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Definitions • Propagule= structure used by an organism to spread or survive • Locus= a physical portion of a chromosome,a gene • Intron= a portion of DNA , a locus that does not code for a protein • Exon= a coding gene Definitions-2 • Alleles= different DNA sequences at the same locus • If a locus has variation in sequence it is polymorphic (many forms) • Polymorphisms are differences in DNA among organisms, the more polymorphisms the easier it is to differentiate organisms • There are more polymorphisms in introns Definitions-3 • Invasive organisms: exotic organism that reproduces and occupies progressively a larger area: – – – – – – – – – Fast reproductive cycle Vectored Hardy Occupy unoccupied niches Different drain on natural resources Make environment favorable for itself and other invaders Linked to disturbances If pathogen , more changes because top of pyramid May hybridize with native species: new taxon is created • MICROBIAL INVASIONS OF NATURAL ECOSYSTEMS: – Cannot be eradicated – Problematic because not noticeable for decades – Can cause limited problems – Can cause major alterations: Because of lack of coevolution between host and pathogen Because they are where similar organisms were not before Introduced organisms • Have a smaller genetic variation than original population • Strong founder effects • Each founder can create a significantly different population if not in equilibrium • Mating will homogenize variation • Mating barriers will increase difference How does DNA help • Identify microbe • Determine whether equally named organism from elsewhere is the same or not • Determine how it is reproducing • Quantify organism • Determine whether it is hybridizing or not Definitions • Phylogeny • Phylogeography • Gene geneaology 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 Nematodes And of course… fungi • Fungi: saprophytic, symbionts, and pathogens • Polyphyletic group in evolutionary terms – Basidiomycetes Ascomycetes Zygomycets Animals Plants Red algae Brown algae Myxomycetes Diversity of fungi, but all have ideal structure for plant infection: – – – – – – – hypha/cord/rhizomorph/infection peg/appressorium Sexual vs. asexual reproduction: can do both Do not photosinthesize Chitin in cell wall Exogenous digestion Indefinite growth Phenotypic plasticity and pleomorphisms Septa Pores Pores CELLS Fungi… again! • ASCOMYCETES • BASIDIOMYCETES • OOMYCETES (fungus-like, water molds) ASCOMYCETES • Yeasts (fermentation, human mycoses) • Truffles, morels • Penicillia (penicillin), Fusaria (potent toxins, damping off of seedlings), molds Ascus is the sack in which the spores are contained Asci can be placed on a disk (apothecium), many apothecia can be together in a fruitbody Morel fruitbody Asci can be carried inside a flask (perithecium) Nectria Ploidy is mostly n BASIDIOMYCETES • Mushrooms. mycorrhizal • Wood decay organisms • Rusts, Smuts • Yeasts and damping off Toadstools and huitacochle are both basidiomycetes Basidium means “club”, it carries the basidiospores (dispersion propagules) naked Most of their life, they are n+n (dikaryons), some rare ones are diploid Oomycetes • Belong to the kingdom Stramenopila, used to be called Chromista • Phytophthora, Pythium, Saprolegnia H20 Oomycetes are not fungi • • • • • • Cellulose in cell wall Ploidy is 2n Result of sexual activity is oospore (2n) Meiosis, somatogamy, caryogamy all occur at the same time • • • Water adapted biology, flagellate phase No septa, holocoenocytic hyphae • • • Chitin in cell wall Ploidy is n, or n+n Result of sexual activity is a spore n Meiosis, somatogamy,caryogamy are usually interupted by vegetative (somatic phase) Better adapted for aerial transmission Septate hyphae Phytophthora • Some important plant pathogens, with very well known history – Phytophthora infestans and the Irish potato famine – Phytopthora cinnamomi and the Jarrah dieback in Australia The Irish Potato Famine • From 1845 to 1850 • Phytophthora infestans • Resulted in the death of 750,000 • Emigration of over 2 million, mainly to the United States. Phytophthora: “plant destructor” • Best known pathogen whose long-distance transport linked to agriculture. – Infected root-stocks – Infested soil – Infected plants 70 species of Phytophthora • 60 until a few years ago, research accelerated, especially by molecular analyses • Differentiated on basis of: – – – – – – Type of sexual intercourse Type of sexual activity Number of hosts Ideal temperature Type of biology Evolutionary history (Waterhouse-Cooke) Hyphae, sporangia, and zoospores of P. ramorum Zoospore Hyphae, sporangia, and zoospores of P. ramorum Most of their lifecycle they are 2n Have cellulose in cell wall Not fungi!!, but look like them because of convergent evolution Fungi do not photosynthesize • • • • Biotrophic: mycorrhyzae, rusts Endophites: clavicipetaceae, Necrotrophic; most pathogens Saprobes: primary (involved in litter decomposition) 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 Cankers by P. ramorum at 3 months from time of inoculation on two coast live oaks 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) 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 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 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 WGR Complexity of forest diseases • At the individual tree level: 3 dimensional • At the landscape level” host diversity, microclimates, etc. • At the temporal level Definitions • Alternatively fixed alleles • Dominant vs. co-dominant markers • Genotype Alternatively fixed alleles: • Two flower species (species 1 and species 2) can have one of two features: – Long (L) or short (s) leaves – Red ( R) or white (w) flowers • Ten individuals from species 1 have the following traits: – LR; LR ;LR ;LR; LR; LR ;LR; sR; sR; sR • Ten individuals from species 2 have the following traits: – sw; sw ;sw ;sw; sw; sw ;sw; Lw; Lw; Lw Which one is the alternatively fixed allele? • Both alleles will differentiate the groups (frequencies are significantly different) • Only one will be diagnostic because alternatively fixed • It is the color of the flower: all flowers in species 1 are R, all flowers in species 2 are w (“all” implies your sampling size is adequate!!) Dominant vs. co-dominant markers • Flowers are red or white or yellow, DNA sequence is agg, agt, agc; DNA fragment is 10, 12 0r 14 bp long (CO-DOMINANT, we know what alternative alleles are) • Flowers are red or non-red, DNA is agg or not, size is 10bp or not. We only see the dominant allele and we express it in binary code 1(present), 0(absent) Limitations of co-dominant markers • Not all non-red flowers are the same, but we assume they are (non red flowers can be orange or yellow) • If at one locus we have a dominant A allele and a recessive a allele, using a codominant marker we would say AA=Aa but not aa. We know in reality AA and Aa are quite different. Genotype • A unique individual as defined by an array of genetic markers. (the more markers you have the less mistaken identity you will have. blonde • Blonde • Blue-eyed • Blonde • Blue-eyed • Hairy • • • • Blonde Blue-eyed Hairy 6 feet tall • • • • • Blonde Blue-eyed Hairy 6 feet tall Missing two molars In the case of microbes it will probably be something like • Genotype A= 01010101 • Genotype B= 00110101 • Genotype C= 00010101 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 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 Removing food base causes infection of roots of other trees Hyphae in plant tissue or soil (shortlived) Melanin-covered rhizomorphs will allow for fungus to move to new food Sources (Armillaria mellea) 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 Janzen-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