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Introduction of new fungicides for Septoria Leaf Blotch Control

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<strong>Introduction</strong> <strong>of</strong> <strong>new</strong> <strong>fungicides</strong> <strong>for</strong><br />

<strong>Septoria</strong> <strong>Leaf</strong> <strong>Blotch</strong> <strong>Control</strong><br />

Andy Leadbeater<br />

Head <strong>of</strong> Fungicide Technical R&D, Basel Switzerland<br />

EPPO Workshop on azole <strong>fungicides</strong> and <strong>Septoria</strong><br />

leaf blotch control, Rothamsted December 2010


2<br />

Agriculture is innovation driven…<br />

Percent <strong>of</strong><br />

sales<br />

14<br />

12<br />

10<br />

8<br />

6<br />

4<br />

2<br />

0<br />

R&D investment as percent <strong>of</strong> sales by sector<br />

Source: Financial Times, Phillips McDougall<br />

2


Loss <strong>of</strong> active substances: Cereal <strong>fungicides</strong> example<br />

Charts show percentages <strong>of</strong> EU-27 arable fungicide value<br />

3<br />

Strobilurin<br />

2002 2008 2014?<br />

Other Triazole<br />

18%<br />

49%<br />

33%<br />

Strobilurins dominate,<br />

followed by triazoles<br />

Strobilurin<br />

Other<br />

31%<br />

8%<br />

Triazole<br />

61%<br />

Triazoles dominate<br />

Strobilurin resistance<br />

widespread<br />

• Strobilurin resistance<br />

continues to grow<br />

• Triazoles significantly<br />

restricted by cut-<strong>of</strong>f<br />

criteria<br />

• Still fewer “other”<br />

alternatives available<br />

Reduced Yields<br />

Loss <strong>of</strong> EU competitiveness<br />

Greater reliance on grain<br />

imports


4<br />

Waves <strong>of</strong> <strong>new</strong> chemistry <strong>for</strong> sustainable disease control<br />

• From broad spectrum and low resistance risk to highly specific and high<br />

resistance risk<br />

• Innovation key <strong>for</strong> solving continuous pathogen adaptation<br />

• Mixtures: tool <strong>for</strong> resistance management program and disease control<br />

security.


“Industry can come up with <strong>new</strong> solutions”.....<br />

● Costs <strong>of</strong> <strong>new</strong> product discovery and development have risen by 39%<br />

from 2000-2008<br />

5


Costs <strong>of</strong> New Product Discovery and Development<br />

6<br />

$M<br />

300<br />

250<br />

200<br />

150<br />

100<br />

50<br />

0<br />

Total $152 m<br />

13<br />

13<br />

18<br />

18<br />

18<br />

10<br />

30<br />

Development 67<br />

Research 72<br />

11<br />

16<br />

18<br />

25<br />

20 36<br />

9<br />

11<br />

44<br />

32<br />

32 41 42<br />

1995 2000 2005-2008<br />

Source: ECPA / Crop Life America 2010<br />

Total $184 m<br />

Development 79<br />

Total $256 m<br />

25<br />

24<br />

32<br />

54<br />

Registration<br />

Environmental Chemistry<br />

Toxicology<br />

Field Trials<br />

Chemistry.<br />

Tox/Env Chemistry<br />

Biology<br />

Chemistry<br />

Development 146<br />

Research 94 Research 85


7<br />

Will <strong>new</strong> chemistry be available to fill the gap?<br />

Drivers <strong>for</strong> Innovation:<br />

Need.. Have..<br />

Rapid time to Market<br />

Stable development costs<br />

Predictable review process<br />

Return on R&D investment<br />

•Increasing delays (average 6 years)<br />

•Increasing number, and complexity<br />

<strong>of</strong> <strong>new</strong> tests<br />

•Significant uncertainty<br />

•Erosion <strong>of</strong> data protection rights


“Industry can come up with <strong>new</strong> solutions”.....<br />

● Costs <strong>of</strong> <strong>new</strong> product discovery and development have risen<br />

by 39% from 2000-2008.<br />

● Number <strong>of</strong> molecules screened to bring 1 to market is<br />

around 140,000.<br />

● Number <strong>of</strong> years between first synthesis and market has<br />

increased to 9.8 years.<br />

● Increased registration requirements thus increase cost and<br />

impact on development workload and time to market<br />

negatively.<br />

● New EU regulations raise the hurdles further <strong>for</strong> <strong>new</strong><br />

product innovation and are likely to reduce the chances <strong>of</strong><br />

success.<br />

8


9<br />

Key Fungicide <strong>Introduction</strong>s<br />

Year Fungicide<br />

1940 - 1960 thiram, zineb, nabam, biphenyl, oxine copper, tecnazene, captan, folpet, fentin<br />

acetate, fentin hydroxide, anilazine, blasticidin S, maneb, dodine, dicloran<br />

