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Viral load of SARS-CoV-2 Omicron BA.5 is lower than that of BA.2 despite the higher infectivity of BA.5
Yuna Takatsuki; Yuta Takahashi; Jun Nakajima; Yumi Iwasaki; Katsutoshi Nagano; Chihiro Tani-Sassa; Sonoka Yuasa; Saki Kanehira; Kazunari Sonobe; Yoko Nukui; Hiroaki Takeuchi; Kousuke Tanimoto; Yukie Tanaka; Akinori Kimura; Naoya Ichimura; Shuji Tohda.
Affiliation
  • Yuna Takatsuki; Tokyo Medical and Dental University
  • Yuta Takahashi; Tokyo Medical and Dental University
  • Jun Nakajima; Tokyo Medical and Dental University
  • Yumi Iwasaki; Tokyo Medical and Dental University
  • Katsutoshi Nagano; Tokyo Medical and Dental University
  • Chihiro Tani-Sassa; Tokyo Medical and Dental University
  • Sonoka Yuasa; Tokyo Medical and Dental University
  • Saki Kanehira; Tokyo Medical and Dental University
  • Kazunari Sonobe; Tokyo Medical and Dental University
  • Yoko Nukui; Tokyo Medical and Dental University
  • Hiroaki Takeuchi; Tokyo Medical and Dental University
  • Kousuke Tanimoto; Tokyo Medical and Dental University
  • Yukie Tanaka; Tokyo Medical and Dental University
  • Akinori Kimura; Tokyo Medical and Dental University
  • Naoya Ichimura; Tokyo Medical and Dental University
  • Shuji Tohda; Tokyo Medical and Dental University
Preprint in En | PREPRINT-MEDRXIV | ID: ppmedrxiv-22281427
ABSTRACT
Sublineage BA.5 of the SARS-CoV-2 Omicron variant rapidly spread and replaced BA.2 in July 2022 in Tokyo. A high viral load can be a possible cause of high transmissibility. Therefore, the copy numbers of SARS-CoV-2 in nasopharyngeal swab samples obtained from all patients visiting the hospital where this research was conducted were measured using quantitative polymerase chain reaction (qPCR). Viral genotypes were determined using PCR-based melting curve analysis. Next, whole-genome sequencing was performed using approximately one-fifth of the samples to verify the viral genotypes determined using PCR. Then, the copy numbers of the BA.1, BA.2, and BA.5 cases were compared. Contrary to expectations, the copy numbers of the BA.5 cases (median 4.7 x 104 copies/L, n = 290) were significantly (p = 0.001) lower than those of BA.2 cases (median 1.1 x 105 copies/L, n = 184). There was no significant difference between the BA.5 and BA.1 cases (median, 3.1 x 104 copies/L; n = 215). The results presented here suggest that the increased infectivity of BA.5 is not caused by higher viral loads, but presumably by other factors such as increased affinity to human cell receptors or immune escape due to its L452R mutation.
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Full text: 1 Collection: 09-preprints Database: PREPRINT-MEDRXIV Language: En Year: 2022 Document type: Preprint
Full text: 1 Collection: 09-preprints Database: PREPRINT-MEDRXIV Language: En Year: 2022 Document type: Preprint