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Development of a PCR-RFLP method for detection of D614G mutation in SARS-CoV-2
In late 2019, an outbreak of respiratory disease named COVID-19 started in the world. To date, thousands of cases of infection are reported worldwide. Most researchers focused on epidemiology and clinical features of COVID-19, and a small part of studies was performed to evaluate the genetic charact...
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Published in: | Infection, genetics and evolution genetics and evolution, 2020-12, Vol.86, p.104625-104625, Article 104625 |
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container_title | Infection, genetics and evolution |
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creator | Hashemi, Seyed Ahmad Khoshi, Amirhosein Ghasemzadeh-moghaddam, Hamed Ghafouri, Majid Taghavi, Mohammadreza Namdar-Ahmadabad, Hasan Azimian, Amir |
description | In late 2019, an outbreak of respiratory disease named COVID-19 started in the world. To date, thousands of cases of infection are reported worldwide. Most researchers focused on epidemiology and clinical features of COVID-19, and a small part of studies was performed to evaluate the genetic characteristics of this virus. Regarding the high price and low availability of sequencing techniques in developing countries, here we describe a rapid and inexpensive method for the detection of D614G mutation in SARS-CoV-2. Using bioinformatics databases and software, we designed the PCR-RFLP method for D614G mutation detection. We evaluated 144 SARS-CoV-2 positive samples isolated in six months in Northeastern Iran. Our results showed that the prevalent type is S-D in our isolates, and a small number of isolated belongs to the S-G type. Of 144 samples, 127 (88.2%) samples have belonged to type S-D, and 13 (9%) samples typed S-G. The first S-G type was detected on 2020 June 10. We have little information about the prevalence of D614G mutation, and it seems that the reason is the lack of cheap and fast methods. We hope that this method will provide more information on the prevalence and epidemiology of D614G mutations worldwide.
•SARS-CoV-2 is the major viral pathogen today.•SARS-CoV-2 has mutations that lead to change in pathogenesis.•The D614G mutation lead to the change of infectivity.•We lack the rapid and inexpensive method for detection of this mutation.•We designed the rapid and inexpensive method for detection of this mutation. |
doi_str_mv | 10.1016/j.meegid.2020.104625 |
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•SARS-CoV-2 is the major viral pathogen today.•SARS-CoV-2 has mutations that lead to change in pathogenesis.•The D614G mutation lead to the change of infectivity.•We lack the rapid and inexpensive method for detection of this mutation.•We designed the rapid and inexpensive method for detection of this mutation.</description><identifier>ISSN: 1567-1348</identifier><identifier>EISSN: 1567-7257</identifier><identifier>DOI: 10.1016/j.meegid.2020.104625</identifier><identifier>PMID: 33166683</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Coronavirus ; COVID-19 - virology ; Humans ; Mutation ; Mutation - genetics ; Polymerase chain reaction ; Polymerase Chain Reaction - methods ; Polymorphism, Restriction Fragment Length - genetics ; Research Paper ; Restriction fragment length polymorphism ; SARS-CoV-2 ; SARS-CoV-2 - genetics ; Spike Glycoprotein, Coronavirus - genetics</subject><ispartof>Infection, genetics and evolution, 2020-12, Vol.86, p.104625-104625, Article 104625</ispartof><rights>2020 Elsevier B.V.</rights><rights>Copyright © 2020 Elsevier B.V. All rights reserved.</rights><rights>2020 Elsevier B.V. All rights reserved. 2020 Elsevier B.V.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c463t-b2c37bc929d92214f592e704fcc545623ff760fbcd5c74602eb55f76ee446d093</citedby><cites>FETCH-LOGICAL-c463t-b2c37bc929d92214f592e704fcc545623ff760fbcd5c74602eb55f76ee446d093</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33166683$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hashemi, Seyed Ahmad</creatorcontrib><creatorcontrib>Khoshi, Amirhosein</creatorcontrib><creatorcontrib>Ghasemzadeh-moghaddam, Hamed</creatorcontrib><creatorcontrib>Ghafouri, Majid</creatorcontrib><creatorcontrib>Taghavi, Mohammadreza</creatorcontrib><creatorcontrib>Namdar-Ahmadabad, Hasan</creatorcontrib><creatorcontrib>Azimian, Amir</creatorcontrib><title>Development of a PCR-RFLP method for detection of D614G mutation in SARS-CoV-2</title><title>Infection, genetics and evolution</title><addtitle>Infect Genet Evol</addtitle><description>In late 2019, an outbreak of respiratory disease named COVID-19 started in the world. To date, thousands of cases of infection are reported worldwide. Most researchers focused on epidemiology and clinical features of COVID-19, and a small part of studies was performed to evaluate the genetic characteristics of this virus. Regarding the high price and low availability of sequencing techniques in developing countries, here we describe a rapid and inexpensive method for the detection of D614G mutation in SARS-CoV-2. Using bioinformatics databases and software, we designed the PCR-RFLP method for D614G mutation detection. We evaluated 144 SARS-CoV-2 positive samples isolated in six months in Northeastern Iran. Our results showed that the prevalent type is S-D in our isolates, and a small number of isolated belongs to the S-G type. Of 144 samples, 127 (88.2%) samples have belonged to type S-D, and 13 (9%) samples typed S-G. The first S-G type was detected on 2020 June 10. We have little information about the prevalence of D614G mutation, and it seems that the reason is the lack of cheap and fast methods. We hope that this method will provide more information on the prevalence and epidemiology of D614G mutations worldwide.
•SARS-CoV-2 is the major viral pathogen today.•SARS-CoV-2 has mutations that lead to change in pathogenesis.•The D614G mutation lead to the change of infectivity.•We lack the rapid and inexpensive method for detection of this mutation.•We designed the rapid and inexpensive method for detection of this mutation.</description><subject>Coronavirus</subject><subject>COVID-19 - virology</subject><subject>Humans</subject><subject>Mutation</subject><subject>Mutation - genetics</subject><subject>Polymerase chain reaction</subject><subject>Polymerase Chain Reaction - methods</subject><subject>Polymorphism, Restriction Fragment Length - genetics</subject><subject>Research Paper</subject><subject>Restriction fragment length polymorphism</subject><subject>SARS-CoV-2</subject><subject>SARS-CoV-2 - genetics</subject><subject>Spike Glycoprotein, Coronavirus - genetics</subject><issn>1567-1348</issn><issn>1567-7257</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9UU1PGzEQtSpQgbT_oEJ75LKpv717QUIJCZWigkLbq7Vrj8HR7jrYm0j9992QNC0XTjN6fvNm_B5CXwgeE0zk19W4BXjydkwx3UFcUvEBnRMhVa6oUCeHnjBenKGLlFYYE4Vp8RGdMUaklAU7R9-nsIUmrFvo-iy4rMoeJst8OVs8ZC30z8FmLsTMQg-m96HbUaaS8HnWbvrqFfFd9nizfMwn4VdOP6FTVzUJPh_qCP2c3f6Y3OWL-_m3yc0iN1yyPq-pYao2JS1tSSnhTpQUFObOGMGFpMw5JbGrjRVGcYkp1EIMEADn0uKSjdD1Xne9qVuwZrg-Vo1eR99W8bcOlddvXzr_rJ_CVivJC1KKQeDqIBDDywZSr1ufDDRN1UHYJE25KBkvC6IGKt9TTQwpRXDHNQTrXRR6pfdR6F0Ueh_FMHb5_4nHob_e__sDDEZtPUSdjIfOgPVxcFvb4N_f8Af3P5nx</recordid><startdate>20201201</startdate><enddate>20201201</enddate><creator>Hashemi, Seyed Ahmad</creator><creator>Khoshi, Amirhosein</creator><creator>Ghasemzadeh-moghaddam, Hamed</creator><creator>Ghafouri, Majid</creator><creator>Taghavi, Mohammadreza</creator><creator>Namdar-Ahmadabad, Hasan</creator><creator>Azimian, Amir</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20201201</creationdate><title>Development of a PCR-RFLP method for detection of D614G mutation in SARS-CoV-2</title><author>Hashemi, Seyed Ahmad ; Khoshi, Amirhosein ; Ghasemzadeh-moghaddam, Hamed ; Ghafouri, Majid ; Taghavi, Mohammadreza ; Namdar-Ahmadabad, Hasan ; Azimian, Amir</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c463t-b2c37bc929d92214f592e704fcc545623ff760fbcd5c74602eb55f76ee446d093</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Coronavirus</topic><topic>COVID-19 - virology</topic><topic>Humans</topic><topic>Mutation</topic><topic>Mutation - genetics</topic><topic>Polymerase chain reaction</topic><topic>Polymerase Chain Reaction - methods</topic><topic>Polymorphism, Restriction Fragment Length - genetics</topic><topic>Research Paper</topic><topic>Restriction fragment length polymorphism</topic><topic>SARS-CoV-2</topic><topic>SARS-CoV-2 - genetics</topic><topic>Spike Glycoprotein, Coronavirus - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hashemi, Seyed Ahmad</creatorcontrib><creatorcontrib>Khoshi, Amirhosein</creatorcontrib><creatorcontrib>Ghasemzadeh-moghaddam, Hamed</creatorcontrib><creatorcontrib>Ghafouri, Majid</creatorcontrib><creatorcontrib>Taghavi, Mohammadreza</creatorcontrib><creatorcontrib>Namdar-Ahmadabad, Hasan</creatorcontrib><creatorcontrib>Azimian, Amir</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Infection, genetics and evolution</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hashemi, Seyed Ahmad</au><au>Khoshi, Amirhosein</au><au>Ghasemzadeh-moghaddam, Hamed</au><au>Ghafouri, Majid</au><au>Taghavi, Mohammadreza</au><au>Namdar-Ahmadabad, Hasan</au><au>Azimian, Amir</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of a PCR-RFLP method for detection of D614G mutation in SARS-CoV-2</atitle><jtitle>Infection, genetics and evolution</jtitle><addtitle>Infect Genet Evol</addtitle><date>2020-12-01</date><risdate>2020</risdate><volume>86</volume><spage>104625</spage><epage>104625</epage><pages>104625-104625</pages><artnum>104625</artnum><issn>1567-1348</issn><eissn>1567-7257</eissn><abstract>In late 2019, an outbreak of respiratory disease named COVID-19 started in the world. To date, thousands of cases of infection are reported worldwide. Most researchers focused on epidemiology and clinical features of COVID-19, and a small part of studies was performed to evaluate the genetic characteristics of this virus. Regarding the high price and low availability of sequencing techniques in developing countries, here we describe a rapid and inexpensive method for the detection of D614G mutation in SARS-CoV-2. Using bioinformatics databases and software, we designed the PCR-RFLP method for D614G mutation detection. We evaluated 144 SARS-CoV-2 positive samples isolated in six months in Northeastern Iran. Our results showed that the prevalent type is S-D in our isolates, and a small number of isolated belongs to the S-G type. Of 144 samples, 127 (88.2%) samples have belonged to type S-D, and 13 (9%) samples typed S-G. The first S-G type was detected on 2020 June 10. We have little information about the prevalence of D614G mutation, and it seems that the reason is the lack of cheap and fast methods. We hope that this method will provide more information on the prevalence and epidemiology of D614G mutations worldwide.
•SARS-CoV-2 is the major viral pathogen today.•SARS-CoV-2 has mutations that lead to change in pathogenesis.•The D614G mutation lead to the change of infectivity.•We lack the rapid and inexpensive method for detection of this mutation.•We designed the rapid and inexpensive method for detection of this mutation.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>33166683</pmid><doi>10.1016/j.meegid.2020.104625</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Coronavirus COVID-19 - virology Humans Mutation Mutation - genetics Polymerase chain reaction Polymerase Chain Reaction - methods Polymorphism, Restriction Fragment Length - genetics Research Paper Restriction fragment length polymorphism SARS-CoV-2 SARS-CoV-2 - genetics Spike Glycoprotein, Coronavirus - genetics |
title | Development of a PCR-RFLP method for detection of D614G mutation in SARS-CoV-2 |
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