1960 - 1970 mancozeb, captafol, dithianon, propineb, thiabendazole, chlorothalonil,<br />

dichl<strong>of</strong>luanid, dodemorph, kasugamycin, polyoxins, pyrazophos, ditalimfos,<br />

carboxin, oxycarboxin, drazoxolon, tolyfluanide, difenphos, benomyl,<br />

fuberidazole, guazatine, dimethirimol, ethirimol, tri<strong>for</strong>ine, tridemorph<br />

1970 - 1980 Iprobenfos, thiophanate, thiophanate-methyl, validamycin, benodanil,<br />

triadimefon, imazalil, iprodione, bupirimate, fenarimol, nuarimol, buthiobate,<br />

vinclozolin, carbendazim, procymidone, cymoxanil, fosetyl-Al, metalaxyl,<br />

furalaxyl, triadimenol, prochloraz, <strong>of</strong>urace, propamocarb, bitertanol<br />

diclobutrazol, etaconazole, propiconazole tolcl<strong>of</strong>os-methy, fenpropimorph<br />

1980 - 2000 benalaxyl, flutolanil, mepronil, pencycuron, cypr<strong>of</strong>uram, triflumizole, flutriafol,<br />

penconazole, flusilazole, diniconazole, oxadixyl, fenpropidin, hexaconazole,<br />

cyproconazole, myclobutanil, tebuconazole, pyrifenox, difenoconazole,<br />

tetraconazole, fenbuconazole, dimethomorph, fenpiclonil, fludioxonil,<br />

epoxyconazole, bromuconazole, pyrimethanil, metconazole, fluquinconazole,<br />

triticonazole, fluazinam, azoxystrobin, kresoxim-methyl, metaminostrobin,<br />

cyprodinil, mepanipyrim, famoxadone, mefenoxam, quinoxyfen, fenhexamid,<br />

fenamidone, trifloxystrobin, cyaz<strong>of</strong>amid (acibenzolar s methyl)<br />

13<br />

24<br />

29<br />

42


Key Fungicide <strong>Introduction</strong>s<br />

10<br />

Year Fungicide<br />

2000 - present picoxystrobin , pyraclostrobin, prothioconazole,<br />

ethaboxam, zoxamide, fluopicolide, flumorph,<br />

benthiavalicarb, iprovalicarb, mandipropamid, boscalid,<br />

silthi<strong>of</strong>am, meptyldinocap, amisulbrom, orysastrobin,<br />

metrafenone, ipconazole, proquinazid, penthiopyrad,<br />

isopyrazam, ametoctradin<br />

Future Many known pipeline products<br />

ca. 20<br />

● Industry continues to invest heavily into providing <strong>new</strong> innovative<br />

solutions, despite increased costs and legislation. Sustainability is<br />

essential to maintain this investment


Fungicide Mode <strong>of</strong> Action Groups Available<br />

<strong>for</strong> Resistance Management in Wheat (adapted from HGCA, 2010)<br />

11<br />

Rusts S tritici S nodorum Mildew Eyespot Ear Blight<br />

DMIs Triazoles **** **** **** ** **** ***<br />

QoI Strobilurins **** * **** * * ***<br />

Amines Amines *** * ***<br />

Chloronitriles Chlorothalonil * *** ** *<br />

APDs Cyprodinil **** *** **<br />

Azanaphthalenes Quinoxyfen<br />

Proquinazid<br />

****<br />

Benz<strong>of</strong>enone Metrafenone * **** **<br />

Phenylacetamides Cyflufenamid ****<br />

Dithiocarbamate Mancozeb * ** ** *<br />

Carboxamides Various<br />

(provisional) **** **** ? *** **** ?<br />

per<strong>for</strong>mance <strong>of</strong> best <strong>fungicides</strong> in each class (adapted from HGCA 2010; modified)<br />

**** excellent *** very good ** moderate * poor (**** resistance losses)<br />

<strong>Septoria</strong> tritici: Very limited possibilities <strong>for</strong> resistance management<br />

Powdery mildew: Good situation with > 6 modes <strong>of</strong> action


12<br />

So What's New??


