4.6 Article

Changes in Fecal Carriage of Extended-Spectrum β-Lactamase Producing Enterobacterales in Dutch Veal Calves by Clonal Spread of Klebsiella pneumoniae

Journal

FRONTIERS IN MICROBIOLOGY
Volume 13, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fmicb.2022.866674

Keywords

veal calves; fecal carriage; Klebsiella pneumoniae; clonal spread; extended-spectrum beta-lactamase producing Enterobacterales

Categories

Funding

  1. Dutch Ministry of Agriculture, Nature and Food Quality [BO-43-111-011]
  2. European Union's Horizon 2020 research and innovation programme through One Health EJP Project Full-Force [773830]
  3. TKI bureau AgriFood

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This study aimed to characterize the changes in fecal carriage of Extended-Spectrum beta-Lactamase (ESBL) producing Enterobacterales (ESBL-PE) over time in Dutch veal calves. The study found a decrease in fecal carriage of cefotaxime-resistant Escherichia coli isolates and an increase of cefotaxime-resistant Klebsiella pneumoniae isolates during the rearing period. The ESBL genes identified differed between the two bacteria. The study also discovered clonal spread of ESBL-K. pneumoniae in some animals.
This study aimed to characterize the changes in fecal carriage of Extended-Spectrum beta-Lactamase (ESBL) producing Enterobacterales (ESBL-PE) in a single Dutch veal calves. During the rearing period at the Dutch veal farm, a decrease in fecal carriage of cefotaxime-resistant Escherichia coli isolates was observed after 2 weeks at the veal farm, while an increase of cefotaxime-resistant Klebsiella pneumoniae isolates was demonstrated. E. coli and K. pneumoniae were isolated from rectal swabs collected from 110 veal calves in week 2, 6, 10, 18, and 24 after their arrival at the farm. ESBL-PE isolates were selectively cultured and identified by MALDI-TOF. ESBL genes were characterized by RT-PCR, PCRs, and amplicon sequencing. A total of 80 E. coli and 174 K. pneumoniae strains were isolated from 104 out of 110 veal calves. The prevalence of ESBL-E. coli decreased from week 2 (61%) to week 6 (7%), while an unexpected increase in ESBL-K. pneumoniae colonization was detected in week 6 (80%). The predominant ESBL genes detected in E. coli isolates were bla(CTX-M-15) and the non-ESBL gene bla(TEM-1a), while in K. pneumoniae bla(CTX-M-14) gene was detected in all isolates. Four cefotaxime-resistant K. pneumoniae isolates were randomly selected and characterized in deep by transformation, PCR-based replicon typing, and whole-genome sequencing (WGS). The clonal relatedness of a subgroup of nine animals carrying K. pneumoniae ESBL genes was investigated by Multi Locus sequence typing (MLST). In four ESBL-K. pneumoniae isolates, bla(CTX-M-14) was located on IncFII(K) and IncFII(NK) plasmid replicons and the isolates were multi-drug resistant (MDR). MLST demonstrated a clonal spread of ESBL-K. pneumoniae ST107. To the best of our knowledge, this is the first study to report a change in fecal carriage of ESBL-PE over time in the same veal calf during the rearing period.

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