Maullinia | |
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E: Resting spores of Maullinia sp. resting spores in Durvillaea antarctica | |
Scientific classification | |
Domain: | Eukaryota |
Clade: | Diaphoretickes |
Clade: | SAR |
Phylum: | Endomyxa |
Class: | Phytomyxea |
Order: | Phagomyxida |
Family: | Phagomyxidae |
Genus: | Maullinia I. Maier, E. R. Parodi, R. Wester-meier et D. G. Müller 2000 |
Maullinia is a genus of intracellular, phytomyxid parasites found across the Southern Hemisphere though primarily in Chile, The Prince Edward Islands, South Africa, Australia, and New Zealand. [1] [2] [3] [4] [5] These parasites infiltrate the cells of their brown algal hosts via cytoplasmic extensions called plasmodia that divide synchronously, [1] becoming increasingly multi-nucleate and engulfing the host cell organelles as they grow. [1] [3] Eventually, as the plasmodia fill the entire cell volume, the host cells become hypertrophied and grow to 3- 4x their original size, [2] showing up as swollen appendages or galls on the host tissue at a macroscopic level. [1] [3] These swollen regions will burst alongside the mature Maullinia plasmodia, releasing biflagellated zoospores to the inter- and extracellular space to disperse the infection further. [6] Zoospores can come from sporangial plasmodia, [1] as in M. ectocarpii, or from resting spores, as in M. braseltonii. [3]
As Maullinia can infect a wide range commercially important brown algal hosts, they present a significant threat to kelp farming and mariculture efforts. [1] These infections could also cause significant harm on a global scale to natural populations, as they are able to disperse over long distances via rafting and tend to thrive in the cooler waters where kelp are often found. [4] [5]
"Maullinia" refers to the Maullín river near Puerto Montt in Chile, from which the genus was first described. [1] The species epithet for M.ectocarpii was chosen in reference to the host organism genus, Ectocarpus [1] . In M. braseltonii, the species epithet was chosen as a dedication to well-renowned phytomyxid specialist James P. Braselton. [3]
Maullinia ectocarpii I. Maier, E. R. Parodi, R. Westermeier et D. G. Müller sp. nov. [1]
For decades, brown algal kelps across the southern hemisphere have been described as having gall-forming infections of unknown origin. [7] [8] [9] The cause of these galls was first investigated purely by chance, when a team of researchers from the University of Konstanz, led by Dr. Ingo Maier, were conducting an epiphytic algal study in Chile. [1] Some specimens of Ectocarpus siliculosus in a Chilean mariculture plantation appeared to have parasitic infections, [1] which piqued the research team's interest. After extensive field and laboratory culture experimentation, a new genus of phytomyxid was described as Maullinia. [1] This was the only phytomyxid parasite of brown algae known to science at the time, [3] and was initially classified as a plasmodiophorid. [1]
Close to a decade later, while investigating gall-forming infections on fronds of the kelp Durvillaeaantarctica, researchers produced the first evidence of a second Maullinia species. [2] Using 18S rRNA molecular data from the parasites causing these gall-forming infections, they constructed a phylogenetic tree which placed the parasite as a sister species to M. ectocarpii. [2] However, not enough evidence was found to constitute a new species description at this time. [3] A few years later, further molecular and morphological experimentation was carried out, providing enough evidence to classify this new Maullinia species as M. braseltonii. [3]
The two species of Maullinia has been shown to successfully parasitize a wide range of brown algal hosts, spanning multiple brown algal orders, such as the Ectocarpales, Fucales, and Laminariales [1] [2] [3] [5] . A table of all known compatible hosts follows.
Orders | Host algal species | M. ectocarpii | M. braseltonii |
Ectocarpales | Acinetospora crinita | compatible | - |
Feldmannia simplex | compatible | - | |
Ectocarpus fasciculatus | compatible | - | |
Ectocarpus siliculosus | compatible | - | |
Hincksia hincksiae | compatible | - | |
Hincksia mitchelliae | compatible | - | |
Kuckuckia spinosa | compatible | - | |
Scytothamnales | Splachnidium rugosum | compatible | - |
Desmarestiales | Desmarestia munda | compatible | - |
Desmarestia distans | compatible | - | |
Laminariales | Macrocystis pyrifera | compatible | - |
Fucales | Durvillaea amatheiae | compatible | - |
Durvillaea antarctica | - | compatible | |
Durvillaea potatorum | compatible | - | |
Durvillaea willana | - | compatible |
Markers of Maullinia infection vary across host species, but all exhibit macroscopic signs of hypertrophy. In filamentous hosts (i.e., Ectocarpus), or hosts in gametophytic stages with microthalli (i.e., Macrocystis), swollen appendages can be found. [1] These appendages are oblong to sub-spherical in shape, extending predominantly from the terminal cell on each main filament axis, but are also seen on the lateral branches. [1] Appendages are unpigmented, with apical openings from which Maullinia zoospores are released. [1] These appendages often occur in proximity to host sporangia, increasing the host's sterility rate and number of abortive sporangia [1] .
