Trajectory of Growth of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Variants in Houston, Texas, January through May 2021, Based on 12,476 Genome Sequences

被引:20
作者
Olsen, Randall J. [1 ,2 ,3 ,4 ]
Christensen, Paul A. [1 ,2 ]
Long, S. Wesley [1 ,2 ,3 ,4 ]
Subedi, Sishir [1 ,2 ]
Hodjat, Parsa [1 ,2 ]
Olson, Robert [5 ,6 ]
Nguyen, Marcus [5 ,6 ]
Davis, James J. [5 ,6 ]
Yerramilli, Prasanti [1 ,2 ]
Saavedra, Matthew O. [1 ,2 ]
Pruitt, Layne [1 ,2 ]
Reppond, Kristina [1 ,2 ]
Shyer, Madison N. [1 ,2 ]
Cambric, Jessica [1 ,2 ]
Gadd, Ryan [1 ,2 ]
Thakur, Rashi M. [1 ,2 ]
Batajoo, Akanksha [1 ,2 ]
Finkelstein, Ilya J. [7 ,8 ]
Gollihar, Jimmy [1 ,2 ,9 ]
Musser, James M. [1 ,2 ,3 ,4 ]
机构
[1] Houston Methodist Res Inst, Ctr Mol & Translat Human Infect Dis Res, Dept Pathol & Genom Med, Houston, TX USA
[2] Houston Methodist Hosp, Houston, TX 77030 USA
[3] Weill Cornell Med Coll, Dept Pathol & Lab Med, New York, NY USA
[4] Weill Cornell Med Coll, Dept Microbiol & Immunol, New York, NY USA
[5] Univ Chicago, Consortium Adv Sci & Engn, Chicago, IL 60637 USA
[6] Argonne Natl Lab, Comp Environm & Life Sci, Lemont, IL USA
[7] Univ Texas Austin, Dept Mol Biosci, Austin, TX 78712 USA
[8] Univ Texas Austin, Inst Mol Biosci, Austin, TX 78712 USA
[9] Univ Texas Austin, Combat Capabil Dev Command CCDC, Army Res Lab South, Austin, TX 78712 USA
关键词
INFECTIONS; LINEAGE; BINDING; B.1.1.7;
D O I
10.1016/j.ajpath.2021.07.002
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Certain genetic variants of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are of substantial concern because they may be more transmissible or detrimentally alter the pandemic course and disease features in individual patients. SARS-CoV-2 genome sequences from 12,476 patients in the Houston Methodist health care system diagnosed from January 1 through May 31, 2021 are reported here. Prevalence of the B.1.1.7 (Alpha) variant increased rapidly and caused 63% to 90% of new cases in the latter half of May. Eleven B.1.1.7 genomes had an E484K replacement in spike protein, a change also identified in other SARS-CoV-2 lineages. Compared with noneB.1.1.7-infected patients, individuals with B.1.1.7 had a significantly lower cycle threshold (a proxy for higher virus load) and significantly higher hospitalization rate. Other variants [eg, B.1.429 and B.1.427 (Epsilon), P.1 (Gamma), P.2 (Zeta), and R.1] also increased rapidly, although the magnitude was less than that in B.1.1.7. Twenty-two patients infected with B.1.617.1 (Kappa) or B.1.617.2 (Delta) variants had a high rate of hospitalization. Breakthrough cases (n = 207) in fully vaccinated patients were caused by a heterogeneous array of virus genotypes, including many not currently designated variants of interest or concern. In the aggregate, this study delineates the trajectory of SARS-CoV-2 variants circulating in a major metropolitan area, documents B.1.1.7 as the major cause of new cases in Houston, TX, and heralds the arrival of B.1.617 variants in the metroplex.
引用
收藏
页码:1754 / 1773
页数:20
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