S. Savocchia, R. Billones-Baaijens, A. Cimmino, A. Evidente

Slides:



Advertisements
Similar presentations
Ash Dieback - Science Update
Advertisements

Terminology Pathogenicity – ability to cause disease Virulence – the degree of pathogenicity.
Terminology Pathogenicity – ability to cause disease Virulence – the degree of pathogenicity.
MtDNA from Human Teeth Samples (05/19/2006) Gel 1: PCR Products of mtDNA Amplification Using Primer Set 1 Gel 2: PCR Products of mtDNA Amplification Using.
Inflammation Due To RA.
Ufedo Ruby Awodi and Greg L. Challis
Overview of Procedures for Biology Project Amplifying the GAPC Gene from Diverse Plant Species.
Disease Resistant Transgenic Grapevine Constitutively Expresses Vitis vinifera Thaumatin-like Protein SA Dhekney, ZT Li, MM Van Aman, M Dutt, J Tattersall,
Antifungal Properties of Cutaneous Bacteria Found on Rana catesbeiana (North American Bullfrog)
Abstract In the fall of 2006, grapevines from two separate vineyards in Southern New Mexico exhibited leaf scorch and dieback symptoms consistent with.
Specific Task Force COST 873 Determination of the Incidence of the Different Pathovars of Pseudomonas syringae in Stone Fruits Interested countries:Belgium.
Characterization of microbial communities in a fluidized-pellet-bed bioreactor by DGGE analysis As an extension of the fluidized pellet bed operation used.
INTRODUCTION In natural conditions plants are continuously exposed to number of pathogens both biotrophs and necrotrophs. Plants respond to invading fungi.
Grapevine Red Blotch Disease This news brochure is intended to provide guidelines to recognize and diagnose Grapevine red blotch disease. For more information,
Introduction Fusarium wilt, also known as Fusarium yellows, is a vascular pathogen with a broad host range including common bean (Phaseolus vulgaris L.),
Molecular methods for molluscan diseases and marine fish virus (VNN)
M. L. Marenzoni1, F. Passamonti1, K. Cappelli1, S. Capomaccio 2, F
Manufacture of Human Interleukin 13 Protein Using a Prokaryotic Expression System Ryan Rupp, York College of Pennsylvania, Department of Biological Sciences.
PCR and Diagnostics Unique sequences of nucleotides if detectable can be used as definitive diagnostic determinants NA hybridisation is the basis for rapid.
Isolating and Purifying Novel Antibiotics from Soil Bacteria Heather Fisher, Department of Biological Sciences, York College of Pennsylvania Introduction.
Background  The soft shell clam, Mya arenaria, currently occupies a large geographical range in the northern hemisphere.  Soft shell clams are found.
Field Results of White Pine Blister Rust Resistance in Sugar Pine and Western White Pine Seedlings Andrew D. Bower and Richard A. Sniezko USDA Forest Service,
Southern Illinois University
Hypotheses H1: A. americanus will have a lower prevalence of Ranavirus than the spotted salamander, Ambystoma maculatum. H2: Prevalence will be highest.
Expanded PLA2G6 Copy Number Variant Analysis in Patients with Infantile Neuroaxonal Dystrophy (INAD) Danielle Crompton, P. K. Rehal, L. MacPherson, K.
Analysis of the Site-of-Action and Evolution of the Host-Selective Toxin Ptr ToxB Wade Holman Dr. Lynda Ciuffetti’s Lab Department of Botany and Plant.
The prevalence of co-infections among Ixodes scapularis harvested from freshly slain deer Paul N. Williams, Dept. of Biology, York College, York, PA
2. Objective To develop early, sensitive and specific detection methods for P. horiana 3. Materials and methods Two different strategies were explored:
Impact of application of endophytic Bacillus spp
Conclusion We were successful in the design of the siRNA vector with AGT-1 insert and transformation of HT115 cells resulting in the silencing of AGT-1.
