Friday, 26 September 2014

INTRODUCTION TO MYCOLOGY


The term "mycology" is derived from Greek word "mykes" meaning mushroom. Therefore mycology is the study of fungi. The ability of fungi to invade plant and animal tissue was observed in early 19th century but the first documented animal infection by any fungus was made by Bassi, who in 1835 studied the muscardine disease of silkworm and proved the that the infection was caused by a fungus Beauveria bassiana.
In 1910 Raymond Sabouraud published his book Les Teignes, which was a comprehensive study of dermatophytic fungi. He is also regarded as father of medical mycology.
Importance of fungi: Fungi inhabit almost every niche in the environment and humans are exposed to these organisms in various fields of life.
General properties of fungi:
·         They are eukaryotic; cells contain membrane bound cell organelles including nuclei, mitochondria, Golgi apparatus, endoplasmic reticulum, lysosomes etc. They also exhibit mitosis.
·         Have ergosterols in their membranes and possesses 80S ribosomes.
·         Have a rigid cell wall and are therefore non-motile, a feature that separates them from animals. All fungi possess cell wall made of chitin.
·         Are chemoheterotrophs (require organic compounds for both carbon and energy sources) and fungi lack chlorophyll and are therefore not autotrophic.
·         Fungi are osmiotrophic; they obtain their nutrients by absorption.
·         They obtain nutrients as saprophytes (live off of decaying matter) or as parasites (live off of living matter).
·         All fungi require water and oxygen and there are no obligate anaerobes.
·         Typically reproduce asexually and/or sexually by producing spores.
·         They grow either reproductively by budding or non-reproductively by hyphal tip elongation.
·         Food storage is generally in the form of lipids and glycogen.
Classification of fungi:
Fungi were initially classified with plants and were a subject of interest for botanists; hence the influence of botany can be seen on their classification. In 1969 R.H Whittaker classified all living organisms into five kingdoms namely
Monera, Protista, Fungi, Plantae and Animalia.
But there are alternate and more practical approaches, one based on sexual reproduction and the other based on morphology of the thallus (vegetative structure).
Based on Sexual reproduction:
v  Zygomycetes: which produce through production of zygospores.
v  Ascomycetes: which produce endogenous spores called ascospores in cells called asci.
v  Basidiomycetes: which produce exogenous spores called basidiospores in cells called basidia.
v  Deuteromycetes (Fungi imperfecti): fungi that are not known to produce any sexual spores (ascospores or basidiospores). This is a heterogeneous group of fungi where no sexual reproduction has yet been demonstrated.
ZYGOMYCETES
Commonly known as bread moulds, these are fast growing, and terrestrial, largely saprophytic fungi. Hyphae are coenocytic and mostly aseptate. Asexual spores include chlamydoconidia, conidia and sporangiospores. Sporangiophores may be simple or branched. Sexual reproduction involves producing a thick-walled sexual resting spore called a zygospore.
Medically important orders and genera include:
·         Entomophthorales: Conidiobolus and Basidiobolus are involved in subcutaneous zygomycosis
·         Mucorales: Rhizopus, Mucor, Rhizomucor, Absidia and Cunninghamella are involved in subcutaneous and systemic zygomycosis (formerly called Mucormycosis)
BASIDIOMYCETES
They exist as saprobes and parasites of plants. Hyphae are dikaryotic and can often be distinguished by the presence of clamp connections over the septa. Sexual reproduction is by the formation of exogenous basidiospores, typically four, on a basidium. Occasional species produce conidia but most are sterile.
Genera of medical importance include:
·         Teleomorph of Cryptococcus neoformans, which is Filobasidiella neoformans
·         Agents of basidiomycosis such as Coprinus and Schizophyllium
·         Mushroom poisoning by Aminita, Lepiota, Coprinus and Psilocybe etc.
ASCOMYCETES
They exist as saprophytes and parasites of plants. Hyphae are septate with simple septal pores. Asexual reproduction is by conidia. Sexual reproduction is by the formation of endogenous ascospores, typically eight, in an ascus.
