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Viral loads and profile of the patients infected with SARS-CoV-2 Delta, Alpha, or R.1 variants in Tokyo.
- Source :
-
Journal of medical virology [J Med Virol] 2022 Apr; Vol. 94 (4), pp. 1707-1710. Date of Electronic Publication: 2021 Dec 02. - Publication Year :
- 2022
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Abstract
- The rapid spread of the Delta variant of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) became a serious concern worldwide in summer 2021. We examined the copy number and variant types of all SARS-CoV-2-positive patients who visited our hospital from February to August 2021 using polymerase chain reaction (PCR) tests. Whole genome sequencing was performed for some samples. The R.1 variant (B.1.1.316) was responsible for most infections in March, replacing the previous variant (B.1.1.214); the Alpha (B.1.1.7) variant caused most infections in April and May; and the Delta variant (B.1.617.2) was the most prevalent in July and August. There was no significant difference in the copy numbers among the previous variant cases (n = 29, median 3.0 × 10 <superscript>4</superscript> copies/µl), R.1 variant cases (n = 28, 2.1 × 10 <superscript>5</superscript> copies/µl), Alpha variant cases (n = 125, 4.1 × 10 <superscript>5</superscript> copies/µl), and Delta variant cases (n = 106, 2.4 × 10 <superscript>5</superscript> copies/µl). Patients with Delta variant infection were significantly younger than those infected with R.1 and the previous variants, possibly because many elderly individuals in Tokyo were vaccinated between May and August. There was no significant difference in mortality among the four groups. Our results suggest that the increased infectivity of Delta variant may be caused by factors other than the higher viral loads. Clarifying these factors is important to control the spread of Delta variant infection.<br /> (© 2021 Wiley Periodicals LLC.)
Details
- Language :
- English
- ISSN :
- 1096-9071
- Volume :
- 94
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Journal of medical virology
- Publication Type :
- Academic Journal
- Accession number :
- 34825717
- Full Text :
- https://doi.org/10.1002/jmv.27479