Genetic Diversity and Antimicrobial Resistance of Extraintestinal E. coli Populations Pre- and Post-Antimicrobial Therapy on Broilers Affected by Colisepticemia

Author:

Pasquali Frédérique1ORCID,Crippa Cecilia1ORCID,Parisi Antonio2ORCID,Lucchi Alex1,Gambi Lucia1,Merlotti Alessandra3ORCID,Remondini Daniel3ORCID,Stonfer Maurizio4,Manfreda Gerardo1

Affiliation:

1. Department of Agricultural and Food Sciences, Alma Mater Studiorum–University of Bologna, 40126 Bologna, Italy

2. Istituto Zooprofilattico Sperimentale di Puglia e Basilicata, 71121 Foggia, Italy

3. Department of Physics and Astronomy, Alma Mater Studiorum–University of Bologna, 40126 Bologna, Italy

4. Bayer Animal Health, 20156 Milan, Italy

Abstract

The aim of the present study was to investigate the genetic diversity and antimicrobial resistance (AMR) of E. coli during enrofloxacin therapy in broilers affected by colisepticemia. Three unrelated farms with ongoing colibacillosis outbreaks were sampled at day 1 before treatment and at days 5, 10 and 24 post-treatment. A total of 179 E. coli isolates were collected from extraintestinal organs and submitted to serotyping, PFGE and the minimum inhibitory concentration (MIC) against enrofloxacin. PFGE clusters shifted from 3–6 at D1 to 10–16 at D5, D10 and D24, suggesting an increased population diversity after the treatment. The majority of strains belonged to NT or O78 and to ST117 or ST23. PFGE results were confirmed with SNP calling: no persistent isolates were identified. An increase in resistance to fluoroquinolones in E. coli isolates was observed along the treatment. Resistome analyses revealed qnrB19 and qnrS1 genes along with mutations in the gyrA, parC and parE genes. Interestingly, despite a fluoroquinolone selective pressure, qnr-carrying plasmids did not persist. On the contrary, two conjugative AMR plasmid clusters (AB233 and AA474) harboring AMR genes other than qnr were persistent since they were identified in both D1 and D10 genomes in two farms. Further studies should be performed in order to confirm plasmid persistence not associated (in vivo) to antimicrobial selective pressure.

Funder

Bayer Animal Health

Publisher

MDPI AG

Subject

General Veterinary,Animal Science and Zoology

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