Transcriptomic landscape of hepatic lymph nodes, peripheral blood lymphocytes and spleen of swamp buffaloes infected with the tropical liver fluke Fasciola gigantica

PLoS Negl Trop Dis. 2022 Mar 23;16(3):e0010286. doi: 10.1371/journal.pntd.0010286. eCollection 2022 Mar.

Abstract

The tropical liver fluke Fasciola gigantica is a parasitic helminth that has been frequently reported to infect mammals, typically involving water buffaloes. In this study, we characterized the tissue transcriptional landscape of buffaloes following infection by F. gigantica. RNAs were isolated from hepatic lymph nodes (hLNs), peripheral blood lymphocytes (pBLs), and spleen at 3-, 42- and 70-days post-infection (dpi), and all samples were subjected to RNA sequencing analyses. At 3 dpi, 2603, 460, and 162 differentially expressed transcripts (DETs) were detected in hLNs, pBLs, and spleen, respectively. At 42 dpi, 322, 937, and 196 DETs were detected in hLNs, pBLs, and spleen, respectively. At 70 dpi, 376, 334, and 165 DETs were detected in hLNs, pBLs, and spleen, respectively. Functional enrichment analysis identified upregulated immune-related pathways in the infected tissues involved in innate and adaptive immune responses, especially in hLNs at 42 and 70 dpi, and pBLs at 3 and 42 dpi. The upregulated transcripts in spleen were not enriched in any immune-related pathway. Co-expression network analysis further identified transcriptional changes associated with immune response to F. gigantica infection. Receiver operating characteristic (ROC) curve analysis showed that 107 genes in hLNs, 32 genes in pBLs, and 36 genes in spleen correlated with F. gigantica load. These findings provide new insight into molecular mechanisms and signaling pathways associated with F. gigantica infection in buffaloes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Buffaloes / parasitology
  • Fasciola hepatica* / genetics
  • Fasciola* / genetics
  • Fascioliasis* / veterinary
  • Lymph Nodes
  • Lymphocytes
  • Spleen
  • Transcriptome

Grants and funding

This work was supported by the National Key Basic Research Program (973 program) of China (Grant No. 2015CB150300) to XQZ, the Yunnan Expert Workstation (Grant No. 202005AF150041) to XQZ, the Veterinary Public Health Innovation Team of Yunnan Province (Grant No. 202105AE160014) to XQZ, and the Fund for Shanxi “1331 Project” (Grant No. 20211331-13) to XQZ. The funders had no role in study design, data collection, and analysis, decision to publish, or preparation of the manuscript.