This document discusses the transmission of plant viruses by fungal pathogens. It notes that five species of fungi can transmit over 30 plant viruses. The fungi transmit viruses both internally, carrying the viruses within their structures, and externally, with viruses attached to the outside. This causes virus symptoms in infected plants. Several major crops are economically impacted by these soil-borne viruses. The document reviews different classes of fungi that can transmit viruses, including plasmodiophoromycetes, chytridiomycetes, and oomycetes. It provides details on the fungal pathogen Polymyxa graminis and its transmission of the Wheat spindle streak mosaic virus. Management strategies to control these soil-borne viruses transmitted by fungi include developing resistant
SURVIVAL AND DISPERSAL OF PHYTOPATHOGENIC BACTERIA.pdfOm Prakash
SURVIVAL OF PHYTOPATHOGENIC BACTERIA
Phytopathogenic bacteria have the ability to survive both for longer & shorter periods including soil, seed, diseased crop debris, weed host, and insect vectors.
DISPERSAL OF PLANT PATHOGENIC BACTERIA
To make a healthy plant diseased, the first requirement of a pathogen is to spread its inoculum (primary as well as secondary) from the source of survival to the susceptible parts of a healthy plant. The spread of a plant pathogen within the general area in which it is already established is called “dispersal” or “dissemination”.
Moving the inoculum only a few inches and transporting it for hundreds of miles both constitute its dispersal or dissemination. However, pathogen dispersal is not necessary only for the spread of diseases but also for the continuity of the life-cycle and evolution of the pathogen. Detailed knowledge of pathogen-dispersal is essential to find out effective control measures for diseases because the possibilities of preventing dispersal and thereby breaking the infection chain always exist.
Symptoms of bacterial infection in plants are much like the symptoms in fungal plant disease.
They include
leaf spots,
blights,
wilts,
scabs,
cankers and a
soft rots of roots,
storage organs and fruit,
SURVIVAL AND DISPERSAL OF PHYTOPATHOGENIC BACTERIA.pdfOm Prakash
SURVIVAL OF PHYTOPATHOGENIC BACTERIA
Phytopathogenic bacteria have the ability to survive both for longer & shorter periods including soil, seed, diseased crop debris, weed host, and insect vectors.
DISPERSAL OF PLANT PATHOGENIC BACTERIA
To make a healthy plant diseased, the first requirement of a pathogen is to spread its inoculum (primary as well as secondary) from the source of survival to the susceptible parts of a healthy plant. The spread of a plant pathogen within the general area in which it is already established is called “dispersal” or “dissemination”.
Moving the inoculum only a few inches and transporting it for hundreds of miles both constitute its dispersal or dissemination. However, pathogen dispersal is not necessary only for the spread of diseases but also for the continuity of the life-cycle and evolution of the pathogen. Detailed knowledge of pathogen-dispersal is essential to find out effective control measures for diseases because the possibilities of preventing dispersal and thereby breaking the infection chain always exist.
Symptoms of bacterial infection in plants are much like the symptoms in fungal plant disease.
They include
leaf spots,
blights,
wilts,
scabs,
cankers and a
soft rots of roots,
storage organs and fruit,
This power-point provides general knowledge on the major wheat disease as
Common bunt of wheat
Fusarium head blight of wheat
Loose smut of wheat
Stagonospora nodorum blotch of wheat
Bacterial streak of wheat
Barley yellow dwarf virus of wheat
Leaf rust of wheat
Stem rust of wheat
Stripe rust of wheat
Powdery mildew of wheat
Septoria tritici blotch of wheat
Stagonospora nodorum blotch
Tan spot
Wheat soilborne mosaic
Wheat spindle streak mosaic
Wheat streak mosaic
Cephalosporium stripe
Common root rot
Fusarium root,
crown, and foot rots
Take-all of wheat
The concept of gene for gene hypothesis was first developed by Flor in 1956 based on his studies of host pathogen interaction in flax, for rust caused by Melampsora lini. The gene for gene hypothesis states that for each gene controlling resistance in the host, there is corresponding gene controlling pathogenicity in the pathogen. The resistance of host is governed by dominant genes and virulence of pathogen by recessive genes. The genotype of host and pathogen determine the disease reaction. When genes in host and pathogen match for all loci, then only the host will show susceptible reaction. If some gene loci remain unmatched, the host will show resistant reaction. Now gene – for –gene relationship has been reported in several other crops like potato, sorghum, wheat, etc. The gene for gene hypothesis is also known as “Flor Hypothesis.”
Thirty soil borne viruses or virus like agents are transmitted by five species of fungal vectors i.e soil inhibiting fungi or protists.
