首页> 美国卫生研究院文献>PLoS Neglected Tropical Diseases >Trypanosoma brucei rhodesiense Transmitted by a Single Tsetse Fly Bite in Vervet Monkeys as a Model of Human African Trypanosomiasis
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Trypanosoma brucei rhodesiense Transmitted by a Single Tsetse Fly Bite in Vervet Monkeys as a Model of Human African Trypanosomiasis

机译:由单个采采蝇蝇叮咬传播的黑尾猴锥虫作为人类非洲锥虫病的模型

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摘要

We have investigated the pathogenicity of tsetse (Glossina pallidipes)-transmitted cloned strains of Trypanosoma brucei rhodesiense in vervet monkeys. Tsetse flies were confirmed to have mature trypanosome infections by xenodiagnosis, after which nine monkeys were infected via the bite of a single infected fly. Chancres developed in five of the nine (55.6%) monkeys within 4 to 8 days post infection (dpi). All nine individuals were successfully infected, with a median pre-patent period of 4 (range = 4–10) days, indicating that trypanosomes migrated from the site of fly bite to the systemic circulation rapidly and independently of the development of the chancre. The time lag to detection of parasites in cerebrospinal fluid (CSF) was a median 16 (range = 8–40) days, marking the onset of central nervous system (CNS, late) stage disease. Subsequently, CSF white cell numbers increased above the pre-infection median count of 2 (range = 0–9) cells/µl, with a positive linear association between their numbers and that of CSF trypanosomes. Haematological changes showed that the monkeys experienced an early microcytic-hypochromic anaemia and severe progressive thrombocytopaenia. Despite a 3-fold increase in granulocyte numbers by 4 dpi, leucopaenia occurred early (8 dpi) in the monkey infection, determined mainly by reductions in lymphocyte numbers. Terminally, leucocytosis was observed in three of nine (33%) individuals. The duration of infection was a median of 68 (range = 22–120) days. Strain and individual differences were observed in the severity of the clinical and clinical pathology findings, with two strains (KETRI 3741 and 3801) producing a more acute disease than the other two (KETRI 3804 and 3928). The study shows that the fly-transmitted model accurately mimics the human disease and is therefore a suitable gateway to understanding human African trypanosomiasis (HAT; sleeping sickness).
机译:我们已经调查了采采蝇(Glossina pallidipes)传播的黑尾锥虫Trypanosoma brucei rhodesiense克隆株的致病性。通过异种诊断,采采蝇被证实具有成熟的锥虫感染,此后,通过叮咬一只被感染的蝇蝇感染了九只猴子。在感染(dpi)后的4到8天内,九只猴子中的五只(55.6%)产生了Chancres。所有九个人均被成功感染,中位专利期为4天(范围== 4-10),这表明锥虫从蝇咬位点迅速迁移到全身循环,而与骨的发育无关。检测脑脊液(CSF)中的寄生虫的时间滞后是中位16天(范围== 8–40)天,标志着中枢神经系统(CNS,晚期)阶段疾病的发作。随后,脑脊液白细胞数目增加到感染前中位计数2(μl= 0-9)细胞/μl以上,并且其数目与脑脊液锥虫的数目呈正线性关系。血液学变化表明,猴子经历了早期的小细胞性低色素性贫血和严重的进行性血小板减少症。尽管粒细胞数增加了3倍达4 dpi,但白斑病在猴子感染中较早发生(8 dpi),这主要取决于淋巴细胞数量的减少。最终,在九个个体中的三个(33%)中观察到白细胞增多。感染持续时间中位数为68天(范围== 22-120天)。在临床和临床病理发现的严重性方面观察到菌株和个体差异,其中两种菌株(KETRI 3741和3801)产生的急性病比其他两种菌株(KETRI 3804和3928)更为严重。研究表明,蝇传模型能准确模拟人类疾病,因此是了解人类非洲锥虫病(HAT;昏睡病)的合适途径。

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