Insect-Plant Interactions: a dynamic
co-evolutionary struggle highly
relevant to future food security
Toby Bruce
University of Nottingham, 12 May 2014
Modern agriculture:
High yielding varieties (?)
High yield –
only if there is adequate crop
protection against pests
Overview of talk:
• Vulnerability of agro-ecosystems to pest attack
Implications for Food Security
• Insect-plant interactions
• Techniques for managing pests
• Future directions
Vulnerability of agro-ecosystems to
pest attack
Lush monocultures of high yielding varieties grown
with fertiliser and irrigation are often more susceptible
to pests
Bruce (2011) J. Exp. Bot. 63: 537-541
fewer
effective
pesticides
reduced
genetic
diversity
in crops
THRIVING
PESTS AND
HIGH CROP
LOSSES
climate change can
make conditions
better for pests
less intrinsic resistance
to insects and
pathogens, and less
competitiveness with
weeds
fertilised crops more
nutritious to insects
and pathogens
broad spectrum
pesticides kill
natural enemies
of pests
Bruce (2011) J. Exp. Bot. 63: 537-541
Impact of Pests, Weeds & Diseases
1965 – staple
cereals
1992 – staple
cereals
42%
lost
36%
lost
SOURCE: Oerke & Dehne (2004) Crop Prot 23:275–285
Crop losses caused by pests have not decreased since the
1960s, even with use of pesticides
Resistance to agrochemicals worldwide
EC Directive 2009-128
A framework “Promoting the use of IPM
and of alternative approaches”
Research on “Alternatives” is urgently
needed
Promoting
IPM and use
of
alternatives
2009/128/EC on the
Sustainable Use of Pesticides
Reducing risks
and impacts of
pesticide use on
human health
and environment
Research on “Alternatives” is urgently
needed
More complicated than just banning
pesticides
Bees
“Impacts of pesticides on human
health and the environment”
… BUT WAIT, some impacts are positive
Human health
► increased affordability of
healthy food (e.g. fruit &
veg)
► less mycotoxin
contamination
Environment
► more food can be
produced on less land
with less water and
fertiliser
► more efficient production
– less GHG
• EU yields decline
• Increased selection pressure for resistance to
remaining pesticides
• Food price increase
• Food production companies move out of Europe
• More land used for agriculture
Unintended consequences
0
1000000
2000000
3000000
4000000
5000000
6000000
7000000
8000000
9000000
10000000
1961 1966 1971 1976 1981 1986 1991 1996 2001 2006 2011 2016 2021 2026 2031 2036 2041 2046
Population(1000s);CerealProduction(x500tonnes)
Will future demand be met?
Source: FAOSTAT
Bruce (2010) Food Security 2: 133-141
To keep pace with
growing demand,
global food
production needs
to increase by an
estimated 70% by
2050 [United
Nations]
New directions for Agriculture in the 21st
Century
Royal Society: “There is a pressing
need for the ‘sustainable
intensification’ of global agriculture in
which yields are increased without
adverse environmental impact and
without the cultivation of more land”.
Royal Society (2009) Policy document 11/09
A second green revolution which is knowledge intensive
rather than input intensive?
So we need to learn more about
insect-plant interactions…
…these are complicated and dynamic
Insect-plant interactions
The different timescales associated
with insect-plant interactions
Bruce (2014) JXB in press
DNA code has evolved over millions of years
- subject to mutations that are deleterious or advantageous according to context
- gene expression is modulated by epigenetic ‘stress imprints’
Insect effectors supress or induce
plant defence (depending if insect or plant is
‘ahead’)
(image courtesy of Saskia Hogenhout)
Plant defence changes over time
(image courtesy of Jurriaan Ton and Marieke van Hulten)
Defences: traditionally divided into
“constitutive” and “induced”
Primed
defence
plant is ready to
mount quicker
or stronger
defences when
subsequently
attacked
Induced
defence
these traits are
always expressed
these traits need a
signal to elicit
them
- attacking organism
- volatile surrogate
(plant activator)
Constitutive
defence
Bruce & Pickett (2007) Current Opinion in
Plant Biology 10: 387-392
primed
not primed
Bruce et al. (2007) Plant Science 173: 603-608
primed
not primed
Bruce et al. (2007) Plant Science 173: 603-608
primed
not primed Does priming
leave an
epigenetic
mark?