Known vectors are from members of class Plamodiophoromycetes in the division Myxomycota & class Chytridiomycetes in the division Eumycota.
This power-point provides general knowledge on the major wheat disease as
Common bunt of wheat
Fusarium head blight of wheat
Loose smut of wheat
Stagonospora nodorum blotch of wheat
Bacterial streak of wheat
Barley yellow dwarf virus of wheat
Leaf rust of wheat
Stem rust of wheat
Stripe rust of wheat
Powdery mildew of wheat
Septoria tritici blotch of wheat
Stagonospora nodorum blotch
Tan spot
Wheat soilborne mosaic
Wheat spindle streak mosaic
Wheat streak mosaic
Cephalosporium stripe
Common root rot
Fusarium root,
crown, and foot rots
Take-all of wheat
The concept of gene for gene hypothesis was first developed by Flor in 1956 based on his studies of host pathogen interaction in flax, for rust caused by Melampsora lini. The gene for gene hypothesis states that for each gene controlling resistance in the host, there is corresponding gene controlling pathogenicity in the pathogen. The resistance of host is governed by dominant genes and virulence of pathogen by recessive genes. The genotype of host and pathogen determine the disease reaction. When genes in host and pathogen match for all loci, then only the host will show susceptible reaction. If some gene loci remain unmatched, the host will show resistant reaction. Now gene – for –gene relationship has been reported in several other crops like potato, sorghum, wheat, etc. The gene for gene hypothesis is also known as “Flor Hypothesis.”
Thirty soil borne viruses or virus like agents are transmitted by five species of fungal vectors i.e soil inhibiting fungi or protists.
Known vectors are from members of class Plamodiophoromycetes in the division Myxomycota & class Chytridiomycetes in the division Eumycota.
This includes detailed explanation with examples on diseases, disease cycle, its importance to study, types of disease cycle and pathogenesis including its components, like, means of survival, dispersal of the plant pathogens, inoculation, type of inoculum, pre-penetration, penetration including different means of entry of pathogens, post-penetration activities of the pathogens inside the plant host and its exit from the host.
Plant viruses transmission through seed, sap and vegetative propagation2013-ag-3253
In this presentation ' Transmission of plant viruses through Seed, Sap and vegetative propagation have been presented. Data is collected primarily from the Mathews plant virology book, however, part of it was also collected from the internet.
Plant Disease Resistant And Genetic EngineeringShweta Jhakhar
Study the adverse effects of different viruses and other fungal diseases on the plants and their growth. Discuss the methods e.g. plant disease resistant and genetic engineering to protect the plants.
Similar to plant virus transmission through the fungal vectors (20)
Richard's entangled aventures in wonderlandRichard Gill
Since the loophole-free Bell experiments of 2020 and the Nobel prizes in physics of 2022, critics of Bell's work have retreated to the fortress of super-determinism. Now, super-determinism is a derogatory word - it just means "determinism". Palmer, Hance and Hossenfelder argue that quantum mechanics and determinism are not incompatible, using a sophisticated mathematical construction based on a subtle thinning of allowed states and measurements in quantum mechanics, such that what is left appears to make Bell's argument fail, without altering the empirical predictions of quantum mechanics. I think however that it is a smoke screen, and the slogan "lost in math" comes to my mind. I will discuss some other recent disproofs of Bell's theorem using the language of causality based on causal graphs. Causal thinking is also central to law and justice. I will mention surprising connections to my work on serial killer nurse cases, in particular the Dutch case of Lucia de Berk and the current UK case of Lucy Letby.
Slide 1: Title Slide
Extrachromosomal Inheritance
Slide 2: Introduction to Extrachromosomal Inheritance
Definition: Extrachromosomal inheritance refers to the transmission of genetic material that is not found within the nucleus.
Key Components: Involves genes located in mitochondria, chloroplasts, and plasmids.
Slide 3: Mitochondrial Inheritance
Mitochondria: Organelles responsible for energy production.
Mitochondrial DNA (mtDNA): Circular DNA molecule found in mitochondria.
Inheritance Pattern: Maternally inherited, meaning it is passed from mothers to all their offspring.
Diseases: Examples include Leber’s hereditary optic neuropathy (LHON) and mitochondrial myopathy.
Slide 4: Chloroplast Inheritance
Chloroplasts: Organelles responsible for photosynthesis in plants.
Chloroplast DNA (cpDNA): Circular DNA molecule found in chloroplasts.
Inheritance Pattern: Often maternally inherited in most plants, but can vary in some species.
Examples: Variegation in plants, where leaf color patterns are determined by chloroplast DNA.
Slide 5: Plasmid Inheritance
Plasmids: Small, circular DNA molecules found in bacteria and some eukaryotes.
