Progress 10/02/14 to 09/30/19
Outputs Target Audience:Professional colleagues (faculty members, students) at other academic institutions, e.g., University of Wisconsin, Madison (Dr. Lyric Bartholomay). Academia-based scientists interested in tick biology and tick-borne pathogens Students enrolled in programs on arthropod-borne zoonotic pathogens Students and scientists studying ticks Changes/Problems:
Nothing Reported
What opportunities for training and professional development has the project provided?
Nothing Reported
How have the results been disseminated to communities of interest?The research results have been published. What do you plan to do during the next reporting period to accomplish the goals?This is the final report. For the renewal project, we willidentify thge insertion sites in the other mutants that were generated. They will be available to other researchers uponrequest, subject to a material transfer agreement.
Impacts What was accomplished under these goals?
(1) Development of parasitic arthropod catalogue/resources: We established and chracterized a mouse model of human ehrlichiosis that recapitulates human disease accurately. For this, we obtained a field isolate of the agent, sequenced its genome, and transformed it to express fluorescent markers suitable for in vitr and in vivo tracking.
Publications
- Type:
Journal Articles
Status:
Published
Year Published:
2019
Citation:
Lynn GE, Burkhardt NY, Felsheim RF, Nelson CM, Oliver JD, Kurtti TJ, Cornax I, O'Sullivan MG, Munderloh UG. Ehrlichia Isolate from a Minnesota Tick: Characterization and Genetic Transformation. Appl Environ Microbiol. 2019 Jul 1;85(14).
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Progress 10/01/17 to 09/30/18
Outputs Target Audience:Academia-based scientists interested in tick biology and tick-borne pathogens Students enrolled in programs on arthropod-borne zoonotic pathogens Students and scientists studying ticks Changes/Problems:
Nothing Reported
What opportunities for training and professional development has the project provided?Graduate student Geoff Lynn accepted a position as scientist at the CDC, and after completion of this government position, moved to the lab of Dr. Errol Fikrig at Yale, to work with Anaplasma phagocytophilum. How have the results been disseminated to communities of interest?Results were published in peer-reviewed journals, and presented at scientific meetings internatiponally and in the US. What do you plan to do during the next reporting period to accomplish the goals?We will continue working with the mouse model of human ehrlichiosis to identify gene function using randommutagenesis and mechanistic analyses.
Impacts What was accomplished under these goals?
We developed a mouse model of human ehrlichiosis that replicates disease in humans accurately, This will allow development of effective treatments and vaccine. Further, the behavior of Ehrlichia muris eauclairensis in its natural reservoir, white-footed mice (Peromuyscus leucopus) was analyzed in detail, and differed from infection in laboratory mic in two ways: white-footed mice were less susceptible to severe dissease than laboratry strains of mice, but the former developed infection of the cerebellum accompanied by neurologic signs such as tremors. Ticks (larval andnymphal Ixodes scapularis) were afficient at acquisition and transmission of the pathogen, and classical co-feeding acquisition (as shown for the European tick-borne encephalitis viruses) was not demonstrated. Thus. E. muris eauclairensis is transmitted by ticks in the same manner as Anaplasmaphagocytophilum. In preparation for studies on th efunction of genes responsible for pathogenesis, we generated~60 mutants ofE. muris eauclairensis.
Publications
- Type:
Journal Articles
Status:
Published
Year Published:
2017
Citation:
Lynn GE, Oliver JD, Cornax I, O'Sullivan MG, Munderloh UG. Experimental evaluation of Peromyscus leucopus as a reservoir host of the Ehrlichia muris-like agent. Parasit Vectors. 2017 Jan 28;10(1):48
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Progress 10/01/16 to 09/30/17
Outputs Target Audience:Academia-based scientists interested in tick biology and tick-borne pathogens Students enrolled in programs on arthropod-borne zoonotic pathogens Students and scientists studying ticks Changes/Problems:
Nothing Reported
What opportunities for training and professional development has the project provided?
Nothing Reported
How have the results been disseminated to communities of interest?Peer-reviewed publication, training of colleagues at other institutions, scientifcmeeting presentations What do you plan to do during the next reporting period to accomplish the goals?Conrtinue dissemination of research materials and knowledge to contribute to goals 1 and 2
Impacts What was accomplished under these goals?
1) Tick cell lines and tick-borne pathogen isolates continue to be made available to the research community. These include specific mutants bearing fluorescent markers for tissue tracking and microscopy 2) The newly identified EMLA has been formally characterized and named Ehrlichia muris eauclairensis
Publications
- Type:
Journal Articles
Status:
Published
Year Published:
2017
Citation:
Pritt BS, Allerdice MEJ, Sloan LM, Paddock CD, Munderloh UG, Rikihisa Y, Tajima T, Paskewitz SM, Neitzel DF, Johnson DKH, Schiffman E, Davis JP, Goldsmith CS, Nelson CM, Karpathy SE. 2017. Proposal to reclassify Ehrlichia muris as Ehrlichia muris subsp. muris subsp. nov. and description of Ehrlichia muris subsp. eauclairensis subsp. nov., a newly recognized tick-borne pathogen of humans in the upper midwestern United States. IJSEM, 67(7):2121-2126.