Bayer presentation IUPAC Congress Melbourn 2010<br />

13<br />

Classification: INTERNAL USE ONLY


14<br />

New QoIs -The Strobilurin Family<br />

(FRAC Code 11)<br />

Company Compound Launch<br />

Syngenta azoxystrobin Sales 2008:<br />

895 mio US$*<br />

BASF pyraclostrobin Sales 2008:<br />

670 mio US$*<br />

Bayer CS trifloxystrobin Sales 2008:<br />

474 mio US$*<br />

Kumiai pyribencarb 2010<br />

Shenyang pyrametostrobin Provisionally<br />

approved<br />

Shenyang coumoxystrobin ?<br />

Shenyang pyraoxystrobin Provisionally<br />

approved<br />

Shenyang triclopyricarb ?<br />

Shenyang dicloaminostrobin ?<br />

* Phillips McDougall 2009


15<br />

Summary (QoI / Strobilurins)<br />

• No <strong>new</strong> breakthrough in the QoI area (<strong>new</strong><br />

compounds show limited biological potential)<br />

• All <strong>new</strong> compounds seem to be x-resistant to the<br />

market strobilurins<br />

• New compounds might be only <strong>of</strong> local importance<br />

e.g. China


Complex II Inhibitors – SDHI Family<br />

Boscalid (BASF) – the first broad spectrum SDHI<br />

16<br />

Chemical Group Pyridine carboxamide (bisphenyltype amide)<br />

Mode <strong>of</strong> Action SDHI (complex II inhibitor)<br />

Spectrum Alternaria (vegis), botrytis (grapes), sclerotinia (lawn,<br />

oilseed rape and lettuce) and eyespot (cereals)<br />

Characteristics Protective, persistent, crop enhancement effects claimed<br />

Registration 2002<br />

Sales First sales 2003<br />

Reinhardsbrunn Symp April 2010<br />

boscalid<br />

O<br />

N<br />

H<br />

N Cl<br />

Cl


1969<br />

carboxin<br />

(Uniroyal)<br />

S<br />

O<br />

O<br />

17<br />

N<br />

Historical Overview <strong>of</strong> SDHIs (source: BASF)<br />

Market entry <strong>of</strong> selected fungicidal SDHI´s & their main targets<br />

1974<br />

benodanil<br />

(BASF)<br />

fenfuram<br />

(Shell/Bayer CS)<br />

O<br />

seed disinfection<br />

(& foliar spray)<br />

O<br />

I<br />

O<br />

N<br />

N<br />

1981<br />

mepronil<br />

(Kumiai)<br />

O<br />

N<br />

O<br />

1986<br />

flutolanil<br />

(Nihon Nohyaku)<br />

O<br />

F<br />

N<br />

F<br />

F<br />

O<br />

1997<br />

furametpyr<br />

(Sumitomo)<br />

N<br />

N<br />

Cl<br />

O<br />

N<br />

O<br />

thifluzamide<br />

(Monsanto/Dow)<br />

F F<br />

O<br />

F<br />

Br O<br />

N<br />

S<br />

N<br />

Br<br />

F<br />

F<br />

F<br />

2003<br />

boscalid<br />

(BASF)<br />

rice diseases specialty crops<br />

N<br />

cereals<br />

O<br />

Cl<br />

N<br />

Cl<br />

2010 – 2012<br />

penthiopyrad<br />

(Mitsui)<br />

fluopyram<br />

(Bayer CS)<br />

penflufen<br />

(Bayer CS) N<br />

sedaxane<br />

(Syngenta)<br />

bixafen<br />

(Bayer CS)<br />

isopyrazam<br />

(Syngenta)<br />

fluxapyroxad<br />

(BASF)<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

O<br />

S<br />

N<br />

O<br />

CF3 Cl CF3 N<br />

CF3 O<br />

F<br />

N<br />

O<br />

CHF 2<br />

O<br />

O<br />

CHF 2<br />

N<br />

Cl<br />

N<br />

CHF O 2<br />

CHF 2<br />

N<br />

F<br />

N<br />

Cl<br />

F<br />

N<br />

F<br />

F


SDHI - Mode <strong>of</strong> Action<br />

inside<br />

Mitochondrial<br />

Membrane<br />

outside<br />

18<br />

AcetylCoA<br />

Oxalacetate<br />

NADH+H + NAD +<br />

I<br />

2 H +<br />

Citrate<br />

Citrate Cycle<br />

Fumarate Succinate<br />

Complex II<br />

Q<br />

2 e-<br />

2 H +<br />

Complex<br />

III<br />

2 H +<br />

½O2 + 4 H + H<br />

-<br />

2O<br />

IV<br />

2 H +<br />

SDHIs Strobilurins<br />

Complex II (Succinate Dehydrogenase)<br />

Respiration Inhibitor - SDHI<br />

ADP + P i ATP<br />

3 H +<br />

3 H +


19<br />

SDHI„s bind to the UQ pocket <strong>of</strong> SQR <strong>of</strong> the complex II<br />