Features: Can carry antibiotic resistance genes and can be transferred between cells through processes like conjugation.
Significance: Important in biotechnology for gene cloning and genetic engineering.
Slide 6: Mechanisms of Extrachromosomal Inheritance
Non-Mendelian Patterns: Do not follow Mendel’s laws of inheritance.
Cytoplasmic Segregation: During cell division, organelles like mitochondria and chloroplasts are randomly distributed to daughter cells.
Heteroplasmy: Presence of more than one type of organellar genome within a cell, leading to variation in expression.
Slide 7: Examples of Extrachromosomal Inheritance
Four O’clock Plant (Mirabilis jalapa): Shows variegated leaves due to different cpDNA in leaf cells.
Petite Mutants in Yeast: Result from mutations in mitochondrial DNA affecting respiration.
Slide 8: Importance of Extrachromosomal Inheritance
Evolution: Provides insight into the evolution of eukaryotic cells.
Medicine: Understanding mitochondrial inheritance helps in diagnosing and treating mitochondrial diseases.
Agriculture: Chloroplast inheritance can be used in plant breeding and genetic modification.
Slide 9: Recent Research and Advances
Gene Editing: Techniques like CRISPR-Cas9 are being used to edit mitochondrial and chloroplast DNA.
Therapies: Development of mitochondrial replacement therapy (MRT) for preventing mitochondrial diseases.
Slide 10: Conclusion
Summary: Extrachromosomal inheritance involves the transmission of genetic material outside the nucleus and plays a crucial role in genetics, medicine, and biotechnology.
Future Directions: Continued research and technological advancements hold promise for new treatments and applications.
Slide 11: Questions and Discussion
Invite Audience: Open the floor for any questions or further discussion on the topic.
This presentation explores a brief idea about the structural and functional attributes of nucleotides, the structure and function of genetic materials along with the impact of UV rays and pH upon them.
Professional air quality monitoring systems provide immediate, on-site data for analysis, compliance, and decision-making.
Monitor common gases, weather parameters, particulates.
Deep Behavioral Phenotyping in Systems Neuroscience for Functional Atlasing a...Ana Luísa Pinho
Functional Magnetic Resonance Imaging (fMRI) provides means to characterize brain activations in response to behavior. However, cognitive neuroscience has been limited to group-level effects referring to the performance of specific tasks. To obtain the functional profile of elementary cognitive mechanisms, the combination of brain responses to many tasks is required. Yet, to date, both structural atlases and parcellation-based activations do not fully account for cognitive function and still present several limitations. Further, they do not adapt overall to individual characteristics. In this talk, I will give an account of deep-behavioral phenotyping strategies, namely data-driven methods in large task-fMRI datasets, to optimize functional brain-data collection and improve inference of effects-of-interest related to mental processes. Key to this approach is the employment of fast multi-functional paradigms rich on features that can be well parametrized and, consequently, facilitate the creation of psycho-physiological constructs to be modelled with imaging data. Particular emphasis will be given to music stimuli when studying high-order cognitive mechanisms, due to their ecological nature and quality to enable complex behavior compounded by discrete entities. I will also discuss how deep-behavioral phenotyping and individualized models applied to neuroimaging data can better account for the subject-specific organization of domain-general cognitive systems in the human brain. Finally, the accumulation of functional brain signatures brings the possibility to clarify relationships among tasks and create a univocal link between brain systems and mental functions through: (1) the development of ontologies proposing an organization of cognitive processes; and (2) brain-network taxonomies describing functional specialization. To this end, tools to improve commensurability in cognitive science are necessary, such as public repositories, ontology-based platforms and automated meta-analysis tools. I will thus discuss some brain-atlasing resources currently under development, and their applicability in cognitive as well as clinical neuroscience.
Seminar of U.V. Spectroscopy by SAMIR PANDASAMIR PANDA
Spectroscopy is a branch of science dealing the study of interaction of electromagnetic radiation with matter.
Ultraviolet-visible spectroscopy refers to absorption spectroscopy or reflect spectroscopy in the UV-VIS spectral region.
Ultraviolet-visible spectroscopy is an analytical method that can measure the amount of light received by the analyte.
