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| Introduction |
The FRAC Azanapthalene (AZN) Working Group was formed in 2010 to generate
common resistance management recommendations for the fungicides quinoxyfen and
proquinazid. The above mentioned fungicides are grouped together under the FRAC
Code No. 13.
CODE |
TARGET SITE OF ACTION |
GROUP NAME |
CHEMICAL GROUP |
COMMON NAME |
COMMENTS |
13 |
Signal transduction (mechanism unknown) |
azanaphthalenes |
aryloxy- quinolines |
quinoxyfen |
Resistance to
quinoxyfen known.
Medium risk.
Resistance
management
required.
Cross resistance
found in Erysiphe
(Uncinula) necator
but not in Blumeria
graminis.
|
quinazolinone |
proquinazid |
Quinoxyfen and proquinazid are Azanaphthalene fungicides with a narrow spectrum of
activity limited to powdery mildew of cereals and broadleaf crops of which grapevines,
cucurbits and fruiting vegetables are key markets segments. Both fungicides act on
early stages of mildew development and are protectant only products. European wheat
powdery mildew baselines were established between 1995 and 1996 for quinoxyfen
(Holloman et al., 1997) and between 1999 and 2002 for proquinazid (Genet & Jaworska,
2009). Baselines for Erysiphe necator were generated in Europe for both molecules
around 1999-2000 (Green & Duriatti, 2005, Genet & Jaworska, 2009). First commercial
sales of quinoxyfen occurred in the EU on wheat and barley in 1997 and on grapevine in
2000. Commercial launch date for proquinazid was in 2006 on cereals and 2007 on
grapevines.
The exact site of action of these two fungicides is not known. Quinoxyfen
effects have been linked to early cell signaling events in wheat powdery mildew (Blumeria graminis)
during germling differentiation (Wheeler et al., 2003). Recent studies have shown that
quinoxyfen appears to target serine esterase activity, with a downstream perturbation in
signal transduction (Lee et al., 2008). Studies conducted on wheat powdery mildew have
shown that proquinazid stimulated the expression of host genes classically associated
with resistance responses including genes in ethylene-mediated response pathways,
phytoalexin biosynthesis, cell-wall strengthening and active oxygen production (Crane et
al., 2008).
Low frequencies of Blumeria graminis isolates with reduced sensitivity to quinoxyfen
were first detected in 2001 whilst a small increase in the frequency of Erysiphe necator
isolates with reduced sensitivity to quinoxyfen was first detected at the start of routine
monitoring in 2003 (Green & Duriatti, 2005). A clear cross-resistance pattern between
quinoxyfen and proquinazid has been demonstrated in grape powdery mildew (Erysiphe
necator) while a looser relationship was observed in Blumeria graminis (Genet &
Jaworska, 2009). The mechanism of resistance is unknown. For resistance management
purposes, quinoxyfen and proquinazid must be managed together under FRAC Group 13:
Powdery mildew is usually regarded as a high-risk pathogen with regard to fungicide
resistance therefore it is important that resistance management recommendations be
strictly followed.
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| Ressistance Monitoring and Use Recommendations |
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| References |
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Crane, V., Beatty, M., Zeka, B., Armstrong, R., Geddens, R. and Sweigard, J. 2008. Proquinazid activates host defense gene expression in
Arabidopsis thaliana. In Modern Fungicides and Antifungal Compounds, Proc. 15th International Rheinhardsbrunn Symposium, 6-10 May 2007, Friedrichroda, Germany, BCPC publications, pp. 19-26.
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Genet, J.-L. and Jaworska, G. 2009. Baseline sensitivity to proquinazid in Blumeria
graminis f.sp. tritici and Erysiphe necator and cross resistance with other fungicides. Pest Management Sci. 65: 878-884.
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Green, E. and Duriatti, A. 2005. Sensitivity of
Uncinula necator isolates to quinoxyfen: baseline studies, validation of baseline method and targeted sensitivity monitoring after several years of commercial use. In Proc. BCPC Internat. Congr. Crop Sci. and Tech., BCPC publications, Alton, Hants, UK, pp 163-168.
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Holloman, D.W., Wheeler, I., Dixon, K., Longhurst, C. and Skylalakis, G. 1997. Defining the resistance risk of the new powdery mildew fungicide quinoxyfen. Pestic. Sci. 51: 347-351.
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Lee, S., Gustafson, G., Skamnioti, P., Baloch, R. and Gurr, S. 2008. Host perception and signal transduction studies in wild-type
Blumeria graminis f.sp. hordei and a quinoxyfen-resistant mutant implicate quinoxyfen in the inhibition of serine esterase activity. Pest Management Sci. 64: 544-555.
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Wheeler, I., Holloman, D.W., Gustafson, G., Mitchell, J,. Longhurst, C., Zhang, Z and Gurr, S. 2003. Quinoxyfen perturbs signal transduction in barley powdery mildew (Blumeria graminis f.sp. hordei). Molecular Plant Pathology 4 (3): 177-186.
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