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. 2013 Oct 3;107(12):806–811. doi: 10.1093/trstmh/trt087

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© The Author 2013. Published by Oxford University Press on behalf of Royal Society of Tropical Medicine and Hygiene. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

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Figure 1. — Real-time reverse transcription PCR for detection of Alkhumra haemorrhagic fever virus (AHFV) RNA in tick cell lines HAE/CTVM9 derived from the hard tick Hyalomma anatolicum, OME/CTVM24 derived from the soft tick Ornithodoros moubata and RAE/CTVM1 derived from the hard tick Rhipicephalus appendiculatus. The graph shows the amount of AHFV RNA detected in each cell line on Days 7, 14, 21 and 28 post inoculation, calculated as the percentage increase compared with the amount present in each culture immediately following inoculation on Day 0. OME/CTVM24 was not tested on Day 21 post inoculation.