Earliest Galaxies in the JADES Origins Field: Luminosity Function and Cosmic ...Sérgio Sacani
We characterize the earliest galaxy population in the JADES Origins Field (JOF), the deepest
imaging field observed with JWST. We make use of the ancillary Hubble optical images (5 filters
spanning 0.4−0.9µm) and novel JWST images with 14 filters spanning 0.8−5µm, including 7 mediumband filters, and reaching total exposure times of up to 46 hours per filter. We combine all our data
at > 2.3µm to construct an ultradeep image, reaching as deep as ≈ 31.4 AB mag in the stack and
30.3-31.0 AB mag (5σ, r = 0.1” circular aperture) in individual filters. We measure photometric
redshifts and use robust selection criteria to identify a sample of eight galaxy candidates at redshifts
z = 11.5 − 15. These objects show compact half-light radii of R1/2 ∼ 50 − 200pc, stellar masses of
M⋆ ∼ 107−108M⊙, and star-formation rates of SFR ∼ 0.1−1 M⊙ yr−1
. Our search finds no candidates
at 15 < z < 20, placing upper limits at these redshifts. We develop a forward modeling approach to
infer the properties of the evolving luminosity function without binning in redshift or luminosity that
marginalizes over the photometric redshift uncertainty of our candidate galaxies and incorporates the
impact of non-detections. We find a z = 12 luminosity function in good agreement with prior results,
and that the luminosity function normalization and UV luminosity density decline by a factor of ∼ 2.5
from z = 12 to z = 14. We discuss the possible implications of our results in the context of theoretical
models for evolution of the dark matter halo mass function.
2. INTRODUCTION:
Thirty soilborne viruses or virus-like agents are transmitted by
five species of fungal vectors
Root-infecting fungal-like organisms, the
plasmodiophoromycetes Polymyxa and Spongospora, and
the chytridiomycete, Olpidium, transmit at least 30 plant
viruses.
Some of these viruses apparently are borne internally in,
whereas others are carried externally on the resting spores
and the zoospores of the fungi. On infection of new host
plants, the fungi introduce the virus and cause symptoms
characteristic of the virus they transmit.
3. IMPORTENCE:
A number of plant viruses in different genera are harboured
in and transmitted through the soil.
They are found throughout the world and several of them
cause significant economic losses to major crops.
Vectors for spread of these viruses are fungal‐like organisms
or plant‐parasitic nematodes, but some viruses can also be
exuded from infected roots and transmitted abiotically,
without the aid of a vector.
The long‐term persistence of these viruses in soil, often for
decades, and a lack of efficient control strategies mean that
diseases caused by these viruses are very difficult to control.
Eradication of inoculum from infected soil is almost
impossible, particularly in those parts of the world where
highly toxic soil fumigant chemicals have been banned in
recent years. Soil‐borne viruses are difficult to study and their
biology is relatively poorly understood at present.
5. Different fungal vectors:
Three different classes of fungi will transmit the fungi:
MYXOMYCOTA:
CLASS:PLASMODIOPHOROMYCETES
ORDER:PLASMODIOPHORALES
FAMILY:PLASMODIOPHORACEAE
Eg : Plasmodiophora ,Polymyxa graminis, Spongospora subterranean
P. graminis : Parasitic on wheat and other cereals. Can transmit plant
viruses ( wheat mosaic)
Spongospora: S. subterranea causing powdery scab of potato tubers.
7. CLASS:PLASMODIOPHOROMYCETES
1. These are obligate endoparasites. Commonly called as endoparasitic
slime molds. Thallus is a plasmodium, Zoospores are anteriorly
biflagellte, whiplash type,unequal in size which are called as
Heterokont zoospores. After swimming for some time, the zoospore
CLASS CHYTRIDIOMYCETES:
1. Thallus
(a) primitive members - unicellular, advanced members with coenocytic
mycelium.
(b) endobiotic (fungus which lives with in the cells of host) or epibiotic
(reproductive organs of the fungus on surface of the host, part or
entire thallus with in the host cell).
(c) holocarpic or eucarpic.
2 .Zoospores are posteriorly uniflagellate whiplash type. Inside the
zoospore, around the nucleus cell ribosomes cluster together to
form a nuclear cap.
3. Asexual reproduction is by zoospores produced in zoosporangia.
8. Oomycetes
(water molds, white rusts, and downy
mildews)
• Have nonseptate elongated mycelium.
Produce zoospores in zoosporangia.
Zoospores have two flagella.
• Sexual resting spores (oospores)
produced by the union of morphologically
different gametangia called antheridia
(male) and oogonia (female).
9.
10. VIRUS TRANSMISSION THROUGH FUNGAL PATHOGENS
They are obligate parasites, live entirely within the host cells, have
similar developmental stages including a plasmodial stage, survive in
soil by formation of resting spores or cysts, and produce motile
zoospores to infect roots of the host plants (Alexopoulos et aI., 1996).
Two types of fungal transmission are distinguished based on either
the mode of acquisition or the site of virus retention (Teakle, 1983).
