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Sensitive tracking of circulating viral RNA through all stages of SARS-CoV-2 infection.
Huang, Zhen; Ning, Bo; Yang, He S; Youngquist, Brady M; Niu, Alex; Lyon, Christopher J; Beddingfield, Brandon J; Fears, Alyssa C; Monk, Chandler H; Murrell, Amelie E; Bilton, Samantha J; Linhuber, Joshua P; Norton, Elizabeth B; Dietrich, Monika L; Yee, Jim; Lai, Weihua; Scott, John W; Yin, Xiao-Ming; Rappaport, Jay; Robinson, James E; Saba, Nakhle S; Roy, Chad J; Zwezdaryk, Kevin J; Zhao, Zhen; Hu, Tony Y.
Afiliação
  • Huang Z; Center for Cellular and Molecular Diagnostics, Tulane University School of Medicine, New Orleans, Louisiana, USA.
  • Ning B; State Key Laboratory of Food Science and Technology, Nanchang University, Nanchang, China.
  • Yang HS; Department of Biochemistry and Molecular Biology, Tulane University School of Medicine, New Orleans, Louisiana, USA.
  • Youngquist BM; Center for Cellular and Molecular Diagnostics, Tulane University School of Medicine, New Orleans, Louisiana, USA.
  • Niu A; Department of Biochemistry and Molecular Biology, Tulane University School of Medicine, New Orleans, Louisiana, USA.
  • Lyon CJ; Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, New York, USA.
  • Beddingfield BJ; Center for Cellular and Molecular Diagnostics, Tulane University School of Medicine, New Orleans, Louisiana, USA.
  • Fears AC; Department of Biochemistry and Molecular Biology, Tulane University School of Medicine, New Orleans, Louisiana, USA.
  • Monk CH; Section of Hematology and Medical Oncology, Tulane University School of Medicine, New Orleans, Louisiana, USA.
  • Murrell AE; Center for Cellular and Molecular Diagnostics, Tulane University School of Medicine, New Orleans, Louisiana, USA.
  • Bilton SJ; Department of Biochemistry and Molecular Biology, Tulane University School of Medicine, New Orleans, Louisiana, USA.
  • Linhuber JP; Division of Microbiology, Tulane National Primate Research Center, Covington, Louisiana, USA.
  • Norton EB; Division of Microbiology, Tulane National Primate Research Center, Covington, Louisiana, USA.
  • Dietrich ML; Department of Microbiology and Immunology.
  • Yee J; Department of Microbiology and Immunology.
  • Lai W; Department of Microbiology and Immunology.
  • Scott JW; Department of Microbiology and Immunology.
  • Yin XM; Department of Microbiology and Immunology.
  • Rappaport J; Department of Pediatrics, and.
  • Robinson JE; Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, New York, USA.
  • Saba NS; State Key Laboratory of Food Science and Technology, Nanchang University, Nanchang, China.
  • Roy CJ; Department of Pathology and Laboratory Medicine, Tulane University School of Medicine, New Orleans, Louisiana, USA.
  • Zwezdaryk KJ; Department of Pathology and Laboratory Medicine, Tulane University School of Medicine, New Orleans, Louisiana, USA.
  • Zhao Z; Department of Microbiology and Immunology.
  • Hu TY; Tulane National Primate Research Center, Covington, Louisiana, USA.
J Clin Invest ; 131(7)2021 04 01.
Article em En | MEDLINE | ID: mdl-33561010
ABSTRACT
BACKGROUNDCirculating severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) RNA may represent a more reliable indicator of infection than nasal RNA, but quantitative reverse transcription PCR (RT-qPCR) lacks diagnostic sensitivity for blood samples.METHODSA CRISPR-augmented RT-PCR assay that sensitively detects SARS-CoV-2 RNA was employed to analyze viral RNA kinetics in longitudinal plasma samples from nonhuman primates (NHPs) after virus exposure; to evaluate the utility of blood SARS-CoV-2 RNA detection for coronavirus disease 2019 (COVID-19) diagnosis in adults cases confirmed by nasal/nasopharyngeal swab RT-PCR results; and to identify suspected COVID-19 cases in pediatric and at-risk adult populations with negative nasal swab RT-qPCR results. All blood samples were analyzed by RT-qPCR to allow direct comparisons.RESULTSCRISPR-augmented RT-PCR consistently detected SARS-CoV-2 RNA in the plasma of experimentally infected NHPs from 1 to 28 days after infection, and these increases preceded and correlated with rectal swab viral RNA increases. In a patient cohort (n = 159), this blood-based assay demonstrated 91.2% diagnostic sensitivity and 99.2% diagnostic specificity versus a comparator RT-qPCR nasal/nasopharyngeal test, whereas RT-qPCR exhibited 44.1% diagnostic sensitivity and 100% specificity for the same blood samples. This CRISPR-augmented RT-PCR assay also accurately identified patients with COVID-19 using one or more negative nasal swab RT-qPCR results.CONCLUSIONResults of this study indicate that sensitive detection of SARS-CoV-2 RNA in blood by CRISPR-augmented RT-PCR permits accurate COVID-19 diagnosis, and can detect COVID-19 cases with transient or negative nasal swab RT-qPCR results, suggesting that this approach could improve COVID-19 diagnosis and the evaluation of SARS-CoV-2 infection clearance, and predict the severity of infection.TRIAL REGISTRATIONClinicalTrials.gov. NCT04358211.FUNDINGDepartment of Defense, National Institute of Allergy and Infectious Diseases, National Institute of Child Health and Human Development, and the National Center for Research Resources.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: RNA Viral / Ácidos Nucleicos Livres / SARS-CoV-2 / COVID-19 Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies Limite: Adolescent / Adult / Aged / Animals / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: RNA Viral / Ácidos Nucleicos Livres / SARS-CoV-2 / COVID-19 Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies Limite: Adolescent / Adult / Aged / Animals / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article