Step 1: Written observation of the symptoms of the fruit and signs of the pathogen.
Symptoms and signs
The fruit that is examined in this study is a strawberry. The infected strawberry in displayed in figure 1, appears to be fully covered in mycelial growth. Mycelial consists of white filaments also known as hyphae (mould), which seems to be growing on the strawberry. Within the branched hyphae there are multiple black spores that surround the fruit. Although the fruit appears to be shriveled, there appears to be an access amount of liquid which remains on the parafilm and the inner components of the fruit are moist and soft. The multiple stages of mycelial that are growing on the fruit in figure 1, demonstrates signs of the pathogen. The
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Sterilize the spatula by holding it over the flame, after cooling proceed to cut 5 mm square block of agar from the unioculated petri dish. Following this step the square of agar was transferred to the centre of the microscope slide. Next, using both the sterile forceps and a scapula a collection of a portion of mycelia mass from the culture and inoculate on both the top and the bottom of the agar cube. After re-flaming and cooling of the spatula and forceps, a sterile cover slip was carefully placed on the upper inoculated surface over the infected agar. The final process includes incubating the closed dish at room temperature until growth was visible (approx. 2-4 days). If there is no visible growth, allow for mould to grow for another 24-48 hours. The closed dish of culture was placed in the fridge until next the session. The new healthy fruit appears to be a ripe, rich red color, with a solid/firm texture and no signs of …show more content…
The slide appears to attain dark hyphae fruiting bodies at the tips. The appearance of spores, sporangiospore and sporangium are visible. Rhizopus is identified in the microscopic analysis of the fruit. The rhizopus is seen as the branching hypha ends in figure 4. The microscope slide demonstrates density of hyphae around the mid region.
Do the Pure Culture Symptoms Observations Match? At the beginning of the experiment, the samples had visible hyphae and black fruiting bodies, which appear to be visible in the re-infected fruit samples. Both the samples have distinct zones of mycelial growth and colonization. In the fruiting and productive zones both samples appear to have increased hyphae density. When samples are analyzed in the microscope they both have evident clusters of sporangia and conidia. When comparing the infect fruit samples it is clear that both the original and re-infected samples are quite similar results including signs and symptoms.
Step 5: Re-isolation of the pathogen in a pure culture and compare to original
This process is done by using several techniques. In the microbiology lab students were given numbered specimens. The number for this report will be specimen number # 24. The Unknown specimen # 24 was to be identified.
The simulation on figure \ref{Fig:3} show the behaviour of the system of susceptible fruits, infected, ascomata and ascospores evolving in time. When the probability of the transmission $\beta$ was varying from $0.001055$ to $0.5$ the observation made agreed with $R_0$ on the basis that as $\beta$ increases so does the infective classes, that is, $I ~~and~~ P_A$ and inversely affects non-infectious $S ~~and~~ P_0$ population classes, during the initial stages the infected class of the host increased at an increasing rate up to a peak of 20000 and ascospores increased up to about 12000 where it reached its carrying capacity then both gradually decrease. We also observed that as the infectious classes were increasing, non-infectious classes were
Question 14: Given what you know about the transmission of cyclosporiasis, on what cultivation or harvesting practices would you focus in the investigation of the raspberry-producing
My results were not what i expected, the results I got were a different fungus than I originally Isolated. The fungus were similar in color and how they grew but the end result was very different looking. Both the fruits I inoculated were the same fungus, and the first fungi inoculation and subculture were the same. The fruit had gotten contaminated before I covered them and it changed my results.
Ascospores can be produced with the help of 0.1 inch of rainfall and temperature of about 500 F. Ascospores are dispersed with the help of wind and primary infection takes place on the host. Secondary infection occurs through conidia, which are produced on infected plant parts (lesion) and dusty powdery growth appears on the surface with whitish mycelial growth. Conidia cause the secondary infection throughout the growing season. Infection can takes place in the temperatures from 590 F to 900 F, but the temperature from 680 to 770 F are optimum temperature for infection. Fungus can overwinter as mycelia inside the dormant bud, which produced disease shoot after breading bud. High relative humidity is conducive for conidia production, but rainfall is not good for infection that reduces the infection by this pathogen (Carrol et al.
Fungi have emerged over the past several decades as major contributors to human disease.(1, 2) As populations of immunocompromised and/or hospitalized patients continue to increase, so will the incidence of invasive fungal infections. A recent study reported that fungemia in the United States increased by 207% between 1979 and 2000.(3) Moreover, as the populations at risk for fungal infection continue to expand, so will the spectrum of pathogens capable of infecting those individuals.
Mushrooms are a good cash crop. It is easy to grow and is brimming with protein, B vitamins and minerals. They even have medicinal properties. Time between spawning and harvesting can be as short as three weeks. Furthermore, after the cultivation, you can still use the substrate as a good soil conditioner. Generally the oyster, shiitake and wood ear mushrooms cultivated .Although many other types of mushrooms can be grown, we have chosen oyster the ones that can easily be cultivated with using appropriate technology. When we choose to grow mushroom we should know the basic knowledge about mushroom. The biology, morphology, species, temperature ranges for fruiting, and market to sell.The life cycle of mushroom (Fungi) multiply by producing millions and millions of spores. When a spore settles in a suitable environment, it can germinate and branch to form a mycelium. When two sexually compatible mycelia meet, they may fuse to form a so-called secondary mycelium, which is capable of forming fruiting bodies.