In non-persistent transmission the virus particles are adsorbed to
the surface of the zoospores and are not present in the resting
spores.
whereas in persistent transmission the virus is carried internally
into the resting spore and zoospores. In addition to the
terminology persistent and non-persistent transmission, the terms
in vivo and in vitro transmission are also still in use. Both the sets
of terms have their flaws (Campbell, 1993, 1996), but the terms
persistent/non-persistent appear to be the currently most
accepted and will therefore be used in the following section.
11. Common name Botanical name Source
Barley Hordeum vulgare Barr, 1979; Rush, 2003
Couch grass, Quackgrass Agropyron repens Barr, 1979
Millet Panicum miliaceum Rush, 2003
Rye Secale cereale Barr, 1979; Rush, 2003
Sorghum Sorghum vulgare Rush, 2003
Wheat Triticum aestivum, T. durum Barr, 1979; Rush, 2003
POLYMYXA GRAMINIS
Polymyxa graminis is an obligate root-infecting organism that was
originally described from wheat by Ledingham (1939). Barr (1979)
examined roots of common weeds for the presence of
plasmodiophoraceous fungi, but was unable to identify a natural
reservoir of host species. The recorded hosts for P. graminis are listed
as.
Recorded plant hosts of Polymyxa graminis
12. As previously stated, P. graminis is the vector for WSSMV. This fungus
is also a vector for the following viral diseases
-Aubian wheat mosaic virus
- Barley mild mosaic virus
- Barley yellow mosaic virus
- Chinese wheat mosaic virus
- Indian peanut clump virus (IPCV)
- Oat golden stripe virus
- Oat mosaic virus
- Peanut clump virus (PCV)
- Rice necrosis mosaic virus
- Rice stripe necrosis virus (RSNV)
- Soil-borne cereal mosaic virus
- Soil-borne wheat mosaic virus
- Sorghum chlorotic spot virus
- Wheat yellow mosaic virus
13. The lifecycle of P. graminis is separated into two phases,
1) the production of zoospores, and
2) the production of resting spores, with each phase initiated by
the attachment and penetration of the plant host epidermal or
root hair cells by zoospores
The zoospores form within zoosporangia located within root hairs
or epidermal cells , and the zoosporangia (resting spores) burst
open releasing the short-lived, motile zoospores into the soil
around the roots The zoospores, with the aid of their two
flagella, swim short distances through the soil moisture film
(moisture between soil particles) to infect roots . 25 fungus
invades the root hairs of young susceptible plants in the autumn
during periods of high soil moisture . The zoospore contents
enlarge within the invaded host cell and undergo several cycles of
synchronous mitotic 'cruciform' nuclear divisions and reduction in
nuclear size .
14. The Polymyxa cytoplasm becomes an irregularly shaped
multinucleate sac (plasmodium),which develops into a
zoosporangium, separated from the host cytoplasm by a distinct
cell wall . The secondary zoospores are cleaved apart, become
rounded when they mature, and the septa between zoosporangial
segments disintegrate later developing into resting spore clusters
(Ward et al).
The fungus forms dark clusters of resting spores in the cortical
tissues within the infected root . These spore balls are released
into the soil when the roots decay , and the fungus survive as
clusters of thick-walled resting spores within the soil for more than
15 years in the absence of access to susceptible hosts . The cycle is
restarted when the resting spores germinate to each produce one
biflagellate zoospore , which, in turn, will infect the root epidermal
cells of a suitable plant host , and behaving in the same manner as
zoospores derived from zoosporangia
15.
16. Transmission of Wheat spindle streak mosaic virus by
Polymyxa graminis
WSSMV particles are thought to be present in viruliferous P.
graminis resting spores and zoospores.
Driskel et al. produced direct evidence that WSSMV is internalised
by P. graminis, as WSSMV coat protein was detected in the resting
spores using immunofluorescence
WSSMV cannot be removed from zoospores by washing, or
inactivated by application of antiserum.
P. graminis resting spores remain viruliferous after treatments with
diluted NaOH and HCl (Kanyuka et al., 2003).
The precise mechanism of virus uptake and transfer is unknow, and
it is also not known whether WSSMV is able to replicate within P.
graminis, although indirect evidence suggests that it does not
Zoospores released from viruliferous P. graminis isolates grown in
virus-resistant host plants no longer contain WSSMV, or loose the
ability to transmit the virus .
17. I. Plant resistant varieties.
II. Postpone fall planting
operations past the Hessian
fly-free date, until mid-
October or later. This delay in
planting means that wheat
seedlings will emerge in
cooler soils that are less
favorable to P. graminis
activity and, thus, conditions
will be less favorable for
infection by WSSMV.
III. Improve internal and
surface drainage of fields
where problems exist.
IV. • Avoid crop production
practices that encourage soil
compaction.