Isopyrazam<br />

F<br />

F<br />

N N<br />

O<br />

N<br />

● Essential TCA cycle reaction<br />

O<br />

O<br />

O<br />

O<br />

O<br />

O<br />

Succinate Ubiquinone<br />

<strong>Septoria</strong> tritici SDH inhibition<br />

150<br />

100<br />

50<br />

-2 2 4<br />

Log (nM) AI<br />

-50<br />

2x e -<br />

● ...can be blocked<br />

O<br />

O<br />

n<br />

H<br />

isopyrazam<br />

SYN 520 (9:1)<br />

Bixafen<br />

Penthiopyrad<br />

Boscalid<br />

Fluopyram


Efficacy <strong>of</strong> Isopyrazam <strong>for</strong> control <strong>of</strong> <strong>Septoria</strong> tritici<br />

20<br />

IZM 1.0+<br />

EPZ 0.5<br />

IZM 1.0<br />

EPZ 1.0<br />

Untreated<br />

0 10 20 30 40 50 60 70 80 90 100<br />

Source: AGRISEARCH, UK<br />

% <strong>Septoria</strong> tritici on leaf 2 (58 DAA2)<br />

Variety: DUXFORD LSD: 19.30<br />

Application: GS30-31 (22/04), GS39-41 (14/05) ,


21<br />

Isopyrazam <strong>for</strong> control <strong>of</strong> <strong>Septoria</strong> tritici<br />

IZM 125g+EPZ 90g<br />

EPZ 90g+Bravo 500g<br />

Rates: gai/ha<br />

IZM 125g<br />

EPZ 125g<br />

Untreated<br />

Location: Terrington, UK<br />

Variety: Consort LSD: 10.83<br />

Applic: GS31/32 (28/04), GS39-45 (21/05)<br />

0 20 40 60 80 100<br />

% <strong>Septoria</strong> tritici on leaf 2, 54DAT2


22<br />

Improved yields from SDHI chemistry<br />

IZM 125g +<br />

EPZ 90g<br />

EPZ 90g<br />

+Bravo 500g<br />

IZM 125g<br />

EPZ 125g<br />

Untreated<br />

Rates: gai/ha<br />

8 8.5 9 9.5 10 10.5 11 11.5 12 12.5 13 13.5 14<br />

Yield (t/ha)<br />

Location: Terrington, UK<br />

Variety: Consort LSD: 0.97<br />

Applic: GS31/32 (28/04), GS39-45 (21/05)


Isopyrazam<br />

Exciting New Chemistry<br />

23<br />

Untreated<br />

IZM, 125 ga/ha


Trials show outstanding brown rust control with<br />

isopyrazam<br />

Advantage 1l/ha high<br />

per<strong>for</strong>ming triazole<br />

Efficacy advantage<br />

24 Source 23 trials various<br />

Advantage<br />

isopyrazam


Resistance risk assessment <strong>for</strong> SDHI <strong>fungicides</strong><br />

● Single site inhibitors<br />

● Mutations in the target genes (sdh genes) lead to resistance<br />

● Compound risk is „medium to high“<br />

● Putative resistance risk<br />

- Mycosphaerella graminicola: medium to high<br />

- Pyrenophora teres: medium<br />

- Rhynchosporium secalis: low to medium<br />

- Puccinia recondita: low<br />

- Ramularia collo-cygni: medium<br />

● SDHIs should always be applied in mixtures or alternations<br />

with an appropriate partner i.e. one that is active in its own<br />

right against current field populations <strong>of</strong> the target pathogen<br />

at the applied dose<br />

25<br />

Source: Sierotzki et al, Reinhardsbrunn 2010


26<br />

Monitored species / SDHIs and reported cases <strong>of</strong> resistance<br />