In non-filamentous algae such as Durvillaea , infected during their mature sporophyte stages, large galls form on the fronds and stipe. [2] [3] These galls are irregular in shape, but most often are circular or ellipsoid with a diameter ranging from 0.5 cm to 7 cm. [2] [3] They are the result of cellular-level hypertrophy, which causes host cells to expand to be 3 – 4x their normal size. [2] These hypertrophied cells are restricted to the sub-cortex, the region between the cortex and the medullary tissue. [3] Hypertrophied cells and the resulting macroscopic galls are paler than healthy tissue, with galls generally having a yellow-brown colouration. [3] They may be solitary or clustered together, but clusters generally indicate a greater extent of Maullinia infection. [3] Individuals which wash ashore tend to have ruptured in areas with these clustered galls, indicating that galls weaken the thallus and make it more susceptible to external damage. [3] There is also strong evidence that Maullinia, as a phytomyxid parasite, adversely affects the reproduction of its hosts. [10]
Maullinia infections of non-filamentous brown algae primarily target adult hosts, and are mostly absent during their reproductive periods. [3] During non-reproductive periods, when adults dominate the populations, an infection rate of up to 40% can be seen. [3] In other words, up to 9 individuals per square meter could be infected. [3]
These infections, regardless of whether the host is filamentous or non-filamentous, can increase viral infection rates as well. [1] Maullinia infections do not appear to trigger significant defense mechanisms in their hosts, [10] only passive protection from the presence of fungal endophytes, [11] and as such provide a vector for viral infections to enter the brown alga alongside Maullinia.
As a parasitic genus, Maullinia derives its nutrition from the host cells it inhabits. Initially, the sole mode of nutrition was thought to be absorptive osmotrophy. [1] In recent years however, new evidence has been revealed supporting intracellular phagotrophy as the primary mode of nutrition, with osmotrophy as a secondary function. [12] Maullinia appears to engulf the host organelles whole as it extends through the cell, with a preference for plastids being clear. [12] This preference could be due to several factors, namely active targeting by Maullinia, the widespread nature of plastids within brown algal cells, or simply a slower digestion process of these complex pigment-containing organelles. [12] Evidence that there is some targeting of plastids comes from the host cell actively producing smaller plastids as the infection proceeds. [12]
Outside of the plastid preference, one of the first intracellular structures to be engulfed is the large storage vacuole. [12] This vacuole contains many complex polysaccharides, and as such its consumption provides the infecting Maullinia with a boost in energy. [12] This energy boost near the beginning of the infection, alongside the loss of a key energy source for the host cell, allows Maullinia to expand quickly.
Maullinia is found across much of the Southern Hemisphere, with infected brown algal populations in Chile, The Prince Edward Islands, South Africa, Australia, and New Zealand currently known. [1] [2] [3] [4] [5] Within these regions Maullinia prevalence increases with latitude, becoming more dominant in southern populations as compared to more tropical ones. [4] This is likely due to a combination of two key factors: the increased density of southern populations and increased Maullinia virulence in cooler waters. [4] While many parasites prefer warmer environments, Maullinia appears to thrive in lower temperatures, having greatest infection rates during the winter months and at greater latitude. [3] [4]
The two species of Maullinia appear to have some preference for habitat, based on the brown algal hosts which they each primarily infect. M. ectocarpii prefers sandy, shallow, sheltered regions where more filamentous brown algae tend to thrive. [3] However, M. ectocarpii is a more generalist species and can adapt to more rocky intertidal species such as Durvillaea amatheiae and Durvillaea potatorum . [4] M. braseltonii is much more specialist, and exclusively infects Durvillaea hosts stemming from rocky intertidal habitats. [4] As many Durvillaea species are buoyant, M. braseltonii is often found infecting drift as well. [3]
The role of drift in distributing Maullinia and providing a vector for novel infections is critical. Rafting is the primary way by which new populations of brown algae are infected by Maullinia, [4] [5] and this process is supported by the physiological changes infected hosts undergo. With the hypertrophied cells forming galls, a greater buoyancy is achieved in infected individuals, allowing them a wider distribution capability. [3] The likelihood of the mechanism is strengthened by the genetic evidence which links the New Zealand population of Maullinia to the Chile population. [5] The role of rafting, alongside the widespread populations separated by thousands of kilometers, implies that Maullinia may be capable of achieving global distribution along cold-temperate coasts. [1]
Life cycles in Maullinia are not completely understood, nor has sexual reproduction been observed. [1] [3] M. ectocarpii and M. braseltonii seem to produce two different forms of plasmodia which develop into unique structures and zoospores not yet observed in the other. Outside of these two plasmodial forms, the life cycle is largely identical.
