Abstract

Simple SummaryKanglang white minnow (KWM, Anabarilius grahami), is a typical “3E” (Endangered, Endemic and Economic) fish species in Yunnan-Guizhou Plateau. As one of the traditional “Four Famous Fishes” in Yunnan province, it has become the major local aquaculture species with increasing demand after the success of artificial breeding. However, this economically important fish is highly susceptible to the infection of a parasite ciliate, Ichthyophthirius multifiliis (Ich), during the practical procedure of artificial breeding. To examine the host immune responses to Ich, we divided the experimental fishes into three groups (including control, early-infected stage, and late-infected stage) for transcriptome sequencing to analyze the differentially expressed genes (DEGs) and immune response mechanisms.The notorious parasite Ichthyophthirius multifiliis (Ich) has been recorded worldwide in fish species and causes white spot disease, posing major threats and resulting in severe losses to international fish production. Extensively effective strategies for treating Ich are not available yet, and genetic mechanisms of hosts in response to the parasite are still largely unknown. In this study, we selected Kanglang white minnow (KWM, Anabarilius grahami) to examine its liver transcriptional changes after Ich infection, as white spot disease is one bottleneck problem in exploring this economically important species. We divided the experimental fishes into three groups (control, early-infected, and late-infected) to examine differentially expressed genes (DEGs). A total of 831 DEGs were identified and classified into 128 significantly enriched GO (Gene Ontology) terms and 71 significantly enriched KEGG (Kyoto Encyclopedia of Genes and Genomes) pathways. Most of these terms or pathways were functionally enriched in immunity, inflammatory response, and apoptosis, such as nucleotide-binding oligomerization domain-like (NOD-like) receptor signaling, tumor necrosis factor (TNF) signaling, interleukin-17 (IL-17) signaling, and apoptosis pathways. We also identified 178 putative antimicrobial peptides (AMPs) and AMP precursors based on our previously reported genome assembly of KWM, and revealed that the expressional patterns varied according to different types. In summary, our work reported the first comprehensive transcriptional changes in KWM in response to the exogenous infection of Ich, which would lay a solid foundation for in-depth studies on disease defense or resistant strains selection in this valuable fish.

Highlights

  • Kanglang white minnow (KWM), Anabarilius grahami, is a typical fish species with “3E”(Endangered, Endemic, and Economic) status and priorities in the Yunnan-Guizhou Plateau ofChina [1]

  • To reveal the potential immune mechanisms of KWM to Ichthyophthirius multifiliis (Ich) infection, we carried out transcriptome sequencing on liver samples from three controls, three early-infected and three late-infected fishes

  • We identified 831 genes that were significantly differentially expressed in KWM in response to the infection of Ich, including 402 activated and 429 suppressed genes

Read more

Summary

Introduction

Kanglang white minnow (KWM), Anabarilius grahami, is a typical fish species with “3E”(Endangered, Endemic, and Economic) status and priorities in the Yunnan-Guizhou Plateau ofChina [1]. Since the wild population of KMW has decreased sharply due to the introduction of an exotic icefish (Neosalanx taihuensis) [4], along with overfishing, destruction of spawning sites and the low fecundity of KMW itself [1]. These anthropogenic causes shifted the KMW from being an abundant economic species to an endangered fish, with evaluations to vulnerable (VU) in the China Species Red List in 2004 [5] and 2015 [6]. Farm-raised KMW are susceptible to exogenous infections of Ichthyophthirius multifiliis (Ich), which has caused heavy damages every year and become one of the major bottleneck problems in the recent exploration of this plateau fish species

Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call