MeMeMeMeMeMeMeMeMeMe
MeMeMeMeMeMeMeMeMeMe
Bruce et al. (2007) Plant Science 173: 603-608
Rapid decisions by insects about plant
colonisation, made in flight
Bruce (2014) JXB in press
How do insects recognise host plants?
1. Species-specific odour
recognition:
taxonomically characteristic volatiles
ORN
Plant Volatile
CNS
ORN
Plant Volatile
CNS
Plant Volatile
Plant Volatile
Plant Volatile
Plant VolatileORN
ORN
ORN
ORN
Bruce et al. (2005) TRENDS in Plant Science 10: 269
2. Ratio-specific odour recognition:
specific combinations of volatiles,
distributed generally among plant
species
GC-linked electroantennography
• The insect antenna is used as a
biological detector
• Delicate manipulation with
microelectrodes to connect an antenna
to an electrical circuit
• Volatiles (GC effluent) passed over
electrophysiological preparation
• There is increased depolarisation when
the insect responds
• Insect released in the centre
• Time spent in treated arm compared
with time spent in control arms
• Insects released at downwind end
• Upwind flight and source contacts recorded
Olfactometer
Wind-tunnel
Behavioural Bioassays
Helicoverpa armigera
• highly polyphagous
• specialises on flowers
H O
H
CH3
CH2
H
O
benzaldehyde phenylacetaldehyde
limonene linalool
Bruce & Cork (2001) J. Chem. Ecol. 27: 1119
Helicoverpa armigera
• host plants
limited to
wheat and a
few related
grasses
Sitodiplosis mosellana
Birkett et al. (2004) J. Chem. Ecol. 30: 1319
3-carene
(Z)-3-hexenyl acetate
acetophenone
Ubiquitous compounds!
Sitodiplosis mosellana
Aphis fabae
• specialist on
beans
• feeds in colonies
(E)-2-hexenal
1-hexanol
(Z)-3-hexen-1-ol
benzaldehyde
6-methyl-5-hepten-2-one
octanal
(Z)-3-hexen-1-yl acetate
(R)-linalool
methyl salicylate
decanal
undecanal
(E)-caryophyllene
(E)-β-farnesene
(S)-(-)-germacrene
(E,E)-4,8,12-trimethyl-1,3,7,11-
tridecatetraene
Webster et al. (2008) J. Chem. Ecol. 34: 1153
Webster et al. (2010) Animal Behaviour 79: 451
Aphis fabae
Timespent(Min)
0
2
-
3
9-comp
syntheti
c blend
*
*
*
* *
*
* * *
*
0.1ng
(E)-2-hexanal
1ng
benzaldehyde
0.01ng
octanal
0.01ng(Z)-3-
hexenyl
acetate
0.1ng(R)-
lianlool
10ngmethyl
salicylate
100ngdecanal
0.01ng(S)-
germacreneD
0.1ngTMTT
Attraction to blends
Bruce & Pickett (2011) Phytochem. 72: 1605
Right mix is needed…
Bruce & Pickett (2011) Phytochem. 72: 1605
Bruce et al. (2005) TRENDS in Plant Science 10: 269
Spatio-temporal resolution of signals
The challenge of host recognition
Insect responses change over time
(image courtesy of Patrizia d'Ettorre and Mauro Patricelli)
Techniques for managing pests
Orange wheat blossom midge
• varies from year to
year
• was difficult to decide
in time which fields
needed treating
• difficult to control with
insecticide
• Females lay eggs, but
larvae die when they start
to feed
• A wound plug is formed at
the feeding site due to
lignification
• Antibiotic action of
phenolic acids by the grain
Resistant varieties
Resistant varieties
Oakley et al 2005 HGCA Project Report No. 363
Now approx. 60% of UK wheat is resistant
Resistant varieties
Yellow rust on wheat OWBM resistant cultivar (Robigus)
Need for multiple resistance
OCOC3H7
OCOC3H7
2,7-nonanediyl dibutyrate
Sex pheromone
Monitoring systems
Bruce et al. (2007) Pest Man. Sci. 63: 49
• Allow rational use of pesticides
• Need based applications save
costs and importantly slow
down the development of
resistance
• sex pheromone traps:
- provide a solution to the
detection problem
- enable more accurate and
effective spray timing
Bruce et al. (2007) Pest Man. Sci. 63: 49
• Pheromone traps widely used by
wheat growers in the UK