Encystment occurs when a Maullinia biflagellated stage settles on a compatible host, and can begin the infection process. Cysts are ellipsoid to kidney-shaped, being approximately 5.8 ± 0.7 μm long and 2.5 ± 0.2 μm wide. [1] They have chitinous cell walls which break open at one end to allow the adhesorium, an infection apparatus, to extend. [1] The adhesorium has no cell wall and develops from a beak-like shape into a narrow neck of 5 – 7 μm in length which punctures the host cell wall. [1] From here, the cyst contents are injected into the host cell cytoplasm, [1] and plasmodial formation begins.
Once cyst contents have been injected into the host cytoplasm, synchronous nuclear divisions occur rapidly to produce large multinucleate plasmodia within the host cell. [1] Each plasmodial nucleus is spherical and contains a distinct, centric nucleolus. [1] Plasmodia continue to grow, via cruciform and non-cruciform mitotic divisions, engulfing host organelles and causing strong host cell hypertrophy. [1] The host nucleus becomes engorged as a result of the hypertrophy, and eventually ceases division. [1] This growth may alter the hosts metabolic functioning, collecting energy-rich compounds within the cell to help feed the Maullinia parasite, [10] although this theory is not proven. [12] After enough plasmodial growth occurs and the host cell is entirely filled, a lobose structure is adopted and plasmodial differentiation occurs. [3]
Mature plasmodia transform into a single sporangium, which develops near the host cell wall and becomes attached to it via deposition of a fine, but dense, fibrillar wall-like material. [1] The size and shape of these sporangia are variable both within and across host species, but on average are club-shaped, 40 – 93 μm long and 27–46 μm wide. [1] In Ectocarpus, these sporangia occur in clusters that mirror the hosts' own growth pattern. [1] Each sporangium produces several hundred zoospores. [1]
Sporangia produce sporangial zoospores, pyriform cells 4.6 ± 0.7 μm long length, 2.3 ± 0.4 μm wide with thick walls and 2 flagella extending from the broad part of the cell. [1] These flagella are of unequal length, with the longer flagellum being more posteriorly oriented and undulating, while the shorter one is more anteriorly oriented and oblique to the midline. [1] Both flagella have short hair tips along them. [1] Sporangial zoospore nuclei have an abundance of condensed chromatin, but no nucleoli. [1] [6] These zoospores are extremely motile and exit singly from a single apical opening on the sporangium. [1] Once released, they disperse and make contact with hosts to begin encystment again. [1]
Resting spores allow for survival in antagonistic environments, which allows M. braseltonii to be more specific about which hosts it chooses to infect as a host cell is not needed for resting spore survival. [2] The plasmodium begins resting spore development by concentrating cytoplasm around the nucleus, allowing the thick, 3-layered wall to start forming. [3] Initially, these resting spores are very irregular and globose to elliptic, but become more regularly spherical as they mature. [3] They have no colour, and will wait to release zoospores until conditions are optimal. [3] These zoospores may be differently structured than their sporangial counterparts, but they have yet to be observed. [3]
Maullinia has hosts of high commercial importance, such as Macrocystis , and as such have the potential of causing devastating effects if an infection were able to spread into a gametophyte mariculture supporting a Macrocystis kelp farm. [1] Examples have been seen already, with the initial description of Maullinia occurring on an infected Chilean Ectocarpus mariculture. [1] These kinds of infections could compound with the delivery of brown algal viruses alongside the parasite, decimating entire kelp cultures in the process. [1]
In addition to its known effects on brown algal hosts, Maullinia has the ability to infect a wide range of hosts that could possibly bridge the marine-terrestrial gap. Phytomyxid parasites have been proven capable of shifting hosts across kingdoms (i.e., from brown algae to angiosperms), and could this introduce completely novel parasites to terrestrial environments. [13]
Brown algae are a large group of multicellular algae comprising the class Phaeophyceae. They include many seaweeds located in colder waters of the Northern Hemisphere. Brown algae are the major seaweeds of the temperate and polar regions. Many brown algae, such as members of the order Fucales, commonly grow along rocky seashores. Most brown algae live in marine environments, where they play an important role both as food and as a potential habitat. For instance, Macrocystis, a kelp of the order Laminariales, may reach 60 m (200 ft) in length and forms prominent underwater kelp forests that contain a high level of biodiversity. Another example is Sargassum, which creates unique floating mats of seaweed in the tropical waters of the Sargasso Sea that serve as the habitats for many species. Some members of the class, such as kelps, are used by humans as food.
