Title: Summary of third class
1Summary of third class
- Unique DNA sequence can be used to identify
target organism by - Designing a taxon specific assay (usullay
employing primers that will only bind to target) - Using BLAST search engine
- Placing sequence in own database and perfor
phylogeographic analysis - DNA loci need to be variable among species and
relatively similar among individuals of the same
species. If sequence (allele) is completely
fixed within one species and variable between
species we call that an alternatively fixed
allele
2Summary of third class
- DNA is amplified through the PCR reaction before
being analyzed (sequenced, electrophoresed,
RFLPed) - With TS-PCR presence of amplified fragment
(amplicon) is a sign that target is present - However size of amplicon is still and normally
used to confirm this - Size is determined through gel or capillary
electrophoreses, by running a size standard
3Summary of third class
- DNA sequences are co-dominant, a single locus
may be sufficient for species determination, but
multiple independent loci are needed to define
individual strains or genotypes - When using DNA information to build trees we
need to know the statistical support for the
clades we see - Too much variation is not necessarily good
because of homoplasy.
4Summary of third class
- P. ramorum case European and North American
individuals are not directly connected because
they are placed on two distinct and strongly
supported clades. If one of them was derived
from the other it would be nested within it - P. ramorum limited genetic diversity in
California when compared to worldwide nursery
pops indicates it is introduced in California
remember that term of comparison is needed as
some microbes display almost no variation
worldwide - Exotic microbes go through a genetic bottleneck
and a strong founder effect.
5- US forest isolates clearly distinct from EU
nursery isolates, also have different mating type - Isolates from nurseries in WA, OR, BC both of
the US and EU types - Potential for XXX sex and recombination in US
nurseries - US forest population is genetically very
homogeneous, trademark of an introduced species
6What about the two readings?
- Heterobasidion
- Armillaria
7The entire genome was sequenced in less than 3
years since discovery of organism
12 SSR loci (di- and tri- repeats identified)
Loci selected to be polymorphic both between
and within continental populations 500
representative isolates analyzed
CCGAAATCGGACCTTGAGTGCGGAGAGAGAGAGAGACTGTACGAGCCCGA
GTCTCGCAT
8Mating Type A1 A2 A2
Growth Rate Fast Slow Fast
9Terminology Genotype Lineage Population
10Results of 1st microsatellite study
- There actually three distinct (genotypically and
phenotypically) lineages of P. ramorum - Very low diversity in US forests (microsats
cannot discriminate among individuals, clonality
confirmed), only one lineage - Several genotypes but only one lineage in EU
nurseries - Three lineages in US nurseries
11Was the pathogen first in US forests or in US
nurseries?
Slide 12
12Was the pathogen first in US forests or in US
nurseries?
Slide 12
nurseries
forests
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14From the genome we learned
- P. ramorum in the US comes from a sexually
reproducing population (heterozygosity rate in
its 2n genome) - P. ramorum appears to have sex only periodically
and then reproduces clonally
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17Co-linearity of P. ramorum and P. sojae
18Further application to track invasion
- First microsatellites could not differentiate
among genotypes, because of clonality - We checked in more variable areas (areas with no
colinearity for instance ) for microsatellites
that would differentiate genotypes - Ability to differentiate even between very
closely related clonal genotypes would allow us
to study patterns of introduction, potential for
local differentiation or evolution, understand
pathogen spread by looking at spread of genes
19We found hypervariable microsatellites that could
do the jobso what did we do?