Decision support system for OWBM
Bruce & Smart (2009) Outlooks Pest Management 20: 89-92
• Identified from winter host volatiles of lettuce
aphid, Nasonovia ribis-nigri
• Emitted by insect infested plants:
– cotton plants damaged by Spodoptera
– potato plants infested with potato aphid
• Biological effects observed >24h after spraying
plants with cis-jasmone
• Non-toxic
• No residue left as it is volatile
cis-Jasmone O
• aphids (Sitobion avenae) released
at downwind end
• numbers settled on wheat seedlings
recorded
• Fewer aphids colonised cis-
jasmone induced plants
0
10
20
30
40
50
60
70
-1 4 9 14 19 24
time after release (h)
%settlement
control
cis-jasmone
Settlement bioassay in simulator
Bruce et al. (2003) Pest Management Science 59: 1031 – 1036
Field plot trial: spray application
0
0.2
0.4
0.6
0.8
1
1.2
28-May 8-Jun 16-Jun 24-Jun 6-Jul
MeanNo.Aphids/Tiller
*
*
control
cis-jasmone
P = 0.036
Bruce et al. (2003) Pest Management Science 59: 1031 – 1036
Wheat Field Trial
significantly longer time spent on
induced plants
0
5
10
15
20
25
Treated Control
min
Aphidius ervi foraging on cis-Jasmone
treated wheat
CYP81D11
• Insect responses to CYP81D11 OE plants are similar to
the responses observed with CJ treated plants
• We still do not know the function of this gene
Bruce et al. (2008) PNAS 105: 4553-4558
Stemborers
(E)-caryophyllene
(E)-4,8-
dimethyl-1,3,7-
nonatriene
Collecting volatiles from plants with
eggs
Bioassay
• insect released in the centre
• time spent in treated arm compared
with time spent in control arms
Response to volatiles collected from plants with and
without eggs?
Maize landrace lines
Tamiru et al. (2011) Ecology Letters 14: 1075
Parasitoid response - landraces
Attracted to plants with eggs
Volatile profiles - landraces
(a) (E)-ocimene, (b) (R)-linalool, (c) (E)-4,8-dimethyl-1,3,7, nonatriene (DMNT), (d) methyl
salicylate, (e) decanal, (f) methyleugenol, (g) (E)-(1R,9S)-caryophyllene, (h) (E)-β-farnesene, (i) (E,E)-
4,8,12-trimethyl-1,3,7,11-tridecatetraene (TMTT).
Tamiru et al. (2011) Ecology Letters 14: 1075
New Project: markers for egg induced
volatile emission trait
Diverse seeds
HIPV induced by eggs in improved line
Improved maize line CKIR12001 emits DMNT when
stemborer eggs are laid on it.
New aphid repellents identified
• Volatiles from Fusarium
graminearum infested wheat
are repellent to grain aphid,
Sitobion avenae
• EAG active compounds:
▫ 2-pentadecanone,
▫ 2-heptanone,
▫ phenyl actetic acid,
▫ α-gurjunene,
▫ 2-tridecanone,
▫ α -cedrene
• Key behaviourally active compounds:
▫ 2-pentadecanone
▫ 2-heptanone
-2.5
-2
-1.5
-1
-0.5
0
0.5
1
1.5
2
- volatiles produced from vegetative
parts and roots can change significantly
following aphid attack
- repellent to subsequent herbivores
- signalling molecules attract natural
enemies
Babikova et al. (2013) Ecology Letters 16: 835-43
Herbivore-Induced Plant Volatiles
Common Mycorrhizal Networks
Hypothesis: Mycorrhizal fungal
networks communicate pest defence
between plants via signalling
through mycelia
Babikova et al. (2013) Ecology Letters 16: 835-43
- arbuscular mycorrhizae are
ubiquitous ancient plant mutualists
-80 % of terrestrial plants
-due to lack of specificity of form
CMNs connecting plants
- CMNs act as conduits of nutrients
and water and also disease
resistance signals
- role in transfer of signals released
in response in insect damage in
multitrophic interactions was
unknown
Babikova et al. (2013) Ecology Letters 16: 835-43
Common Mycorrhizal Networks
Donor
plant with
aphids
No barrier. Root and
hyphal contact
Static 40 µm mesh.
