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DISEASES AND TREES • What exactly is a disease? It is the outcome of an interaction between a plant and the environment, resulting in an altered physiology of the host • Sustained interaction=biotic • Single event= abiotic What is a pathogen? • Strictly speaking a pathogen is the causal agent of disease • Bacteria • Viruses • Nematodes • Stramenopiles • Algae • Phytoplasmas • Higher plants And of course… fungi • Fungi: saprophytic, symbionts, and pathogens • Polyphyletic group in evolutionary terms – Basidiomycetes Ascomycetes Zygomycets Animals Plants Red algae Brown algae Myxomycetes Fungi… again! • Filamentous somatic (vegetative body) – High surface, good for extrogenous digestion – Good infection structures, infection peg, appressoria, rhizomorphs Chitin in cell wall Nuclear ploidy very unique Reproduction by spores: asexual mode very well represented Small nuclei, but with a lot of plasticity Hyphae, sporangia, and zoospores of P. ramorum Fungi do not photosynthesize • • • • Biotrophic: mycorrhyzae, rusts Endophites: clavicipetaceae, Necrotrophic; most pathogens Saprobes: primary (involved in litter decomposition) Some pathogen roles in natural plant communities • Selection of individuals best suited for the site • Maintenance of genetic diversity and stability in host plant populations • Establishment or maintenance of host geographic ranges • Natural succession • Regulation of stand density, structure, and composition DISEASE!! • Symptoms vs. signs; e.g. chlorosis vs. fruitbody • The disease triangle host-pathogen-environment • Susceptibility of individuals or of portions of individuals • Genetic variability • Basic compatibility (susceptibility) between host and pathogen • Ability to withstand physiological alterations Genetic resistance in host Length of lesion Proportion of stem (mm) girdled (%) Nicasio\ China Camp 42.5a 40.5a 0.71a 0.74a San Diego 27.8b 0.41b Ojai Interior live oak (Maricopa) 25.0b 14.1b 0.47b 0.33b host-pathogen-environment • • • • • Basic compatibility with host (virulence) Ability to maintain diversity: sex vs. no sex Size of genetic pool Agressiveness (pathogenicity) towards hosts Ability to survive without host Chlamydospores of P. ramorum 93 100 0.1 Pr75 Qa Monterey Pr87 Am Marin Pr86b Am Marin Pr86a Am Marin Pr84 Soil Marin Pr82 Vo Marin Pr80 Vo Marin Pr72 Rh Alameda Pr65 Qp Santa Cruz Pr58 Vo Marin Pr50 Qa Sonoma Pr201b Rh Santa Cruz Pr201a Rh Santa Cruz Pr47b Qa Sonoma Pr47a Qa Sonoma Pr35 Qa Sonoma Pr28 Ld Sonoma Pr24 Qa Sonoma Pr22 Qa Sonoma Pr20 Qa Sonoma Pr19 Qa Napa Pr16 Qa Santa Cruz Pr13 Qa Santa Cruz Clone group Pr11b Qa Monterey Pr11a Qa Monterey Pr10 Ld Monterey Pr08 Qa Napa Pr06 Qa Marin Pr05 Ld Marin Pr04 Qk Marin Pr03 Ld Marin Pr88 Uc Sonoma Pr89 Uc Sonoma Pr90 Qa Marin Pr91 Uc Sonoma Pr97 Qa Napa Pr102 Qa Marin Pr103 Ld Marin Pr104 Ld Marin Pr107 Uc Sonoma Pr110 Uc Marin Pr112 Uc Marin Pr113 Uc Marin Pr114 Uc Marin Pr115 Uc Marin Pr116 Uc Marin Pr136 Uc Marin Pr156 Ld Oregon Pr157 Ld Oregon Pr158 Ld Oregon PrJL3.1 Ss Sonoma PrSDC21.6 Ss Sonoma Pr36 Qa Sonoma Pr27 Qa Marin Pr57 Ld Santa Clara Pr70 Vo Marin Pr159 Ld Oregon Pr52a Rh Santa Cruz 67 Pr52b Rh Santa Cruz 89 PrCoen Rh Santa Cruz PrJL3.5.3 Ss Sonoma 96 Pr106 Uc Sonoma Pr71 Qa Sonoma Pr01 Qa Marin PrE9/95 Rh Germany PrE16/99 Vb Germany PrE12/98 Rh Germany PrE104 Water Germany European group PrE69082 Rh Germany PrE9/3 Water Germany PrE14/98-a Rh Germany Pl33 Cl Del Norte Pl16 Soil Josephine P. lateralis Pl27 Tb Del Norte (outgroup) NJ P. lateralis E33LAT E27LAT E16LAT 0.005 changes 4 11 12 13 16 20 22 23a 23b 27 36 63 77 88 98 119 140 195a 195b 201Ca 201Cb 203 240 265 288 326 331 339 344leaves 344stem 351 354 355 357 362 441 463 469 472 478 488 491 492 493 496 507 570 661 662 663 112 291 275 142 664 237 217a 217b coen 477 279 e1 e4 e7 e9 e10 e2 West Coast Europe host-pathogen-environment • • • • • • Temperatures Shading Relative humidity Free standing water pH and any potentially predisposing factors Nutrient status Colony diameter (mm) at 13 days Presence of free water Between 6 and 12 hours required for infection of bay leaves Human activities affecting disease incidence in forests • Introduction of exotic pathogens • Planting trees in inappropriate sites • Changing stand density, age structure, composition, fire frequency • Wound creation • Pollution, etc. Effects of fire exclusion DISEASE: plant microbe interaction • Basic compatibility need to be present • Chemotaxis, thighmotropy • Avirulence in pathogen matched by resistance in host according to the gene for gene model • Pathogenicity factors such as toxins and enzymes important in the infection process Effects of diseases on host mortality, growth and reproduction • Young plants killed before reaching reproductive age • Affect reproductive output • Directly affect flowers and fruits Complexity of forest diseases • At the individual tree level: 3 dimensional • At the landscape level” host diversity, microclimates, etc. • At the temporal level Complexity of forest diseases • Primary vs. secondary • Introduced vs. native • Air-dispersed vs. splash-dispersed, vs. animal vectored • Root disease vs. stem. vs. wilt, foliar • Systemic or localized Progression of cankers Older canker with dry seep Hypoxylon, a secondary sapwood decayer will appear Stem canker on coast live oak Cankers by P. ramorum at 3 months from time of inoculation on two coast live oaks Root disease center in true fir caused by H. annosum Categories of wild plant diseases • • • • • • • • Seed decay Seedling diseases Foliage diseases Systemic infections Parasitic plants Cankers, wilts , and diebacks Root and butt rots Floral diseases Seed diseases • Up to 88% mortality in tropical Uganda • More significant when seed production is episodic Seedling diseases • Specific diseases, but also diseases of adult trees can affect seedlings • Pythium, Phytophthora, Rhizoctonia, Fusarium are the three most important ones • Pre- vs. post-emergence • Impact: up to 65% mortality in black cherry. These diseases build up in litter • Shady and moist environment is very conducive to these diseases Foliar diseases • In general they reduce photosynthetic ability by reducing leaf area. At times this reduction is actually beneficial • Problem is accentuated in the case of small plants and in the case other health issues are superimposed • Often, e.g. with anthracnose,needle cast and rust diseases leaves are point of entry for twig and branch infection with permanent damage inflicted Systemic infections • Viral? • Phytoplasmas • Peronospora and smuts can lead to over 50% mortality • Endophytism: usually considered beneficial Grass endophytes • Clavicipetaceae and grasses, e.g. tall fescue • Mutualism: antiherbivory, protection from drought, increased productivity • Classic example of coevolutionary development: Epichloe infects “flowers” of sexually reproducing fescue, Neotyphodium is vertically transmitted in species whose sexual reproductive ability has been aborted Parasitic plants • True (Phoradendron) and dwarf mistletoe (Arceuthobium) • Effects: – Up to 65% reduction in growth (Douglas-fir) – 3-4 fold mortality rate increase – Reduced seed and cone production Problem accentuated in multistoried uneven aged forests Cankers, wilts, and die-backs • Includes extremely aggressive, often easy to import tree diseases: pine pitch canker, Dutch elm disease, Chestnut blight, White pine blister rust • Lethal in most cases, generally narrow host range with the exception of Sudden Oak Death Root diseases • Extremely common, probably represent the most economically damaging type of diseases • Effects: tree mortality (direct and indirect), cull, effect on forest structure, effect on composition, stand density, growth rate • Heterobasidion, Armillaria, Phellinus weirii, Phytophthora cinnamomi Floral diseases • Pollinator vectored smut on silene offers an example of well known dynamic interaction in which pathogen drives genetic variability of hosts and is affected by environmental condition • Puccinia monoica produces pseudoflowers that mimic real flowers. Effects: reduction in seed production, reduction in pollinators visits POPULATION DYNAMICS Species interactions and diversity Density-dependence • Most diseases show positive density dependence • Negative dependence likely to be linked to limited inoculum: e.g. vectors limited • If pathogen is host-specific overall density may not be best parameter, but density of susceptible host/race • In some cases opposite may be true especially if alternate hosts are taken into account Counterweights to numerical effects • Compensatory response of survival can exceed negative effect of pathogen • “carry over” effects? – NEGATIVE: progeny of infected individuals less fit; – POSITIVE; progeny more resistant (shown with herbivory) Disease and competition • Competition normally is conducive to increased rates of disease: limited resources weaken hosts, contagion is easier • Pathogens can actually cryptically drive competition, by disproportionally affecting one species and favoring another Diseases and succession • Soil feedbacks; normally it’s negative. Plants growing in their own soil repeatedly have higher mortality rate. This is the main reason for agricultural rotations and in natural systems ensures a trajectory towards maintaining diversity • Phellinus weirii takes out Douglas fir and hemlock leaving room for alder Janzel-Connol • Regeneration near parents more at riak of becoming infected by disease because of proximity to mother (Botryosphaeria, Phytophthora spp.). Maintains spatial heterogeneity in tropical forests • Effects are