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Development and Validation of Three Automated High-Throughput Molecular Tests to Detect Monkeypox Virus Infections.
Anderson, Mark; Hodges, Austin; Luk, Ka-Cheung; Olivo, Ana; Forberg, Kenn; Meyer, Todd V; Strobel, Carolyn; Kim, Mark; Toolsie, Dan; Moore, Nicholas M; Goldstein, Yitzchak; Rodgers, Mary; Lucic, Danijela; Cloherty, Gavin.
Afiliação
  • Anderson M; Infectious Disease Research, Abbott Diagnostics Division, Abbott Park, Illinois, USA.
  • Hodges A; Abbott Pandemic Defense Coalition, Abbott Park, Illinois, USA.
  • Luk KC; Infectious Disease Research, Abbott Diagnostics Division, Abbott Park, Illinois, USA.
  • Olivo A; Abbott Pandemic Defense Coalition, Abbott Park, Illinois, USA.
  • Forberg K; Infectious Disease Research, Abbott Diagnostics Division, Abbott Park, Illinois, USA.
  • Meyer TV; Abbott Pandemic Defense Coalition, Abbott Park, Illinois, USA.
  • Strobel C; Infectious Disease Research, Abbott Diagnostics Division, Abbott Park, Illinois, USA.
  • Kim M; Abbott Pandemic Defense Coalition, Abbott Park, Illinois, USA.
  • Toolsie D; Infectious Disease Research, Abbott Diagnostics Division, Abbott Park, Illinois, USA.
  • Moore NM; Abbott Pandemic Defense Coalition, Abbott Park, Illinois, USA.
  • Goldstein Y; Infectious Disease Research, Abbott Diagnostics Division, Abbott Park, Illinois, USA.
  • Rodgers M; Abbott Pandemic Defense Coalition, Abbott Park, Illinois, USA.
  • Lucic D; Infectious Disease Research, Abbott Diagnostics Division, Abbott Park, Illinois, USA.
  • Cloherty G; Abbott Pandemic Defense Coalition, Abbott Park, Illinois, USA.
J Infect Dis ; 229(Supplement_2): S137-S143, 2024 Mar 26.
Article em En | MEDLINE | ID: mdl-37739785
BACKGROUND: The 2022 outbreak of the clade IIb monkeypox virus and subsequent global spread lead to an urgent need for the development of high-throughput, sensitive, and reproducible diagnostic tests. METHODS: We developed 3 assays to detect monkeypox virus, 2 (MPXV+ and MPXV) for m2000 RealTime and 1 (MPXV) for Alinity m platforms. Dual targets in E9L and B6R (MPXV+) and J2L and B7R (MPXV) increased mutation resistance. In silico prediction indicates MPXV+ cross-reactivity with orthopox viruses and specific monkeypox virus detection with MPXV. RESULTS: m2000 RealTime MPXV+ and MPXV assay sensitivity was determined to be 3.2 plaque-forming units/mL using a reference virus culture diluted into universal transport medium (UTM). Alinity m MPXV lower limit of detection was 200 copies/mL using monkeypox virus plasmids in pooled UTM matrix. m2000 RealTime MPXV+ and MPXV assays were validated with lesion swabs in UTM and 1:1 saliva to UTM mixtures. Commercially available and remnant clinical lesion specimens in UTM were tested with RealTime MPXV+, RealTime MPXV and Alinity m MPXV assays and demonstrated high agreement to known mpox (MPX)-positive specimens. CONCLUSIONS: RealTime MPXV+, RealTime MPXV, and Alinity MPXV are high throughput and sensitive assays used for the detection of monkeypox virus. These assays maybe useful during MPX outbreaks.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Mpox Limite: Humans Idioma: En Revista: J Infect Dis Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Mpox Limite: Humans Idioma: En Revista: J Infect Dis Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos