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Inactivation of African Swine Fever Virus by reagents commonly used in containment laboratories

Inactivation of African Swine Fever Virus by reagents commonly used in containment laboratories
Inactivation of African Swine Fever Virus by reagents commonly used in containment laboratories
Rapid and effective virus inactivation is an essential step for safe diagnostic testing and for research and vaccine development using infectious viruses. We characterised the reduction of African Swine Fever Virus (ASFV) infectivity using Virkon™ S (Lanxess) 1% w/v disinfectant, FACS™ Lysing buffer (BD), and AVL™ buffer (Qiagen), using porcine cell culture. No virus was detected following a 30 s 20:1 v/v mixing ratio of Virkon™ S 1% with high titre ASFV, supporting its effective use as a laboratory surface disinfectant. FACS™ Lysing and AVL™ buffers also inactivated ASFV, permitting safe removal of treated infected samples from high containment facilities.
0166-0934
McCleary, Stephen
d9ff45c6-8a8f-4b69-b37d-828a1fc1e43a
McCarthy, Ronan R.
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Strong, Rebecca
66abc51c-3f2a-44b1-bcaa-21477bfd67e9
Edwards, Jane
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Crooke, Helen
8bd844c0-1104-4dfb-a326-9973970bc7c0
McCleary, Stephen
d9ff45c6-8a8f-4b69-b37d-828a1fc1e43a
McCarthy, Ronan R.
0b2cf2e0-b0ff-4c92-aa04-92d91182d1f2
Strong, Rebecca
66abc51c-3f2a-44b1-bcaa-21477bfd67e9
Edwards, Jane
4f3ac03d-6393-4459-a2c3-55153be4f8b1
Crooke, Helen
8bd844c0-1104-4dfb-a326-9973970bc7c0

McCleary, Stephen, McCarthy, Ronan R., Strong, Rebecca, Edwards, Jane and Crooke, Helen (2021) Inactivation of African Swine Fever Virus by reagents commonly used in containment laboratories. Journal of Virological Methods, 295, [114203]. (doi:10.1016/j.jviromet.2021.114203).

Record type: Article

Abstract

Rapid and effective virus inactivation is an essential step for safe diagnostic testing and for research and vaccine development using infectious viruses. We characterised the reduction of African Swine Fever Virus (ASFV) infectivity using Virkon™ S (Lanxess) 1% w/v disinfectant, FACS™ Lysing buffer (BD), and AVL™ buffer (Qiagen), using porcine cell culture. No virus was detected following a 30 s 20:1 v/v mixing ratio of Virkon™ S 1% with high titre ASFV, supporting its effective use as a laboratory surface disinfectant. FACS™ Lysing and AVL™ buffers also inactivated ASFV, permitting safe removal of treated infected samples from high containment facilities.

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Published date: 15 June 2021

Identifiers

Local EPrints ID: 506146
URI: http://eprints.soton.ac.uk/id/eprint/506146
ISSN: 0166-0934
PURE UUID: 5f6b087f-b8e1-42bf-96c3-d38fb7051bb5
ORCID for Ronan R. McCarthy: ORCID iD orcid.org/0000-0002-7480-6352

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Date deposited: 29 Oct 2025 17:36
Last modified: 01 Nov 2025 03:12

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Contributors

Author: Stephen McCleary
Author: Ronan R. McCarthy ORCID iD
Author: Rebecca Strong
Author: Jane Edwards
Author: Helen Crooke

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