20Genotyped approximately 300 isolates from 17
forest sites and from a number of nurseries
21Distribution of Phytophthora ramorum in December
2002
22Distribution of Phytophthora ramorum in December
2006
Map from www.suddenoakdeath.org M. Kelly,
UC-Berkeley
23We stratified our sampling in the following
way1- Sites gt 10 years2- Sites infested for
10-5 years 3- New infestations
24Infestations differ in composition of genotypes,
even if they are in the same county. ( 13 sites,
Contingency analysis Plt0.0001)
2
1
6
2
2
25High diversity (high Fst) indicates migration
among sites is limited. Dynamics of medium range
spread based on rare successful movement of
infectious propagules, followed by local
differentiation
26Overlap of genotypes between nursery and old
wild populations
Marin
P0.16, Fst almost 0
Santa Cruz
Sonoma
Populations are at tens of miles from one another
27When we constructed an unrooted cladogram using
PHIst
New sites
Intermediate sites
Nurseries and old sites
28Mantel test among all individuals. Morans I vs
ln (geographic distance)
29DNA applications to study ecology of pathogen
- Culturing and direct observation unreliable
- DNA based test doe not mean organism is alive or
active - Reverse transciptase PCR targets messanger RNA
and allows for quantification of signal, we can
actually study whether organism is active (many
copies of mRNA), alive but dormant (few copies),
or dead no copies
30Mt DNA
- gtP. ramorum COXI (925bp)
- TTAATTTTATTTCAACTATTTATAATATGCGAGCTCCTGGTTT
AAGTTTCCATAGATTACCTTTATTTGTTTGGTCTGTATTAATTACAGCTT
TTCTTTTATTATTAACATTACCTGTTTTAGCTGGTGCAATTACTATGTTA
TTAACTGATAGAAATTTAAATACTTCTTTTTATGATCCATCAGGCGGAGG
TGATCCTGTGTTATATCAACATTTATTTTGGTTTTTTGGTCACCCTGAAG
TTTATATTTTAATTTTACCAGCATTTGGTATTATTAGTCAAGTTTCTGCA
GCTTTTGCTAAAAAAAATGTATTTGGTTATTTAGGTATGGTTTATGCTAT
GTTATCTATAGGTTTATTAGGTTCTATTGTTTGGGCACATCATATGTTTA
CTGTAGGTTTAGATGTAGATACTAGAGCTTATTTTTCTGCAGCTACTATG
ATTATTGCTGTACCTACAGGTATTAAAATTTTTAGTTGGTTAGCTACTTT
ATGGGGTGGTTCATTAAAATTTGAAACACCTTTATTATTTACCTTAGGTT
TTATTTTATTATTTGTTATGGGTGGAGTAACA
Ram Reverse
COX I 925 bp
Ram Forward
Amplicon 138 bp
Cytochrome c oxidase is large transmembrane
protein, found in the mitochondrion, which acts
as the terminal enzyme of respiratory chain.
31RT-PCR from symptomatic bay leaves (China Camp
Oct-2005)
32EFFECTS OF SOD
- Ecological disaster tanoaks at risk of
extinction change in forest structure and
composition - Biota linked to vanishing trees highly impacted
- Hydrogeological impact
- Climate and nutrient cycle impact
- Hazard to humans and properties
- Added cost because of intense regulation of
pathogen cleanisng, prescriptions, testing - Affecting trade
33Emergent Disease
- Previously unknown pathogen
- Unknown Biology and Epidemiology
- Ecology of California coastal forests little
understood
ALL RESEARCH USEFUL FOR MGMT.
34Adaptive management
- Need to act even with imperfect knowledge
- Mgmt. changes as understanding increases
- Adapt strategies from similar situations
- Strategies may vary depending on situation
- Real world testing?
35Scale Dependent Research and Management
- Individual tree protect individuals but do
little to slow epidemic, timing and understanding
of specific pathways essential - Landscape protect a stand, make local
environment unfavorable to pathogen, scaling
essential - Regional to continental change distribution and
composition of species, prevention and modeling
essential
36Introduction phase 1- Escape of pathogen
from Infected nursery plants at two locations
Mount Tamalpais (Marin County), and
Scotts Valley (Santa Cruz County) 2- Nurseries
and two sites have identical strain composition,
but distance between sites is impossible for
natural spread of organism
37Rhododendron In EU mostly a nursery issue, but
also present in nurseries in US and Canada
Stem canker
Leaf necrosis
38Bay/Oak association
Coast Live Oak (no sporulation)
Bay (highly infectious)
Canker margin in phloem
Bleeding canker
Sporangia
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40Bimodal spread pattern50 reduction at 10 m200
m in absence of wind1-5 km in presence of
strong winds
Scale of dispersal essential to scale control
41ERADICATION in OREGON
42Jay Smith Road
- 50 acres, 4 units
- Thinning
- Thinning Burning
- Monitor sprouts and new seedlings over 2 years
- Monitor rainwater and soil populations of P.
ramorum
Source Y. Valachovic, C. Lee
43Before
After
44Thinning and inoculum load
45AgriFos and PentraBark Topical Application
46Zoospore Inoculator for P. Ramorum
Zoospores are in Direct Contact with Tree for 24
hrs.
Grafting Wax Creates a Water Tight Seal
47Agrifos vs. Azomite Treatments (efficacy 1 - 24
months)
a
a
Canker Size (mm)
b
48Statewide tanoak resistance program
Tanoak Petiole Plug Assay
Less susceptible
More susceptible
49Some conclusions
- Understanding of biology and ability to detect
pathogen essential for individual treatment of
trees and early eradication - Scale of dispersal makes landscape level control
and eradication difficult because spread from
hotspots can coalesce (a couple of miles) - Regional level management difficult because
costly in these mostly unmanaged forests disease
management has to fit with overall goals of
landowner
50Bicycles for Cargo Transport
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