Medically important genera include the:
·         Teleomorphs of known pathogenic fungi e.g. Arthroderma (of Trichophyton and Microsporum), Ajellomyces dermatitidis (of Blastomyces dermatitidis), Pseudallescheria boydii (of Scedosporium apiospermum)
·         Agents of mycetoma, like Leptosphaeria
·         Agents of black piedra, like Piedraia hortae.
DEUTEROMYCETES
Deuteromycetes are also known as Fungi Imperfecti because of absence of sexually reproducing forms (teleomorph or perfect stage). As their teleomorph continue to be discovered, they would be classified among the previous categories, until then this remains an artificial and heterogeneous group.
There are three classes of Fungi Imperfecti.
·         Blastomycetes: These include asexual budding forms of Cryptococcus, Candida, Torulopsis and Rhodotorula. Depending on the presence of melanin in their cell walls, they may be non-dematiaceous or dematiaceous.
·         Hyphomycetes: A class of mycelial moulds which reproduce asexually by conidia on hyphae. Hyphae are septate. This class contains the majority of medically important fungi. Dematiaceous hyphomycetes are those conidial fungi that produce dark brown, green-black, or black colonies and are the causative agents of phaeohyphomycosis. Hyaline hyphomycetes include those conidial fungi, which are not darkly pigmented; colonies may be colourless or brightly coloured. These include the agents of hyalohyphomycosis, aspergillosis, dermatophytosis and the dimorphic pathogens, like Histoplasma capsulatum.
·         Coelomycetes: These produce acervuli, which are tightly bound mats of hyphae on which conidia are produced.
Based on Morphology:
v  Moulds (Molds): Filamentous fungi Eg: Aspergillus sps, Trichophyton rubrum
v  Yeasts: Single celled cells that buds Eg: Cryptococcus neoformans, Saccharomyces cerviciae
v  Yeast like: Similar to yeasts but produce pseudohyphae Eg: Candida albicans
v  Dimorphic: Fungi existing in two different morphological forms at two different environmental conditions. They exist as yeasts in tissue and in vitro at 37oC and as moulds in their natural habitat and in vitro at room temperature. Eg: Histoplasma capsulatum, Blastomyces dermatidis, Paracoccidiodes brasiliensis, Coccidioides immitis
Some 200 "human pathogens" have been recognized from among an estimated 1.5 million species of fungi.
Morphology of fungi:
Fungi exist in two fundamental forms; the filamentous (hyphal) and single celled budding forms (yeast). But, for the classification sake they are studied as moulds, yeasts, yeast like and dimorphic fungi. All fungi have typical eukaryotic morphology. They have rigid cell wall composed of chitin, which may be layered with mannans, glucans and other polysaccharides in association with polypeptides. Some lower fungi possess cellulose in their cell wall. Some fungi such as Cryptococcus and yeast form of Histoplasma capsulatum possess polysaccharide capsules that help them to evade phagocytosis.
Inner to the cell wall is the plasma membrane that is a typical bi-layered membrane in addition to the presence of sterols. Fungal membranes possess ergosterol in contrast to cholesterol found in mammalian cells. The cytoplasm consists of various organelles such as mitochondria, golgi apparatus, ribosomes, endoplasmic reticulum, lysosomes, microtubules and a membrane enclosed nucleus. A unique property of nuclear membrane is that it persists throughout the metaphase of mitosis unlike in plant and animal cells where it dissolves and re-forms. The nucleus possesses paired chromosomes.
Moulds:
The thallus of mould is made of hyphae, which are cylindrical tube like structures that elongates by growth at tips. A mass of hyphae is known as mycelium. It is the hypha that is responsible for the filamentous nature of mould. The hyphae may be branched or unbranched. They may be septate or aseptate. Hyphae usually have cross walls that divide them into numerous cells. These cross walls, called septa have small pores through which cytoplasm is continuous throughout the hyphae. Therefore all hyphal fungi tend to be coenocytic (multinucleate). With exception of zygomycetes (Rhizopus, Mucor), all moulds are septate. Non-septate hyphae are considered to be more primitive because if a hyphal strand is damaged the entire strand dies. When a septate hyphal strand is damaged, the pores between adjacent compartments can be plugged, thus preventing death of the whole hyphal strand.
