Batrachochytrium

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Batrachochytrium
Zoosporangia of Batrachochytrium dendrobatidis growing on a freshwater arthropod (a) and on algae (b). The scale bars represent 30 µm.
Scientific classification e
Kingdom:Fungi
Division:Chytridiomycota
Class:Chytridiomycetes
Order:Rhizophydiales
Genus:Batrachochytrium
Binomial name
Batrachochytrium dendrobatidis
Longcore, Pessier & D.K. Nichols (1999)
 
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Batrachochytrium
Zoosporangia of Batrachochytrium dendrobatidis growing on a freshwater arthropod (a) and on algae (b). The scale bars represent 30 µm.
Scientific classification e
Kingdom:Fungi
Division:Chytridiomycota
Class:Chytridiomycetes
Order:Rhizophydiales
Genus:Batrachochytrium
Binomial name
Batrachochytrium dendrobatidis
Longcore, Pessier & D.K. Nichols (1999)

Batrachochytrium dendrobatidis, also known as Bd or the amphibian chytrid fungus, is a chytrid fungus that causes the disease chytridiomycosis in amphibians. In the decade after it was first discovered in 1998,[1] the disease devastated amphibian populations around the world, in a global decline towards multiple extinctions, part of the Holocene extinction. A recently-described second species, B. salamandrivorans, also cause chytridiomycosis and death in salamanders.

Some amphibian species appear to have an innate capacity to withstand chytridiomycosis infection. Even within species that generally succumb, some populations survive, possibly demonstrating that these traits or alleles of species are being subjected to evolutionary selection.

Etymology[edit]

The generic name is derived from the latin words batrachos (frog) and chytra (earthen pot), while the specific epithet is derived from the genus of frogs from which the original confirmation of pathogenicity was made (Dendrobates).[2]

Systematics[edit]

Batrachochytrium dendrobatidis was until recently considered the single species of the genus Batrachochytrium. The initial classification of the pathogen as a chytrid was based on zoospore ultrastructure. DNA analysis of the ssu-rDNA has corroborated the view, with the closest match to Chytridium confervae. A second species of Batrachochytrium was discovered in 2013: B. salamandrivorans, which mainly affects salamanders and also causes chytridiomycosis.[3] B. salamandrivorans differs from B. dendrobatidis primarily in the formation of germ tubes in vitro, the formation of colonial thalli with multiple sporangia in vivo, and a lower thermal preference.[3]

Morphology[edit]

B. dendrobatidis infects the keratinized skin of amphibians. The fungus in the epidermis has a thallus bearing a network of rhizoids and smooth-walled, roughly spherical, inoperculate (without an operculum) sporangia. Each sporangium produces a single tube to discharge spores.

Zoospore structure[edit]

Zoospores of B. dendrobatidis, which are typically 3-5 µm in size, have an elongate–ovoidal body with a single, posterior flagellum (19-20 µm long), and possess a core area of ribosomes often with membrane-bound spheres of ribosomes within the main ribosomal mass.[2] A small spur has been observed, located at the posterior of the cell body, adjacent to the flagellum, but this may be an artifact in the formalin-fixed specimens. The core area of ribosomes is surrounded by a single cisterna of endoplasmic reticulum, two to three mitochondria, and an extensive microbody–lipid globule complex. The microbodies closely appose and almost surround four to six lipid globules (three anterior and one to three laterally), some of which appear bound by a cisterna. Some zoospores appear to contain more lipid globules (this may have been a result of a plane-of-sectioning effect, because the globules were often lobed in the zoospores examined). A rumposome has not been observed.[2]

Flagellum structure[edit]

A nonfunctioning centriole lies adjacent to the kinetosome. Nine interconnected props attach the kinetosome to the plasmalemma, and a terminal plate is present in the transitional zone. An inner ring-like structure attached to the tubules of the flagellar doublets within the transitional zone has been observed in transverse section. No roots associated with the kinetosome have been observed. In many zoospores, the nucleus lies partially within the aggregation of ribosomes and was invariably situated laterally. Small vacuoles and a Golgi body with stacked cisternae occurred within the cytoplasm outside the ribosomal area. Mitochondria, which often contain a small number of ribosomes, are densely staining with discoidal cristae.[2]

Life cycle[edit]

B. dendrobatidis sporangia in the skin of an Atelopus varius. The arrows indicate discharge tubes through which zoospores exit the host cell. Scale bar = 35 µm.

B. dendrobatidis has two primary life stages: a sessile, reproductive zoosporangium and a motile, uniflagellated zoospore released from the zoosporangium. The zoospores are known to be active only for a short period of time, and can travel short distances of one to two centimeters.[4] However, the zoospores are capable of chemotaxis, and can move towards a variety of molecules that are present on the amphibian surface, such as sugars, proteins and amino acids.[5] B. dendrobatidis also contains a variety of proteolytic enzymes and esterases that help it digest amphibian cells and use amphibian skin as a nutrient source.[6] Once the zoospore reaches its host, it forms a cyst underneath the surface of the skin, and initiates the reproductive portion of its life cycle. The encysted zoospores develop into zoosporangia, which may produce more zoospores that can reinfect the host, or be released into the surrounding aquatic environment.[7] The amphibians infected with these zoospores are shown to die from cardiac arrest.[citation needed]

Physiology[edit]