Hyphal contact, no
root contact
0.5 µm mesh. No
hyphal contact, no
root contact
Rotated 40 µm
mesh. No hyphal
contact, no root contact
Roots
AM fungi
Babikova et al. (2013) Ecology Letters 16: 835-43
Experimental mesocosm
No hyphal connection
Receiver plants (no aphids)
0.5 µm 40 µm
rotated
40 µm
static
no
barrier
Donor
(with
aphids)
Timespent[min]
-3
-2
-1
0
1
2
3
Pea aphid
Aphidius ervi
Hyphal connection
Attractive
Repellent
a
a
b
b b
z
z
y y
y
Response of pea aphid and its parasitoid wasp (Aphidius
ervi) to volatiles in olfactometer bioassays: time spent in
treated arm minus control (mean)
3
-2
-1
0
1
2
With
MeS
Without
MeS
Attractive
Repellent
Timespent
[min]
***
-3
amountofmethylsalicylate[ng/ml]
0
2
4
6
8
10
Methylsalicylate
[ng/ml]
Response of pea aphid to volatiles in olfactometer
bioassays: time spent in treated arm minus control (mean)
Babikova et al. (2013) Ecology Letters 16: 835-43
Future directions
Biocontrol with natural enemies
• Natrual enemies of pests can
be released to control them
• Successful in glasshouses e.g.
Almaria in Spain
• Harder to use in open field
environments
New Agri-tech Catalyst project:
Lure-and-kill technology to manage beetle pests of field
beans and peas
4-Methylheptane-3,5-dione
Beauveria bassiana spores adhering to
Entostat particles
Sitona lineatus
adults
♂ produced
aggregation
pheromone that
attracts ♀s and
♂s
The main non-chemical control of aphids is based on parasitoids - either by
release in glasshouses or encouraging natural populations outside.
Biocontrol in edible protected crops 2010/11
(UK)
Aphidius ervi used on 2072 ha:
350 ha tomatoes,
131 ha of cucumbers,
1511 ha of peppers
Data from Fera Pesticide Usage survey (ha are treated hectares and include repeat
treatments)
Aphidius colemani used on 3160 ha:
2235 ha peppers,
487 ha of cucumbers,
426 other vegetables
Aphidius
Aphelinus
Praon
Dendrocerus Alloxysta PachyneuronAsaphes
0
1
2
3
4
5
6
Treated Control
Time(mins)
Significant
Attraction in
Olfactometer
Bioassay
*
Attractant
Introgressing resistance?
at least 10,000 years ago
wild einkorn wheat
(Triticum urartu)
wild goat grass
related to Aegilops
speltoides
Triticum diccocoides,
wild emmer wheat
prehistoric times
goat grass
(Aegilops
tauschii)
Bread wheat,
Triticum
aestivum
Blight resistant potato +Rpi-vnt1
5 fungicide sprays
to protect
No pesticide needed
Aphid resistant wild potatoes
0
10
20
30
40
50
60
70
80
90
100
% Nymph
survival
(after 7 days)
0
2
4
6
8
10
12
Nymphs
produced
(after 24h)
0
0.5
1
1.5
2
2.5
3
3.5
4
4.5
5
Adults settled
(after 24h)
Two of the ten lines tested were very
resistant with 0% aphid survival after 7 days.
Molecular recognition system in insects
Molecular recognition system in plants
Understanding resistance mechanisms
(image courtesy of Saskia Hogenhout)
Conclusion
Intensified agriculture is more
dependent on crop protection
Lush monocultures of high yielding varieties grown
with fertiliser are often more susceptible to pests
Value of Crop Protection – UK wheat
Oerke EC (2006) Crop losses to pests. The
Journal of Agricultural Science 144:31-43.
