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牛副流感3型病毒的气溶胶稳定性

Aerosol stability of bovine parainfluenza type 3 virus.

作者信息

Elazhary M A, Derbyshire J B

出版信息

Can J Comp Med. 1979 Jul;43(3):295-304.

Abstract

Aerosols of bovine parainfluenza type 3 virus were generated with a Devilbiss 40 nebulizer from Eagle's minimum essential medium and nasal secretion from a non-infected calf and stored in a rotating drum at temperatures of 6 degrees C or 32 degrees C and relative humidities of 30% or 90%. The aerosols were sampled at seven minutes, one, two and three hours after the start of generation with an all glass impinger (AGI-30) and titrated for infectivity in cell cultures. Physical decay was determined by a rhodamine tracer technique. Media, temperature or relative humidity had little effect on the survival of parainfluenza type 3 virus during spraying (zero to seven minutes). During aging of aerosols at 32 degrees C and 30% relative humidity, parainfluenza type 3 virus was less stable in Eagle's minimum essential medium than in nasal secretion from a noninfected calf, but at 6 degrees C and 30% relative humidity, the virus was more stable in Eagle's minimum essential medium. At 32 degrees C, the virus was less stable during aging at 90% relative humidity than at 30% relative humidity. The virus was consistently more stable during aging of aerosols at 6 degrees C than at 32 degrees C.

摘要

使用德维比斯40型雾化器,以伊格尔氏最低限度基本培养基和未感染小牛的鼻分泌物为原料,生成牛副流感3型病毒气溶胶,并将其储存在转鼓中,温度为6摄氏度或32摄氏度,相对湿度为30%或90%。在生成气溶胶开始后的7分钟、1小时、2小时和3小时,用全玻璃撞击式采样器(AGI - 30)对气溶胶进行采样,并在细胞培养中测定其感染性。通过罗丹明示踪技术确定物理衰减。培养基、温度或相对湿度对喷雾过程中(0至7分钟)牛副流感3型病毒的存活影响很小。在32摄氏度和30%相对湿度下气溶胶老化过程中,牛副流感3型病毒在伊格尔氏最低限度基本培养基中的稳定性低于在未感染小牛的鼻分泌物中的稳定性,但在6摄氏度和30%相对湿度下,该病毒在伊格尔氏最低限度基本培养基中更稳定。在32摄氏度时,该病毒在90%相对湿度下老化期间的稳定性低于在30%相对湿度下的稳定性。在6摄氏度下气溶胶老化过程中,该病毒始终比在32摄氏度下更稳定。

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本文引用的文献

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SURVIVAL OF MEASLES VIRUS IN AIR.麻疹病毒在空气中的存活情况
Nature. 1964 Mar 7;201:1054-5. doi: 10.1038/2011054a0.
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Appl Microbiol. 1973 Aug;26(2):146-8. doi: 10.1128/am.26.2.146-148.1973.
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Aerosol stability of three acute respiratory disease viruses.三种急性呼吸道疾病病毒的气溶胶稳定性
Proc Soc Exp Biol Med. 1967 May;125(1):222-7. doi: 10.3181/00379727-125-32054.

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