Crop rotation as a management
tool to reduce the incidence of
disease
Manipulation of planting dates,
irrigation schedules and paddock
drainage by avoiding exposure of
crops to high risk low-lying wet
areas could reduce virus
incidence .
although many sources of
resistance to WSSMV have been
identified in commercial wheat
varieties and in wild Triticum
species, with the resistance trait
being highly heritable
Polymyxa graminis
wheat spindle streak mosic
virus
18. Peanut Clump virus transmission by Polymyxa graminis under
controlled conditions.
Dieryck B1, Weyns J, Van Hese V, Bragard C, Legrève A.
Author information
Abstract
More than fifteen soil-borne viruses belonging to the Beny-, Bymo-,
Furo- or Pecluvirus, causing diseases on cereals and groundnut, are
transmitted by the soil-borne protist root endoparasite Polymyxo
graminis.
Barley yellow mosaic virus is plant pathogenic virus that causes
the yellow mosaic disease of barleyThe virus is transmitted
via Polymyxa graminis, which is a plasmodiophorid protist,
through the resting spores that survive in the soil, and
eventually zoospores.[2]
19. Spongospora subterranea
Spongospora subterranea is the causal agent of powdery scab on
potato. Though this disease can reduce yield somewhat, the true
economic effect is due to the unmarketable, scabbed appearance
Host range and distribution
Spongospora subterranea can be found worldwide, wherever
potatoes are consistently grown. Other than potato
(Solanum tuberosum), few hosts have been reported. But it is
assumed that solanaceous plants are susceptible including reports
of tomato (Lycopersicon esculentum) and
other Solanumsp. such as nightshade
(S. demissum). Nasturtium sp. has also been reported as a host
20. Ecology and life cycle
Starting with a biflagellate, uninucleate zoospore (n) there are two
paths possible. The zoospore can directly infect the root, encyst, and
form a uninucleate plasmodium which will multiply and develop into
a multinucleate plasmodium, though all nuclei will remain identical
(n). The plasmodium will develop into a thin-walled zoosporangium
containing many new zoospores, all identical .
Resting spores can persist in the soil for up to ten years. The cell
walls contain three layers, aiding in the spore’s longevity. Zoospores
swim through water films and therefore require free water in order
to infect. After emergence, they swim to a host but only survive for
about two hours. Infected seed tubers are a source of inoculum as
well as infested soils where the organism persists for long periods of
time. Symptomatic tubers will, therefore, not be accepted for seed
22. MODE OF TRANSMISSION OF POTATO MOP TOP VIRUS BY
SPONGOSPORA:
Zoospores of Spongospora subterranea introduce the virus into the
potato plant when they infect the roots, stolons and/or young tubers.
Systemic movement of the virus within the plant is generally slow and
erratic. The critical period for infection and development of powdery
scab on tubers is early in the growth cycle, at stolon formation and
tuber set, a period that lasts about 3-4 weeks. Tubers which have
matured beyond this period are resistant to infection by zoospores.
Little or no spread occurs in areas where soil temperatures are above
20°C, or where moisture is lacking. When PMTV-infected tubers are
planted as seed, the virus is passed on as a secondary infection to
only limited numbers of progeny tubers (30 - 50%). Therefore, spread
via the obligate vector, powdery scab is the most important means of
transmission.
23. Resistance and control
Varietal susceptibility of potatoes to powdery scab varies
considerably but no varieties are immune to either powdery
scab or PMTV.
Resistance to powdery scab and to PMTV are genetically
independent traits. , control of PMTV is generally directed at
its vector,Spongospora subterranea.
Using clean seed and minimising the spread of soil and other
forms of contamination restricts spread of the pathogen.
Infection may be reduced by environmental control such as
improved drainage, reduced irrigation during early tuber
development, delayed planting until soils are warmer or drier
and crop rotation with brassicas and other crops.
Seed and soil treatments may also help reduce the spread of
the pathogen from infected seed and reduce numbers of viable
spores.
25. Table 2. Major examples of plant viruses that can be vectored by
zoospores
Virus name Virus host Vector
Tobacco necrosis group (isometric)
Tobacco necrosis
virus
Many hosts O. brassicae
Cucumber necrosis
virus
Cucumber Olpidium sp.