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Progress 10/01/15 to 09/30/16
Outputs Target Audience:Academia-based scientists interested in tick biology and tick-borne pathogens Students enrolled in programs on arthropod-borne zoonotic pathogens Students and scientists studying ticks Changes/Problems:
Nothing Reported
What opportunities for training and professional development has the project provided?
Nothing Reported
How have the results been disseminated to communities of interest?Publicagtion of journal articles, presentation of talks at the meeting of the American Society for Rickettsiology What do you plan to do during the next reporting period to accomplish the goals?Distribute tick cell lines to additional labs. Design n-counter or multiplex-PCR-based tool for identification of pathogens. Establish routine to identify mosquitoes and ticks using barcodes.
Impacts What was accomplished under these goals?
Tick cell lines have been distributed to participating labs requesting them, and training has been provided in their cultivation.
Publications
- Type:
Journal Articles
Status:
Published
Year Published:
2016
Citation:
Nair AS, Chen C, Ganta CK, Sanderson MW, Alleman AR, Munderloh UG, Ganta RR. 2016. Comparative Experimental Infection Study in Dogs with Ehrlichia canis, E. chaffeensis, Anaplasma platys and A. phagocytophilum. PLoS One. 11(2):e0148239
- Type:
Journal Articles
Status:
Under Review
Year Published:
2017
Citation:
Lynn GE, Burkhardt NY, Felsheim RF, Nelson CM, Oliver JD, Kurtti TJ, Munderloh UG. In revision. Characterization and genetic transformation of an Ehrlichia isolated from a Minnesota tick. Applied and Environmental Microbiology.
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Progress 10/02/14 to 09/30/15
Outputs Target Audience:Academia-based scientists interested in tick biology and tick-borne pathogens Students enrolled in programs on arthropod-borne zoonotic pathogens Students and scientists studying ticks Changes/Problems:
Nothing Reported
What opportunities for training and professional development has the project provided?Training for one postdoctoral research associate in Entomology. Training included molecular microbiology and cell biology techniques, manuscript and grant writing, meeting presentations. How have the results been disseminated to communities of interest?Peer-reviewed publications, meeting presentations. What do you plan to do during the next reporting period to accomplish the goals?Investigating the interaction of different tick-borne pathogens and tick symbionts in individual ticks, acquisition from infected rodents by blood feeding and directly during co-feeding of infected and uninfected ticks on the same animal.
Impacts What was accomplished under these goals?
Aim #2 - ticks Prepared by Jonathan Oliver for Ulrike Munderloh Several collaborative efforts were proposed regarding Aim 2. 1. Some contributors mentioned that they had difficulty in preserving the quality of extracted tick DNA for later diagnostic tests. This led to a discussion of establishing standardized protocols for tick extraction and common pathogen PCR protocols. It can be difficult for new experimenters to determine what published protocols will work accurately and consistently. Having standardized protocols established which are known to work consistently may produce more reliable results in this field. In our experience, we find the Qiagen Blood and Tissue DNA extraction kits together with pre-washing and dissecting ticks produces DNA that does not rapidly degrade. In the future, we are willing to contribute a consolidated list of the primer sets and thermocycler recipes our laboratory uses for detection of tick-borne pathogens. 2. Dr. Goudarz Molaei of the Connecticut Agricultural Experiment Station demonstrated interest in acquiring some of our tick cell lines and pathogen strains. Follow-up telephone and email conversation have continued to solidify this exchange of materials. 3. Overlapping with Aim 1, we provided Jimmy Becnel with a list of the tick cell lines we have made available to other researchers. This is for his compilation of resources available for arthropod-borne disease of veterinary significance. It was decided that actual pathogenic organisms would not be included in this list at this time, but may be added later.
Publications
- Type:
Journal Articles
Status:
Accepted
Year Published:
2016
Citation:
Oliver JD, Lynn GE, Burkhardt NY, Price LD, Nelson CM, Kurtti TJ, Munderloh UG. Accepted. Infection of Immature Ixodes scapularis (Acari: Ixodidae) by Membrane Feeding. J. Med. Ent.
- Type:
Journal Articles
Status:
Published
Year Published:
2015
Citation:
Wang J, Dyachenko V, Munderloh UG, Straubinger RK. 2015. Transmission of Anaplasma phagocytophilum from endothelial cells to peripheral granulocytes in vitro under shear flow conditions. Med Microbiol and Immunol 204(5):593-603
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