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Development of an immunochromatographic kit to detect severe acute respiratory syndrome coronavirus 2.
Oshiro, Satoshi; Tabe, Yoko; Funatogawa, Keiji; Saito, Kaori; Tada, Tatsuya; Hishinuma, Tomomi; Mizutani, Naeko; Akiwa, Makoto; Sekiguchi, Jun-Ichiro; Miida, Takashi; Kirikae, Teruo.
  • Oshiro S; Department of Microbiology, Juntendo University School of Medicine, Tokyo, Japan.
  • Tabe Y; Department of Clinical Laboratory Medicine, Juntendo University School of Medicine, Tokyo, Japan.
  • Funatogawa K; Tochigi Prefectural Institute of Public Health and Environmental Science, Utsunomiya, Tochigi, Japan.
  • Saito K; Department of Clinical Laboratory Medicine, Juntendo University School of Medicine, Tokyo, Japan.
  • Tada T; Department of Microbiology, Juntendo University School of Medicine, Tokyo, Japan.
  • Hishinuma T; Department of Microbiology, Juntendo University School of Medicine, Tokyo, Japan.
  • Mizutani N; Department of Microbiology, Juntendo University School of Medicine, Tokyo, Japan.
  • Akiwa M; Microbiology Research Division, Kohjin Bio Co., Ltd., Saitama, Japan.
  • Sekiguchi JI; Microbiology Research Division, Kohjin Bio Co., Ltd., Saitama, Japan.
  • Miida T; Department of Clinical Laboratory Medicine, Juntendo University School of Medicine, Tokyo, Japan.
  • Kirikae T; Department of Microbiology, Juntendo University School of Medicine, Tokyo, Japan. Electronic address: t-kirikae@juntendo.ac.jp.
J Virol Methods ; 294: 114183, 2021 08.
Article in English | MEDLINE | ID: covidwho-1225322
ABSTRACT

BACKGROUND:

The novel severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) is responsible for the worldwide coronavirus disease-19 (COVID-19) pandemic, starting in late 2019. The standard diagnostic methods to detect SARS-CoV-2 are PCR-based genetic assays. Antigen-antibody-based immunochromatographic assays are alternative methods of detecting this virus. Rapid diagnosis kits to detect SARS-CoV-2 are urgently needed. STUDY

DESIGN:

Three monoclonal antibodies against SARS-CoV-2 nucleocapsid (N) protein were used to develop an antigen-antibody-based immunochromatographic kit to detect SARS-CoV-2. These assays were evaluated using  nasopharyngeal swab specimens collected from patients suspected of having COVID-19.

RESULTS:

These assays detected recombinant SARS-CoV-2 N protein at concentrations >0.2 ng/mL within 10 min after protein loading, but did not detect the N proteins of Middle East respiratory syndrome coronavirus (MERS-CoV), human coronaviruses OC43 (HCoV-OC43) and 299E (HCoV-229E) and other pathogens causing respiratory infections. Nasopharyngeal swab specimens obtained 1~3, 4~9, and ≥ 10 days after symptom onset from COVID-19 patients diagnosed by RT-PCR showed positivity rates of 100 %, >80 %, and <30 %, respectively.

CONCLUSIONS:

Kits using this immunochromatographic assay may be a rapid and useful tool for point-of-care diagnosis of COVID-19 when samples are obtained from patients 1~9 days after symptom onset.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Immunoassay / Coronavirus Nucleocapsid Proteins / COVID-19 Type of study: Diagnostic study / Experimental Studies Topics: Long Covid Limits: Animals / Humans Language: English Journal: J Virol Methods Year: 2021 Document Type: Article Affiliation country: J.jviromet.2021.114183

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Immunoassay / Coronavirus Nucleocapsid Proteins / COVID-19 Type of study: Diagnostic study / Experimental Studies Topics: Long Covid Limits: Animals / Humans Language: English Journal: J Virol Methods Year: 2021 Document Type: Article Affiliation country: J.jviromet.2021.114183