Value of UK wheat production in 2011
(Defra - Agiculture in the UK dataset) £ 2 210 million
Crop losses with no crop protection
(from Oerke 2006) %
weeds 23 £ 508 million
pests 8.7 £ 192 million
diseases 18.1 £ 400 million
TOTAL £1100 million
0
1000000
2000000
3000000
4000000
5000000
6000000
7000000
8000000
9000000
10000000
Population(1000s);Cereal
Production(x500tonnes)
Source: FAOSTAT
Will Future Demand be
Met?
Consider resources,
planetary boundaries
and climate change
Questions… ?

Insect plant interactions

  • 1.
    Insect-Plant Interactions: adynamic co-evolutionary struggle highly relevant to future food security Toby Bruce University of Nottingham, 12 May 2014
  • 2.
  • 3.
    High yield – onlyif there is adequate crop protection against pests
  • 4.
    Overview of talk: •Vulnerability of agro-ecosystems to pest attack Implications for Food Security • Insect-plant interactions • Techniques for managing pests • Future directions
  • 5.
    Vulnerability of agro-ecosystemsto pest attack Lush monocultures of high yielding varieties grown with fertiliser and irrigation are often more susceptible to pests
  • 6.
    Bruce (2011) J.Exp. Bot. 63: 537-541
  • 7.
    fewer effective pesticides reduced genetic diversity in crops THRIVING PESTS AND HIGHCROP LOSSES climate change can make conditions better for pests less intrinsic resistance to insects and pathogens, and less competitiveness with weeds fertilised crops more nutritious to insects and pathogens broad spectrum pesticides kill natural enemies of pests Bruce (2011) J. Exp. Bot. 63: 537-541
  • 8.
    Impact of Pests,Weeds & Diseases 1965 – staple cereals 1992 – staple cereals 42% lost 36% lost SOURCE: Oerke & Dehne (2004) Crop Prot 23:275–285 Crop losses caused by pests have not decreased since the 1960s, even with use of pesticides
  • 9.
  • 10.
    EC Directive 2009-128 Aframework “Promoting the use of IPM and of alternative approaches”
  • 11.
    Research on “Alternatives”is urgently needed Promoting IPM and use of alternatives 2009/128/EC on the Sustainable Use of Pesticides Reducing risks and impacts of pesticide use on human health and environment
  • 12.
  • 13.
    More complicated thanjust banning pesticides Bees
  • 14.
    “Impacts of pesticideson human health and the environment” … BUT WAIT, some impacts are positive
  • 15.
    Human health ► increasedaffordability of healthy food (e.g. fruit & veg) ► less mycotoxin contamination Environment ► more food can be produced on less land with less water and fertiliser ► more efficient production – less GHG
  • 16.
    • EU yieldsdecline • Increased selection pressure for resistance to remaining pesticides • Food price increase • Food production companies move out of Europe • More land used for agriculture Unintended consequences
  • 17.
    0 1000000 2000000 3000000 4000000 5000000 6000000 7000000 8000000 9000000 10000000 1961 1966 19711976 1981 1986 1991 1996 2001 2006 2011 2016 2021 2026 2031 2036 2041 2046 Population(1000s);CerealProduction(x500tonnes) Will future demand be met? Source: FAOSTAT Bruce (2010) Food Security 2: 133-141 To keep pace with growing demand, global food production needs to increase by an estimated 70% by 2050 [United Nations]
  • 18.
    New directions forAgriculture in the 21st Century Royal Society: “There is a pressing need for the ‘sustainable intensification’ of global agriculture in which yields are increased without adverse environmental impact and without the cultivation of more land”. Royal Society (2009) Policy document 11/09 A second green revolution which is knowledge intensive rather than input intensive?
  • 20.
    So we needto learn more about insect-plant interactions… …these are complicated and dynamic
  • 21.
  • 22.
    The different timescalesassociated with insect-plant interactions Bruce (2014) JXB in press
  • 23.
    DNA code hasevolved over millions of years - subject to mutations that are deleterious or advantageous according to context - gene expression is modulated by epigenetic ‘stress imprints’
  • 25.
    Insect effectors supressor induce plant defence (depending if insect or plant is ‘ahead’) (image courtesy of Saskia Hogenhout)
  • 26.
    Plant defence changesover time (image courtesy of Jurriaan Ton and Marieke van Hulten)
  • 27.
