Abstract

Chicken peripheral blood mononuclear cells (PBMCs) exhibit wide-ranging cell types, but current understanding of their subclasses, immune cell classification, and function is limited and incomplete. Here we performed single-cell RNA sequencing (scRNA-seq) of PBMCs in Avian leukosis virus subgroup J (ALV-J) infected and control chickens at 21 days post infection (DPI) to determine chicken PBMCs subsets and their specific molecular and cellular characteristics. Eight cell populations and their potential marker genes were identified in PBMCs. T cell populations had the strongest response to (ALV-J) infection, based on the detection of the largest number of differentially expressed genes (DEGs), and could be further grouped into four subsets: activated CD4+ T cells, Th1-like cells, Th2-like cells, and cytotoxic CD8+ T cells. Furthermore, pseudotime analysis results suggested that chicken CD4+ T cells could potentially differentiate into Th1-like and Th2-like cells. Moreover, ALV-J infection activated CD4+ T cell was probably inclined to differentiate into Th1-like cells. Compared to the control PBMCs, ALV-J infection also had an obvious impact on PBMCs composition. B cells showed inconspicuous response and their numbers decreased in PBMCs from ALV-J infected chicken. Proportions of cytotoxic Th1-like cells and CD8+ T cells increased in the T cell population of PBMCs from ALV-J infected chicken, which were potentially key mitigating effectors against ALV-J infection. More importantly, our results provide a rich resource of gene expression profiles of chicken PBMCs subsets for a systems-level understanding of their function in homeostatic condition as well as in response to viral infection.

Highlights

  • Adaptive immunity is known to play a vital protective role against avian viral infections

  • We found that Avian leukosis virus subgroup J (ALV-J) viremia was eliminated by 21 days post infection (DPI) when a significantly up-regulated CD8+T cell proportion and a very low serum antibody level in the peripheral blood were detected (Dai et al, 2020a)

  • We used the 10x Genomics platforms to perform 3 scRNAseq on peripheral blood mononuclear cells (PBMCs) collected from ALV-J infected and PBStreated control chickens at 21 DPI, respectively

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Summary

Introduction

Adaptive immunity is known to play a vital protective role against avian viral infections. Many interesting scientific questions about avian T cell or B cell immunity remain unresolved (Dai et al, 2019). Many important marker genes of the chicken immune cells are unknown, including effector or memory T cells and B cells. The Th1-Th2 paradigm is reported to exist in chickens (Degen et al, 2005). Whether this paradigm holds true at the cellular and molecular levels and whether chicken Th cells can become terminally polarized to a Th1 or Th2 phenotype remain to be verified. It is important and interesting to thoroughly characterize the molecular signatures of the CD4+ T, CD8+ T cells, and B cells during homeostasis and after pathogen exposure

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