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Abstract
Effective implementation of antibiotic stewardship, especially in critical care, is limited by a lack of direct comparative investigations on how different antibiotics impact the microbiota and antibiotic resistance rates. We investigated the impact of two commonly used antibiotics, third-generation cephalosporins (3GC) and piperacillin/tazobactam (TZP) on the endotracheal, perineal and faecal microbiota of intensive care patients in Australia. Patients exposed to either 3GC, TZP, or no β-lactams (control group) were sampled over time and 16S rRNA amplicon sequencing was performed to examine microbiota diversity and composition. While neither treatment significantly affected diversity, numerous changes to microbiota composition were associated with each treatment. The shifts in microbiota composition associated with 3GC exposure differed from those observed with TZP, consistent with previous reports in animal models. This included a significant increase in Enterobacteriaceae and Enterococcaceae abundance in endotracheal and perineal microbiota for those administered 3GC compared to the control group. Culture-based analyses did not identify any significant changes in the prevalence of specific pathogenic or antibiotic-resistant bacteria. Exposure to clinical antibiotics has previously been linked to reduced microbiota diversity and increased antimicrobial resistance, but our results indicate that these effects may not be immediately apparent after short-term real-world exposures.
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1 Macquarie University, Department of Molecular Sciences, Sydney, Australia (GRID:grid.1004.5) (ISNI:0000 0001 2158 5405)
2 The University of Sydney and Westmead Hospital, Centre for Infectious Diseases and Microbiology, The Westmead Institute for Medical Research, Sydney, Australia (GRID:grid.1013.3) (ISNI:0000 0004 1936 834X)
3 The University of Sydney and Westmead Hospital, Centre for Infectious Diseases and Microbiology, The Westmead Institute for Medical Research, Sydney, Australia (GRID:grid.1013.3) (ISNI:0000 0004 1936 834X); Westmead Breast Cancer Institute, Westmead Hospital, Sydney, Australia (GRID:grid.413252.3) (ISNI:0000 0001 0180 6477)
4 Westmead Hospital and The University of Sydney, Intensive Care Unit, Sydney, Australia (GRID:grid.1013.3) (ISNI:0000 0004 1936 834X)
5 The University of Sydney and Westmead Hospital, Centre for Infectious Diseases and Microbiology, The Westmead Institute for Medical Research, Sydney, Australia (GRID:grid.1013.3) (ISNI:0000 0004 1936 834X); NSW Health Pathology, Centre for Infectious Diseases and Microbiology Laboratory Services, Sydney, Australia (GRID:grid.416088.3) (ISNI:0000 0001 0753 1056)
6 NSW Health Pathology, Centre for Infectious Diseases and Microbiology Laboratory Services, Sydney, Australia (GRID:grid.416088.3) (ISNI:0000 0001 0753 1056)
7 The University of Sydney and Westmead Hospital, Charles Perkins Centre, Sydney, Australia (GRID:grid.1013.3) (ISNI:0000 0004 1936 834X)
8 Nepean Hospital, Sydney University Medical School (Nepean), The University of Sydney, Department of Intensive Care Medicine Unit, Sydney, Australia (GRID:grid.1013.3) (ISNI:0000 0004 1936 834X); Macquarie University, Department of Clinical Medicine, Sydney, Australia (GRID:grid.1004.5) (ISNI:0000 0001 2158 5405)