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Aerosolized avian influenza virus by laboratory manipulations

BACKGROUND: Avian H5N1 influenza viruses present a challenge in the laboratory environment, as they are difficult to collect from the air due to their small size and relatively low concentration. In an effort to generate effective methods of H5N1 air removal and ensure the safety of laboratory perso...

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Autores principales: Li, Zhiping, Li, Jinsong, Zhang, Yandong, Li, Lin, Ma, Limin, Li, Dan, Gao, Feng, Xia, Zhiping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3439333/
https://www.ncbi.nlm.nih.gov/pubmed/22866888
http://dx.doi.org/10.1186/1743-422X-9-146
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author Li, Zhiping
Li, Jinsong
Zhang, Yandong
Li, Lin
Ma, Limin
Li, Dan
Gao, Feng
Xia, Zhiping
author_facet Li, Zhiping
Li, Jinsong
Zhang, Yandong
Li, Lin
Ma, Limin
Li, Dan
Gao, Feng
Xia, Zhiping
author_sort Li, Zhiping
collection PubMed
description BACKGROUND: Avian H5N1 influenza viruses present a challenge in the laboratory environment, as they are difficult to collect from the air due to their small size and relatively low concentration. In an effort to generate effective methods of H5N1 air removal and ensure the safety of laboratory personnel, this study was designed to investigate the characteristics of aerosolized H5N1 produced by laboratory manipulations during research studies. RESULTS: Normal laboratory procedures used to process the influenza virus were carried out independently and the amount of virus polluting the on-site atmosphere was measured. In particular, zootomy, grinding, centrifugation, pipetting, magnetic stirring, egg inoculation, and experimental zoogenetic infection were performed. In addition, common accidents associated with each process were simulated, including breaking glass containers, syringe injection of influenza virus solution, and rupturing of centrifuge tubes. A micro-cluster sampling ambient air pollution collection device was used to collect air samples. The collected viruses were tested for activity by measuring their ability to induce hemagglutination with chicken red blood cells and to propagate in chicken embryos after direct inoculation, the latter being detected by reverse-transcription PCR and HA test. The results showed that the air samples from the normal centrifugal group and the negative-control group were negative, while all other groups were positive for H5N1. CONCLUSIONS: Our findings suggest that there are numerous sources of aerosols in laboratory operations involving H5N1. Thus, laboratory personnel should be aware of the exposure risk that accompanies routine procedures involved in H5N1 processing and take proactive measures to prevent accidental infection and decrease the risk of virus aerosol leakage beyond the laboratory.
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spelling pubmed-34393332012-09-12 Aerosolized avian influenza virus by laboratory manipulations Li, Zhiping Li, Jinsong Zhang, Yandong Li, Lin Ma, Limin Li, Dan Gao, Feng Xia, Zhiping Virol J Research BACKGROUND: Avian H5N1 influenza viruses present a challenge in the laboratory environment, as they are difficult to collect from the air due to their small size and relatively low concentration. In an effort to generate effective methods of H5N1 air removal and ensure the safety of laboratory personnel, this study was designed to investigate the characteristics of aerosolized H5N1 produced by laboratory manipulations during research studies. RESULTS: Normal laboratory procedures used to process the influenza virus were carried out independently and the amount of virus polluting the on-site atmosphere was measured. In particular, zootomy, grinding, centrifugation, pipetting, magnetic stirring, egg inoculation, and experimental zoogenetic infection were performed. In addition, common accidents associated with each process were simulated, including breaking glass containers, syringe injection of influenza virus solution, and rupturing of centrifuge tubes. A micro-cluster sampling ambient air pollution collection device was used to collect air samples. The collected viruses were tested for activity by measuring their ability to induce hemagglutination with chicken red blood cells and to propagate in chicken embryos after direct inoculation, the latter being detected by reverse-transcription PCR and HA test. The results showed that the air samples from the normal centrifugal group and the negative-control group were negative, while all other groups were positive for H5N1. CONCLUSIONS: Our findings suggest that there are numerous sources of aerosols in laboratory operations involving H5N1. Thus, laboratory personnel should be aware of the exposure risk that accompanies routine procedures involved in H5N1 processing and take proactive measures to prevent accidental infection and decrease the risk of virus aerosol leakage beyond the laboratory. BioMed Central 2012-08-06 /pmc/articles/PMC3439333/ /pubmed/22866888 http://dx.doi.org/10.1186/1743-422X-9-146 Text en Copyright ©2012 Li et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Li, Zhiping
Li, Jinsong
Zhang, Yandong
Li, Lin
Ma, Limin
Li, Dan
Gao, Feng
Xia, Zhiping
Aerosolized avian influenza virus by laboratory manipulations
title Aerosolized avian influenza virus by laboratory manipulations
title_full Aerosolized avian influenza virus by laboratory manipulations
title_fullStr Aerosolized avian influenza virus by laboratory manipulations
title_full_unstemmed Aerosolized avian influenza virus by laboratory manipulations
title_short Aerosolized avian influenza virus by laboratory manipulations
title_sort aerosolized avian influenza virus by laboratory manipulations
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3439333/
https://www.ncbi.nlm.nih.gov/pubmed/22866888
http://dx.doi.org/10.1186/1743-422X-9-146
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