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Phylodynamic signatures in the emergence of community-associated MRSA.
Steinig, Eike; Aglua, Izzard; Duchene, Sebastian; Meehan, Michael T; Yoannes, Mition; Firth, Cadhla; Jaworski, Jan; Drekore, Jimmy; Urakoko, Bohu; Poka, Harry; Wurr, Clive; Ebos, Eri; Nangen, David; Müller, Elke; Mulvey, Peter; Jackson, Charlene; Blomfeldt, Anita; Aamot, Hege Vangstein; Laman, Moses; Manning, Laurens; Earls, Megan; Coleman, David C; Greenhill, Andrew; Ford, Rebecca; Stegger, Marc; Syed, Muhammad Ali; Jamil, Bushra; Monecke, Stefan; Ehricht, Ralf; Smith, Simon; Pomat, William; Horwood, Paul; Tong, Steven Y C; McBryde, Emma.
Afiliación
  • Steinig E; Department of Infectious Diseases, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, VIC, 3000, Australia.
  • Aglua I; Australian Institute of Tropical Health and Medicine, James Cook University, Townsville and Cairns, QLD, 4810, Australia.
  • Duchene S; Sir Joseph Nombri Memorial-Kundiawa General Hospital, Kundiawa, 461, Simbu Province, Papua New Guinea.
  • Meehan MT; Department of Infectious Diseases, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, VIC, 3000, Australia.
  • Yoannes M; Australian Institute of Tropical Health and Medicine, James Cook University, Townsville and Cairns, QLD, 4810, Australia.
  • Firth C; Papua New Guinea Institute of Medical Research, Goroka, 441, Eastern Highlands Province, Papua New Guinea.
  • Jaworski J; Australian Institute of Tropical Health and Medicine, James Cook University, Townsville and Cairns, QLD, 4810, Australia.
  • Drekore J; Sir Joseph Nombri Memorial-Kundiawa General Hospital, Kundiawa, 461, Simbu Province, Papua New Guinea.
  • Urakoko B; Simbu Children's Foundation, Kundiawa, 461, Simbu Province, Papua New Guinea.
  • Poka H; Sir Joseph Nombri Memorial-Kundiawa General Hospital, Kundiawa, 461, Simbu Province, Papua New Guinea.
  • Wurr C; Sir Joseph Nombri Memorial-Kundiawa General Hospital, Kundiawa, 461, Simbu Province, Papua New Guinea.
  • Ebos E; Surgical Department, Goroka General Hospital, Goroka, 441, Eastern Highlands Province, Papua New Guinea.
  • Nangen D; Surgical Department, Goroka General Hospital, Goroka, 441, Eastern Highlands Province, Papua New Guinea.
  • Müller E; Surgical Department, Goroka General Hospital, Goroka, 441, Eastern Highlands Province, Papua New Guinea.
  • Mulvey P; Leibniz Institute of Photonic Technology, 07743 Jena, Germany.
  • Jackson C; InfectoGnostics Research Campus, 07743 Jena, Germany.
  • Blomfeldt A; Australian Institute of Tropical Health and Medicine, James Cook University, Townsville and Cairns, QLD, 4810, Australia.
  • Aamot HV; US National Poultry Research Center, Agricultural Research Service, US Department of Agriculture, Athens, GA 30605.
  • Laman M; Department of Microbiology and Infection Control, Akershus University Hospital, 1478 Lørenskog, Norway.
  • Manning L; Department of Microbiology and Infection Control, Akershus University Hospital, 1478 Lørenskog, Norway.
  • Earls M; Papua New Guinea Institute of Medical Research, Goroka, 441, Eastern Highlands Province, Papua New Guinea.
  • Coleman DC; Department of Infectious Diseases, Fiona Stanley Hospital, Murdoch, WA, 6150, Australia.
  • Greenhill A; Medical School, University of Western Australia, Harry Perkins Research Institute, Fiona Stanley Hospital, Murdoch, WA, 6150, Australia.
  • Ford R; Microbiology Research Unit, Division of Oral Biosciences, University of Dublin, Trinity College, D02 PN40 Dublin, Ireland.
  • Stegger M; Microbiology Research Unit, Division of Oral Biosciences, University of Dublin, Trinity College, D02 PN40 Dublin, Ireland.
  • Syed MA; Papua New Guinea Institute of Medical Research, Goroka, 441, Eastern Highlands Province, Papua New Guinea.
  • Jamil B; Department of Microbiology, Federation University Australia, Ballarat, VIC, 3350, Australia.
  • Monecke S; Papua New Guinea Institute of Medical Research, Goroka, 441, Eastern Highlands Province, Papua New Guinea.
  • Ehricht R; Department of Bacteria, Parasites and Fungi, Statens Serum Institut, 2300 Copenhagen, Denmark.
  • Smith S; Department of Microbiology, University of Haripur, 22620 Haripur, Pakistan.
  • Pomat W; BJ Micro Lab (SMC Private) Limited, 46000 Islamabad, Pakistan.
  • Horwood P; Leibniz Institute of Photonic Technology, 07743 Jena, Germany.
  • Tong SYC; Technical University of Dresden, 01187 Dresden, Germany.
  • McBryde E; Leibniz Institute of Photonic Technology, 07743 Jena, Germany.
Proc Natl Acad Sci U S A ; 119(45): e2204993119, 2022 Nov 08.
Article en En | MEDLINE | ID: mdl-36322765
ABSTRACT
Community-associated, methicillin-resistant Staphylococcus aureus (MRSA) lineages have emerged in many geographically distinct regions around the world during the past 30 y. Here, we apply consistent phylodynamic methods across multiple community-associated MRSA lineages to describe and contrast their patterns of emergence and dissemination. We generated whole-genome sequencing data for the Australian sequence type (ST) ST93-MRSA-IV from remote communities in Far North Queensland and Papua New Guinea, and the Bengal Bay ST772-MRSA-V clone from metropolitan communities in Pakistan. Increases in the effective reproduction number (Re) and sustained transmission (Re > 1) coincided with spread of progenitor methicillin-susceptible S. aureus (MSSA) in remote northern Australian populations, dissemination of the ST93-MRSA-IV genotype into population centers on the Australian East Coast, and subsequent importation into the highlands of Papua New Guinea and Far North Queensland. Applying the same phylodynamic methods to existing lineage datasets, we identified common signatures of epidemic growth in the emergence and epidemiological trajectory of community-associated S. aureus lineages from America, Asia, Australasia, and Europe. Surges in Re were observed at the divergence of antibiotic-resistant strains, coinciding with their establishment in regional population centers. Epidemic growth was also observed among drug-resistant MSSA clades in Africa and northern Australia. Our data suggest that the emergence of community-associated MRSA in the late 20th century was driven by a combination of antibiotic-resistant genotypes and host epidemiology, leading to abrupt changes in lineage-wide transmission dynamics and sustained transmission in regional population centers.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Infecciones Estafilocócicas / Infecciones Comunitarias Adquiridas / Staphylococcus aureus Resistente a Meticilina Tipo de estudio: Risk_factors_studies Límite: Humans País/Región como asunto: Asia / Oceania Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2022 Tipo del documento: Article País de afiliación: Australia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Infecciones Estafilocócicas / Infecciones Comunitarias Adquiridas / Staphylococcus aureus Resistente a Meticilina Tipo de estudio: Risk_factors_studies Límite: Humans País/Región como asunto: Asia / Oceania Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2022 Tipo del documento: Article País de afiliación: Australia