4.7 Article

Novel single nucleotide polymorphisms in the bovine leukemia virus genome are associated with proviral load and affect the expression profile of viral non-coding transcripts

Journal

VETERINARY MICROBIOLOGY
Volume 261, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.vetmic.2021.109200

Keywords

BLV; Long non-coding RNA; miRNA; Proviral load; AS1

Funding

  1. Ministry of Agriculture, Forestry and Fisheries of Japan [JPJ008617.17935709]
  2. JSPS KAKENHI [20K15687]
  3. Grants-in-Aid for Scientific Research [20K15687] Funding Source: KAKEN

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This study identified novel SNPs in the AS1 coding region and showed that individuals infected with BLV carrying minor SNPs exhibited low proviral load. Construction of infectious clones with these SNPs indicated changes in the expression profile of AS1 RNA, with an increase in the AS1-L isoform. Prediction analysis suggested that the introduced SNPs altered the secondary structure of AS1 RNA.
Bovine leukemia virus (BLV) infects bovine B-cells and causes malignant lymphoma, resulting in severe economic losses in the livestock industry. To control the spread of BLV, several studies have attempted to clarify the molecular mechanisms of BLV pathogenesis, but the details of the mechanism are still enigmatic. Currently, viral non-coding RNAs are attracting attention as a novel player for BLV pathogenesis because these transcripts can evade the host immune response and are persistently expressed in latent infection. One of the viral non-coding RNA, AS1, is encoded in the antisense strand of the BLV genome and consists of two isoforms, AS1-L and AS1-S. Although the function of the AS1 is still unknown, the AS1 RNA might also have some roles because it keeps expressing in tumor tissues. In the present study, we identified novel single nucleotide polymorphisms (SNPs) located in the AS1 coding region and indicated that individuals infected with BLV with minor SNPs showed low proviral load. To evaluate the effect of identified SNPs, we constructed infectious clones with these SNPs and found that their introduction affected the expression profile of AS1 RNA; the amount of AS1-L isoform increased compared with the wild type, although the total amount of AS1 RNA remained unchanged. Prediction analysis also suggested that the introduction of SNPs changed the secondary structure of AS1 RNA. These results explain part of the relationship between BLV expansion in vivo and the expression profile of AS1, although further analysis is required.

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