AI Article Synopsis

  • A Δ J11 mutant strain was created from a low pathogenic avian pathogenic Escherichia coli (APEC) to enhance protein content in bacterial biomimetic vesicles (BBVs) and outer membrane vesicles (OMVs) for vaccination studies.
  • Immunization in chickens with either OMVs or BBVs through intranasal routes resulted in high levels of specific antibodies and significantly improved survival rates against a severe APEC strain, with 66.67% survival compared to just 16.67% in controls.
  • The study suggests that intranasal vaccination with BBVs can induce a strong immune response similar to OMVs, indicating potential for developing effective APEC vaccines.

Article Abstract

To evaluate the immunoprotective effect of bacterial biomimetic vesicles (BBVs) against avian pathogenic (APEC), a Δ J11 mutant strain was generated by deleting the gene in the low pathogenic O78 serotype J11 strain. The total protein content of outer membrane vesicles (OMVs) derived from the Δ J11 strain exhibited a sevenfold increase compared to the wild-type strain. Additionally, high-pressure homogenization technology was employed to produce BBVs, resulting in a sixfold increase in total protein content compared to spontaneously secreted OMVs from Δ J11. The immunogenicity of both OMVs and BBVs was assessed through intranasal or intramuscular immunization in specific pathogen-free (SPF) chickens. Results demonstrated that intranasal immunization with OMVs or BBVs in chickens elicited specific IgY antibodies against APEC outer membrane proteins and specific sIgA antibodies in the nasal cavity and trachea, as well as a significant increase in the proliferation response of chicken peripheral blood lymphocytes. The bacterial load in the blood and various organs of the challenged chickens were significantly reduced, resulting in a 66.67% and 58.30% survival rate against a high pathogenic serotype O78 strain challenge, while the control group exhibited only a 16.67% survival rate. The intramuscular immunization with OMVs or BBVs in chickens only induced specific IgY antibodies, with a survival rate of only 33.33% for challenged chickens during the same period. Therefore, intranasal vaccination of the highly productive BBVs is capable of eliciting an immune response similar to that of OMVs and providing protection against APEC infection, thus offering innovative insights for the advancement of APEC vaccines.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11593933PMC
http://dx.doi.org/10.3390/ijms252212055DOI Listing

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Article Synopsis
  • A Δ J11 mutant strain was created from a low pathogenic avian pathogenic Escherichia coli (APEC) to enhance protein content in bacterial biomimetic vesicles (BBVs) and outer membrane vesicles (OMVs) for vaccination studies.
  • Immunization in chickens with either OMVs or BBVs through intranasal routes resulted in high levels of specific antibodies and significantly improved survival rates against a severe APEC strain, with 66.67% survival compared to just 16.67% in controls.
  • The study suggests that intranasal vaccination with BBVs can induce a strong immune response similar to OMVs, indicating potential for developing effective APEC vaccines.
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