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Next Generation DNA Sequencing of Tissues from Infected Diabetic Foot Ulcers.
Malone, M; Johani, K; Jensen, S O; Gosbell, I B; Dickson, H G; Hu, H; Vickery, K.
Affiliation
  • Malone M; High Risk Foot Service, Liverpool Hospital, South West Sydney LHD, Sydney, Australia; Liverpool Diabetes Collaborative Research Unit, Ingham Institute of Applied Medical Research, Sydney, Australia; Molecular Medicine Research Group, Microbiology & Infectious Diseases, School of Medicine, Wester
  • Johani K; Surgical Infection Research Group, Faculty of Medicine and Health Sciences, Macquarie University, Sydney, Australia.
  • Jensen SO; Molecular Medicine Research Group, Microbiology & Infectious Diseases, School of Medicine, Western Sydney University, Sydney, Australia; Antimicrobial Resistance and Mobile Elements Group, Ingham Institute of Applied Medical Research, Sydney, Australia.
  • Gosbell IB; Molecular Medicine Research Group, Microbiology & Infectious Diseases, School of Medicine, Western Sydney University, Sydney, Australia; Antimicrobial Resistance and Mobile Elements Group, Ingham Institute of Applied Medical Research, Sydney, Australia; Department of Microbiology and Infectious
  • Dickson HG; Liverpool Diabetes Collaborative Research Unit, Ingham Institute of Applied Medical Research, Sydney, Australia; Ambulatory Care Department (PIXI), Liverpool Hospital, South West Sydney LHD, Sydney, Australia.
  • Hu H; Surgical Infection Research Group, Faculty of Medicine and Health Sciences, Macquarie University, Sydney, Australia.
  • Vickery K; Surgical Infection Research Group, Faculty of Medicine and Health Sciences, Macquarie University, Sydney, Australia.
EBioMedicine ; 21: 142-149, 2017 Jul.
Article in En | MEDLINE | ID: mdl-28669650
ABSTRACT
We used next generation DNA sequencing to profile the microbiome of infected Diabetic Foot Ulcers (DFUs). The microbiota was correlated to clinical parameters and treatment outcomes to determine if directed antimicrobial therapy based on conventional microbiological cultures are relevant based on genomic analysis. Patients≥18years presenting with a new Diabetic Foot Infection (DFI) who had not received topical or oral antimicrobials in the two weeks prior to presentation, were eligible for enrolment. Tissue punch biopsies were obtained from infected DFUs for analysis. Demographics, clinical and laboratory data were collected and correlated against microbiota data. Thirty-nine patients with infected DFUs were recruited over twelve-months. Shorter duration DFUs (Staphylococcus aureus in three cases and Streptococcus agalactiae in two. Longer duration DFUs (≥six weeks) were diversely polymicrobial (p<0.01) with an average of 63 (range 19-125) bacterial species. Severe DFIs had complex microbiomes and were distinctly dissimilar to less severe infections (p=0.02), characterised by the presence of low frequency microorganisms. Nineteen patients (49%) during the study period experienced antimicrobial treatment failure, but no overall differences existed in the microbiome of patients who failed therapy and those who experienced treatment success (p=0.2). Our results confirm that short DFUs have a simpler microbiome consisting of pyogenic cocci but chronic DFUs have a highly polymicrobial microbiome. The duration of a DFU may be useful as a guide to directing antimicrobial therapy.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Diabetic Foot / Metagenome / Metagenomics / Microbiota Type of study: Diagnostic_studies Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: EBioMedicine Year: 2017 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Diabetic Foot / Metagenome / Metagenomics / Microbiota Type of study: Diagnostic_studies Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: EBioMedicine Year: 2017 Document type: Article