difficult to measure if there is little host diversity, not enough host-specificity on the pathogen side, and if periodic disturbances play an important role in the life of the ecosystem The red queen hypothesis • Coevolutionary arm race • Dependent on: – Generation time has a direct effect on rates of evolutionary change – Genetic variability available – Rates of outcrossing (Hardy-weinberg equilibrium) – Metapopulation structure Frequency-, or density dependent, or balancing selection • New alleles, if beneficial because linked to a trait linked to fitness will be positively selected for. – Example: two races of pathogen are present, but only one resistant host variety, suggests second pathogen race has arrived recently Diseases as strong forces in plant evolution • Selection pressure • Co-evolutionary processes – Conceptual: processes potentially leading to a balance between different ecosystem components – How to measure it: parallel evolution of host and pathogen • Rapid generation time of pathogens. Reticulated evolution very likely. Pathogens will be selected for INCREASED virulence • In the short/medium term with long lived trees a pathogen is likely to increase its virulence • In long term, selection pressure should result in widespread resistance among the host More details on: • How to differentiate linear from reticulate evolution: comparative studies on topology of phylogenetic trees will show potential for horizontal transfers. Phylogenetic analysis neeeded to confirm horizontal transmission NJ 11.10 SISG CA Geneaology of “S” DNA insertion into P ISG confirms horizontal transfer. 2.42 SISG CA BBd SISG WA F2 SISG MEX Time of “cross-over” uncertain NA S BBg SISG WA 14a2y SISG CA 15a5y M6 SISG CA 6.11 SISG CA 9.4 SISG CA AWR400 SPISG CA 9b4y SISG CA 15a1x M6 PISG CA 1M PISG MEX 9b2x PISG CA A152R FISG EU A62R SISG EU 890 bp CI>0.9 A90R SISG EU EU S A93R SISG EU J113 FISG EU J14 SISG EU J27 SISG EU J29 SISG EU 0.0005 substitutions/site EU F NA P NJ Phylogenetic relationships within the Heterobasidion complex Het INSULARE Fir-Spruce True Fir EUROPE Spruce EUROPE True Fir NAMERICA Pine Europe Pine EUROPE Pine N.Am. Pine NAMERICA 0.05 substitutions/site HOST-SPECIFICITY • • • • • Biological species Reproductively isolated Measurable differential: size of structures Gene-for-gene defense model Sympatric speciation: Heterobasidion, Armillaria, Sphaeropsis, Phellinus, Fusarium forma speciales NJ Phylogenetic relationships within the Heterobasidion complex Het INSULARE Fir-Spruce True Fir EUROPE Spruce EUROPE True Fir NAMERICA Pine Europe Pine EUROPE Pine N.Am. Pine NAMERICA 0.05 substitutions/site SEX • Ability to recombine and adapt • Definition of population and metapopulation • Different evolutionary model • Why sex? Clonal reproductive approach can be very effective among pathogens The “scale” of disease • Dispersal gradients dependent on propagule size, resilience, ability to dessicate, NOTE: not linear • Important interaction with environment, habitat, and niche availability. Examples: Heterobasidion in Western Alps, Matsutake mushrooms that offer example of habitat tracking • Scale of dispersal (implicitely correlated to metapopulation structure)---two examples: Heterobasidion in California, and Coriolopsis in Panama From Garbelotto and Chapela, Evolution and biogeography of matsutakes Biodiversity within species as significant as between species S-P ratio in stumps is highly dependent on distance from true fir and hemlock stands . . San Diego White mangroves: Corioloposis caperata Coco Solo Mananti Ponsok David Coco Solo 0 237 273 307 Mananti Ponsok David 0 60 89 0 113 0 Distances between study sites White mangroves: Corioloposis caperata Forest fragmentation can lead to loss of gene flow among previously contiguous populations. The negative repercussions of such genetic isolation should most severely affect highly specialized organisms such as some plantparasitic fungi. AFLP study on single spores Coriolopsis caperata on Laguncularia racemosa Site # of isolates # of loci % fixed alleles Coco Solo 11 113 2.6 David 14 104 3.7 Bocas 18 92 15.04 Coco Solo Coco Solo Bocas David 0.000 0.000 0.000 Bocas 0.2083 0.000 0.000 David 0.1109 0.2533 0.000 Distances =PhiST between pairs of populations. Above diagonal is the Probability Random d istance > Observed distance (1000 iterations). From the population level to the individual • Autoinfection vs. alloinfection • Primary spread=by spores • Secondary spread=vegetative, clonal spread, same genotype . Completely different scales Coriolus Heterobasidion Armillaria Phellinus Recognition of self vs. non self • Intersterility genes: maintain species gene pool. Homogenic system • Mating genes: recognition of “other” to allow for recombination. Heterogenic system • Somatic compatibility: protection of the individual.