The Oomycetes, or Oomycota, form a distinct phylogenetic lineage of fungus-like eukaryotic microorganisms within the Stramenopiles. They are filamentous and heterotrophic, and can reproduce both sexually and asexually. Sexual reproduction of an oospore is the result of contact between hyphae of male antheridia and female oogonia; these spores can overwinter and are known as resting spores. Asexual reproduction involves the formation of chlamydospores and sporangia, producing motile zoospores. Oomycetes occupy both saprophytic and pathogenic lifestyles, and include some of the most notorious pathogens of plants, causing devastating diseases such as late blight of potato and sudden oak death. One oomycete, the mycoparasite Pythium oligandrum, is used for biocontrol, attacking plant pathogenic fungi. The oomycetes are also often referred to as water molds, although the water-preferring nature which led to that name is not true of most species, which are terrestrial pathogens.
The Phytomyxea are a class of parasites that are cosmopolitan, obligate biotrophic protist parasites of plants, diatoms, oomycetes and brown algae. They are divided into the orders Plasmodiophorida and Phagomyxida. Plasmodiophorids are best known as pathogens or vectors for viruses of arable crops.
Synchytrium endobioticum is a chytrid fungus that causes the potato wart disease, or black scab. It also infects some other plants of the genus Solanum, though potato is the only cultivated host.
Phycodnaviridae is a family of large (100–560 kb) double-stranded DNA viruses that infect marine or freshwater eukaryotic algae. Viruses within this family have a similar morphology, with an icosahedral capsid. As of 2014, there were 33 species in this family, divided among 6 genera. This family belongs to a super-group of large viruses known as nucleocytoplasmic large DNA viruses. Evidence was published in 2014 suggesting that specific strains of Phycodnaviridae might infect humans rather than just algal species, as was previously believed. Most genera under this family enter the host cell by cell receptor endocytosis and replicate in the nucleus. Phycodnaviridae play important ecological roles by regulating the growth and productivity of their algal hosts. Algal species such Heterosigma akashiwo and the genus Chrysochromulina can form dense blooms which can be damaging to fisheries, resulting in losses in the aquaculture industry. Heterosigma akashiwo virus (HaV) has been suggested for use as a microbial agent to prevent the recurrence of toxic red tides produced by this algal species. Phycodnaviridae cause death and lysis of freshwater and marine algal species, liberating organic carbon, nitrogen and phosphorus into the water, providing nutrients for the microbial loop.
Powdery scab is a disease of potato tubers. It is caused by the cercozoan Spongospora subterranea f. sp. subterranea and is widespread in potato growing countries. Symptoms of powdery scab include small lesions in the early stages of the disease, progressing to raised pustules containing a powdery mass. These can eventually rupture within the tuber periderm. The powdery pustules contain resting spores that release anisokont zoospores to infect the root hairs of potatoes or tomatoes. Powdery scab is a cosmetic defect on tubers, which can result in the rejection of these potatoes. Potatoes which have been infected can be peeled to remove the infected skin and the remaining inside of the potato can be cooked and eaten.
Durvillaea is a genus of large brown algae in the monotypic family Durvillaeaceae. All members of the genus are found in the southern hemisphere, including Australia, New Zealand, South America, and various subantarctic islands. Durvillaea, commonly known as southern bull kelps, occur on rocky, wave-exposed shorelines and provide a habitat for numerous intertidal organisms. Many species exhibit a honeycomb-like structure in their fronds that provides buoyancy, which allows individuals detached from substrates to raft alive at sea, permitting dispersal for hundreds of days over thousands of kilometres. Durvillaea species have been used for clothing, tools and as a food source by many indigenous cultures throughout the South Pacific, and they continue to play a prominent role in Chilean cuisine.
Durvillaea antarctica, also known as cochayuyo and rimurapa, is a large, robust species of southern bull kelp found on the coasts of Chile, southern New Zealand, and Macquarie Island. D. antarctica, an alga, does not have air bladders, but floats due to a unique honeycomb structure within the alga's blades, which also helps the kelp avoid being damaged by the strong waves.
