Skip to main content

Comparison of the Respiratory Resistomes and Microbiota in Children Receiving Short versus Standard Course Treatment for Community-Acquired Pneumonia.

Publication ,  Journal Article
Pettigrew, MM; Kwon, J; Gent, JF; Kong, Y; Wade, M; Williams, DJ; Creech, CB; Evans, S; Pan, Q; Walter, EB; Martin, JM; Gerber, JS; Hofto, ME ...
Published in: mBio
April 26, 2022

Pediatric community-acquired pneumonia (CAP) is often treated with 10 days of antibiotics. Shorter treatment strategies may be effective and lead to less resistance. The impact of duration of treatment on the respiratory microbiome is unknown. Data are from children (n = 171), ages 6 to 71 months, enrolled in the SCOUT-CAP trial (NCT02891915). Children with CAP were randomized to a short (5 days) versus standard (10 days) beta-lactam treatment strategy. Throat swabs were collected at enrollment and the end of the study and used for shotgun metagenomic sequencing. The number of beta-lactam and multidrug efflux resistance genes per prokaryotic cell (RGPC) was significantly lower in children receiving the short compared to standard treatment strategy at the end of the study (Wilcoxon rank sum test, P < 0.05 for each). Wilcoxon effect sizes were small for beta-lactam (r: 0.15; 95% confidence interval [CI], 0.01 to 0.29) and medium for multidrug efflux RGPC (r: 0.23; 95% CI, 0.09 to 0.37). Analyses comparing the resistome at the beginning and end of the trial indicated that in contrast to the standard strategy group, the resistome significantly differed in children receiving the short course strategy. Relative abundances of commensals such as Neisseria subflava were higher in children receiving the standard strategy, and Prevotella species and Veillonella parvula were higher in children receiving the short course strategy. We conclude that children receiving 5 days of beta-lactam therapy for CAP had a significantly lower abundance of antibiotic resistance determinants than those receiving standard 10-day treatment. These data provide an additional rationale for reductions in antibiotic use when feasible. IMPORTANCE Antibiotic resistance is a major threat to public health. Treatment strategies involving shorter antibiotic courses have been proposed as a strategy to lower the potential for antibiotic resistance. We examined relationships between the duration of antibiotic treatment and its impact on resistance genes and bacteria in the respiratory microbiome using data from a randomized controlled trial of beta-lactam therapy for pediatric pneumonia. The randomized design provides reliable evidence of the effectiveness of interventions and minimizes the potential for confounding. Children receiving 5 days of therapy for pneumonia had a lower prevalence of two different types of resistance genes than did those receiving the 10-day treatment. Our data also suggest that children receiving longer durations of therapy have a greater abundance of antibiotic resistance genes for a longer period of time than do children receiving shorter durations of therapy. These data provide an additional rationale for reductions in antibiotic use.

Duke Scholars

Altmetric Attention Stats
Dimensions Citation Stats

Published In

mBio

DOI

EISSN

2150-7511

Publication Date

April 26, 2022

Volume

13

Issue

2

Start / End Page

e0019522

Location

United States

Related Subject Headings

  • beta-Lactams
  • Pneumonia
  • Microbiota
  • Infant
  • Humans
  • Community-Acquired Infections
  • Child, Preschool
  • Child
  • Anti-Bacterial Agents
  • 3207 Medical microbiology
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Pettigrew, M. M., Kwon, J., Gent, J. F., Kong, Y., Wade, M., Williams, D. J., … Antibacterial Resistance Leadership Group, . (2022). Comparison of the Respiratory Resistomes and Microbiota in Children Receiving Short versus Standard Course Treatment for Community-Acquired Pneumonia. MBio, 13(2), e0019522. https://doi.org/10.1128/mbio.00195-22
Pettigrew, M. M., J. Kwon, J. F. Gent, Y. Kong, M. Wade, D. J. Williams, C. B. Creech, et al. “Comparison of the Respiratory Resistomes and Microbiota in Children Receiving Short versus Standard Course Treatment for Community-Acquired Pneumonia.MBio 13, no. 2 (April 26, 2022): e0019522. https://doi.org/10.1128/mbio.00195-22.
Pettigrew MM, Kwon J, Gent JF, Kong Y, Wade M, Williams DJ, et al. Comparison of the Respiratory Resistomes and Microbiota in Children Receiving Short versus Standard Course Treatment for Community-Acquired Pneumonia. mBio. 2022 Apr 26;13(2):e0019522.
Pettigrew, M. M., et al. “Comparison of the Respiratory Resistomes and Microbiota in Children Receiving Short versus Standard Course Treatment for Community-Acquired Pneumonia.MBio, vol. 13, no. 2, Apr. 2022, p. e0019522. Pubmed, doi:10.1128/mbio.00195-22.
Pettigrew MM, Kwon J, Gent JF, Kong Y, Wade M, Williams DJ, Creech CB, Evans S, Pan Q, Walter EB, Martin JM, Gerber JS, Newland JG, Hofto ME, Staat MA, Fowler VG, Chambers HF, Huskins WC, Antibacterial Resistance Leadership Group. Comparison of the Respiratory Resistomes and Microbiota in Children Receiving Short versus Standard Course Treatment for Community-Acquired Pneumonia. mBio. 2022 Apr 26;13(2):e0019522.

Published In

mBio

DOI

EISSN

2150-7511

Publication Date

April 26, 2022

Volume

13

Issue

2

Start / End Page

e0019522

Location

United States

Related Subject Headings

  • beta-Lactams
  • Pneumonia
  • Microbiota
  • Infant
  • Humans
  • Community-Acquired Infections
  • Child, Preschool
  • Child
  • Anti-Bacterial Agents
  • 3207 Medical microbiology