Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2019 Feb 5:10:153.
doi: 10.3389/fimmu.2019.00153. eCollection 2019.

Comparative Study of Immune Reaction Against Bacterial Infection From Transcriptome Analysis

Affiliations
Review

Comparative Study of Immune Reaction Against Bacterial Infection From Transcriptome Analysis

Shun Maekawa et al. Front Immunol. .

Abstract

Transcriptome analysis is a powerful tool that enables a deep understanding of complicated physiological pathways, including immune responses. RNA sequencing (RNA-Seq)-based transcriptome analysis and various bioinformatics tools have also been used to study non-model animals, including aquaculture species for which reference genomes are not available. Rapid developments in these techniques have not only accelerated investigations into the process of pathogenic infection and defense strategies in fish, but also used to identify immunity-related genes in fish. These findings will contribute to fish immunotherapy for the prevention and treatment of bacterial infections through the design of more specific and effective immune stimulants, adjuvants, and vaccines. Until now, there has been little information regarding the universality and diversity of immune reactions against pathogenic infection in fish. Therefore, one of the aims of this paper is to introduce the RNA-Seq technique for examination of immune responses in pathogen-infected fish. This review also aims to highlight comparative studies of immune responses against bacteria, based on our previous findings in largemouth bass (Micropterus salmoides) against Nocardia seriolae, gray mullet (Mugil cephalus) against Lactococcus garvieae, orange-spotted grouper (Epinephelus coioides) against Vibrio harveyi, and koi carp (Cyprinus carpio) against Aeromonas sobria, using RNA-seq techniques. We demonstrated that only 39 differentially expressed genes (DEGs) were present in all species. However, the number of specific DEGs in each species was relatively higher than that of common DEGs; 493 DEGs in largemouth bass against N. seriolae, 819 DEGs in mullets against L. garvieae, 909 in groupers against V. harveyi, and 1471 in carps against A. sobria. The DEGs in different fish species were also representative of specific immune-related pathways. The results of this study will enhance our understanding of the immune responses of fish, and will aid in the development of effective vaccines, therapies, and disease-resistant strains.

Keywords: RNA-Seq; bacteria; fish disease; immune response; transcriptome.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Venn diagrams showing overlaps of up and down regulated genes among each fish with bacterial challenge. The numbers indicate up (red arrow) and down (blue arrow) regulated genes in each categories.
Figure 2
Figure 2
Pathway map of Notch signaling (A) and Th1 differentiation (B) in KEGG. In each gene boxes, the gene expression levels are shown in 4 fish (C, Carp; G, Grouper; L, Largemouth bass; M, Mullet) spleen 1 day after infection with A. sobria, V. harveyi, N. seriolae, and L. garvieae, respectively, when compared to the control group. The lower expression levels of genes are shown in green, and the higher expression levels of genes are shown in red. Undetected genes are shown by white coloring (see color legend in figure).

Similar articles

Cited by

References

    1. Wang Z, Gerstein M, Snyder M. RNA-Seq: a revolutionary tool for transcriptomics. Nat Rev Genet. (2009) 10:57–63. 10.1038/nrg2484 - DOI - PMC - PubMed
    1. Qian X, Ba Y, Zhuang Q, Zhong G. RNA-Seq technology and its application in fish transcriptomics. OMICS (2014) 18:98–110. 10.1089/omi.2013.0110 - DOI - PMC - PubMed
    1. Martin SA, Dehler CE, Krol E. Transcriptomic responses in the fish intestine. Dev Comp Immunol. (2016) 64:103–17. 10.1016/j.dci.2016.03.014 - DOI - PubMed
    1. Jacobson G, Muncaster S, Mensink K, Forlenza M, Elliot N, Broomfield G, et al. . Omics and cytokine discovery in fish: presenting the Yellowtail kingfish (Seriola lalandi) as a case study. Dev Comp Immunol. (2017) 75:63–76. 10.1016/j.dci.2017.04.001 - DOI - PubMed
    1. Petit J, David L, Dirks R, Wiegertjes GF. Genomic and transcriptomic approaches to study immunology in cyprinids: what is next? Dev Comp Immunol. (2017) 75:48–62. 10.1016/j.dci.2017.02.022 - DOI - PubMed

MeSH terms