During 2013-2014 growing seasons, forty three isolates of Pestalotiopsis spp were recovered from guava leaves and fruits showed scab symptoms from different regions in EL-Beheira governorate. Five Pestalotiopsis species were recognized according to the morphological characteristics of fungal colony (Colony color, Size and number of acervulii) and conidia (Length, Width, and Color of median cells, Length and the number of apical and basal appendages); they were P. psidii, P. microspora, P. clavispora, P. neglecta and Pestalotiosis sp. All the isolates recovered were pathogenic to the cv. Balady of guava fruits. However, P.psidii isolates were the most highly pathogenic followed by P. neglecta, P. clavispora, P. microspora and Pestalotiopsis sp, respectively. RAPD-PCR analysis using five random oligonucleotide primers revealed DNA fingerprints and considerable variations were revealed with primers tested. Bar marker showed a common band for all Pestalotiopsis isolates and species at 500bp, while BAQ, 18 and A9B4 exhibited banding pattern similar for all isolates of the same species which were different from that of the other species. Scab disease control of infected fruits by chitosan as s natural product was tested. The in vitro 2.5% chitosan application significantly inhibited the growth of Pestalotiopsis spp tested by 86.53% on agar plates.
Morphology: Encrusting thallus of 170 – 190 µm in diameter. It is rarely recorded as fruticose growth forms.
Analyses of macro and micro-morphological characteristics accommodated the isolate F.2.1.4 in the genus Myceliophthora due to the presence of spreading colonies with dense aerial mycelium and blastic conidia often borne in ampulliform swellings (Van Oorschot, 1980). Particularly, this isolate produced pulverulent pale mycelium, obovoid conida measuring 5.65-7.91 x 3.39-4.52 μm as well as conidia walls finely ornamented. Based on such
Xanthomonas axonopodis is the bacterium which causes the sickness named Citrus canker that influences Citrus species. Because of contamination sores on the leaves, products of the soil can been seen on citrus trees including grapefruits,
Protozoa are unicellular aerobic eukaryotes. They have a nucleus, complex organelles, and obtain nourishment by absorption or ingestion through specialized structures. They make up the largest group of organisms in the world in terms of numbers, biomass, and diversity. Their cell walls are made up of cellulose. Protozoa have been traditionally divided based on their mode of locomotion: flagellates produce their own food and use their whip-like structure to propel forward, ciliates have tiny hair that beat to produce movement, amoeboids have false feet or pseudopodia used for feeding and locomotion, and sporozoans are non-motile. They also have different means of nutrition, which groups them as autotrophs or heterotrophs.
Hyphae are very tiny and grow at the tip, dividing repeatedly along their length which create long, branching chains. The Hyphae will keep growing until a network of threads is formed. This is called a mycelium. It is less common yet still possible for fungi to produce spores sexually. Two mating cells from hyphae of different strains of fungi can fuse together and form a spore stalk, this is mating. The spores eventually burst causing the spores to drop in the same area or be carried by wind or rain to a new area. They will then germinate like seeds.
Puccinia psidii is a fungi, indigenous to Brazil. In 1884, it was first observed in the guava fruit and hence was named as guava rust. Later in 1934, the disease spread to Central America and Caribbean island causing a major devastation. The reason behind this spread is still unclear (Tommerup et al., 2003). This fungi is found in China, Southern and Central America, Japan, Africa and Australia (Jolanda Roux et al., 2013). It is notable that a similar type of fungi, ‘Puccinia asparagi’ causing rust entered New Zealand from Australia in 1973 (Viljanen et al., 2006).
They then gradually spread and form ring of necrotizing tissue (Sedlakova et al 2011). At first the plant will look healthy before the lesions are visible on the outside. This is also a challenge for the farmers because they will not know if their produce is unhealthy until it is visible. By the time they can cut of the plant the disease would have spread to the neighboring plants as well. P. infestans are produced through sexual and asexual mating. The two mating types are known as A1 and A2 ( Nowicki et al 2012). When mycelia of both types interact they produce oospores sexually. Mycelia is the branched filament of fungi (Encyclopaedia Britannica 2017). Oospores are spores that have a thick coating that allows them to survive harsh environmental conditions for a long period (Nowicki et al 2012). When both these types mate they produce a worse isolate compared to only if A1 mating occurs. The production of these more harmful isolates was detected by researchers in United States which has made controlling this pathogen more difficult (Fall et al 2015). Sporangia of P. infectans also produce zoospores through asexual mating. Sexual and asexual mating is influenced by the environment. Asexual is mating is encouraged when the weather is a warmer and oospores are produced in cooler weather hence for the thick coating of oospores.