B. dendrobatidis can grow within a wide temperature range (4-25°C), with optimal temperatures being between 17-25°C.[8] The wide temperature range for growth, including the ability to survive at 4°C gives the fungus the ability to overwinter in its hosts, even where temperatures in the aquatic environments are low. The species does not grow well above temperatures of 25°C, and growth is halted above 28°C.[8] Infected red-eyed treefrogs (Litoria chloris) recovered from their infections when incubated at a temperature of 37°C.[9]

Varying forms[edit]

B. dendrobatidis has occasionally been found in forms distinct from its traditional zoospore and sporangia stages. For example, before the 2003 European heat wave that decimated populations of the water frog Rana lessonae through chytridiomycosis, the fungus existed on the amphibians as spherical, unicellular organisms, confined to minute patches (80-120 meters across). These organisms, unknown at the time, were subsequently identified as B. dendrobatidis. Characteristics of the organisms were suggestive of encysted zoospores; they may have embodied a resting spore, a saprobe, or a parasitic form of the fungus that is non-pathogenic.[10]

Habitat and relationship to amphibians[edit]

The fungus grows on amphibian skin and produces aquatic zoospores.[11] It is widespread and ranges from lowland forests to cold mountain tops. It is sometimes a non-lethal parasite and possibly a saprophyte. The fungus is associated with host mortality in highlands or during winter, and becomes more pathogenic at lower temperatures.[12]

Geographic distribution[edit]

It has been suggested that B. dendrobatidis originated in Africa and subsequently spread to other parts of the world by trade in African clawed frogs (Xenopus laevis).[13] In this study, 697 archived specimens of three species of Xenopus, previously collected from 1879 to 1999 in southern Africa were examined. The earliest case of chytridiomycosis was found in a X. laevis specimen from 1938. The study also suggests that chytridiomycosis had been a stable infection in southern Africa from 23 years prior to finding any infected outside of Africa.[13]

American bullfrogs (Rana catesbiana), also widely distributed, are also thought to be carriers of the disease due to their inherent low susceptibility to B. dendrobatidis infection.[14][15] The bullfrog often escapes captivity and can establish feral populations where it may introduce the disease to new areas.[4] It has also been shown that B. dendrobatidis can survive and grow in moist soil and on bird feathers, suggesting that B. dendrobatidis may also be spread in the environment by birds and transportation of soils.[16] Infections have been linked to mass mortalities of amphibians in North America, South America, Central America, Europe and Australia.[17][18][19] B. dendrobatidis has been implicated in the extinction of the sharp-snouted day frog (Taudactylus acutirostris) in Australia.[20]

A wide variety of amphibian hosts have been identified as being susceptible to infection by B. dendrobatidis, including wood frogs (Rana sylvatica),[21] the mountain yellow-legged frog (Rana muscosa)[22] the southern two-lined salamander (Eurycea cirrigera),[23] San Marcos Salamander (Eurycea nana) Texas Salamander (Eurycea neotenes) Blanco River Springs Salamander (Eurycea pterophila) Barton Springs Salamander (Eurycea sosorum) Jollyville Plateau Salamander (Eurycea tonkawae) [24] Ambystoma jeffersonianum,[25] the western chorus frog (Pseudacris triseriata), the southern cricket frog (Acris gryllus), the eastern spadefoot toad (Scaphiopus holbrooki), the southern leopard frog (Rana sphenocephala),[26] the Rio Grande Leopard frog (Lithobates berlandieri),[27] and the Sardinian newt (Euproctus platycephalus).[28]

Southeast Asia[edit]

While most studies concerning B. dendrobatidis have been performed in various locations across the world, the presence of the fungus in Southeast Asia remains a relatively recent development. The exact process through which the fungus was introduced to Asia is not known, however, as mentioned above, it has been suggested transportation of asymptomatic carrier species (e.g. Lithobates catesbeianus, the American Bullfrog) may be a key component in the dissemination of the fungus, at least in China.[29] Initial studies demonstrated the presence of the fungus on island states/countries such as Hong Kong,[30] Indonesia,[31] Taiwan,[32] and Japan.[33] Soon thereafter, mainland Asian countries such as Thailand,[34] South Korea,[35] and China[36] reported incidences of B. dendrobatidis among their amphibian populations. Much effort has been put into classifying herpetofauna in countries like Cambodia, Vietnam, and Laos where new species of frogs, toads, and other amphibians and reptiles are being discovered on a frequent basis. Scientists simultaneously are swabbing herptofauna in order to determine if these newly discovered animals possess traces of the fungus.

In Cambodia, a study showed B. dendrobatidis to be prevalent throughout the country in areas near Phnom Penh (in a village <5 km), Sihanoukville (frogs collected from the local market), Kratie (frogs collected from streets around the town), and Siem Reap (frogs collected from a national preserve: Angkor Centre for Conservation of Biodiversity).[37] Another study in Cambodia questioned the potential anthropological impact in the dissemination of B. dendrobatidis on local amphibian populations in 3 different areas in relation to human interaction: low (an isolated forest atop a mountain people rarely visit), medium (a forest road ~15km from a village that is used at least once a week), and high (a small village where humans interact with their environment on a daily basis). Using quantitative PCR, evidence of B. dendrobatidis was found in all 3 sites with the highest percentage of amphibians positive for the fungus from the forest road (medium impact; 50%), followed by the mountain forest (low impact; 44%) and village (high impact; 36%).[38] Human influence most likely explains detection of the fungus in the medium and high areas, however it does not provide an adequate explanation why even isolated amphibians were positive for B. dendrobatidis. This may go unanswered until more research is performed on transmission of the fungus across landscapes.

See also[edit]

References[edit]

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Further reading[edit]

External links[edit]