Susceptibility to Ranavirus Through Frogs and Salamanders Using q-PCR For Detection and Quantification Thomas Brigman Department of Biology, York College.
Molecular Techniques in Microbiology These include 9 techniques (1) Standard polymerase chain reaction Kary Mullis invented the PCR in 1983 (USA)Kary.
Development and Application of SNP markers in Genome of shrimp (Fenneropenaeus chinensis) Jianyong Zhang Marine Biology.
Pain in the Neck: An Investigation of TSHr Gene Expression in a Population with Abundant Hypothyroidism Wesley Anderson and Ronald Kaltreider, Ph.D. Department.
Background Gregory Fischer Julie Anderson Daniel Herman  Department of Biology  University of Wisconsin-Eau Claire Heterologous expression of MBP1 from.
Department of Plant Pathology  Faculty of Agriculture ESCA OF GRAPEVINES IN SOUTH AFRICA Chana-Lee White Francois Halleen and Lizel Mostert Presented.
Expression of Deer Adenovirus Spike Protein By: Dang Duong.
Synthesis of Biologically Active Thiadiazole Analogs Lillian Nordahl 2006.
Genetic Variation of Renibacterium salmoninarum genes in infected salmonids Jeffrey Burnett HHMI Summer Investigator Dr. Dan Rockey Laboratory Biomedical.
Cosegregation of CAPS with Disease Phenotypes in Barley Abstract This project was designed to identify cleaved amplified polymorphic sequence (CAPS) markers.
GOAL 1: Appropriate Technologies developed and disseminated Objective 1.2 Appropriate management technologies for food and industrial crops developed.
Relationship Between STAT3 Inhibition and the Presence of p53 on Cyclin D1 Gene Expression in Human Breast Cancer Cell Lines Introduction STAT3 and p53.
Microbes and disease Microbes and Disease: Establishing a Connection History and Relevance of Koch's Postulates And The Germ Theory of Infectious Disease.
Rapid detection of resistant Gram- negatives directly from specimens Dr Gemma Vanstone Royal Free Hampstead NHS Trust.
Something to Smile About: DNA Barcoding of St. John’s Wort Herbal Supplements Authors: Justin Rubino, Gus Moody Mentor: Vanaja Zacharopoulos, PhD Friends.
DNA Profiling Using PCR Sara Small, Sarah Petroni, Annelise Yackow.
Unit 1.1 Review MI.
The role of basic research in antibiotic discovery and development Prof Jeff Errington FMedSci FRS Centre for Bacterial Cell Biology, Newcastle University.
Entomopathogenic Fungi on Hemiberlesia pitysophila Chengqun Lv*, Baoling Huang, Mengji Qiao, Jiguang Wei, Bo Ding Entomopathogenic Fungi on Hemiberlesia.
Polymerase Chain Reaction
Introduction Conclusion References Aim of the work
Grape “ESCA” Pruning Disease
Grapevine Trunk Diseases
Overview Wednesday Thursday Labs 12, 13 & 14 due March 7th
The use of Torulaspora delbrueckii yeast strains for the production
The bacterial ecology of the sheep mammary gland
1. Diseased plant identification and coppicing
288 Fungicide resistance profiles and virulence of Stagonosporopsis species isolates from watermelon and melon in eastern China M. Newark1, N. Dufault1,
Allan J. Somers, Elizabeth Rutledge PhD., Salish Kootenai College
Listeria Experiment Name:PCR nr 114_05_listeria_hly
Gilda Carvalho, Cláudia Galinha, Teresa Crespo and Maria Reis
Molecular characterisation of five metalloproteases (Mep1-5)
Phaeomoniella chlamydospora on grapevine
CHESTNUT BREEDING PROGRAM
RESULTS AND DISCUSSION
VWF sequence variants: innocent until proven guilty
Ants Effect on Soil Composition
ETIOLOGY OF PLANT DISEASES. ETIOLOGY OF DISEASE Study of causation or origination Study of causation or origination -Greek word “aitiolologia” -Greek.
(A) The result of a qPCR assay comparing fluorescence with cycle number. (A) The result of a qPCR assay comparing fluorescence with cycle number. The results.
Multiplex PCR assay to detect common resistance determinants in B
Presentation transcript:

