Literature DB >> 33713379

Staphylococcus aureus genotype variation among and within periprosthetic joint infections.

Dongzhu Ma1, Kimberly M Brothers1, Patrick L Maher1, Nathan J Phillips2, Deborah Simonetti3, Anthony William Pasculle4, Anthony R Richardson5, Vaughn S Cooper2, Kenneth L Urish1.   

Abstract

Staphylococcus aureus is a common organism in orthopedic infections, but little is known about the genetic diversity of strains during an infectious process. Using periprosthetic joint infection (PJI) as a model, a prospective study was designed to quantify genetic variation among S. aureus strains both among and within patients. Whole genome sequencing and multilocus sequence typing was performed to genotype these two populations at high resolution. In nasal cultures, 78% of strains were of clonal complexes CC5, CC8, and CC30. In PJI cultures, only 63% could be classified in these common clonal complexes. The PJI cultures had a larger proportion of atypical strains, and these atypical strains were associated with poor host status and compromised immune conditions. Mutations in genes involved in fibronectin binding (ebh, fnbA, clfA, and clfB) systematically distinguished later PJI isolates from the first PJI isolate from each patient. Repeated mutations in S. aureus genes associated with extracellular matrix binding were identified, suggesting adaptive, parallel evolution of S. aureus during the development of PJI.
© 2021 Orthopaedic Research Society.

Entities:  

Keywords:  Ebh; MSCRAMM binding; Periprosthetic joint infection; Staphylococcus aureus; fibrinogen; fibronectin; nasal carriage

Mesh:

Year:  2021        PMID: 33713379      PMCID: PMC8435540          DOI: 10.1002/jor.25031

Source DB:  PubMed          Journal:  J Orthop Res        ISSN: 0736-0266            Impact factor:   3.494


  50 in total

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Journal:  N Engl J Med       Date:  2001-01-04       Impact factor: 91.245

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7.  Giant extracellular matrix binding protein expression in Staphylococcus epidermidis is regulated by biofilm formation and osmotic pressure.

Authors:  Jacqueline C Linnes; Hongyan Ma; James D Bryers
Journal:  Curr Microbiol       Date:  2013-02-05       Impact factor: 2.188

8.  The Toxin-Antitoxin MazEF Drives Staphylococcus aureus Biofilm Formation, Antibiotic Tolerance, and Chronic Infection.

Authors:  Dongzhu Ma; Jonathan B Mandell; Niles P Donegan; Ambrose L Cheung; Wanyan Ma; Scott Rothenberger; Robert M Q Shanks; Anthony R Richardson; Kenneth L Urish
Journal:  mBio       Date:  2019-11-26       Impact factor: 7.867

9.  The epidemiology of revision total knee arthroplasty in the United States.

Authors:  Kevin J Bozic; Steven M Kurtz; Edmund Lau; Kevin Ong; Vanessa Chiu; Thomas P Vail; Harry E Rubash; Daniel J Berry
Journal:  Clin Orthop Relat Res       Date:  2009-06-25       Impact factor: 4.176

10.  Genomic characterization and outcome of prosthetic joint infections caused by Staphylococcus aureus.

Authors:  Peter Wildeman; Staffan Tevell; Carl Eriksson; Amaya Campillay Lagos; Bo Söderquist; Bianca Stenmark
Journal:  Sci Rep       Date:  2020-04-03       Impact factor: 4.379

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  2 in total

1.  Synovial Fluid-Induced Aggregation Occurs across Staphylococcus aureus Clinical Isolates and is Mechanistically Independent of Attached Biofilm Formation.

Authors:  Amelia Staats; Peter W Burback; Mostafa Eltobgy; Dana M Parker; Amal O Amer; Daniel J Wozniak; Shu-Hua Wang; Kurt B Stevenson; Kenneth L Urish; Paul Stoodley
Journal:  Microbiol Spectr       Date:  2021-09-15

2.  Microbiological and Molecular Features Associated with Persistent and Relapsing Staphylococcus aureus Prosthetic Joint Infection.

Authors:  Irene Muñoz-Gallego; María Ángeles Meléndez-Carmona; Jaime Lora-Tamayo; Carlos Garrido-Allepuz; Fernando Chaves; Virginia Sebastián; Esther Viedma
Journal:  Antibiotics (Basel)       Date:  2022-08-18
  2 in total

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