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. 2017 May 22;114(23):5994–5999. doi: 10.1073/pnas.1703546114

Table S1.

Primers used in this study

Primer Sequence, 5′-3′ Application
16S-27F AGAGTTTGATCCTGGCTCAG PCR of eubacterial 16S rRNA gene
16S-1492R TACGGYTACCTTGTTACGACTT
16SF TCCTACGGGAGGCAGCAGT qPCR of eubacterial 16S rRNA gene
16SR GGACTACCAGGGTATCTAATCCTGTT
SmF1 ACGTTCATCAATTGACGTTACTCGCA qPCR of S. marcescens16S rRNA gene
SmR1 AACCGCCTGCGTGCGCTTTA
338F ACTCCTACGGGAGGCAGCA PCR of V3 and V4 hypervariable regions of eubacterial 16S rRNA gene
806R GGACTACHVGGGTWTCTAAT
cDNA S7F AGAACCAGCAGACCACCATC qPCR of AsS7 as endogenous control for quantification of relative expression of immune genes
cDNA S7R CGACGCACAGTAGCACAAAC
gDNA AsS7F TCCTGGAGCTGGAAATGAAC qPCR of AsS7 as endogenous control for quantification of midgut bacteria
gDNA AsS7R GCCGGGTCTGAACCTTCTGG
GAM1F GTACGTCAGCCGGAAGGGAG qPCR of Gambicin 1
GAM1R CGTAATGAACGAGGACGAACAGC
CEC1F GGAAGCGGGACGCCTGAA qPCR of Cecropin 1
CEC1R CCTTGACACCTGCCACCACC
DEF1F AGTCGTGGTCCTGGCGGCTCT qPCR of Defensin 1
DEF1R ACGAGCGATGCAATGCGCGGCA
ATTF AAAGCCAGAGCGGCAACAC qPCR of Attacin
ATTR TCAGTAACCGTGCGTGAAAGTC
FBN9F AACAATCTGACCGCACTGC qPCR of Fbn9
FBN9R TGTGACGCATTCCCTGTAG
DuoxF GGAACTGTTCTCGGCTGTCA qPCR of Duox
DuoxR TGATGTCCCAGAGCGTGAAC
gpdF CCCAGAACATCATTCCCAGC qPCR of fungal gpd for quantification of B. bassiana
gpdR TCAATGCGGGCAGTCAAGTC
dsDuoxF TAATACGACTCACTATAGGGGCTCGTCGGAAGTTTGTGAAAAA RNAi of mosquito Duox
dsDuoxR TAATACGACTCACTATAGGGTCGCATCATCTCACTCAGCTCTCC
dsGFPF TAATACGACTCACTATAGGGAGATGGTGAGCAAGGGCGAGGAGCTGT RNAi of GFP as negative control
dsGFPR TAATACGACTCACTATAGGGAGTTACTTGTACAGCTCGTCCATGCCG

F, forward; R, reverse.