SEQUENCING OF BAC ENDS FROM A RHIPICEPHALUS MICROPLUS BAC LIBRARY
Tick and Biting Fly Research
2012 Annual Report
1a.Objectives (from AD-416):
Our project objective is to study the tick vector-pathogen interface using the experimental system of Boophilus microplus, the southern cattle tick, and Anaplasma marginale, a rickettsial pathogen of cattle which is transmitted by B. microplus. Development of pathogen infectivity in the tick vector is coordinated with tick feeding, thus ensuring an efficient transmission of the pathogen to susceptible livestock. The long term objective is an enhanced understanding of pathogensis in this system leading to development of technologies to block disease transmission. We expect to have identified specific pathways that are regulated at the time when pathogen infectivity develops and transmission occurs.
1b.Approach (from AD-416):
Integrated A. marginale-B. microplus microarrays will be developed using the completed A. marginale genome sequence and the existing B. microplus gene index database of expressed sequence tags. The microarrays will be used to identify networks of pathogen and tick vector gene expression profiles during the development of A. marginale infectivity within B. microplus. Differential gene transcription in the tick will be assayed using midguts and salivary glands of B. microplus, comparing RNA isolated from tissues of ticks reared in conditions under which infectivity develops or fails to develop. Lastly, we will veify the integrated pathogen and tick vector gene expression patterns by proteomic and quantitative PCR analysis.
Based in part on this collaboration with ARS, the University of Houston-Clear Lake was able to secure NSF funding to upgrade their DNA sequencing capabilities to sequence R. microplus BAC clone ends.