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Characterization of Antibiotic Administration Factors Associated with Microbiome Disruption and Subsequent
Samantha Franklin1, Corina Ramont2, Maliha Batool3
1Interdisciplinary Graduate Program in Genetics and Genomics, Texas A&M University, College Station, TX 77843, USA.
Background:
Broad-spectrum antibiotics are often used for suspected infections in patients with hematologic malignancies due to the risk of severe infections. Although antibiotic use can lead to antimicrobial resistance and microbiome dysbiosis, the effects of antibiotics on the microbiome and resistome in patients with acute myeloid leukemia (AML) undergoing remission induction chemotherapy (RIC) are not well understood.
Methods:
Various statistical models were utilized to examine the effects of antibiotic administration on the microbiome and resistome over time, as well as differences in AR-infection (ARI) and colonization (ARC) by important CDC-threats in 119 AML patients.
Results:
A greater number of unique antibiotic classes administered correlated with a loss of unique antibiotic resistance genes (ARGs) (R = -0.39, p = 0.008). Specifically, although a greater number of oxazolidinone administrations was correlated with a greater loss of diversity (R = -0.58, p < 0.001), each additional day of linezolid reduced the risk of ARC by ~30% (HR: 0.663, p = 0.047) and decreased the odds of acquiring genes predicted to confer macrolide (HR: 0.50, p = 0.026) resistance.
Conclusions:
The number of antibiotic administrations and the types of antibiotics used can influence the risk of antibiotic resistance gene (ARG) expansion and ARC events in AML patients undergoing RIC. While certain antibiotics may reduce microbial diversity, they are not always linked to an increase in ARGs or ARC events.
Insights
Antibiotic use in acute myeloid leukemia (AML) patients undergoing chemotherapy impacts microbial diversity and resistance. Certain antibiotics may reduce resistance gene acquisition, but overall effects vary.
Area of Science:
- Microbiology
- Oncology
- Pharmacology
Background:
- Broad-spectrum antibiotics are crucial for suspected infections in hematologic malignancy patients.
- Antibiotic use can lead to antimicrobial resistance and microbiome dysbiosis.
- Impacts of antibiotics on the microbiome and resistome in acute myeloid leukemia (AML) patients undergoing remission induction chemotherapy (RIC) are not well understood.
Purpose of the Study:
- To investigate the effects of antibiotic administration on the microbiome and resistome in AML patients undergoing RIC.
- To analyze the differences in antibiotic resistance-infections (ARI) and colonization (ARC) by CDC-threats.
Main Methods:
- Statistical models were used to examine changes in the microbiome and resistome over time.
- Analysis included 119 AML patients undergoing RIC.
- Investigated correlations between antibiotic classes, diversity, and antibiotic resistance genes (ARGs).
Main Results:
- More unique antibiotic classes correlated with fewer unique ARGs (R = -0.39, p = 0.008).
- Oxazolidinone use correlated with reduced microbial diversity (R = -0.58, p < 0.001).
- Each day of linezolid reduced ARC risk by ~30% (HR: 0.663, p = 0.047) and macrolide resistance gene acquisition odds (HR: 0.50, p = 0.026).
Conclusions:
- Antibiotic administration and type influence ARG expansion and ARC events in AML patients.
- Some antibiotics may decrease microbial diversity without increasing ARGs or ARC events.
- Understanding these dynamics is key for managing infections and resistance in AML patients.
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