4.7 Article

Multidrug-Resistant Methicillin-Resistant Staphylococcus aureus Associated with Bacteremia and Monocyte Evasion, Rio de Janeiro, Brazil

Journal

EMERGING INFECTIOUS DISEASES
Volume 27, Issue 11, Pages 2825-2835

Publisher

CENTERS DISEASE CONTROL & PREVENTION
DOI: 10.3201/eid2711.210097

Keywords

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Funding

  1. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq) [140774/2019-0, 443804/2018-4, 307672/2019-0]
  2. Fundacao Carlos Chagas Filho de Amparo a Pesquisa do Estado do Rio de Janeiro [E-26/210.193/2014, E-26/010.001280/2016, E-26.202.803/2017, E-26/010.002435/2019]
  3. Bill & Melinda Gates Foundation [OPP1193112]
  4. US National Institutes of Health [1R01AI137526-01]

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Researchers investigated 600 methicillin-resistant Staphylococcus aureus (MRSA) isolates collected in 51 hospitals in the Rio de Janeiro, Brazil, metropolitan area from 2014 to 2017, and identified an emerging multidrug-resistant MRSA sublineage named the Rio de Janeiro (RdJ) clone. The study also found that the RdJ clone, which began spreading in 2009, more effectively evaded immune function compared to other related isolates.
We typed 600 methicillin-resistant Staphylococcus aureus (MRSA) isolates collected in 51 hospitals in the Rio de Janeiro, Brazil, metropolitan area during 2014-2017. We found that multiple new clonal complex (CC) 5 sequence types had replaced previously dominant MRSA lineages in hospitals. Whole-genome analysis of 208 isolates revealed an emerging sublineage of multidrug-resistant MRSA, sequence type 105, staphylococcal cassette chromosome mec II, spa t002, which we designated the Rio de Janeiro (RdJ) clone. Using molecular clock analysis, we hypothesized that this lineage began to expand in the Rio de Janeiro metropolitan area in 2009. Multivariate analysis supported an association between bloodstream infections and the CC5 lineage that includes the RdJ clone. Compared with other closely related isolates, representative isolates of the RdJ clone more effectively evaded immune function related to monocytic cells, as evidenced by decreased phagocytosis rate and increased numbers of viable unphagocytosed (free) bacteria after in vitro exposure to monocytes.

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