Investigation of Variants In SARS-CoV-2 Infections after Three Doses of COVID-19 Vaccine

Burcu GÜRER GİRAY, Gökçe GÜVEN AÇIK
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 Objective: Our study focused on retrospectively assessing variant of concern, specified by the World Health Organization (WHO), with one-step reverse transcription and real-time polymerase chain reaction (RT-PCR) test in SARS-CoV-2 positive patients after three doses of attenuated COVID-19 vaccine.
 Methods: 8.520 samples transported with viral nucleic acid buffer (vNAT) tubes between June 2021 and January 31, 2022, were tested and included in the study. All the patients whose samples were included in our research had 3 doses of CoronaVac (Sinovac Life Science Co, Ltd, Beijing, China). Gender distribution was 4686 (55%) female and 3834 ( 45%) males. Variant specific genome regions only found in B.1.351, P.1 and B.1.1.7 as well as ORF1ab and N gene regions are investigated by the Bio-Speedy® Emerging Plus kit (Bioeksen AR-GE Technologies, Turkey) used to identify the variants in the study.
 Results: All 8.520 samples were SARS-CoV-2 RT-PCR positive. Our study detected alpha and delta variants in 1460 (17.14%) and 3570 (41.9%) patients respectively. 2570 (30.16%) patients did not have any variants according to test results. It was observed that the spread of beta, gamma and other suspicious variants remained at relatively low rates.
 Conclusion: The delta variant became dominant from July until to the end of the year. Declining delta variant rates and increasing cases of suspected variants towards the beginning of December 2021 suggest the omicron variant. Therefore, molecular surveillance studies that are planned to take epidemiological data into consideration and to examine the prevalence and gene-based analysis of local and worldwide variants are required.","PeriodicalId":15449,"journal":{"name":"Journal of contemporary medicine","volume":"3 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of contemporary medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.16899/jcm.1343574","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

Abstract Objective: Our study focused on retrospectively assessing variant of concern, specified by the World Health Organization (WHO), with one-step reverse transcription and real-time polymerase chain reaction (RT-PCR) test in SARS-CoV-2 positive patients after three doses of attenuated COVID-19 vaccine. Methods: 8.520 samples transported with viral nucleic acid buffer (vNAT) tubes between June 2021 and January 31, 2022, were tested and included in the study. All the patients whose samples were included in our research had 3 doses of CoronaVac (Sinovac Life Science Co, Ltd, Beijing, China). Gender distribution was 4686 (55%) female and 3834 ( 45%) males. Variant specific genome regions only found in B.1.351, P.1 and B.1.1.7 as well as ORF1ab and N gene regions are investigated by the Bio-Speedy® Emerging Plus kit (Bioeksen AR-GE Technologies, Turkey) used to identify the variants in the study. Results: All 8.520 samples were SARS-CoV-2 RT-PCR positive. Our study detected alpha and delta variants in 1460 (17.14%) and 3570 (41.9%) patients respectively. 2570 (30.16%) patients did not have any variants according to test results. It was observed that the spread of beta, gamma and other suspicious variants remained at relatively low rates. Conclusion: The delta variant became dominant from July until to the end of the year. Declining delta variant rates and increasing cases of suspected variants towards the beginning of December 2021 suggest the omicron variant. Therefore, molecular surveillance studies that are planned to take epidemiological data into consideration and to examine the prevalence and gene-based analysis of local and worldwide variants are required.
三剂COVID-19疫苗后SARS-CoV-2感染变异的调查
摘要# x0D;目的:采用一步反转录和实时聚合酶链反应(RT-PCR)检测方法,回顾性评估世界卫生组织(WHO)指定的SARS-CoV-2阳性患者接种三剂COVID-19减毒疫苗后的关注变异。方法:对2021年6月至2022年1月31日期间用病毒核酸缓冲液(vNAT)管运输的8.520份样本进行检测并纳入研究。所有纳入我们研究样本的患者均使用3剂CoronaVac(北京科兴生命科学有限公司,中国)。性别分布为女性4686人(55%),男性3834人(45%)。仅在B.1.351, P.1和B.1.1.7中发现的变异特异性基因组区域以及ORF1ab和N基因区域使用Bio-Speedy®Emerging Plus试剂盒(Bioeksen AR-GE Technologies,土耳其)进行研究,用于识别研究中的变异。 结果:8.520份样本均为SARS-CoV-2 RT-PCR阳性。我们的研究分别在1460例(17.14%)和3570例(41.9%)患者中检测到α和δ变异。2570例(30.16%)患者检测结果未发现任何变异。据观察,β、γ和其他可疑变异的传播速度仍然相对较低。结论:从7月到年底,δ型变异占主导地位。到2021年12月初,delta变异率下降,疑似变异病例增加,这表明是组粒变异。因此,需要计划进行分子监测研究,以考虑流行病学数据,并检查本地和全球变异的患病率和基于基因的分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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