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Original Article

Interference between Escherichia coli genotypes from the E. coli peritonitis syndrome given simultaneously to productive SPF White Leghorn hens by intratracheal inoculation

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Received 06 Feb 2024, Accepted 19 Mar 2024, Published online: 11 Apr 2024
 

ABSTRACT

The purpose of the present study was to examine if potentiation of mortality occurred after simultaneous administration of several Escherichia coli genotypes, each capable of inducing the E. coli peritonitis syndrome, in comparison with single genotype application. Five groups of productive specified pathogen free White Leghorn hens were housed in isolators. Groups 1–4 consisted of 32 hens each, group 5 of 10 hens. At 32 weeks of age all groups were inoculated intratracheally. Groups 1 and 2 were inoculated with a mix of four E. coli genotypes and groups 3 and 4 with a mix of four other genotypes. Groups 1 and 3 were given 1 median lethal dose (LD50) of each genotype per hen and groups 2 and 4 had a dose of 0.1 LD50 per genotype per hen; group 5 was mock inoculated. The experiment ended one week after inoculations. In Group 5, no mortality occurred and gross lesions were absent at post-mortem examination. Mortality in groups 1 and 3 was 84% and 81%, respectively; in groups 2 and 4 59% and 66%, respectively. Although mortality in groups 1 and 3 exceeded the expected 50%, this could not be due to potentiation as cluster analysis of reisolates showed that in individual hens only one genotype was found, indicating interference between E. coli genotypes. In groups all four or only two genotypes were recovered, showing that not all genotypes will induce colibacillosis in all experimental groups. Therefore, broad protection can be best assessed by challenging with various single genotypes.

RESEARCH HIGHLIGHTS

  • All four or only two E. coli genotypes were found in groups of hens given mixes of four genotypes.

  • In contrast, only one genotype was found in individual hens.

  • E. coli genotypes interfere with each other in hens after given as a mix.

  • Interference is likely based on a random process.

  • Broad protection can best be assessed by challenging with single genotypes.

Acknowledgements

We thank Max Schellekens and Refke Peerboom for their skilful technical assistance and Carolyn Moonen for her help with the analysis of the FT-IR results.

Disclosure statement

No potential conflict of interest was reported by the authors.

Additional information

Funding

We also thank Stichting Avined, Nieuwegein, the Netherlands for funding this study.

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