Tick cell culture isolation and growth of Rickettsia raoultii from Dutch Dermacentor reticulatus ticks

被引:39
作者
Alberdi, M. Pilar [1 ,2 ]
Nijhof, Ard M. [3 ]
Jongejan, Frans [3 ,4 ]
Bel-Sakyi, Lesley [1 ,2 ]
机构
[1] Univ Edinburgh, Roslin Inst, Roslin EH25 9RG, Midlothian, Scotland
[2] Univ Edinburgh, Royal Dick Sch Vet Studies, Roslin EH25 9RG, Midlothian, Scotland
[3] Univ Utrecht, Fac Vet Med, Utrecht Ctr Tick Borne Dis, NL-3584 CL Utrecht, Netherlands
[4] Univ Pretoria, Fac Vet Sci, Dept Vet Trop Dis, ZA-0110 Onderstepoort, South Africa
基金
英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
Dermacentor reticulatus; Ticks; Tick cell lines; Rickettsia raoultii; Endosymbionts; FEVER GROUP RICKETTSIA; MOUNTAIN WOOD TICK; PHYLOGENETIC ANALYSIS; BORRELIA-BURGDORFERI; IXODES-SCAPULARIS; SP-NOV; ANDERSONI; ENDOSYMBIONT; LINES; PEACOCKII;
D O I
10.1016/j.ttbdis.2012.10.020
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Tick cell lines play an important role in research on ticks and tick-borne pathogenic and symbiotic microorganisms. In an attempt to derive continuous Dermacentor reticulatus cell lines, embryo-derived primary cell cultures were set up from eggs laid by field ticks originally collected as unfed adults in The Netherlands and maintained for up to 16 months. After several months, it became evident that cells in the primary cultures were infected with a Rickettsia-like intracellular organism. Supernatant medium containing some D. reticulatus cells was inoculated into cultures of 2 Rhipicephalus (Boophilus) microplus cell lines, BME/CTVM2 and BME/CTVM23, where abundant growth of the bacteria occurred intracellularly on transfer to both cell lines. Bacterial growth was monitored by light (live, inverted microscope, Giemsa-stained cytocentrifuge smears) and transmission electron microscopy revealing heavy infection with typical intracytoplasmic Rickettsia-like bacteria, not present in uninfected cultures. DNA was extracted from bacteria-infected and uninfected control cultures, and primers specific for Rickettsia 16S rRNA, ompB, and sca4 genes were used to generate PCR products that were subsequently sequenced. D. reticulatus primary cultures and both infected tick cell lines were positive for all 3 Rickettsia genes. Sequencing of PCR products revealed 99-100% identity with published Rickettsia raoultii sequences. The R. raoultii also grew abundantly in the D. nitens cell line ANE58, poorly in the D. albipictus cell line DALBE3, and not at all in the D. andersoni cell line DAE15. In conclusion, primary tick cell cultures and cell lines are useful systems for isolation and propagation of fastidious tick-borne microorganisms. In vitro isolation of R. raoultii from Dutch D. reticulatus confirms previous PCR-based detection in field ticks, and. presence of the bacteria in the tick eggs used to initiate the primary cultures confirms that transovarial transmission of this Rickettsia occurs. (C) 2012 Elsevier GmbH. All rights reserved.
引用
收藏
页码:348 / 353
页数:6
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