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Candida tropicalis (Castell.) Berkhout 1923

Candida tropicalis ( 德語 )

由wikipedia DE提供

Candida tropicalis ist ein asexueller diploider pathogener Candida-Stamm, der zu etwa 10 % der erfassten systemischen Pilzinfektionen führt. Er wurde ubiquitär auch in Umwelt-Isolationen von Kot, Erde, Garnelen, Kefir, Boden, Wasser, Wein, Fischen, Kakao, Früchten und Beeren, Konfitüre und Joghurt gefunden.[1]

Beschreibung

Auf Sabouraud-Agar gezüchtete Kolonien sind weiß bis cremefarben, glatt, kahl oder leicht faltig und hefeartig in ihrer Erscheinung. Der Rand der Kolonie wird oft von Mycel umgeben. Die Zellen sind kugelig bis subsphärisch ähnlich der Bäckerhefe und werden 3,0–5,5 × 4,0–9,0 µm groß. Auf RAT (Reis-Agar-Tween) ist reichlich Pseudomycel vorhanden, das baumartig aussieht und einzelne oder kurze Ketten oder Trauben von Blastosporen trägt.[2][3]

Gentechnik

Ähnlich wie bei vielen anderen Candida-Stämmen entspricht einem CUG-Codon in C. tropicalis ein Serin-Rückstand anstatt des universellen Leucins. Die genaue Genomgröße und Chromosomenzahl von C. tropicalis sind nicht bekannt, aber Schätzungen zufolge hat das Genom eine Größe von 15 MBp, in fünf oder sechs Chromosomen organisiert. Die Zahl der Protein-Gene beträgt 6254.[4] Auch der Protein-Export wurde erforscht.[5] Die 2-Enoyl-CoA-Hydratase[6] 3 von C. tropicalis ist ein Teil eines multifunktionalen Enzyms des Typs 2[7] Das KEGG-Genom[8] wurde online publiziert[9] wie auch die Proteinstrukturen.[10]

Klinische Bedeutung

Candida tropicalis ist eine der Hauptursachen für Sepsis und verbreitete Candidiasis, vor allem in Patienten mit Lymphomen, Leukämien und Diabetes. Krankheitsbilder sind Sepsis, Harnwegsinfekte, pulmonale Manifestationen, Haut- und Nagelmykosen und Sinusitis.[11] C. tropicalis ist neben C. albicans der zweithäufigstauftretende medizinische Candida-Stamm mit steigender Relevanz als Erreger systemischer Mykosen.[12] Saccharose negative Varianten von C. tropicalis wurden auch zunehmend in Fällen von Kandidose gefunden. Er tritt vor allem bei immungeschwächten Patienten mit oft höherer Virulenz als Candida albicans auf und ist für ca. 30 % der Sprosspilzerkrankungen bei Patienten mit malignen hämatologischen Erkrankungen verantwortlich.[13]

Diagnose

Zur Diagnose bieten sich an:[14][15]

  • Kulturen mit begleitendem Pilz-Antibiogramm
  • IG-A
  • Feine Längstrukturen und Verwerfungen im Nagel deuten auf Nagelbettinfektion hin
  • PCR[16]

Zur Untersuchung dienen Proben aus Blut, Urin, Sputum, Vaginalabstrichen, Nägeln, Bronchiallavagen und Sinusflüssigkeit und Stuhl.[17]

Behandlung

Wirksame Antimykotika-Medikamente sind Fluconazol[18], Voriconazol, Caspofungin[19] und Anidulafungin sowie das frei käufliche Nystatin und aus der Naturheilkunde Cineol (Eukalyptusöl). C. tropicalis hat durch die oft höhere Virulenz als Candida albicans vor allem bei geschwächten Patienten an klinischer Bedeutung gewonnen. Die hohe Resistenz gegen Medikamente hat bei Nystatin schon zu Therapieversagen und Resistenz[20] geführt (Ahearn u. a. 1984).

