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More cell culture passaged Camelpox virus sequences found resembling those of vaccinia virus

BACKGROUND: Camelpox is the most infectious and economically important disease of camelids that causes significant morbidity and mortality rates. Several live attenuated vaccines against Camelpox virus (CMLV) are produced worldwide by passaging field isolates in cell culture. Sequence of a high pass...

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Autores principales: Khalafalla, Abdelmalik I., Al Hosani, Mohamed A., Ishag, Hassan Zackaria Ali, Al Muhairi, Salama S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Faculty of Veterinary Medicine 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7419068/
https://www.ncbi.nlm.nih.gov/pubmed/32821659
http://dx.doi.org/10.4314/ovj.v10i2.4
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author Khalafalla, Abdelmalik I.
Al Hosani, Mohamed A.
Ishag, Hassan Zackaria Ali
Al Muhairi, Salama S.
author_facet Khalafalla, Abdelmalik I.
Al Hosani, Mohamed A.
Ishag, Hassan Zackaria Ali
Al Muhairi, Salama S.
author_sort Khalafalla, Abdelmalik I.
collection PubMed
description BACKGROUND: Camelpox is the most infectious and economically important disease of camelids that causes significant morbidity and mortality rates. Several live attenuated vaccines against Camelpox virus (CMLV) are produced worldwide by passaging field isolates in cell culture. Sequence of a high passage Saudi isolate of CMLV was previously found closely resembled Vaccinia virus (VACV). AIM: To determine whether other high cell culture passage CMLV isolates are genetically resemble VACV and further to explore the possible mechanism of the resemblance. METHODS: We performed polymerase chain reaction and DNA sequence analysis of A-type inclusion body protein (ATIP), L1R, and open reading frame (ORF) 185 genes on different cell culture passage levels of a field isolate, two high passage vaccines, wild-type, and reference strains of CMLV. RESULTS: We demonstrate that additional two high passage attenuated vaccine candidate from Sudan and UAE likewise contain sequences resembling VACV more than CMLV. Furthermore, sequence analysis of the ATIP gene of selected virus passages in cell culture revealed that the shift to VACV-like occurred between passage 11 and 20 and up to the 10th passage the genome still resembles wild-type virus. This observation was further confirmed by recombination analysis which indicated recombination events at ATIP and ORF185 genes occurred at higher passages. CONCLUSION: We confirmed that the cell culture passage CMLV turns to resemble VACV after cell culture passage and concluded that the resemblance may not be a result of contamination or misidentification as previously thought but could be due to recombination events that occurred during the passage process.
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spelling pubmed-74190682020-08-19 More cell culture passaged Camelpox virus sequences found resembling those of vaccinia virus Khalafalla, Abdelmalik I. Al Hosani, Mohamed A. Ishag, Hassan Zackaria Ali Al Muhairi, Salama S. Open Vet J Original Research BACKGROUND: Camelpox is the most infectious and economically important disease of camelids that causes significant morbidity and mortality rates. Several live attenuated vaccines against Camelpox virus (CMLV) are produced worldwide by passaging field isolates in cell culture. Sequence of a high passage Saudi isolate of CMLV was previously found closely resembled Vaccinia virus (VACV). AIM: To determine whether other high cell culture passage CMLV isolates are genetically resemble VACV and further to explore the possible mechanism of the resemblance. METHODS: We performed polymerase chain reaction and DNA sequence analysis of A-type inclusion body protein (ATIP), L1R, and open reading frame (ORF) 185 genes on different cell culture passage levels of a field isolate, two high passage vaccines, wild-type, and reference strains of CMLV. RESULTS: We demonstrate that additional two high passage attenuated vaccine candidate from Sudan and UAE likewise contain sequences resembling VACV more than CMLV. Furthermore, sequence analysis of the ATIP gene of selected virus passages in cell culture revealed that the shift to VACV-like occurred between passage 11 and 20 and up to the 10th passage the genome still resembles wild-type virus. This observation was further confirmed by recombination analysis which indicated recombination events at ATIP and ORF185 genes occurred at higher passages. CONCLUSION: We confirmed that the cell culture passage CMLV turns to resemble VACV after cell culture passage and concluded that the resemblance may not be a result of contamination or misidentification as previously thought but could be due to recombination events that occurred during the passage process. Faculty of Veterinary Medicine 2020 2020-04-23 /pmc/articles/PMC7419068/ /pubmed/32821659 http://dx.doi.org/10.4314/ovj.v10i2.4 Text en http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Khalafalla, Abdelmalik I.
Al Hosani, Mohamed A.
Ishag, Hassan Zackaria Ali
Al Muhairi, Salama S.
More cell culture passaged Camelpox virus sequences found resembling those of vaccinia virus
title More cell culture passaged Camelpox virus sequences found resembling those of vaccinia virus
title_full More cell culture passaged Camelpox virus sequences found resembling those of vaccinia virus
title_fullStr More cell culture passaged Camelpox virus sequences found resembling those of vaccinia virus
title_full_unstemmed More cell culture passaged Camelpox virus sequences found resembling those of vaccinia virus
title_short More cell culture passaged Camelpox virus sequences found resembling those of vaccinia virus
title_sort more cell culture passaged camelpox virus sequences found resembling those of vaccinia virus
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7419068/
https://www.ncbi.nlm.nih.gov/pubmed/32821659
http://dx.doi.org/10.4314/ovj.v10i2.4
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