Abstract

Efficient vaccines are the main strategy to control the avian coronavirus (AvCoV), although several drawbacks related to traditional attenuated and inactivated vaccines have been reported. These counterpoints highlight the importance of developing new alternative vaccines against AvCoV, especially those able to induce long-lasting immune responses. This study evaluated and compared two inactivated vaccines formulated with AvCoV BR-I variants, one composed of chitosan nanoparticles (AvCoV-CS) and the second by Montanide oily adjuvant (AvCoV-O). Both developed vaccines were administered in a single dose or associated with the traditional Mass attenuated vaccine. The AvCoV-CS vaccine administered alone or associated with the Mass vaccine was able to induce strong humoral and cell-mediated immune (CMI) responses and complete protection against IBV virulent infection, wherein single administration was characterized by high IgA antibody levels in the mucosa, whereas when associated with the Mass vaccine, the serum IgG antibody was predominantly observed. On the other hand, single administration of the oily vaccine presented poor humoral and CMI responses and consequently incomplete protection against virulent challenge, but when associated with the Mass vaccine, immune responses were developed, and complete protection against infection was observed. Both of our experimental vaccines were able to induce full protection against virulent IBV challenge. A single dose of AvCoV-CS vaccine was sufficient to achieve complete protection, while AvCoV-O required a previous priming by a Mass strain to complete the protection.

Highlights

  • Live attenuated and inactivated vaccines, containing the most epidemiologically important strains of the avian coronavirus (AvCoV), have been extensively used for the control of infectious bronchitis (IB) in poultry

  • Chickens single immunized with the chitosan nanoparticle vaccine containing an inactivated BR-I strain of AvCoV (Nano group) had earlier and higher levels of local IgA anti-AvCoV antibodies after challenge and higher expression levels of memory compared to cell-mediated immune (CMI)-related genes, such as the CD8β and Granzyme A genes in the trachea at 1 dpi

  • Chickens primed with the attenuated Mass vaccine followed by the AvCoV-CS vaccine (L+Nano) presented a stronger response of systemic IgG anti-AvCoV antibodies and higher levels of expression of CMI-related genes during the post-challenge period, characterized by the increased expression of the CD8β and Granzyme A genes in tracheal and renal samples at 5 and 11 dpi, respectively

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Summary

Introduction

Live attenuated and inactivated vaccines, containing the most epidemiologically important strains of the avian coronavirus (AvCoV), have been extensively used for the control of infectious bronchitis (IB) in poultry. Despite the constant increase in new vaccines, there are still several reports of incomplete protection against emerging new variants, mainly due to poor cross-protective immune responses developed in the respiratory mucosa, which is the portal of entry for this virus [1,2,3,4]. Alternative inactivated antigenic delivery and adjuvant systems are required, especially for those targeting the enhancement of the immunogenic responses. In this context, new adjuvants and/or carrier systems for AvCoV inactivated vaccines may constitute relevant approaches to replace traditional adjuvants, well known to be associated with increased toxicity, lower immunogenicity, and adverse reactions [11,12]

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