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Persistence of SARS-CoV-2 infection on personal protective equipment (PPE).
Córdoba-Lanús, Elizabeth; García-Pérez, Omar; Cazorla-Rivero, Sara; Rodríguez-Esparragón, Francisco; Piñero, José-Enrique; Clavo, Bernardino; Lorenzo-Morales, Jacob.
  • Córdoba-Lanús E; Instituto Universitario de Enfermedades Tropicales y Salud Pública de Canarias de La Universidad de La Laguna, La Laguna, Tenerife, Spain. acordoba@ull.edu.es.
  • García-Pérez O; Departamento de Medicina Interna, Dermatología y Psiquiatría, Universidad de La Laguna, La Laguna, Tenerife, Spain. acordoba@ull.edu.es.
  • Cazorla-Rivero S; Red Cooperativa de Enfermedades Tropicales (RICET), Instituto de Salud Carlos III, Madrid, Spain. acordoba@ull.edu.es.
  • Rodríguez-Esparragón F; CIBER de Enfermedades Infecciosas, Instituto de Salud Carlos III, 28029, Madrid, Spain. acordoba@ull.edu.es.
  • Piñero JE; Instituto Universitario de Enfermedades Tropicales y Salud Pública de Canarias de La Universidad de La Laguna, La Laguna, Tenerife, Spain.
  • Clavo B; Departamento de Medicina Interna, Dermatología y Psiquiatría, Universidad de La Laguna, La Laguna, Tenerife, Spain.
  • Lorenzo-Morales J; Red Cooperativa de Enfermedades Tropicales (RICET), Instituto de Salud Carlos III, Madrid, Spain.
BMC Infect Dis ; 21(1): 1169, 2021 Nov 19.
Article in English | MEDLINE | ID: covidwho-1526606
ABSTRACT

BACKGROUND:

SARS-CoV-2 stability and infection persistence has been studied on different surfaces, but scarce data exist related to personal protective equipment (PPE), moreover using realist viral loads for infection. Due to the importance for adequate PPE management to avoid risk of virus infection, RNA stability was evaluated on PPE.

METHODS:

Persistence of SARS-CoV-2 infection and detection of genomic RNA in PPE (gowns and face masks) were determined by in-vitro assays and RT-qPCR, respectively. Samples were infected with a clinical sample positive for SARS-CoV-2 (Clin-Inf), and with a heat-inactivated SARS-CoV-2 strain sample (Str-Inf) as a control.

RESULTS:

PPE samples infected with Clin-Inf were positive for the 3 viral genes on gowns up to 5 days post-infection, whereas these overall genes were detected up to 30 days in the case of face masks. However, gowns and FFP2 masks samples contaminated with Clin-Inf showed a cytopathic effect over VERO cells up to 5-7 days post-infection.

CONCLUSIONS:

SARS-CoV-2 RNA was detected on different PPE materials for 5 to 30 days, but PPE contaminated with the virus was infectious up to 5-7 days. These findings demonstrate the need to improve PPE management and to formulate strategies to introduce viricidal compounds in PPE fabrics.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Personal Protective Equipment / COVID-19 Type of study: Experimental Studies / Observational study / Prognostic study Limits: Animals / Humans Language: English Journal: BMC Infect Dis Journal subject: Communicable Diseases Year: 2021 Document Type: Article Affiliation country: S12879-021-06861-7

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Personal Protective Equipment / COVID-19 Type of study: Experimental Studies / Observational study / Prognostic study Limits: Animals / Humans Language: English Journal: BMC Infect Dis Journal subject: Communicable Diseases Year: 2021 Document Type: Article Affiliation country: S12879-021-06861-7