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SARS-CoV-2 genome variations and evolution patterns in Egypt: a multi-center study

A serious global public health emergency emerged late November 2019 in Wuhan City, China, by a new highly pathogenic virus, SARS-CoV-2. The virus evolution spread has been tracked by three developing databases: GISAID, Nextstrain and PANGO to understand its circulating variants. In this study, 110 d...

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Autores principales: Jalal, Deena, Elzayat, Mariam G., El-Shqanqery, Hend E., Diab, Aya A., Yahia, Abdelrahman, Samir, Omar, Bakry, Usama, Amer, Khaled, ElNaqeeb, Mostafa, Hassan, Wael, Talat, Hala S., Farawela, Hala M., Hamdy, Mona S., Soliman, May S., El Sissy, Maha H., Ezzelarab, Moushira H., El khateeb, Sara M., Soliman, Lamyaa H., Haddad, Sara E., Hatem, Ashraf, Ismail, Mohamed S., Hossam, Maha, Mansour, Tarek, Shalaby, Lobna, Soliman, Sonia, Hassan, Reem, Hammad, Mahmoud, Abdo, Ibrahim, Magdeldin, Sameh, ElHaddad, Alaa, Abouelnaga, Sherif, Sayed, Ahmed A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9403952/
https://www.ncbi.nlm.nih.gov/pubmed/36008511
http://dx.doi.org/10.1038/s41598-022-18644-4
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author Jalal, Deena
Elzayat, Mariam G.
El-Shqanqery, Hend E.
Diab, Aya A.
Yahia, Abdelrahman
Samir, Omar
Bakry, Usama
Amer, Khaled
ElNaqeeb, Mostafa
Hassan, Wael
Talat, Hala S.
Farawela, Hala M.
Hamdy, Mona S.
Soliman, May S.
El Sissy, Maha H.
Ezzelarab, Moushira H.
El khateeb, Sara M.
Soliman, Lamyaa H.
Haddad, Sara E.
Hatem, Ashraf
Ismail, Mohamed S.
Hossam, Maha
Mansour, Tarek
Shalaby, Lobna
Soliman, Sonia
Hassan, Reem
Hammad, Mahmoud
Abdo, Ibrahim
Magdeldin, Sameh
ElHaddad, Alaa
Abouelnaga, Sherif
Sayed, Ahmed A.
author_facet Jalal, Deena
Elzayat, Mariam G.
El-Shqanqery, Hend E.
Diab, Aya A.
Yahia, Abdelrahman
Samir, Omar
Bakry, Usama
Amer, Khaled
ElNaqeeb, Mostafa
Hassan, Wael
Talat, Hala S.
Farawela, Hala M.
Hamdy, Mona S.
Soliman, May S.
El Sissy, Maha H.
Ezzelarab, Moushira H.
El khateeb, Sara M.
Soliman, Lamyaa H.
Haddad, Sara E.
Hatem, Ashraf
Ismail, Mohamed S.
Hossam, Maha
Mansour, Tarek
Shalaby, Lobna
Soliman, Sonia
Hassan, Reem
Hammad, Mahmoud
Abdo, Ibrahim
Magdeldin, Sameh
ElHaddad, Alaa
Abouelnaga, Sherif
Sayed, Ahmed A.
author_sort Jalal, Deena
collection PubMed
description A serious global public health emergency emerged late November 2019 in Wuhan City, China, by a new highly pathogenic virus, SARS-CoV-2. The virus evolution spread has been tracked by three developing databases: GISAID, Nextstrain and PANGO to understand its circulating variants. In this study, 110 diagnosed positive COVID-19 patient’s samples, were collected from Kasr Al-Aini Hospital and the Children Cancer Hospital Egypt 57357 between May 2020 and January 2021, with clinical severity ranging from mild to severe. The viral genomes were sequenced by next generation sequencing, and phylogenetic analysis was performed to understand viral transmission dynamics. According to Nextstrain clades, most of our sequenced samples belonged to clades 20A and 20D, which in addition to clade 20B were present from the beginning of sample collection in May 2020. Clades 19A and 19B, on the other hand, appeared in the mid and late 2020 respectively, followed by the disappearance of clade 20B at the end of 2020. We identified a relatively high prevalence of the D614G spike protein variant and novel patterns of mutations associated together and with different clades. We also identified four mutations, spike H49Y, ORF3a H78Y, ORF8 E64stop and nucleocapsid E378V, associated with higher disease severity. Altogether, our study contributes genetic, phylogenetic, and clinical correlation data about the spread of the SARS-CoV-2 pandemic in Egypt.
