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Pathogenicity of three genetically distinct and highly pathogenic Egyptian H5N8 avian influenza viruses in chickens

In late 2016, Egypt encountered multiple cases of the highly pathogenic avian influenza (HPAI) virus of the H5N8 subtype. In a previous study, three distinct genotypes, including A/common-coot/Egypt/CA285/2016 (H5N8) (CA285), A/duck/Egypt/SS19/2017 (H5N8) (SS19), and A/duck/Egypt/F446/2017 (H5N8) (F...

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Autores principales: Yehia, Nahed, Erfan, Ahmed M., Adel, Amany, El-Tayeb, Ahmed, Hassan, Wafaa M.M., Samy, Ahmed, Abd El-Hack, Mohamed E., El-Saadony, Mohamed T., El-Tarabily, Khaled A., Ahmed, Kawkab A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8808262/
https://www.ncbi.nlm.nih.gov/pubmed/35093769
http://dx.doi.org/10.1016/j.psj.2021.101662
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author Yehia, Nahed
Erfan, Ahmed M.
Adel, Amany
El-Tayeb, Ahmed
Hassan, Wafaa M.M.
Samy, Ahmed
Abd El-Hack, Mohamed E.
El-Saadony, Mohamed T.
El-Tarabily, Khaled A.
Ahmed, Kawkab A.
author_facet Yehia, Nahed
Erfan, Ahmed M.
Adel, Amany
El-Tayeb, Ahmed
Hassan, Wafaa M.M.
Samy, Ahmed
Abd El-Hack, Mohamed E.
El-Saadony, Mohamed T.
El-Tarabily, Khaled A.
Ahmed, Kawkab A.
author_sort Yehia, Nahed
collection PubMed
description In late 2016, Egypt encountered multiple cases of the highly pathogenic avian influenza (HPAI) virus of the H5N8 subtype. In a previous study, three distinct genotypes, including A/common-coot/Egypt/CA285/2016 (H5N8) (CA285), A/duck/Egypt/SS19/2017 (H5N8) (SS19), and A/duck/Egypt/F446/2017 (H5N8) (F446), were isolated from wild birds, a backyard, and a commercial farm, respectively, during the first wave of infection. In this current study, we investigated the differences in the pathogenicity, replication and transmissibility of the three genotypes and A/chicken/Egypt/15S75/2015 (H5N1) (S75) was used as the control. The intravenous pathogenicity index was between 2.68 and 2.9. The chicken lethal dose 50 values of F446, SS19 and CA285 were 10(3.7), 10(3.7), an 10(4) with a natural route of infection, respectively. These strains took longer than S75 to cause death when infection was carried out through the natural route (HPAI H5N1). After inoculation with the original concentration of 10(5) and 10(6) egg infective dose 50 (EID(50)), F446 had a higher mortality rate with short mean death times of 4, and 7 days, respectively compared with the other H5N8 viruses. Chickens inoculated with F446 and contacted exposed chickens infected with F446 showed the highest viral titer with remarkable differences in all H5N8 tested swabs at 2-4 days postinfection (dpi) compared to S75 at 2 dpi. This indicates that F446 had a more efficient transmission and spread from contact exposed birds to other birds. All H5N8 viruses were able to replicate systematically in all organs (trachea, brain, lung, and spleen) of the chicken with high viral titer with significantly different and more pathological changes observed in F446 than in other H5N8 viruses at 2 and 4 dpi. Compared with H5N1, we recorded a significantly high viral titer in the samples obtained from the lung, brain and both cloacal and tracheal swabs at 2 and 4 dpi, respectively and in the samples obtained from the spleen at 2 and 4 dpi among the experimental chicken. The comparative pathogenesis study revealed that in comparison with the other HPAI H5N8 viruses, the genotype F446 was more pathogenic, and showed more efficient viral replication and transmissibility in chickens in Egypt. The genotype F446 also showed a high viral titer than HPAI H5N1 and short mean death time at the third day after inoculation with 10(6) and 10(5) EID50, which revealed a conservation of certain H5N8 genotypes and a decrease in the incidence of H5N1.