Melon necrotic spot
virus
Melon, cucumber Olpidium radicale
Tobacco stunt type (rigid tubular; double-stranded RNA)
Tobacco stunt virus Nicotiana Olpidium brassicae
Lettuce big vein
26. Barley yellow mosaic group (filamentous)
Barley yellow
mosaic virus
Hordeum spp. Polymyxa graminis
Wheat spindle
streak mosaic
virus
Triticum spp. P. graminis
Oat mosaic virus Avena spp. P. graminis
Wheat yellow
mosaic virus
Triticum spp. P. graminis
Rice necrotic
mosaic virus
Oryza spp. P. graminis
Virus host vector
27. Furovirus group (Fungally transmitted rod-shaped viruses; single-stranded
RNA)
Soil-borne wheat
mosaic virus
Triticum spp. Polymyxa graminis
Beet necrotic
yellow vein virus
Beta spp. Polymyxa betae
Potato mop top
virus
Solanum spp. Spongospora subterranea
Oat golden stripe
virus
Avena spp. P. graminis
Peanut clump virus Peanut P. graminis
Broad bean
necrosis virus
Broad bean P. graminis
28. Olpidium brassicae
Morphology and biology:
Olpidium brassicae Vegetative body is
ameboid, turning into zoosporangium
inside host plant cells.
In host plant the cell can form to 12
zoosporangia. In the spring the zoospores
go to the surface of host plant through
aerotropical channels. Zoospores are
spherical, 3 microns in diameter.
This cycle of asexual reproduction takes
several days. When the sexual reproduction
is taking place, the zoospores leaving
different zoosporangia merge in pairs,
forming biflagellate zygote that fastens to
surface of a host cell after a dormant
period, crusts and turns into cyst.
29. Hosts Infects cabbage and other cruciferous species, and also flax,
cucumbers, tomato, salad, tobacco, and other plants.
Olphidium transmitted viral diseases:
Introduction Olpidium brassicae is a root-infecting plant parasite
and widespread in temperate areas of the world. It was reported
to cause a damping-off disease of cabbage, but the disease may
be caused by other pathogens. O.brassicaes.l. is economically
important because O.brassicaes transmits several destructive plant
viruses, such as Tobacco necrosis virus, Tobacco stunt virus, Tulip
mild mottle mosaic virus, Lettuce big-vein associated virus
(LBVaV)(syn.=Lettucebig-veinvirus), Mirafiori lettuce big-vein
virus
31. MANAGEMENT : control of Olpidium brassicae, the vector of
cucumher systemic necrosis and bean stipple streak virus diseases
Under laboratory conditions cucumber systemic necrosis virus
(CSNV) and bean stipple streak virus (BSSV) were controlled by
fumigation of soils naturally infected with the vector Olpidium
brassicae, using methyl bromide at 9.76 kg/100 m, steam, or an
air-steam mixture.
CSNV and BSSV were not effectively controlled with the soil
fumigants chloropicrin and dazomet.Incorporation of the
fungicides benomyl, captan, and zineb into naturally infected soil
gave some control at high rates of application; copper oxychloride
in the soil had no effect on disease incidence.
Methyl bromide fumigation of naturally infected soils with 12.20
kg/100 m and 14.64 kg/100m eradicated CSNV and BSSV from
commercial glasshouses.
32.
33. SYNCHITRIUM ENDOBIOTICUM
synchytrium is a large genus of plant pathogens within the phylum Chytridiomycota.
Species are commonly known as false rust or wart disease. Approximately
200 species are described
Lifecycle
S. endobioticum is an obligate parasite which does not produce hyphae, but
sporangia containing 200-300 motile zoospores. In the spring, at temperatures
above 8°C and given sufficient moisture, the winter (i.e. long-lived) sporangium in
decaying warts in the soil germinates and releases uninucleate zoospores. The latter
possess a single flagellum enabling them to move in soil water and reach the living
host.
zoospore penetrates the host cell. This becomes greatly enlarged and the enclosed
fungus forms a short-lived, quickly reproducing stage, the summer sporangium,
Under certain conditions of stress, such as water shortage, the zoospores may fuse
in pairs to form a zygote; the host cell in which it forms does not swell but divides.
The host cell wall remains closely attached, forming an outer layer to the resistant,
thick-walled winter sporangium. This matures and is released into the soil from
rotting warts. Winter sporangia can remain viable for at least 30 years and are found
at depths of up to 50 cm.
35. Potato virus x and synchytrium endobioticum :
Both the virus and fungus are presumably of long association with the potato plant
, since both are present in the Andes of south America, the probably home of this
plant ,as well as in many other countries. However the evidence implicating S.
endobioticum as a vector of potato virus x is derived from laboratory studies in
Europe only.
Nienhus and stille found the zoospore suspension taken from potato plant
onfected by both the wart fungus and potato virus x transmitted the virus to shoot
of healthy tubers. No transmission of the virus was achieved if zoospores are
inactivated before testing, or if zoospores from virus free plants were mixed with a
potato virus x suspension.