Mycelium are of three kinds:
·         Vegetative mycelium are those that penetrates the surface of the medium and absorbs nutrients.
·         Aerial mycelium are those that grow above the agar surface
·         Fertile mycelium are aerial hyphae that bear reproductive structures such as conidia or sporangia.
TYPES OF HYPHAE
Since hypha is the structural unit of mould, the mycelium imparts colour, texture and topography to the colony. Those fungi that possess melanin pigments in their cell wall are called phaeoid or dematiaceous and their colonies are coloured grey, black or olive. Examples are species of Bipolaris, Cladosporium, Exophiala, Fonsecaea, Phialophora and Wangiella those hyphae that don't possess any pigment in their cell wall are called hyaline. Hyphae may have some specialized structure or appearance that aid in identification. Some of these are:
a) Spiral hyphae: These are spirally coiled hyphae commonly seen in Trichophyton mentagrophytes.
b) Pectinate body: These are short, unilateral projections from the hyphae that resemble a broken comb. Commonly seen in Microsporum audouinii.
c) Favic chandelier: These are the group of hyphal tips that collectively resemble a chandelier or the antlers of the deer (antler hyphae). They occur in Trichophyton schoenleinii and Trichophyton violaceum.
d) Nodular organ: This is an enlargement in the mycelium that consists of closely twisted hyphae. Often seen in Trichophyton mentagrophytes and Microsporum canis.
e) Racquet hyphae: There is regular enlargement of one end of each segment with the opposing end remaining thin. Seen in Epidermophyton floccosum, Trichophyton mentagrophytes.
f) Rhizoides: These are the root like structures seen in portions of vegetative hyphae in some members of zygomycetes.
There are structures in the hyphae, which arise out of modification of a single cell and transform into thick walled resting cells. Chlamydospore (or chlamydoconidia), which are produced by Trichophyton schoenleinii and Trichophyton verrucosum are thick walled cells that are larger than other cells and arranged singly or in groups. In some fungi such as Trichosporon beigeilli and Coccidioides immitis some alternating cells become thick walled and subsequently the intervening cells disintegrate leaving behind arthrospores (or arthroconidia).
























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Yeasts are unicellular spherical to ellipsoid cells. They reproduce by budding, which result in blastospore (blastoconidia) formation. In some cases, as the cells buds the buds fail to detach and elongate thus forming a chain of elongated hyphae like filament called pseudohyphae. This property is seen in Candia albicans. The same species also have the ability to produce true hypha, which is seen as germ tube. The difference between the two is that there is a constriction in psueudohyphae at the point of budding, while the germ tube has no constriction.
·         Some yeast such as Cryptococcus and the yeast form of Blastomyces dermatatidis produce polysaccharide capsule.
·         Some yeasts are pigmented. Rhodotorula sps produces pink colonies due to carotenoid pigments while some yeasts such as Phaeoannellomyces werneckii and Piedraia hortae are dematiaceous, producing brown to olivaceous colonies.
·         True yeasts such as Saccharomyces cerviciae don't produce pseudohyphae. Yeast-like fungi may be basidiomycetes, such as Cryptococcus neoformans or ascomycetes such as Candida albicans.
Reproduction in fungi:
Fungi reproduce by asexual, sexual and parasexual means.
Asexual reproduction is the commonest mode in most fungi with fungi participating in sexual mode only under certain circumstances. The form of fungus undergoing asexual reproduction is known as anamorph (or imperfect stage) and when the same fungus is undergoing sexual reproduction, the form is said to be teleomorph (or perfect stage). The whole fungus, including both the forms is referred as holomorph. (Taxonomically, the teleomorph or the holomorph is used, but practically it is more convenient to use the anamorph.)
Asexual reproduction:
Asexual spores are produced following mitosis whereas sexual spores are produced following meiosis.