Ectocarpus siliculosus is a filamentous brown alga. Its genome was the first brown macroalgal genome to be sequenced, with the expectation that E. siliculosus will serve as a genetic and genomic model for brown macroalgae.
Hematodinium is a genus of dinoflagellates. Species in this genus, such as Hematodinium perezi, the type species, are internal parasites of the hemolymph of crustaceans such as the Atlantic blue crab and Norway lobster. Species in the genus are economically damaging to commercial crab fisheries, including causing bitter crab disease in the large Tanner or snow crab fisheries of the Bering Sea.
Ceratiomyxa is a genus of plasmodial slime mould within the Eumycetozoa, first described by Pier Antonio Micheli. They are widely distributed and commonly found on decaying wood.
Parvilucifera is a genus of marine alveolates that behave as endoparasites of dinoflagellates. It was described in 1999 by biologists Fredrik Norén and Øjvind Moestrup, who identified the genus among collections of Dinophysis dinoflagellates off the coast of Sweden. Initially mistaken for products of sexual reproduction, the round bodies found within these collections were eventually recognized as sporangia, spherical structures that generate zoospores of a parasitic protist. This organism was later identified as P. infectans, the type species. The examination of this organism and its close genetic relationship to Perkinsus led to the creation of the Perkinsozoa phylum within the Alveolata group.
Ectocarpus is a genus of filamentous brown alga that is a model organism for the genomics of multicellularity. Among possible model organisms in the brown algae, Ectocarpus was selected for the relatively small size of its mature thallus and the speed with which it completes its life cycle. Tools available for Ectocarpus as a model species include a high quailty genome sequence and both forward and reverse genetic methodologies, the latter based on CRISPR-Cas9.
Plasmodiophora bicaudata is a marine pathogen, an obligate parasite of seagrass of the genus Zostera and the causal agent of wasting disease in the genus. These marine plants grow in fine sediment in shallow seas and the pathogen seems to have a worldwide distribution.
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, and all are obligate parasites of angiosperms, ferns, or mosses. Early species were mistakenly classified among the higher fungi because of their superficial similarity to the rust fungi. Anton de Bary and Mikhail S. Woronin recognized the true nature of these fungi and established the genus to accommodate Synchytrium taraxaci, which grows on dandelions, and S. succisae, which grows on Succisa pratensis. Synchytrium taraxaci is the type of the genus. The genus has been divided into 6 subgenera based on differences in life cycles.
Physoderma is a genus of chytrid fungi. Described by German botanist Karl Friedrich Wilhelm Wallroth in 1833, the genus contains some species that are parasitic on vascular plants, including P. alfalfae and P. maydis, causative agents of crown wart of alfalfa and brown spot of corn, respectively. Of the chytrid genera, Physoderma is the oldest. However, species were confused with the rust fungi, the genus Synchytrium, and the genus Protomyces of Ascomycota. Members of Physoderma are obligate parasites of pteridophytes and angiosperms. There are approximately 80 species within this genus.
Pythium porphyrae, is a parasitic species of oomycete in the family Pythiaceae. It is the cause of red rot disease or red wasting disease, also called akagusare (赤ぐされ) in Japanese. The specific epithet porphyrae (πορφυρα) stems from the genus of one of its common hosts, Porphyra, and the purple-red color of the lesions on the thallus of the host. However, many of its hosts have been moved from the genus Porphyra to Pyropia.
Phagomyxids are a group of obligate endoparasitic protists belonging to the subphylum Endomyxa in Cercozoa. Taxonomically, they are united under a single family Phagomyxidae, order Phagomyxida, sister to the plasmodiophores.
Tetramyxa parasitica is a species of parasitic cercozoan, member of the plasmodiophorids, that causes gall formation on multiple genera of aquatic plants. It was first discovered on roots of Ruppia and described by Karl von Goebel in 1884 in his work Flora, where it became the type species of the genus Tetramyxa.
Aphelidium tribonemae is a species within the Aphelid group. Their classification in the kingdom Fungi is a subject of controversy. Some argue for the classification of aphelids as ‘fungal animals', and for a period of time in the 1950s, aphids were classified as protists due to their amoeboid stage. Recently, molecular phylogenetics placed the aphelids within Opisthosporidia, a super phylum within Opisthokonta. Aphelids have posterior uniflagellate zoospores which place them as Opisthokonts. They are an early diverging lineage in Kingdom Fungi. While the aphelid group only contains three genera, it spans many both freshwater and marine ecosystems.
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