id	author	title	date	pages	extension	mime	words	sentences	flesch	summary	cache	txt
cord-269466-9hnal9ad	Agbeci, Maxime	Contribution of Host Intracellular Transport Machineries to Intercellular Movement of Turnip Mosaic Virus	2013-10-03		.txt	text/plain	7184	391	49	In this study, we used a novel dual gene cassette construct that differentiated primary infected cells from cells infected after virus intercellular movement to show that the early as well as the late secretory pathway, but not endocytosis, was important for TuMV transport. By using a dual cassette of genes encoding fluorescent proteins that can differentiate between primary infected cells and cells infected after intercellular transport, we provide evidence that turnip mosaic virus (TuMV) needs a functional secretory pathway where pre-and post-Golgi trafficking and the actomyosin network are important for its movement. Fig. 2E shows that that there was no significant difference in the ratio of red over green fluorescence during BFA and CMA treatments compared with the no inhibitor treatment (TuMV alone) at 4 dpinf, indicating that viral protein production in the primary infected cells was not affected by the drug treatments.	./cache/cord-269466-9hnal9ad.txt	./txt/cord-269466-9hnal9ad.txt