Dissertation/Thesis Abstract

Identification of Dermacentor andersoni saliva proteins that modulate mammalian phagocyte function
by Mudenda, Lwiindi, Ph.D., Washington State University, 2015, 75; 3717421
Abstract (Summary)

Ticks are obligate blood sucking parasites which transmit a wide range of pathogens worldwide including protozoa, bacteria and viruses. Additionally, tick feeding alone may result in anemia, dermatosis and toxin-induced paralysis. Dermacentor andersoni is a species of tick found in the western United States that transmits pathogens of public health importance including Rickettsia rickettsii, Francisella tularensis, and Colorado Tick Fever Virus, as well as Anaplasma marginale, a rickettsial pathogen that causes economic losses in both the dairy and beef industries worldwide. D. andersoni ticks are obligate blood sucking parasites that require a blood meal through all stages of their lifecycle. During feeding, ticks secrete factors that modulate both innate and acquired immune responses in the host which enables them to feed for several days without detection. The pathogens transmitted by ticks exploit these immunomodulatory properties to facilitate invasion of and replication in the host. Molecular characterization of these immunomodulatory proteins secreted in tick saliva offers an opportunity to develop novel anti-tick vaccines as well as anti-inflammatory drug targets. To this end we performed deep sequence analysis on unfed ticks and ticks fed for 2 or 5 days. The pooled data generated a database of 21,797 consensus sequences. Salivary gland gene expression levels of unfed ticks were compared to 2- and 5-day fed ticks to identify genes upregulated early during tick feeding. Next we performed mass spectrometry on saliva from 2- and 5-day fed ticks and used the database to identify 677 proteins. We cross referenced the protein data with the transcriptome data to identify 157 proteins of interest for immunomodulation and blood feeding. Both proteins of unknown function and known immunomodulators were identified. We expressed four of these proteins and tested them for inhibition of macrophage activation and/or cytokine expression in vitro. The results showed diverse effects of the various test proteins on the inflammatory response of mouse macrophage cell lines. The proteins upregulated some cytokines while downregulating others. However, all the proteins upregulated the regulatory cytokine IL-10.

Indexing (document details)
Advisor: Brown, Wendy
Commitee: Brayton, Kelly A., Owen, Jeb P., Palmer, Guy H., Scoles, Glen A.
School: Washington State University
Department: Veterinary Microbiology and Pathology
School Location: United States -- Washington
Source: DAI-B 76/11(E), Dissertation Abstracts International
Subjects: Molecular biology, Bioinformatics, Immunology
Keywords: Gene expression, Mass spectrometry, Proteomics, Saliva proteins, Tick, Transcriptomics
Publication Number: 3717421
ISBN: 9781321968972
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