The immune response to lumpy skin disease virus in cattle is influenced by inoculation route

Petra Fay, Najith Wijesiriwardana, Henry Munyanduki, Beatriz Sanz Bernardo, Isabel Lewis, Ismar Haga, Katy Moffat, Arnoud H M van Vliet, Jayne Hope, Simon P. Graham, Pip Beard

Research output: Contribution to journalArticlepeer-review

Abstract

Lumpy skin disease virus (LSDV) causes severe disease in cattle and water buffalo and is transmitted by hematophagous arthropod vectors. Detailed information of the adaptive and innate immune response to LSDV is limited, hampering the development of tools to control the disease. This study provides an in-depth analysis of the immune responses of calves experimentally inoculated with LSDV via either needle-inoculation or arthropod-inoculation using virus-positive Stomoxys calcitrans and Aedes aegypti vectors.
Seven out of seventeen needle-inoculated calves (41%) developed clinical disease characterised by multifocal necrotic cutaneous nodules. In comparison 8/10 (80%) of the arthropod‐inoculated calves developed clinical disease. A variable LSDV‐specific IFN‐γ immune response was detected in the needle-inoculated calves from 5 days post inoculation (dpi) onwards, with no difference between clinical calves (developed cutaneous lesions) and nonclinical calves (did not develop cutaneous lesions). In contrast a robust and uniform cell-mediated immune response was detected in all eight clinical arthropod-inoculated calves, with little response detected in the two nonclinical arthropod-inoculated calves. Neutralising antibodies against LSDV were detected in all inoculated cattle from 5-7 dpi. Comparison of the production of anti-LSDV IgM and IgG antibodies revealed no difference between clinical and nonclinical needle-inoculated calves, however a strong IgM response was evident in the nonclinical arthropod-inoculated calves but absent in the clinical arthropod-inoculated calves. This suggests that early IgM production is a correlate of protection in LSD. This study presents the first evidence of differences in the immune response between clinical and nonclinical cattle and highlights the importance of using a relevant transmission model when studying LSD.
Original languageEnglish
Article number1051008
Pages (from-to)1-21
Number of pages21
JournalFrontiers in Immunology
Volume13
Early online date28 Nov 2022
DOIs
Publication statusPublished - 28 Nov 2022

Keywords / Materials (for Non-textual outputs)

  • Humoral immunity
  • Lumpy Skin Disease
  • bovine immunity
  • cell-mediated immunity
  • neutralising antibodies
  • poxvirus
  • virus

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