虫体数量、繁殖力、肝脏和肠道虫卵计数、肝脏和脾脏重量以及纤维化面积方面存在显著差异,但在肉芽肿大小方面无差异。器官重量的差异可由虫卵负荷以及独立于虫卵负荷的内在寄生虫因素来解释。我们发现受感染小鼠品系在细胞因子(IFN-γ、TNF-α)、嗜酸性粒细胞、淋巴细胞和单核细胞计数方面存在显著差异。
本研究表明,寄生虫和宿主基因型均会影响感染结果。虽然宿主基因型解释了免疫性状的大部分变异,但寄生虫基因型解释了寄生虫学性状的大部分变异,并且宿主和寄生虫基因型均会影响免疫病理学结果。