These results indicate that the virus may be thallus acquired by the potato wart
fungus and carried internally in the zoospores. The soil borne tobamoviruses and
potyvirus which have this relationship can persist in the resting spores of their
vectors of years. Such a persistant relationship would have a useful function in the
soil survival of the rather unstable particles of potato virus x , although the
common carry-over of the virus in the tubers would reduce the importence of this
36. MANAGEMENT
Control Tomato varieties with resistance to PVX (and ToMV) are
available. Consult with your local extension agent to determine
those suitable in your region. Avoid growing tomatoes near potato
fields. Workers who handle potato plants or tubers should change
clothes and wash thoroughly with soap and water before working
with tomatoes. Similarly, tools and equipment used with potatoes
should be thoroughly cleaned before being used in tomatoes.
PVX
37. Pythium ultimum
Pythium ultimum is a plant pathogen. It causes the damping-off and root rot
diseases of hundreds of diverse plant hosts including corn, soybean, potato, wheat,
fir, and many ornamental species.
Ecology and lifecycle
P. ultimum can grow saprophytically and survive as resistant resting structures in
the soil and in root residues. When conditions are favorable, the fungi begin to
infect the seeds and/or root tips of plants. Vegetative hyphae can directly penetrate
plant cells. Mycelial growth and the movement of zoospores can facilitate the
spread of P. ultimum to other susceptible plants. P. ultimum can reproduce both
sexually and asexually. For asexual reproduction, sack-like sporangia will be formed .
Sporangia can directly germinate as hyphae. For sexual reproduction,
an oogonium and a club-shaped antheridium) will be produced. When they contact
with each other, the nuclei of this two structures will form a zygote, then a thick-wall
oospore will be formed. Both sporangia and zoospores are short-lived in soils, while
oospores can be survived in the soil for longer periods. For example, sporangia of P.
ultimum were found to remain viable for 11 months in the, while oospores can
survive in the soil for nearly 12 years.
38. Pea False Leaf Roll and Pythium ultimum
This suspected virus is unusual is being reported to be
transmissible by sap, seed, Myzus persicae and Pythium ultimum (
Thottappilly and schmutterer, 1968)
When the mixture of healthy and diseased seed was planted in the
same pot, the disease incidence was increased from 10-12 % to 50-
60%.
Replanting infested soil without prior steaming resulted in 40%
disease incidence , compared with no infection in steamed soil.
Seed treatment with certain fungicide greatly reduce the spread of
the disease.
The disease spread from diseased to healthy pea seedlings placed
iin water on opposite sides of a petri dish.
Pythium ultimum caused the disease when its mycelium infected
healthy seedlings.
40. Management of disease is challenging but focuses on
sanitation, fungicides, and biological control.
Fungicides include mefenoxam, thiadiazole, etridiazole,
propamocarb, dimethomorph, and phosphonates.
Biological control agents include the bacteria Bacillus subtilis,
Streptomyces griseoviridis, and the fungi Candida oleophila,
Gliocladium catenulatum, Trichoderma
harziamum, and Trichoderma virens.
Effective resistance in the plant host is generally not available.
Sanitation is very important since the pathogen can be easily
introduced into pasteurized soil or even soil-free potting
mixes on dirty tools or pots.
Especially in greenhouses, fungus gnats may also help move
the pathogen from place to place.
42. Acknowledge
I acknowledge the scientists who spent valuable time in
generating information on various aspects of plant pathology
and displayed the same on internet for use by teachers and
researchers.
CONCLUSION:
By understanding the different viruses are transmitted by
fungi we recommend the proper chemical to control fungi and
vectors in crop management there by increasing yield and
income
we concluded that research on fungi which transmit viruses is
not sufficient to identify the correct symptoms of disease and
favourable conditions. We need study on the soil born viruses
which are transmitted by fungi
43. REFERENCE:
HANDBOOK OF PLANT VIROLOGY – Jawaid A.Khan, Jeanna Dijkstra
PLANT VIRUS VECTORS, EPIDEMELOGY AND MANAGEMENT-S.Mukhopadhyay
link.springer.com/chapter/10.1007%2F978-3-540-78826-3_24
www.sipav.org/main/jpp/volumes/0305/030501.pdf
hillagric.ac.in/.../Lect.%207%20Pl%20Path%20502%20Plant%20virus%...
www.annualreviews.org › ... › List of Issues › Volume 34, 1996
onlinelibrary.wiley.com/doi/10.1002/9780471729259.../pd
Vectors of Plant Pathogens
edited by Kerry F. Harris, Karl Maramorosch
MOLECULAR BIOLOGY OF PLANT VIRUSES edited by c. L. Mandahar Botany
Department Panjab University, India
COMPARATIVE PLANT VIROLOGY SECOND EDITION
ROGER HULL Emeritus Fellow Department of Disease and Stress Biology