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<p>This study aimed to evaluate the virulence and infection response of <i>Campylobacter jejuni</i> (CJ) strains isolated from chickens, as well as a standard strain isolated from humans, to understand better the pathogen-host relationship between CJ and chicken embryos (CE) with an active immune system. With its well-developed vascular structures, the CE model offers a valuable method for studying complex biological systems. We assessed embryo mortality, weight, macroscopic and microscopic lesions, bacterial multiplication within the embryo, and macrophage and lymphocyte (T and B cell) counts using flow cytometry. Additionally, histopathological lesions were examined. CJ killed CE at a dose of 3.7 log CFU/CE; however, lower doses (2.5 log CFU/CE) did not result in embryo death but instead caused macroscopic damage along with mild to moderate lesions. Certain strains were also capable of stimulating the immune system; however, this response varied depending on the strain. These findings underscore the importance of studying the virulence, infection dynamics, and immune responses of various CJ strains, highlighting the utility of the CE model for these investigations.</p>

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Virulence and Immune Response of Campylobacter jejuni Strains in Chicken Embryo Model

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年2月20日

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  • Paula Fernanda de Sousa Braga,
  • Emília Rezende Vaz,
  • Simone Sommerfeld,
  • Fabiana de Almeida Araújo Santos,
  • Gabriela Ribeiro da Silva,
  • Alessandra Castro Rodrigues,
  • Isabelle Ezequiel Pedrosa,
  • Alessandra Aparecida Medeiros Ronchi,
  • Adriana Freitas Neves,
  • Belchiolina Beatriz Fonseca

摘要

This study aimed to evaluate the virulence and infection response of Campylobacter jejuni (CJ) strains isolated from chickens, as well as a standard strain isolated from humans, to understand better the pathogen-host relationship between CJ and chicken embryos (CE) with an active immune system. With its well-developed vascular structures, the CE model offers a valuable method for studying complex biological systems. We assessed embryo mortality, weight, macroscopic and microscopic lesions, bacterial multiplication within the embryo, and macrophage and lymphocyte (T and B cell) counts using flow cytometry. Additionally, histopathological lesions were examined. CJ killed CE at a dose of 3.7 log CFU/CE; however, lower doses (2.5 log CFU/CE) did not result in embryo death but instead caused macroscopic damage along with mild to moderate lesions. Certain strains were also capable of stimulating the immune system; however, this response varied depending on the strain. These findings underscore the importance of studying the virulence, infection dynamics, and immune responses of various CJ strains, highlighting the utility of the CE model for these investigations.