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spelling pubmed-94039522022-08-25 SARS-CoV-2 genome variations and evolution patterns in Egypt: a multi-center study Jalal, Deena Elzayat, Mariam G. El-Shqanqery, Hend E. Diab, Aya A. Yahia, Abdelrahman Samir, Omar Bakry, Usama Amer, Khaled ElNaqeeb, Mostafa Hassan, Wael Talat, Hala S. Farawela, Hala M. Hamdy, Mona S. Soliman, May S. El Sissy, Maha H. Ezzelarab, Moushira H. El khateeb, Sara M. Soliman, Lamyaa H. Haddad, Sara E. Hatem, Ashraf Ismail, Mohamed S. Hossam, Maha Mansour, Tarek Shalaby, Lobna Soliman, Sonia Hassan, Reem Hammad, Mahmoud Abdo, Ibrahim Magdeldin, Sameh ElHaddad, Alaa Abouelnaga, Sherif Sayed, Ahmed A. Sci Rep Article A serious global public health emergency emerged late November 2019 in Wuhan City, China, by a new highly pathogenic virus, SARS-CoV-2. The virus evolution spread has been tracked by three developing databases: GISAID, Nextstrain and PANGO to understand its circulating variants. In this study, 110 diagnosed positive COVID-19 patient’s samples, were collected from Kasr Al-Aini Hospital and the Children Cancer Hospital Egypt 57357 between May 2020 and January 2021, with clinical severity ranging from mild to severe. The viral genomes were sequenced by next generation sequencing, and phylogenetic analysis was performed to understand viral transmission dynamics. According to Nextstrain clades, most of our sequenced samples belonged to clades 20A and 20D, which in addition to clade 20B were present from the beginning of sample collection in May 2020. Clades 19A and 19B, on the other hand, appeared in the mid and late 2020 respectively, followed by the disappearance of clade 20B at the end of 2020. We identified a relatively high prevalence of the D614G spike protein variant and novel patterns of mutations associated together and with different clades. We also identified four mutations, spike H49Y, ORF3a H78Y, ORF8 E64stop and nucleocapsid E378V, associated with higher disease severity. Altogether, our study contributes genetic, phylogenetic, and clinical correlation data about the spread of the SARS-CoV-2 pandemic in Egypt. Nature Publishing Group UK 2022-08-25 /pmc/articles/PMC9403952/ /pubmed/36008511 http://dx.doi.org/10.1038/s41598-022-18644-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International lLicense, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Jalal, Deena
Elzayat, Mariam G.
El-Shqanqery, Hend E.
Diab, Aya A.
Yahia, Abdelrahman
Samir, Omar
Bakry, Usama
Amer, Khaled
ElNaqeeb, Mostafa
Hassan, Wael
Talat, Hala S.
Farawela, Hala M.
Hamdy, Mona S.
Soliman, May S.
El Sissy, Maha H.
Ezzelarab, Moushira H.
El khateeb, Sara M.
Soliman, Lamyaa H.
Haddad, Sara E.
Hatem, Ashraf
Ismail, Mohamed S.
Hossam, Maha
Mansour, Tarek
Shalaby, Lobna
Soliman, Sonia
Hassan, Reem
Hammad, Mahmoud
Abdo, Ibrahim
Magdeldin, Sameh
ElHaddad, Alaa
Abouelnaga, Sherif
Sayed, Ahmed A.
SARS-CoV-2 genome variations and evolution patterns in Egypt: a multi-center study
title SARS-CoV-2 genome variations and evolution patterns in Egypt: a multi-center study
title_full SARS-CoV-2 genome variations and evolution patterns in Egypt: a multi-center study
title_fullStr SARS-CoV-2 genome variations and evolution patterns in Egypt: a multi-center study
title_full_unstemmed SARS-CoV-2 genome variations and evolution patterns in Egypt: a multi-center study
title_short SARS-CoV-2 genome variations and evolution patterns in Egypt: a multi-center study
title_sort sars-cov-2 genome variations and evolution patterns in egypt: a multi-center study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9403952/
https://www.ncbi.nlm.nih.gov/pubmed/36008511
http://dx.doi.org/10.1038/s41598-022-18644-4
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