    Defences: traditionally dividedinto “constitutive” and “induced” Primed defence plant is ready to mount quicker or stronger defences when subsequently attacked Induced defence these traits are always expressed these traits need a signal to elicit them - attacking organism - volatile surrogate (plant activator) Constitutive defence Bruce & Pickett (2007) Current Opinion in Plant Biology 10: 387-392
  • 28.
    primed not primed Bruce etal. (2007) Plant Science 173: 603-608
  • 29.
    primed not primed Bruce etal. (2007) Plant Science 173: 603-608
  • 30.
    primed not primed Doespriming leave an epigenetic mark? MeMeMeMeMeMeMeMeMeMe MeMeMeMeMeMeMeMeMeMe Bruce et al. (2007) Plant Science 173: 603-608
  • 32.
    Rapid decisions byinsects about plant colonisation, made in flight Bruce (2014) JXB in press
  • 33.
    How do insectsrecognise host plants? 1. Species-specific odour recognition: taxonomically characteristic volatiles ORN Plant Volatile CNS ORN Plant Volatile CNS Plant Volatile Plant Volatile Plant Volatile Plant VolatileORN ORN ORN ORN Bruce et al. (2005) TRENDS in Plant Science 10: 269 2. Ratio-specific odour recognition: specific combinations of volatiles, distributed generally among plant species
  • 34.
    GC-linked electroantennography • Theinsect antenna is used as a biological detector • Delicate manipulation with microelectrodes to connect an antenna to an electrical circuit • Volatiles (GC effluent) passed over electrophysiological preparation • There is increased depolarisation when the insect responds
  • 35.
    • Insect releasedin the centre • Time spent in treated arm compared with time spent in control arms • Insects released at downwind end • Upwind flight and source contacts recorded Olfactometer Wind-tunnel Behavioural Bioassays
  • 36.
    Helicoverpa armigera • highlypolyphagous • specialises on flowers
  • 37.
    H O H CH3 CH2 H O benzaldehyde phenylacetaldehyde limonenelinalool Bruce & Cork (2001) J. Chem. Ecol. 27: 1119 Helicoverpa armigera
  • 38.
    • host plants limitedto wheat and a few related grasses Sitodiplosis mosellana
  • 39.
    Birkett et al.(2004) J. Chem. Ecol. 30: 1319 3-carene (Z)-3-hexenyl acetate acetophenone Ubiquitous compounds! Sitodiplosis mosellana
  • 40.
    Aphis fabae • specialiston beans • feeds in colonies
  • 41.
  • 42.
    Webster et al.(2010) Animal Behaviour 79: 451 Aphis fabae Timespent(Min) 0 2 - 3 9-comp syntheti c blend * * * * * * * * * * 0.1ng (E)-2-hexanal 1ng benzaldehyde 0.01ng octanal 0.01ng(Z)-3- hexenyl acetate 0.1ng(R)- lianlool 10ngmethyl salicylate 100ngdecanal 0.01ng(S)- germacreneD 0.1ngTMTT
  • 43.
    Attraction to blends Bruce& Pickett (2011) Phytochem. 72: 1605
  • 44.
    Right mix isneeded… Bruce & Pickett (2011) Phytochem. 72: 1605
  • 45.
    Bruce et al.(2005) TRENDS in Plant Science 10: 269 Spatio-temporal resolution of signals
  • 46.
    The challenge ofhost recognition
  • 47.
    Insect responses changeover time (image courtesy of Patrizia d'Ettorre and Mauro Patricelli)
  • 48.
  • 50.
    Orange wheat blossommidge • varies from year to year • was difficult to decide in time which fields needed treating • difficult to control with insecticide
  • 51.
    • Females layeggs, but larvae die when they start to feed • A wound plug is formed at the feeding site due to lignification • Antibiotic action of phenolic acids by the grain Resistant varieties
  • 53.
    Resistant varieties Oakley etal 2005 HGCA Project Report No. 363 Now approx. 60% of UK wheat is resistant Resistant varieties
  • 54.
    Yellow rust onwheat OWBM resistant cultivar (Robigus) Need for multiple resistance
  • 55.
  • 56.