The asexual spores of zygomycetes, which are known as sporangiospores form within sac like structure known as sporangia. The sporangiospores result from the mitotic cleavage of cytoplasm in the sporangium. The sporangia are borne on special hyphae called sporangiophore. This endogenous process of spore formation within a sac is known as sporogenesis.
Conidia arise either by budding off conidiogenous hyphae or by differentiation of preformed hyphae. These develop following mitosis of a parent nucleus and are formed in any manner except involving cytoplasmic cleavage. This exogenous process is known as conidiogenesis, a process that occurs both in yeasts and moulds. Conidia are borne on specialised structures called conidiophore.
Conidia production may be blastic or thallic. In blastic development the conidium begins to enlarge and a septum is formed. Here the conidium originates from part of parent. In thallic mode of development the conidium is differentiated by a septum before its differentiation. Thus the conidium results from the conversion of entire parent cell into the conidium.
The cell that gives rise to a conidium is called a conidiogenous cell. Conidiophores are specialised hyphae that bear conidia or conidiogenous cells. In many cases conidiogenous cells are referred as phialides.
Sexual Reproduction:
Sexual propagules are produced by the fusion of two nuclei that then generally undergo meiosis.
The first step in sexual methods of reproduction involves plasmogamy (cytoplasmic fusion of two cells). The second step is karyogamy (fusion of two compatible nuclei), resulting in production of diploid or zygote nucleus. This is followed by genetic recombination and meiosis. The resulting four haploid spores are said to be sexual spores, e.g. zygospores, ascospores and basidiospores.
If a sexual spore is produced only by fusion of a nucleus of one mating type with a nucleus of another mating type (+ and - strains), the fungus is said to be heterothallic. In contrast, homothallic moulds produce sexual sporesfollowing the fusion of two nuclei from the same strain. For sexual reproduction to occur, two compatible isolates are required.
Zygospores, which are the sexual spores of zygomycetes are round, thick walled reproductive structures that result from the union of two gamentagia. Ascomycetes produce sexual spores called ascospores in a special sac like cell known as ascus. In basidiomycetes the basidiospores are released from basidium, which is the terminal cell of a hyphae.
Parasexual reproduction:
Parasexual reproduction, first seen in Aspergillus is known to occur in basidiomycetes, ascomycetes and deuteromycetes. The process involves genetic recombination without the requirement of specific sexual structures.

Importance of Spores:
A. Biological
·         Allows for dissemination
·         Allows for reproduction
·         Allows the fungus to move to new food source.
·         Allows fungus to survive periods of adversity.
·         Means of introducing new genetic combinations into a population
B. Practical
·         Rapid identification (also helps with classification)
·         Source of inocula for human infection
·         Source of inocula for contamination
Beneficial Effects of Fungi:
·         Decomposition - nutrient and carbon recycling.
·         Biosynthetic factories. The fermentation property is used for the industrial production of alcohols, fats, citric, oxalic and gluconic acids.
·         Important sources of antibiotics, such as Penicillin.
·         Model organisms for biochemical and genetic studies. Eg: Neurospora crassa
·         Saccharomyces cerviciae is extensively used in recombinant DNA technology, which includes the Hepatitis B Vaccine.
·         Some fungi are edible (mushrooms).
·         Yeasts provide nutritional supplements such as vitamins and cofactors.
·         Penicillium is used to flavour Roquefort and Camembert cheeses.
·         Ergot produced by Claviceps purpurea contains medically important alkaloids that help in inducing uterine contractions, controlling bleeding and treating migraine.
·         Fungi (Leptolegnia caudate and Aphanomyces laevis) are used to trap mosquito larvae in paddy fields and thus help in malaria control.
Harmful Effects of Fungi:
·         Destruction of food, lumber, paper, and cloth.
·         Animal and human diseases, including allergies.
·         Toxins produced by poisonous mushrooms and within food (Mycetism and Mycotoxicosis).
·         Plant diseases.
·         Spoilage of agriculture produce such as vegetables and cereals in the godown.

·         Damage the products such as magnetic tapes and disks, glass lenses, marble statues, bones and wax.

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