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Exhaled breath SARS-CoV-2 shedding patterns across variants of concern.
Raymenants, Joren; Duthoo, Wout; Stakenborg, Tim; Verbruggen, Bert; Verplanken, Julien; Feys, Jos; Van Duppen, Joost; Hanifa, Rabea; Marchal, Elisabeth; Lambrechts, Andy; Maes, Piet; André, Emmanuel; Van den Wijngaert, Nik; Peumans, Peter.
  • Raymenants J; Laboratory of Clinical Microbiology, Department of Microbiology, Immunology and Transplantation, KU Leuven, 3000, Leuven, Belgium; Department of general internal medicine, University Hospitals Leuven, 3000, Leuven, Belgium. Electronic address: Joren.raymenants@kuleuven.be.
  • Duthoo W; Imec Solutions department, imec, 3001, Leuven, Belgium.
  • Stakenborg T; Life Science Technologies department, imec, 3001, Leuven, Belgium.
  • Verbruggen B; Imec Solutions department, imec, 3001, Leuven, Belgium.
  • Verplanken J; Enabling Digital Transformations department, imec, 9000, Ghent, Belgium.
  • Feys J; Department of Clinical and Epidemiological Virology (Rega Institute), 3000, Leuven, Belgium.
  • Van Duppen J; Life Science Technologies department, imec, 3001, Leuven, Belgium.
  • Hanifa R; Life Science Technologies department, imec, 3001, Leuven, Belgium.
  • Marchal E; Life Science Technologies department, imec, 3001, Leuven, Belgium.
  • Lambrechts A; Imec Solutions department, imec, 3001, Leuven, Belgium.
  • Maes P; KU Leuven, 3000, Leuven, Belgium.
  • André E; Laboratory of Clinical Microbiology, Department of Microbiology, Immunology and Transplantation, KU Leuven, 3000, Leuven, Belgium; Department of laboratory medicine, University Hospitals Leuven, 3000, Leuven, Belgium.
  • Van den Wijngaert N; Imec Solutions department, imec, 3001, Leuven, Belgium.
  • Peumans P; Life Science Technologies department, imec, 3001, Leuven, Belgium.
Int J Infect Dis ; 123: 25-33, 2022 Oct.
Article in English | MEDLINE | ID: covidwho-1966626
ABSTRACT

OBJECTIVES:

We performed exhaled breath (EB) and nasopharyngeal (NP) quantitative polymerase chain reaction (qPCR) and NP rapid antigen testing (NP RAT) of SARS-CoV-2 infections with different variants.

METHODS:

We included immuno-naïve alpha-infected (n = 11) and partly boosted omicron-infected patients (n = 8) as high-risk contacts. We compared peak NP and EB qPCR cycle time (ct) values between cohorts (Wilcoxon-Mann-Whitney test). Test positivity was compared for three infection phases using Cochran Q test.

RESULTS:

Peak median NP ct was 11.5 (interquartile range [IQR] 10.1-12.1) for alpha and 12.2 (IQR 11.1-15.3) for omicron infections. Peak median EB ct was 25.2 (IQR 24.5-26.9) and 28.3 (IQR 26.4-30.8) for alpha and omicron infections, respectively. Distributions did not differ between cohorts for NP (P = 0.19) or EB (P = 0.09). SARS-CoV-2 shedding peaked on day 1 in EB (confidence interval [CI] 0.0 - 4.5) and day 3 in NP (CI 1.5 - 6.0). EB qPCR positivity equaled NP qPCR positivity on D0-D1 (P = 0.44) and D2-D6 (P = 1.0). It superseded NP RAT positivity on D0-D1 (P = 0.003) and D2-D6 (P = 0.008). It was inferior to both on D7-D10 (P < 0.001).

CONCLUSION:

Peak EB and nasopharynx shedding were comparable across variants. EB qPCR positivity matched NP qPCR and superseded NP RAT in the first week of infection.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Cohort study / Diagnostic study / Observational study / Prognostic study Topics: Variants Limits: Humans Language: English Journal: Int J Infect Dis Journal subject: Communicable Diseases Year: 2022 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Cohort study / Diagnostic study / Observational study / Prognostic study Topics: Variants Limits: Humans Language: English Journal: Int J Infect Dis Journal subject: Communicable Diseases Year: 2022 Document Type: Article