S. Savocchia, R. Billones-Baaijens, A. Cimmino, A. Evidente Isolation and characterisation of phytotoxins produced by Botryosphaeriaceae and their role in grapevine trunk diseases PIERLUIGI REVEGLIA PhD Candidate Supervisors: S. Savocchia, R. Billones-Baaijens, A. Cimmino, A. Evidente

Botryosphaeria dieback (BD) INTRODUCTION Botryosphaeria dieback (BD) A serious problem of grapevines worldwide Ranked in the top five priority diseases of the Australian wine grape industry Caused by species of fungi – Botryosphaeriaceae 11 species reported in Australian vineyards Causes cankers, dieback and eventually death of vines Photo: W. Pitt

Photo: L. Mugnai In Europe, the disease also produces foliar symptoms associated with phytotoxins produced by BD pathogens

No foliar symptoms have been observed in Australian vineyards to date Investigate the role of phytotoxins in the pathogenicity and symptom expression of Botryosphaeria dieback pathogens in Australian vineyards

RESEARCH QUESTIONS Do Australian Botryosphaeriaceae spp. produce phytotoxins in vitro and in planta? Are these phytotoxins the same/different from those reported in other countries? Are the phytotoxins involved in pathogenicity and virulence of these pathogens? What is their role in the symptomatology observed in vineyards? What gene families are involved in phytotoxin production?

OBJECTIVE 1: Identify and biologically and chemically characterise the phytotoxic metabolites produced by Botryosphaeriaceae spp. Botryosphaeria spp. Botryosphaeria dothidea Diplodia mutila Diplodia seriata Dothiorella vidmadera Dothiorella sp. Neofusicoccum australe Neofusicoccum luteum Neofusicoccum parvum Spencermartinsia viticola Liquid cultures Liquid extraction TLC analysis Grapevine leaf assays

Production of phytotoxic metabolites PURIFICATION CHARACTERISATION Silica gel column Preparative TLC 1D and 2D NMR spectroscopy ESI/LC MS Reveglia et al., Natural Product Research, 2018 (accepted)

Phytotoxins from Spencermartinsia viticola Reveglia et al., Arab. J. Chem., 2018 doi.org/10.1016/j.arabjc.2018.01.014.

Phytotoxins from Dothiorella vidmadera Reveglia et al., J. Agr. Food Chem., 2018, 66, 1760-1764.

FIRST CONCLUSIONS: ….WHAT’S NEXT? The most virulent and widespread Australian Botryosphaeriaceae spp. are capable to produce phytotoxins in vitro. They can produce already known and novel phytotoxins. ….WHAT’S NEXT? Are the phytotoxins produced in planta ? Are they involved in pathogenicity and virulence of these pathogens? What is their role in the symptomatology observed in vineyards? What gene families are involved in phytotoxin production?

Botryosphaeriaceae spp.: D. seriata (H142a) S. viticola (L19) OBJECTIVE 2: Production and translocation of PMs in artificially-inoculated and naturally-infected plants Botryosphaeriaceae spp.: D. seriata (H142a) S. viticola (L19) Do. vidmadera (L5) Varieties: Chardonnay Cabernet Sauvignon inoculate with mycelia plugs 12 plants per variety-treatment sub-samples will be collected at 6, 9 and 12 months. Naturally infected plants: Tumbaramba and Harden

EXPERIMENTS IN PROGRESS: Isolation Phytotoxins extraction and LC-QqQ analysis DNA extraction and qPCR

OBJECTIVE 3: Investigate the Genetic mechanisms involved in the production of phytotoxins by Botryosphaeriaceae spp. Amplification of (R)-mellein gene, SN477 (Chooi et al. 2015). Designed 7 different primers: NP 1 – NP 7.   DNA extraction  (R)-mellein gene detection  Only NP 1 was amplified for Neofusicoccum parvum, no amplification for Diplodia seriata.  ….WHAT’S NEXT? Purify PCR product and sequence. Design novel primers for D. seriata

ACKNOWLEDGEMENTS