Abstract

Infectious bronchitis is a highly contagious, acute viral respiratory disease of chickens, regardless of the strain, and its infection may lead to considerable economic losses to the poultry industry. New nephropathogenic infectious bronchitis virus (NIBV) strains have increasingly emerged in recent years; hence, evaluating their infection-influenced immune function changes and the alteration of metabolite profiling is important. Initially, chickens were randomly distributed into two groups: the control group (Con) and the disease group (Dis). Here, the partial cytokines were examined, and the metabolome alterations of the bursa of Fabricius (BF) in NIBV infections in chickens were profiled by gas chromatography time-of-flight/mass spectrometry (GC-TOF/MS). The results revealed that the NIBV infection promotes the mRNA expression of inflammatory cytokines. Metabolic profile analysis indicated that clustering differed between the two groups and there were 75 significantly different metabolites detected between the two groups, suggesting that the host metabolism was significantly changed by NIBV infection. Notably, the following 12 metabolites were identified as the potential biomarkers: 3-phenyllactic acid, 2-deoxytetronic acid, aminomalonic acid, malonamide 5, uric acid, arachidonic acid, 2-methylglutaric acid, linoleic acid, ethanolamine, stearic acid, N-alpha-acetyl-l-ornithine, and O-acetylserine. Furthermore, the results of the correlation analysis showed that a strong correlation existed between metabolic biomarkers and inflammatory cytokines. Our results describe an immune and metabolic profile for the BF of chickens when infected with NIBV and provide new biomarkers of NIBV infection as potential targets and indicators of indicating therapeutic efficacy.

Highlights

  • Infectious bronchitis virus (IBV) is a gamma coronavirus in the family Coronaviridae that consists of a positive-stranded RNA of 27.6 kb in length, which has been recognized as a pathogen of infectious bronchitis (IB), as well as respiratory and urogenital diseases in the commercial poultry industry worldwide [1,2,3]

  • Given that the immune organ is usually associated with variations in the expression levels of cytokines in viral infection states, we aimed to test whether nephropathogenic infectious bronchitis virus (NIBV) infection promoted bursa of Fabricius (BF) proinflammatory expression

  • Studies by several scholars have shown that severe pathological damages caused by virulent IBV strains in immune organs are related to high levels of virus replication and strong inflammation [33, 34]

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Summary

Introduction

Infectious bronchitis virus (IBV) is a gamma coronavirus in the family Coronaviridae that consists of a positive-stranded RNA of 27.6 kb in length, which has been recognized as a pathogen of infectious bronchitis (IB), as well as respiratory and urogenital diseases in the commercial poultry industry worldwide [1,2,3]. All strains of IBV can replicate on most chicken epithelial surfaces, such as those of the trachea, lungs, kidney, oviduct, alimentary, and proventriculus [4, 5]. Necropsy of chickens that died after NIBV infection revealed enlarged and pale kidneys, with urate deposits in the collecting tubule, making it a major cause of economic losses within the commercial poultry industry [9]

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