    Monitoring systems Bruce etal. (2007) Pest Man. Sci. 63: 49 • Allow rational use of pesticides • Need based applications save costs and importantly slow down the development of resistance • sex pheromone traps: - provide a solution to the detection problem - enable more accurate and effective spray timing
  • 57.
    Bruce et al.(2007) Pest Man. Sci. 63: 49 • Pheromone traps widely used by wheat growers in the UK
  • 58.
    Decision support systemfor OWBM Bruce & Smart (2009) Outlooks Pest Management 20: 89-92
  • 60.
    • Identified fromwinter host volatiles of lettuce aphid, Nasonovia ribis-nigri • Emitted by insect infested plants: – cotton plants damaged by Spodoptera – potato plants infested with potato aphid • Biological effects observed >24h after spraying plants with cis-jasmone • Non-toxic • No residue left as it is volatile cis-Jasmone O
  • 61.
    • aphids (Sitobionavenae) released at downwind end • numbers settled on wheat seedlings recorded • Fewer aphids colonised cis- jasmone induced plants 0 10 20 30 40 50 60 70 -1 4 9 14 19 24 time after release (h) %settlement control cis-jasmone Settlement bioassay in simulator
  • 62.
    Bruce et al.(2003) Pest Management Science 59: 1031 – 1036 Field plot trial: spray application
  • 63.
    0 0.2 0.4 0.6 0.8 1 1.2 28-May 8-Jun 16-Jun24-Jun 6-Jul MeanNo.Aphids/Tiller * * control cis-jasmone P = 0.036 Bruce et al. (2003) Pest Management Science 59: 1031 – 1036 Wheat Field Trial
  • 64.
    significantly longer timespent on induced plants 0 5 10 15 20 25 Treated Control min Aphidius ervi foraging on cis-Jasmone treated wheat
  • 65.
    CYP81D11 • Insect responsesto CYP81D11 OE plants are similar to the responses observed with CJ treated plants • We still do not know the function of this gene Bruce et al. (2008) PNAS 105: 4553-4558
  • 67.
  • 68.
    Collecting volatiles fromplants with eggs
  • 69.
    Bioassay • insect releasedin the centre • time spent in treated arm compared with time spent in control arms Response to volatiles collected from plants with and without eggs?
  • 70.
    Maize landrace lines Tamiruet al. (2011) Ecology Letters 14: 1075 Parasitoid response - landraces Attracted to plants with eggs
  • 71.
    Volatile profiles -landraces (a) (E)-ocimene, (b) (R)-linalool, (c) (E)-4,8-dimethyl-1,3,7, nonatriene (DMNT), (d) methyl salicylate, (e) decanal, (f) methyleugenol, (g) (E)-(1R,9S)-caryophyllene, (h) (E)-β-farnesene, (i) (E,E)- 4,8,12-trimethyl-1,3,7,11-tridecatetraene (TMTT). Tamiru et al. (2011) Ecology Letters 14: 1075
  • 72.
    New Project: markersfor egg induced volatile emission trait
  • 74.
  • 75.
    HIPV induced byeggs in improved line Improved maize line CKIR12001 emits DMNT when stemborer eggs are laid on it.
  • 77.
    New aphid repellentsidentified • Volatiles from Fusarium graminearum infested wheat are repellent to grain aphid, Sitobion avenae • EAG active compounds: ▫ 2-pentadecanone, ▫ 2-heptanone, ▫ phenyl actetic acid, ▫ α-gurjunene, ▫ 2-tridecanone, ▫ α -cedrene
  • 78.
    • Key behaviourallyactive compounds: ▫ 2-pentadecanone ▫ 2-heptanone -2.5 -2 -1.5 -1 -0.5 0 0.5 1 1.5 2
  • 80.
    - volatiles producedfrom vegetative parts and roots can change significantly following aphid attack - repellent to subsequent herbivores - signalling molecules attract natural enemies Babikova et al. (2013) Ecology Letters 16: 835-43 Herbivore-Induced Plant Volatiles
  • 81.
    Common Mycorrhizal Networks Hypothesis:Mycorrhizal fungal networks communicate pest defence between plants via signalling through mycelia Babikova et al. (2013) Ecology Letters 16: 835-43
  • 82.