Pathogen Field Sensitivity Pathogen Field Sensitivity<br />

A. alternata R (US), Pistachio E. necator S<br />

B. cinerea R (in grapes and<br />

strawberries, apple storage<br />

etc.)<br />

C. cassiicola R (cucurbits, Japan) M. fijiensis S<br />

P. xanthii R (cucurbits) V. inaequalis S<br />

M. graminicola S<br />

P. teres S<br />

R. secalis S<br />

R. collo-cygni S<br />

Tapesia spp. S<br />

M. nivale S<br />

U. nuda S?<br />

S. sclerotiorum S (R, single isolate from OSR<br />

in 2008 but not re-found<br />

(FRAC))<br />

P. leucotricha S


SDHI Sensitivity Monitoring<br />

● 2010 monitoring in cereals (all FRAC Working Group companies) show<br />

a continuing fully sensitive situation <strong>for</strong> SDHIs against all pathogens<br />

including M graminicola.<br />

● All values are within the estabished baseline sensitivity range. No<br />

change <strong>for</strong> isopyrazam since 2004 (start <strong>of</strong> monitoring).<br />

27<br />

C


SDHI FRAC Working Group recommendations<br />

SDHI Guidelines – Cereals 2011<br />

● Apply SDHI <strong>fungicides</strong> always in mixtures applied as tank mix or as a c<strong>of</strong>ormulated<br />

mixture<br />

● The mixture partner:<br />

28<br />

- should provide satisfactory disease control when used alone on the<br />

target disease<br />

- must have a different mode <strong>of</strong> action<br />

● Apply a maximum <strong>of</strong> 2 SDHI fungicide containing sprays per cereal crop.<br />

● Apply the SDHI fungicide preventively or as early as possible in the<br />

disease cycle. Do not rely only on the curative potential <strong>of</strong> SDHI<br />

<strong>fungicides</strong>.<br />

● Strongly reduced rate programs including multiple applications must not<br />

be used. Refer to manufacturers’ recommendations <strong>for</strong> rates.


Summary (Broad spectrum Compounds/SDHIs)<br />

● Boscalid is so far the most significant SDHI in<br />

market, in many crops, also used in cereals.<br />

● Penthiopyrad, bixafen, fluopyram, isopyrazam,<br />

fluxapyroxad are broad-spectrum, high potential<br />

SDHI <strong>fungicides</strong> expected to be significant in the<br />

market. For seed treatment sedaxane and<br />

penflufen are expected.<br />

● Bixafen, isopyrazam, penthiopyrad, fluxapyroxad<br />

used in mixtures with other <strong>fungicides</strong> expected to<br />

be important in cereals based upon published<br />

in<strong>for</strong>mation<br />

29


30<br />

WHAT'S NEXT AFTER THE SDHIs?


What's next?<br />

● Company published pipeline in<strong>for</strong>mation shows a number <strong>of</strong> potential<br />

<strong>new</strong> <strong>fungicides</strong>, <strong>of</strong> undisclosed chemistry and mode <strong>of</strong> action<br />

● These <strong>fungicides</strong> may or may not be novel in terms <strong>of</strong> mode <strong>of</strong> action<br />

● Based upon investor presentations alone these seem to be quite some<br />

time away from market at present (6-9 years??)<br />

● There is no guarantee that these willl pass regulatory hurdles and will<br />

make it to the market.<br />

● Key message – Industry is continuing to innovate but hurdles are high<br />

and it seems we will have to wait a while be<strong>for</strong>e the next wave <strong>of</strong> modes<br />

<strong>of</strong> action <strong>for</strong> cereals after the SDHIs hits the market.<br />

31


Conclusions – New Fungicides <strong>for</strong> <strong>Septoria</strong> <strong>Control</strong><br />

● There are few modes <strong>of</strong> action available <strong>for</strong> M. graminicola<br />

control.<br />

● The "next generation" <strong>of</strong> cereal <strong>fungicides</strong> is based around<br />

SDHIs.<br />

● A very good number <strong>of</strong> high per<strong>for</strong>ming SDHIs will be launched<br />

and will need to be managed well to ensure longevity. Triazoles,<br />

chlorothalonil etc will be essential <strong>for</strong> resistance management.<br />

● Chemistry / MOA following the SDHIs, is not yet clear.<br />

● New EU regulations raise the hurdles further <strong>for</strong> <strong>new</strong> product<br />

innovation and are likely to reduce the chances <strong>of</strong> success..<br />

● R&D search criteria will be changed, hazard criteria designed in<br />

earlier in the process (will tend to reduce success)<br />

● Drive to lower per<strong>for</strong>ming but lower hazard solutions (not lower<br />

risk!) e.g. biologicals<br />

32

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