Revealing the Tick Microbiome: Insights into Midgut and Salivary Gland Microbiota of Female Ticks.

Anna Wiesinger, Jasmin Wenderlein, Sebastian Ulrich, Stephanie Hiereth, Lidia Chitimia-Dobler, Reinhard K Straubinger
Author Information
  1. Anna Wiesinger: Chair of Bacteriology and Mycology, Institute for Infectious Diseases and Zoonosis, Department of Veterinary Sciences, Faculty of Veterinary Medicine, LMU Munich, 80539 Munich, Germany. ORCID
  2. Jasmin Wenderlein: Chair of Bacteriology and Mycology, Institute for Infectious Diseases and Zoonosis, Department of Veterinary Sciences, Faculty of Veterinary Medicine, LMU Munich, 80539 Munich, Germany. ORCID
  3. Sebastian Ulrich: Chair of Bacteriology and Mycology, Institute for Infectious Diseases and Zoonosis, Department of Veterinary Sciences, Faculty of Veterinary Medicine, LMU Munich, 80539 Munich, Germany. ORCID
  4. Stephanie Hiereth: Chair of Bacteriology and Mycology, Institute for Infectious Diseases and Zoonosis, Department of Veterinary Sciences, Faculty of Veterinary Medicine, LMU Munich, 80539 Munich, Germany.
  5. Lidia Chitimia-Dobler: Bundeswehr Institute of Microbiology (InstMikroBioBw), Neuherbergstraße 11, 80937 Munich, Germany.
  6. Reinhard K Straubinger: Chair of Bacteriology and Mycology, Institute for Infectious Diseases and Zoonosis, Department of Veterinary Sciences, Faculty of Veterinary Medicine, LMU Munich, 80539 Munich, Germany. ORCID

Abstract

The ectoparasite is an important vector for many tick-borne diseases (TBD) in the northern hemisphere, such as Lyme borreliosis, rickettsiosis, human granulocytic anaplasmosis, or tick-borne encephalitis virus. As climate change will lead to rising temperatures in the next years, we expect an increase in tick activity, tick population, and thus in the spread of TBD. Consequently, it has never been more critical to understand relationships within the microbial communities in ticks that might contribute to the tick's fitness and the occurrence of TBD. Therefore, we analyzed the microbiota in different tick tissues such as midgut, salivary glands, and residual tick material, as well as the microbiota in complete ticks using 16S rRNA gene amplicon sequencing. By using a newly developed DNA extraction protocol for tick tissue samples and a self-designed mock community, we were able to detect endosymbionts and pathogens that have been described in the literature previously. Further, this study displayed the usefulness of including a mock community during bioinformatic analysis to identify essential bacteria within the tick.

Keywords

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MeSH Term

Animals
Female
Humans
Ixodes
RNA, Ribosomal, 16S
Lyme Disease
Salivary Glands
Tick-Borne Diseases
Microbiota

Chemicals

RNA, Ribosomal, 16S

Word Cloud

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