    - arbuscular mycorrhizaeare ubiquitous ancient plant mutualists -80 % of terrestrial plants -due to lack of specificity of form CMNs connecting plants - CMNs act as conduits of nutrients and water and also disease resistance signals - role in transfer of signals released in response in insect damage in multitrophic interactions was unknown Babikova et al. (2013) Ecology Letters 16: 835-43 Common Mycorrhizal Networks
  • 83.
    Donor plant with aphids No barrier.Root and hyphal contact Static 40 µm mesh. Hyphal contact, no root contact 0.5 µm mesh. No hyphal contact, no root contact Rotated 40 µm mesh. No hyphal contact, no root contact Roots AM fungi Babikova et al. (2013) Ecology Letters 16: 835-43 Experimental mesocosm
  • 84.
    No hyphal connection Receiverplants (no aphids) 0.5 µm 40 µm rotated 40 µm static no barrier Donor (with aphids) Timespent[min] -3 -2 -1 0 1 2 3 Pea aphid Aphidius ervi Hyphal connection Attractive Repellent a a b b b z z y y y Response of pea aphid and its parasitoid wasp (Aphidius ervi) to volatiles in olfactometer bioassays: time spent in treated arm minus control (mean) 3 -2 -1 0 1 2 With MeS Without MeS Attractive Repellent Timespent [min] *** -3 amountofmethylsalicylate[ng/ml] 0 2 4 6 8 10 Methylsalicylate [ng/ml] Response of pea aphid to volatiles in olfactometer bioassays: time spent in treated arm minus control (mean) Babikova et al. (2013) Ecology Letters 16: 835-43
  • 85.
  • 87.
    Biocontrol with naturalenemies • Natrual enemies of pests can be released to control them • Successful in glasshouses e.g. Almaria in Spain • Harder to use in open field environments
  • 88.
    New Agri-tech Catalystproject: Lure-and-kill technology to manage beetle pests of field beans and peas 4-Methylheptane-3,5-dione Beauveria bassiana spores adhering to Entostat particles Sitona lineatus adults ♂ produced aggregation pheromone that attracts ♀s and ♂s
  • 89.
    The main non-chemicalcontrol of aphids is based on parasitoids - either by release in glasshouses or encouraging natural populations outside.
  • 90.
    Biocontrol in edibleprotected crops 2010/11 (UK) Aphidius ervi used on 2072 ha: 350 ha tomatoes, 131 ha of cucumbers, 1511 ha of peppers Data from Fera Pesticide Usage survey (ha are treated hectares and include repeat treatments) Aphidius colemani used on 3160 ha: 2235 ha peppers, 487 ha of cucumbers, 426 other vegetables
  • 91.
  • 92.
  • 95.
  • 96.
    at least 10,000years ago wild einkorn wheat (Triticum urartu) wild goat grass related to Aegilops speltoides Triticum diccocoides, wild emmer wheat prehistoric times goat grass (Aegilops tauschii) Bread wheat, Triticum aestivum
  • 97.
    Blight resistant potato+Rpi-vnt1 5 fungicide sprays to protect No pesticide needed
  • 98.
    Aphid resistant wildpotatoes 0 10 20 30 40 50 60 70 80 90 100 % Nymph survival (after 7 days) 0 2 4 6 8 10 12 Nymphs produced (after 24h) 0 0.5 1 1.5 2 2.5 3 3.5 4 4.5 5 Adults settled (after 24h) Two of the ten lines tested were very resistant with 0% aphid survival after 7 days.
  • 99.
  • 100.
  • 101.
    Understanding resistance mechanisms (imagecourtesy of Saskia Hogenhout)
  • 102.
  • 103.
    Intensified agriculture ismore dependent on crop protection Lush monocultures of high yielding varieties grown with fertiliser are often more susceptible to pests
  • 104.
    Value of CropProtection – UK wheat Oerke EC (2006) Crop losses to pests. The Journal of Agricultural Science 144:31-43. Value of UK wheat production in 2011 (Defra - Agiculture in the UK dataset) £ 2 210 million Crop losses with no crop protection (from Oerke 2006) % weeds 23 £ 508 million pests 8.7 £ 192 million diseases 18.1 £ 400 million TOTAL £1100 million
  • 106.
  • 107.