In silico prediction and expression analysis of vaccine candidate genes of Campylobacter jejuni

• Published in: Poultry science 2023-05, Vol.102 (5), p.102592-102592, Article 102592
• Main Authors: Poudel, Sabin, Jia, Linan, Arick, Mark A., Hsu, Chuan-Yu, Thrash, Adam, Sukumaran, Anuraj T., Adhikari, Pratima, Kiess, Aaron S., Zhang, Li
• Format: Article
• Language: English
• Subjects: Animals; Campylobacter; Campylobacter Infections - genetics; Campylobacter Infections - prevention & control; Campylobacter Infections - veterinary; Campylobacter jejuni - genetics; Chickens - genetics; Genes, Bacterial; GENETICS AND MOLECULAR BIOLOGY; host-pathogen interaction; Humans; Poultry; reverse vaccinology, Campylobacter jejuni; RT-qPCR; Vaccines
• ISSN: 0032-5791; 1525-3171
• DOI: 10.1016/j.psj.2023.102592

Campylobacter jejuni (C. jejuni) is the most common food-borne pathogen that causes human gastroenteritis in the United States. Consumption of contaminated poultry products is considered as the major source of human Campylobacter infection. An effective vaccine would be a promising alternative to antibiotic supplements to curb C. jejuni colonization in poultry gastrointestinal (GI) tract. However, the genetic diversity among the C. jejuni isolates makes vaccine production more challenging. Despite many attempts, an effective Campylobacter vaccine is not yet available. This study aimed to identify suitable candidates to develop a subunit vaccine against C. jejuni, which could reduce colonization in the GI tract of the poultry. In the current study, 4 C. jejuni strains were isolated from retail chicken meat and poultry litter samples and their genomes were sequenced utilizing next-generation sequencing technology. The genomic sequences of C. jejuni strains were screened to identify potential antigens utilizing the reverse vaccinology approach. In silico genome analysis predicted 3 conserved potential vaccine candidates (phospholipase A [PldA], TonB dependent vitamin B12 transporter [BtuB], and cytolethal distending toxin subunit B [CdtB]) suitable for the development of a vaccine. Furthermore, the expression of predicted genes during host-pathogen interaction was analyzed by an infection study using an avian macrophage-like immortalized cell line (HD11). The HD11 was infected with C. jejuni strains, and the RT-qPCR assay was performed to determine the expression of the predicted genes. The expression difference was analyzed using ΔΔCt methods. The results indicate that all 3 predicted genes, PldA, BtuB, and CdtB, were upregulated in 4 tested C. jejuni strains irrespective of their sources of isolation. In conclusion, in silico prediction and gene expression analysis during host-pathogen interactions identified 3 potential vaccine candidates for C. jejuni.