Role of Nucleocapsid Protein Antigen Detection for Safe End of Isolation of SARS-CoV-2 Infected Patients with Long Persistence of Viral RNA in Respiratory Samples.

RT-PCR SARS-CoV-2 antigen test isolation and discharge recommendations virus culture

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
07 Sep 2021
Historique:
received: 17 08 2021
revised: 31 08 2021
accepted: 03 09 2021
entrez: 28 9 2021
pubmed: 29 9 2021
medline: 29 9 2021
Statut: epublish

Résumé

In SARS-CoV-2 infection, viral RNA may persist in respiratory samples for several weeks after the resolution of symptoms. Criteria to assess the end of infectivity are not unequivocally defined. In some countries, time from diagnosis is the unique criterion used, in addition to symptom cessation. This study evaluates the role of the Lumipulse A total of 671 nasopharyngeal swabs from patients diagnosed with infection at least 21 days before were assessed by RT-PCR and LAA, and the role of LAA in predicting the absence of infectivity was evaluated by virus cell culture. Viable virus was present in 10/138 cultured samples. Eight out of ten infective patients suffered from a concomitant disease, predisposing them to long-term shedding of infective virus. In particular, infectious virus was isolated from 10/20 RT-PCR+/LAA+ cultured samples, whereas no viable virus was found in all 118 RT-PCR+/LAA- cultured swabs. LLA and RT-PCR agreed in 484/671 (72.1%) samples, with 100% and 26.7% concordance in RT-PCR negative and positive samples, respectively. Viable virus can be found ≥21 days after diagnosis in immunocompromised or severely ill patients. LAA better than RT-PCR predicts non-infectivity of patients and can be safely used to end isolation in cases with long persistence of viral RNA in the respiratory tract.

Sections du résumé

BACKGROUND BACKGROUND
In SARS-CoV-2 infection, viral RNA may persist in respiratory samples for several weeks after the resolution of symptoms. Criteria to assess the end of infectivity are not unequivocally defined. In some countries, time from diagnosis is the unique criterion used, in addition to symptom cessation. This study evaluates the role of the Lumipulse
METHODS METHODS
A total of 671 nasopharyngeal swabs from patients diagnosed with infection at least 21 days before were assessed by RT-PCR and LAA, and the role of LAA in predicting the absence of infectivity was evaluated by virus cell culture.
RESULTS RESULTS
Viable virus was present in 10/138 cultured samples. Eight out of ten infective patients suffered from a concomitant disease, predisposing them to long-term shedding of infective virus. In particular, infectious virus was isolated from 10/20 RT-PCR+/LAA+ cultured samples, whereas no viable virus was found in all 118 RT-PCR+/LAA- cultured swabs. LLA and RT-PCR agreed in 484/671 (72.1%) samples, with 100% and 26.7% concordance in RT-PCR negative and positive samples, respectively.
CONCLUSIONS CONCLUSIONS
Viable virus can be found ≥21 days after diagnosis in immunocompromised or severely ill patients. LAA better than RT-PCR predicts non-infectivity of patients and can be safely used to end isolation in cases with long persistence of viral RNA in the respiratory tract.

Identifiants

pubmed: 34575147
pii: jcm10184037
doi: 10.3390/jcm10184037
pmc: PMC8469917
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Fondazione Cassa di Risparmio di Perugia
ID : 19663

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Auteurs

Antonella Mencacci (A)

Department of Medicine and Surgery, Microbiology and Clinical Microbiology, Santa Maria Della Misericordia" Hospital, University of Perugia, 06129 Perugia, Italy.

Alessio Gili (A)

Public Health Section, Department of Medicine and Surgery, University of Perugia, 06129 Perugia, Italy.

Anna Gidari (A)

Department of Medicine and Surgery, Infectious Diseases Clinic, "Santa Maria della Misericordia" Hospital, University of Perugia, 06129 Perugia, Italy.

Elisabetta Schiaroli (E)

Department of Medicine and Surgery, Infectious Diseases Clinic, "Santa Maria della Misericordia" Hospital, University of Perugia, 06129 Perugia, Italy.

Carla Russo (C)

Department of Medicine and Surgery, Microbiology and Clinical Microbiology, Santa Maria Della Misericordia" Hospital, University of Perugia, 06129 Perugia, Italy.

Elio Cenci (E)

Department of Medicine and Surgery, Microbiology and Clinical Microbiology, Santa Maria Della Misericordia" Hospital, University of Perugia, 06129 Perugia, Italy.

Barbara Camilloni (B)

Department of Medicine and Surgery, Microbiology and Clinical Microbiology, Santa Maria Della Misericordia" Hospital, University of Perugia, 06129 Perugia, Italy.

Alessandro Graziani (A)

Department of Medicine and Surgery, Microbiology and Clinical Microbiology, Santa Maria Della Misericordia" Hospital, University of Perugia, 06129 Perugia, Italy.

Arduino Melelli-Roia (A)

Department of Medicine and Surgery, Microbiology and Clinical Microbiology, Santa Maria Della Misericordia" Hospital, University of Perugia, 06129 Perugia, Italy.

Daniela Francisci (D)

Department of Medicine and Surgery, Infectious Diseases Clinic, "Santa Maria della Misericordia" Hospital, University of Perugia, 06129 Perugia, Italy.

Fabrizio Stracci (F)

Public Health Section, Department of Medicine and Surgery, University of Perugia, 06129 Perugia, Italy.

Classifications MeSH