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Survival of SARS Virus in Vitro

机译:SARS病毒的体外存活

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Objective Evaluate the stability and infectious of SARS virus in patient's excrements and contaminated objects in vitro. Method Two strains of SARS virus were used in this study, one was BJ - 01 isolated from the lung tissue of one patient in Beijing, The other was GZF isolated from sputum of one patient in Guangzhou, The virus were cultured and propagated with Vero - E6 cell, the medium was DMEM supplemented with 10% fetal bovine serum. (1) Adding SARS virus (10~6TCID_(50)) to the specimen of faeces, urine, sputum, and plasma collected from healthy individuals, depositing in the cleaning area of BSL - 31ab, sampling 0. 5ml after definite time points, centrifuging, filtering and titering in Vero - E6 cell, observing CPE. (2) Smearing 10~6TCID_(50) SARS virus on the surface of sterilized steel slice, glass slice, plastics slice, paper slice, fabric slice and wood slice, adding the virus to sterilized water and soil. Rinsing and infecting Vero - E6 cell after definite time points. (3) The experiments were repeated three times. Result (1) SARS virus survival at least 3 days in the analogue sputum of SARS patient. The virus is stable at least 4 days in the analogue faeces of SARS patients. The virus keep high liter as long as 10 days in the analogue urine and plasma of SARS patients. (2) SARS virus keep infectious at least 48 - 72 hr in the analogue contaminated steel slice, glass slice and plastics slice, The infectious liter reduced about 5log within 48 hours. The virus can survival 4 - 6hr in the analogue conlaminal-ed paper slice, fabric slice and wood slice, 8hr in contaminated soil, 10 days in contaminated water. (3) The survival lime of BJ - 01 slrain and GZF strain in those specimens mentioned above were nol significantly difference. Conclusion SARS virus can survival long lime after discharge outside human body. It might be transmitted by faeces - oral mode and by contaminated environment. It is very important to sterilize patient' s excrement and contaminated objects effectively.
机译:目的评估SARS病毒在患者粪便和受污染物体中的稳定性和感染性。方法采用两株SARS病毒,一株是从北京一名患者的肺组织中分离出的BJ-01,另一株是从广州某患者的痰中分离出的GZF,并用Vero-培养和繁殖。 E6细胞,培养基是补充有10%胎牛血清的DMEM。 (1)在从健康个体收集的粪便,尿液,痰液和血浆标本中添加SARS病毒(10〜6TCID_(50)),沉积在BSL-31ab的清洁区域中,在确定的时间点采样0. 5ml,在Vero-E6细胞中进行离心,过滤和滴定,观察CPE。 (2)在灭菌的钢片,玻璃片,塑料片,纸片,织物片和木片的表面涂上10〜6TCID_(50)SARS病毒,并将其添加到灭菌的水和土壤中。在确定的时间点后漂洗和感染Vero-E6细胞。 (3)实验重复3次。结果(1)SARS病毒在SARS患者的类似痰中存活至少3天。该病毒在SARS患者的类似粪便中至少稳定4天。该病毒在SARS患者的类似尿液和血浆中可保持长达10天的高升。 (2)SARS病毒在类似的被污染的钢片,玻璃片和塑料片中至少保持48-72 hr的传染性,在48小时之内感染量减少了约5log。该病毒可以在类似的带棱片的纸片,织物片和木片中存活4-6小时,在被污染的土壤中存活8小时,在被污染的水中存活10天。 (3)在上述标本中,BJ-01滑坡的存活石灰和GZF应变的存活率无显着差异。结论SARS病毒在人体内排出后能存活很长的时间。它可能通过粪便传播-口服模式和受污染的环境。有效地对患者的排泄物和被污染的物体进行消毒非常重要。

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