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spelling pubmed-88082622022-02-04 Pathogenicity of three genetically distinct and highly pathogenic Egyptian H5N8 avian influenza viruses in chickens Yehia, Nahed Erfan, Ahmed M. Adel, Amany El-Tayeb, Ahmed Hassan, Wafaa M.M. Samy, Ahmed Abd El-Hack, Mohamed E. El-Saadony, Mohamed T. El-Tarabily, Khaled A. Ahmed, Kawkab A. Poult Sci IMMUNOLOGY, HEALTH AND DISEASE In late 2016, Egypt encountered multiple cases of the highly pathogenic avian influenza (HPAI) virus of the H5N8 subtype. In a previous study, three distinct genotypes, including A/common-coot/Egypt/CA285/2016 (H5N8) (CA285), A/duck/Egypt/SS19/2017 (H5N8) (SS19), and A/duck/Egypt/F446/2017 (H5N8) (F446), were isolated from wild birds, a backyard, and a commercial farm, respectively, during the first wave of infection. In this current study, we investigated the differences in the pathogenicity, replication and transmissibility of the three genotypes and A/chicken/Egypt/15S75/2015 (H5N1) (S75) was used as the control. The intravenous pathogenicity index was between 2.68 and 2.9. The chicken lethal dose 50 values of F446, SS19 and CA285 were 10(3.7), 10(3.7), an 10(4) with a natural route of infection, respectively. These strains took longer than S75 to cause death when infection was carried out through the natural route (HPAI H5N1). After inoculation with the original concentration of 10(5) and 10(6) egg infective dose 50 (EID(50)), F446 had a higher mortality rate with short mean death times of 4, and 7 days, respectively compared with the other H5N8 viruses. Chickens inoculated with F446 and contacted exposed chickens infected with F446 showed the highest viral titer with remarkable differences in all H5N8 tested swabs at 2-4 days postinfection (dpi) compared to S75 at 2 dpi. This indicates that F446 had a more efficient transmission and spread from contact exposed birds to other birds. All H5N8 viruses were able to replicate systematically in all organs (trachea, brain, lung, and spleen) of the chicken with high viral titer with significantly different and more pathological changes observed in F446 than in other H5N8 viruses at 2 and 4 dpi. Compared with H5N1, we recorded a significantly high viral titer in the samples obtained from the lung, brain and both cloacal and tracheal swabs at 2 and 4 dpi, respectively and in the samples obtained from the spleen at 2 and 4 dpi among the experimental chicken. The comparative pathogenesis study revealed that in comparison with the other HPAI H5N8 viruses, the genotype F446 was more pathogenic, and showed more efficient viral replication and transmissibility in chickens in Egypt. The genotype F446 also showed a high viral titer than HPAI H5N1 and short mean death time at the third day after inoculation with 10(6) and 10(5) EID50, which revealed a conservation of certain H5N8 genotypes and a decrease in the incidence of H5N1. Elsevier 2021-12-10 /pmc/articles/PMC8808262/ /pubmed/35093769 http://dx.doi.org/10.1016/j.psj.2021.101662 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle IMMUNOLOGY, HEALTH AND DISEASE
Yehia, Nahed
Erfan, Ahmed M.
Adel, Amany
El-Tayeb, Ahmed
Hassan, Wafaa M.M.
Samy, Ahmed
Abd El-Hack, Mohamed E.
El-Saadony, Mohamed T.
El-Tarabily, Khaled A.
Ahmed, Kawkab A.
Pathogenicity of three genetically distinct and highly pathogenic Egyptian H5N8 avian influenza viruses in chickens
title Pathogenicity of three genetically distinct and highly pathogenic Egyptian H5N8 avian influenza viruses in chickens
title_full Pathogenicity of three genetically distinct and highly pathogenic Egyptian H5N8 avian influenza viruses in chickens
title_fullStr Pathogenicity of three genetically distinct and highly pathogenic Egyptian H5N8 avian influenza viruses in chickens
title_full_unstemmed Pathogenicity of three genetically distinct and highly pathogenic Egyptian H5N8 avian influenza viruses in chickens
title_short Pathogenicity of three genetically distinct and highly pathogenic Egyptian H5N8 avian influenza viruses in chickens
title_sort pathogenicity of three genetically distinct and highly pathogenic egyptian h5n8 avian influenza viruses in chickens
topic IMMUNOLOGY, HEALTH AND DISEASE
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8808262/
https://www.ncbi.nlm.nih.gov/pubmed/35093769
http://dx.doi.org/10.1016/j.psj.2021.101662
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