Literatur

  • B. Chattopadhyay: Candida tropicalis meningitis: a case report. In: The Journal of Laryngology & Otology, 95, 1981, S. 1149–1151.
  • N. L. Dawson, H. A. Robles, S. Alvarez: Recurrent Candida tropicalis meningitis. In: Clinical Neurology and Neurosurgery, 107, 2005, S. 243–245.
  • S. R. Ahuja, S. Karande, M. V. Kulkarni, U. Tendolkar: Candida tropicalis meningitis in a young infant. In: Indian J Pediat., 70, 2003, S. 925–927.
  • D. W. Chadwick, E. Hartley, M. Mackinnon: Candida tropicalis meningitis. In: Arch Neurol., 37, 1980, S. 175–176.
  • E. Hernig, M. Djaldetti, J. Pinkhas, A. Vries: Candida tropicalis meningitis in Hodking’s disease. In: JAMA, 119, 1967, S. 214–215.
  • Candidose der Haut. (Memento vom 28. März 2014 im Internet Archive)
  • Candida tropicalis and Candida Albicans fungemia in children with leukemitis. In: Cancer, 68, 1991, S. 594.
  • G. Butler u. a.: Evolution of pathogenicity and sexual reproduction in eight Candida genomes. In: Journal Nature, 459, 2009, S. 657–662.

Einzelnachweise

  1. Candida-Arten (außer C. albicans) Candida-Arten
  2. Candida tropicalis – Pathogenic hemiascomycete yeast used in industry and sequenced for a comparative genomics study Pathogenic hemiascomycete yeast
  3. Candida tropicalis (Memento des Originals vom 5. März 2011 im Internet Archive)  src= Info: Der Archivlink wurde automatisch eingesetzt und noch nicht geprüft. Bitte prüfe Original- und Archivlink gemäß Anleitung und entferne dann diesen Hinweis.@1@2Vorlage:Webachiv/IABot/www.mycology.adelaide.edu.au Candida tropicalis Mycology online C. tropicalis
  4. G. Butler, M. D. Rasmussen, u. a.: Evolution of pathogenicity and sexual reproduction in eight Candida genomes. In: Nature. Band 459, Nummer 7247, Juni 2009, S. 657–662, doi:10.1038/nature08064, PMID 19465905, PMC 2834264 (freier Volltext).
  5. Protein export - Candida tropicalis
  6. hydratase
  7. M. K. Koski, A. M. Haapalainen, J. K. Hiltunen, T. Glumoff: Crystallization and preliminary crystallographic data of 2-enoyl-CoA hydratase 2 domain of Candida tropicalis peroxisomal multifunctional enzyme type 2. In: Acta crystallographica. Section D, Biological crystallography. Band 59, Pt 7Juli 2003, S. 1302–1305. PMID 12832794.
  8. Candida tropicalis Candida tropicalis MYA-3404
  9. Candida tropicalis: CTRG_05871 (Memento vom 28. März 2014 im Internet Archive)
  10. Candida Gene Order Browser
  11. Candida-Arten (außer C. albicans)
  12. W. G. Merz u. a.: Increased incidence of fungemia caused by Candida crusei. In: J Clin Micro. 24, 1986, S. 581.
  13. T. Kashimoto, H. Kitagawa, H. Kachi: Candida Tropicalis Vertebral Osteomyelitis and Discitis: A Case Report and Discussion on the Diagnosis and Treatment. (Abstract)
  14. Candida-Nachweis Diagnose
  15. Orale Candidose. (Memento vom 28. März 2014 im Internet Archive) → Diagnostik
  16. Identifizierung von Candida-Spezies und -Stämmen durch den Nachweis von polymorphen DNA-Regionen in der PCR. (PDF) Dissertation
  17. Hefepilze / Blastomyceten (Memento vom 14. September 2012 im Internet Archive)
  18. Was von der Antibiotika-Therapie übrig bleibt …. – opportunistische Pilzinfektionen durch Candida (Memento vom 23. April 2007 im Internet Archive) Antibiotikamonitor
  19. Neue Standards für die Therapie von Pilzinfektionen
  20. Eintrag zu Nystatin in der DrugBank der University of Alberta, abgerufen am 28. Januar 2017.
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wikipedia DE

Candida tropicalis: Brief Summary ( 德語 )

由wikipedia DE提供

Candida tropicalis ist ein asexueller diploider pathogener Candida-Stamm, der zu etwa 10 % der erfassten systemischen Pilzinfektionen führt. Er wurde ubiquitär auch in Umwelt-Isolationen von Kot, Erde, Garnelen, Kefir, Boden, Wasser, Wein, Fischen, Kakao, Früchten und Beeren, Konfitüre und Joghurt gefunden.

