4.6 Article

Replication Kinetics of Rickettsia raoultii in Tick Cell Lines

Journal

MICROORGANISMS
Volume 9, Issue 7, Pages -

Publisher

MDPI
DOI: 10.3390/microorganisms9071370

Keywords

vector-borne disease; Rickettsia raoultii; infectious disease; tick cell line

Categories

Funding

  1. Newton-Ungku Omar Fund partnership [332192305]
  2. UK Department of Business, Energy and Industrial Strategy (BEIS)
  3. UK Department of Business, Energy and Industrial Strategy
  4. Malaysian Industry-Government Group for High Technology (MIGHT)
  5. Ministry of Education, Malaysia [MO002-2019]
  6. Universiti Malaya, Malaysia [RU008-2018, UM.00000188/HGA.GV]
  7. United Kingdom Biotechnology and Biological Sciences Research Council [BB/P024270/1, BB/P024378/1]

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The study investigated the growth characteristics of R. raoultii in different tick cell lines and found variations in the growth kinetics among the cell lines tested, with IDE8 cells tolerating the highest level of R. raoultii replication. Further studies are needed to better understand the persistence of R. raoultii within tick populations.
Rickettsia raoultii is one of the causative agents of tick-borne lymphadenopathy in humans. This bacterium was previously isolated and propagated in tick cell lines; however, the growth characteristics have not been investigated. Here, we present the replication kinetics of R. raoultii in cell lines derived from different tick genera (BME/CTVM23, RSE/PILS35, and IDE8). Tick cell cultures were infected in duplicate with cryopreserved R. raoultii prepared from homologous cell lines. By 12-14 days post infection, 100% of the cells were infected, as visualized in Giemsa-stained cytocentrifuge smears. R. raoultii growth curves, determined by rickettsiae-specific gltA qPCR, exhibited lag, exponential, stationary and death phases. Exponential phases of 4-12 days and generation times of 0.9-2.6 days were observed. R. raoultii in BME/CTVM23 and RSE/PILS35 cultures showed, respectively, 39.5- and 37.1-fold increases compared to the inoculum. In contrast, multiplication of R. raoultii in the IDE8 cultures was 110.1-fold greater than the inoculum with a 7-day stationary phase. These findings suggest variation in the growth kinetics of R. raoultii in the different tick cell lines tested, amongst which IDE8 cells could tolerate the highest levels of R. raoultii replication. Further studies of R. raoultii are needed for a better understanding of its persistence within tick populations.

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