. 2020 Aug 3;15(8):e0237044. doi: 10.1371/journal.pone.0237044

Table 2. Vero cells infected with PS-exosomes or PS-exosome depleted stool.

Virus	Sample	Time-point	Mean ± SEM	Significance
GII.4 Sydney	PS-exosomes	0h	1.00 ± 0.12	–
	PS-exosomes	72h	1.43 ± 0.12	*
	PS-depleted	0h	1.00 ± 0.09	–
	PS-depleted	72h	1.94 ± 0.13	****
GII.3	PS-exosomes	0h	1.00 ± 0.08	–
	PS-exosomes	72h	1.42 ± 0.17	*
	PS-depleted	0h	1.00 ± 0.09	–
	PS-depleted	72h	2.67 ± 0.28	****
GII.4 Den Haag	stool	0h	1.01 ± 0.13	–
	stool	72h	1.28 ± 0.17	ns
	PS-exosomes	0h	1.00 ± 0.14	–
	PS-exosomes	72h	1.22 ± 0.18	ns
	PS-depleted	0h	0.96 ± 0.07	–
	PS-depleted	72h	0.99 ± 0.13	ns

qRT-PCR analysis after a 72h infection (MOI = 0.1). Mean fold-changes over 0h time-points displayed. Significant differences between 0h and 72h time-points were calculated. Magnetic bead partitioning was used to isolate PS-exosomes and generate PS-depleted stool samples. Data represent n = 3 ± SEM.