. 2014 Nov 21;5:636. doi: 10.3389/fmicb.2014.00636

Table 4.

Transcriptional data of SQR9 when confronted with different fungal pathogens.

Gene	Relative gene expression (fold change)
	M	VDK	SS	FOC	RSK	FS	PP
bmyD	0.247 ± 0.006^c	0.243 ± 0.004^c	1.732 ± 0.002^d	2.603 ± 0.006^f	0.180 ± 0.001^b	0.120 ± 0.006^a	1.990 ± 0.001^e
fenA	0.924 ± 0.006^c	12.807 ± 0.006^f	0.920 ± 0.001^c	2.932 ± 0.002^d	0.80 ± 0.001^b	0.640 ± 0.001^a	3.210 ± 0.001^e
srfA	0.860 ± 0.001^b	0.672 ± 0.003^b	3.763 ± 0.005^e	0.111 ± 0.001^a	3.053 ± 0.003^d	1.488 ± 0.577^c	1.551 ± 0.001^c
dhbA	0.885 ± 0.006^b	15.121 ± 0.001^g	2.692 ± 0.002^c	10.233 ± 0.003^f	3.295 ± 0.005^d	0.88 ± 0.001^a	4.732 ± 0.001^e

^a−b

Means and standard deviations were calculated from relative gene expression of SQR9 classified into different genes. Small letters in brackets indicate significant differences as determined by One-Way ANOVA and Duncan's multiple range tests.

QRT-PCR result of SQR9 monoculture is represented as m, QRT-PCR results of SQR9 confronted with Verticillium dahliae Kleb, Sclerotinia sclerotiorum, Fusarium oxysporum, Rhizoctonia solani, Fusarium solani, Phytophthora parasitica var. nicotianae are represented as VDK, SS, FOC, RSK, FS, and PP, respectively. B. amyloliquefaciens SQR9-recA was used as an internal reference gene. Data are expressed as log10 relative quantification (RQ) (−2^{ΔΔ CT}). Data represent the mean value ± standard error from three replicates. The data obtained were analyzed by One-Way ANOVA analysis and means were analyzed by the Duncan's multiple range tests at P ≤ 0.05.