Barley |
Biotrophic |
Blumeria graminis
|
Effector gene Avra10
|
Reduced fungal development |
Nowara et al. (2010) |
Barley |
Biotrophic |
B. graminis
|
50 Blumeria effector candidates |
Eight were identified contributing to infection |
Pliego et al. (2013) |
Wheat |
Biotrophic |
Puccinia striiformis f. sp. tritici
|
Calcineurin homologs Pscna1/Pscnb1
|
Slower extension of fungal hyphae and reduced production of urediospores |
Zhang et al. (2012) |
Wheat |
Biotrophic |
P. striiformis f. sp. tritici
|
MAPK kinase gene PsFUZ7
|
Hyphal development strongly restricted, necrosis of plant cells in resistance responses induced |
Zhu et al. (2017) |
Wheat |
Biotrophic |
P. striiformis f. sp. tritici
|
PKA catalytic subunit gene PsCPK1
|
Significant reduction in the length of infection hyphae and disease phenotype |
Qi et al. (2018) |
Wheat |
Biotrophic |
Puccinia triticina
|
MAP kinase (PtMAPK1), cyclophilin (PtCYC1), and calcineurin B (PtCNB) |
Disease suppression, compromising fungal growth and sporulation |
Panwar et al. (2013a) |
Wheat |
Biotrophic |
P. triticina
|
Three predicted pathogenicity genes encoding MAPK, cyclophilin, and calcineurin regulatory subunit |
Suppressed disease phenotype |
Panwar et al. (2013b) |
Wheat |
Biotrophic |
Puccinia graminis f. sp. tritici
|
Haustoria‐enriched genes |
Reduced fungi development |
Yin et al. (2015) |
Lettuce |
Biotrophic oomycete |
Bremia lactucae
|
Highly abundant message #34 (HAM34), cellulose synthase (CES1) |
Greatly reduced growth and inhibition of sporulation |
Govindarajulu et al. (2015) |
Potato |
Biotrophic oomycete |
Phytophthora infestans
|
Three genes important in the infection, PiGPB1, PiCESA2, and PiPEC, together with PiGAPDH taking part in basic cell maintenance |
Hp‐PiGBP1 targeting the G protein β‐subunit (PiGPB1) important for pathogenicity resulted in most restricted disease progress |
Jahan et al. (2015) |
Potato |
Biotrophic oomycete |
P. infestans
|
RXLR effector Avr3a gene |
Imparted partial resistance to late blight disease |
Sanju et al. (2015) |
Arabidopsis, barley |
Hemibiotrophic |
Fusarium graminearum
|
Fungal cytochrome P450 lanosterol C‐14α‐demethylase (CYP51) genes |
Inhibition of fungal growth |
Koch et al. (2013) |
Banana |
Hemibiotrophic |
Fusarium oxysporum f. sp. cubense
|
Velvet, Fusarium transcription factor 1
|
Resisted disease at 8 months post‐inoculation |
Ghag et al. (2014) |
Arabidopsis
|
Hemibiotrophic |
F. oxysporum
|
F‐box protein required for pathogenicity 1 (FRP1), F. oxysporum Wilt 2 (FOW2), plant 12‐oxophytodienoate‐10,11‐reductase gene (OPR) |
Survival rates after fungal infection were higher in the transgenic lines |
Hu et al. (2015) |
Wheat |
Hemibiotrophic |
F. graminearum
|
Chitin synthase (Chs) 3b
|
High levels of stable, consistent resistance to both fusarium head blight and fusarium stem blight throughout the T3 to T5 generations |
Cheng et al. (2015) |
Wheat |
Hemibiotrophic |
F. graminearum
|
β‐1,3‐glucan synthase gene FcGls1
|
Aberrant, swollen fungal hyphae |
Chen, Kastner et al. (2016) |
Arabidopsis, barley |
Hemibiotrophic |
F. graminearum
|
CYP51 genes |
Spray‐induced gene silencing also conferred resistance against F. graminearum in unsprayed distal leaf parts |
Koch et al. (2016), Wang and Jin (2017) |
Wheat, barley |
Hemibiotrophic |
F. graminearum
|
TRI6, a transcription factor that positively regulates deoxynivalenol synthesis |
Silencing of TRI6
|
Hunter et al. (2018) |
Cotton |
Hemibiotrophic |
Verticillium dahliae
|
Two V. dahliae genes encoding a Ca2+‐dependent cysteine protease (Clp‐1) and an isotrichodermin C‐15 hydroxylase (HiC‐15) |
Cotton plants increased production of microRNA 166 (mir166) and mir159 that silence Clp‐1 and hic‐15
|
Zhang et al. (2016) |
Cotton |
Hemibiotrophic |
V. dahliae
|
V. dahliae
hygrophobins1 (VdH1) gene |
Induced silencing of the target mRNA and conferred resistance to V. dahliae infection |
Zhang et al. (2016) |
Arabidopsis, tomato |
Hemibiotrophic |
V. dahliae
|
Three previously identified virulence genes of V. dahliae (Ave1, Sge1, and NLP1) |
Reduced verticillium wilt disease in two of the three targets |
Song and Thomma (2018) |
Arabidopsis, tomato |
Necrotrophic |
Botrytis cinerea
|
B. cinerea Dicer‐like protein encoding genes: Bc‐DCL1 and Bc‐DCL2
|
Silenced Bc‐DCL genes and attenuated fungal pathogenicity and growth |
Weiberg et al. (2014), Wang et al. (2016) |
Arabidopsis
|
Necrotrophic |
B. cinerea
|
small RNAs‐containing vesicles accumulate at the infection sites and are taken up by the fungal cells |
Transferred host sRNAs induced silencing of fungal genes critical for pathogenicity |
Cai et al. (2018) |
Tall fescue |
Necrotrophic |
Rhizoctonia solani
|
Genes encoding RNA polymerase, importin beta‐1 subunit, Cohesin complex subunit Psm1, and a ubiquitin E3 ligase |
Lesion size was reduced by as much as 90% |
Zhou et al. (2016) |
Tobacco |
Necrotrophic |
Sclerotinia sclerotiorum
|
Chitin synthase (Chs) |
Reduction in disease severity |
Andrade et al. (2016) |
Maize |
Saprotrophic |
Aspergillus species |
AflC gene encodes an enzyme in the Aspergillus aflatoxin biosynthetic pathway |
Aflatoxin could not be detected |
Thakare et al. (2017) |