Natural blood feeding and temperature shift modulate the global transcriptional profile of Rickettsia rickettsii infecting its tick vector

PLoS One. 2013 Oct 14;8(10):e77388. doi: 10.1371/journal.pone.0077388. eCollection 2013.

Abstract

Rickettsia rickettsii is an obligate intracellular tick-borne bacterium that causes Rocky Mountain Spotted Fever (RMSF), the most lethal spotted fever rickettsiosis. When an infected starving tick begins blood feeding from a vertebrate host, R. rickettsii is exposed to a temperature elevation and to components in the blood meal. These two environmental stimuli have been previously associated with the reactivation of rickettsial virulence in ticks, but the factors responsible for this phenotype conversion have not been completely elucidated. Using customized oligonucleotide microarrays and high-throughput microfluidic qRT-PCR, we analyzed the effects of a 10°C temperature elevation and of a blood meal on the transcriptional profile of R. rickettsii infecting the tick Amblyomma aureolatum. This is the first study of the transcriptome of a bacterium in the genus Rickettsia infecting a natural tick vector. Although both stimuli significantly increased bacterial load, blood feeding had a greater effect, modulating five-fold more genes than the temperature upshift. Certain components of the Type IV Secretion System (T4SS) were up-regulated by blood feeding. This suggests that this important bacterial transport system may be utilized to secrete effectors during the tick vector's blood meal. Blood feeding also up-regulated the expression of antioxidant enzymes, which might correspond to an attempt by R. rickettsii to protect itself against the deleterious effects of free radicals produced by fed ticks. The modulated genes identified in this study, including those encoding hypothetical proteins, require further functional analysis and may have potential as future targets for vaccine development.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bacterial Secretion Systems / genetics
  • Computer Simulation
  • Feeding Behavior / physiology*
  • Female
  • Gene Expression Profiling*
  • Genes, Bacterial / genetics
  • Guinea Pigs
  • Insect Vectors / microbiology*
  • Microfluidics
  • Oligonucleotide Array Sequence Analysis
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Reproducibility of Results
  • Reverse Transcriptase Polymerase Chain Reaction
  • Rickettsia Infections / genetics
  • Rickettsia Infections / microbiology
  • Rickettsia rickettsii / genetics*
  • Rickettsia rickettsii / physiology*
  • Temperature*
  • Ticks / microbiology*

Substances

  • Bacterial Secretion Systems
  • RNA, Messenger

Grants and funding

This work was supported by funds from the São Paulo Research Foundation (FAPESP; Grant 2008/053570-0), the Coordination for the Improvement of Higher Education Personnel (CAPES), and the National Council for Scientific and Technological Development [CNPq; the National Institutes of Science and Technology Program in Molecular Entomology (INCT-EM)].The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.