Department of Infectious Diseases and College of Veterinary Medicine, University of Georgia, Athens, Georgia, USA.
Department of Pathology, College of Veterinary Medicine, University of Georgia, Athens, Georgia, USA.
Vector Borne Zoonotic Dis. 2021 Aug;21(8):586-592. doi: 10.1089/vbz.2020.2761. Epub 2021 Jun 14.
As one of the causative agents of lymphatic filariasis in humans, has been established as the laboratory model of choice for studying this infection owing to its viability in small animal hosts, with the domestic cat being significant among these. The usefulness of individual feline infections is highly dependent on the levels of circulating microfilariae in the blood; thus, characterizing the course of microfilaremia benefits our understanding of this model. In -endemic regions, cats are also known reservoirs of infection, and describing microfilaremia in a controlled setting may improve transmission modeling. We followed the course of infection in 10 experimentally infected cats from inoculation to ultimate resolution. Seven cats developed patency, with a peak microfilaria concentration of 6525/mL. In addition, to identify cellular responses with potential value as predictors of patency, we measured the peripheral blood leukocyte counts during the first 8 months of infection and tested for correlations with lifelong microfilaria production. No strong relationships were observed, though cell values did appear to shift with the maturation phases of the parasite. The data we present reflect the course of microfilaremia in an important laboratory model under controlled conditions.
作为人类淋巴丝虫病的病原体之一,已被确立为研究该感染的首选实验室模型,因为它在小型动物宿主中具有活力,其中家猫尤为重要。单个猫感染的有用性高度依赖于血液中循环微丝蚴的水平;因此,描述微丝蚴血症的过程有助于我们理解该模型。在流行地区,猫也是感染的重要储存宿主,在受控环境中描述微丝蚴血症可能会改善传播建模。我们从接种到最终解决的过程中跟踪了 10 只实验感染猫的感染过程。7 只猫出现了通透性,微丝蚴浓度峰值为 6525/mL。此外,为了确定具有作为通透性预测因子潜在价值的细胞反应,我们在感染的前 8 个月测量外周血白细胞计数,并测试与终生微丝蚴产生的相关性。虽然细胞值似乎随着寄生虫的成熟阶段而变化,但没有观察到很强的相关性。我们提出的数据反映了在受控条件下重要实验室模型中微丝蚴血症的过程。