4.7 Article

Identification of microRNAs in the Lyme Disease Vector Ixodes scapularis

Journal

Publisher

MDPI
DOI: 10.3390/ijms23105565

Keywords

Ixodes scapularis; salivary glands; microRNA; RNA sequencing; Borrelia burgdorferi

Funding

  1. USDA NIFA award [2017-67017-26171]
  2. Pakistan-US Science and Technology Cooperation award (US Department of State)
  3. Mississippi INBRE, an institutional Award (IDeA) from the National Institute of General Medical Sciences of the National Institutes of Health [P20GM103476]
  4. NIH NIAID [AI135049]
  5. NIFA [914701, 2017-67017-26171] Funding Source: Federal RePORTER

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MicroRNAs (miRNAs) play a crucial role in various biological processes, including immune responses to infections. This study focused on the differentially expressed miRNAs in the black-legged tick Ixodes scapularis after infection with Borrelia burgdorferi, the causative agent of Lyme disease. The findings provide valuable insights into the miRNAs expressed in the tick's salivary glands and their potential use in preventing or treating B. burgdorferi infection.
MicroRNAs (miRNAs) are a class of small non-coding RNAs involved in many biological processes, including the immune pathways that control bacterial, parasitic, and viral infections. Pathogens probably modify host miRNAs to facilitate successful infection, so they might be useful targets for vaccination strategies. There are few data on differentially expressed miRNAs in the black-legged tick Ixodes scapularis after infection with Borrelia burgdorferi, the causative agent of Lyme disease in the United States. Small RNA sequencing and qRT-PCR analysis were used to identify and validate differentially expressed I. scapularis salivary miRNAs. Small RNA-seq yielded 133,465,828 (>= 18 nucleotides) and 163,852,135 (>= 18 nucleotides) small RNA reads from Borrelia-infected and uninfected salivary glands for downstream analysis using the miRDeep2 algorithm. As such, 254 miRNAs were identified across all datasets, 25 of which were high confidence and 51 low confidence known miRNAs. Further, 23 miRNAs were differentially expressed in uninfected and infected salivary glands: 11 were upregulated and 12 were downregulated upon pathogen infection. Gene ontology and network analysis of target genes of differentially expressed miRNAs predicted roles in metabolic, cellular, development, cellular component biogenesis, and biological regulation processes. Several Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways, including sphingolipid metabolism; valine, leucine and isoleucine degradation; lipid transport and metabolism; exosome biogenesis and secretion; and phosphate-containing compound metabolic processes, were predicted as targets of differentially expressed miRNAs. A qRT-PCR assay was utilized to validate the differential expression of miRNAs. This study provides new insights into the miRNAs expressed in I. scapularis salivary glands and paves the way for their functional manipulation to prevent or treat B. burgdorferi infection.

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