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wikipedia DE

Candida tropicalis ( 英語 )

由wikipedia EN提供

Candida tropicalis is a species of yeast in the genus Candida. It is a common pathogen in neutropenic hosts, in whom it may spread through the bloodstream to peripheral organs.[1] For invasive disease, treatments include amphotericin B, echinocandins, or extended-spectrum triazole antifungals.[2]

History and taxonomy

In the history of fungi, the name of genus Candida, derived from the family Debaryomycetaceae,[3] comes from the Latin term "candidus" which has the meaning of “glowing white” and also refers to as smooth and glistering.[4] Genus Candida referred to any asexual yeast without any of the following characteristics: production of acetic acid, pigments of colours red, pink or orange, arthroconidia, unipolar or bipolar budding, enteroblastic-basipetal budding, blastoconidia formation on sympodulae, buds formation on stalks, triangular cells, needle-shaped terminal conidia, and having the ability to grow on inositol as a sole carbon source.[3] Although there are 200 species identified in this genus,[3] the taxonomy remains undefined and incomplete due to several reasons such as changing the words for some representations, the finding of new species and the reclassification of identified old species.[4] This genus no longer includes species that test positive to diazonium blue B (DBB).[3] The defunct genera Oidium and Monilia were used to represent the genus Candida.[4]

In the genus Candida, there are other species that are similar to Candida tropicalis. Candida albicans is taxonomically close to C. tropicalis sharing many pathogenic traits[5] whereas C. maltosa and C. sake are physiologically similar to C. tropicalis but they can be differentiated by the growth at 35 °C (only C. sake showing negative) and assimilation of soluble starch (only C. tropicalis showing positive starch assimilation).[6]

Identification

C. tropicalis is easily identified using phenotypic and molecular methods.[7] The identification of species in the genus Candida relies on morphological and physiological features. Species in the genus are vegetative cells which reproduce asexually by budding, and the structure, shape, septation, color and arrangement of buds is useful for identification.[8] The production and appearance of pseudohyphae and blastoconidia may also be useful for identification.[8] Physiological profiles relating to carbon and nitrogen utilization are of value in determining species, as are the presence certain distinctive biochemical features.[6] Increasingly, molecular genetic methods such as DNA sequencing are used as primary tools for the accurate determination of species identifications in this group.[6]

Growth and morphology

Colony of C. tropicalis on a Petri dish.

C. tropicalis is a vegetative cell[9] with the shape from round to oval ranging from approximately 2 – 10 micrometers.[3] A mould exhibits dimorphism[8] forming a single-celled yeast or so-called blastoconidia which reproduces by simple budding.[8] Conidia are the asexual units that are produced by budding of the tips or walls of the hyphae.[8] Conidia are types of simple and unicellular bodies that could also take the form of multicellular cells with different shapes, sizes, and colors.[8] Microconidia refer to small and unicellular conidia whereas macroconidia refer to large and multicellular conidia.[8]

There are different media on which C. tropicalis can grow effectively. A common medium used is the Sabouraud’s agar which contains peptone and sugar. This is enough for identifying the species but with a disadvantage of promoting mycelial growth and suppressing conidia formation.[8] Another commonly used medium is the cornmeal agar which is useful in inducing formation of conidia.[8] Potato-glucose, potato-carrot, tomato juice, lima bean and others are also types of media used for growth.[8] The optimal temperature for growth is between 25–35 °C (77–95 °F)[4] and growth is enhanced if sugar or fat is added in the medium. Colony of C. tropicalis are white, smooth and butyrous with a fringed border.[6][9]

Physiology

C. tropicalis reproduces asexually by the production of blastoconidia through budding. As blastoconidia increase in number they may elongate in shape producing structures called the pseudohyphae.[3][4] Under specific conditions of reduced oxygen level in host tissues, submerged colonies in agar medium, or in the presence of 5-10% CO2, true, septate hyphae may form.[9][3]

Physiological characteristics of C. tropicalis

Growth

Fermentation

Urea hydrolysis

This test is to detect yeast’s ability to produce enzyme urease. Once there's a compatible substrate, urease will split urea to produce ammonia increasing the pH. C. tropicalis is found to be urease negative.[3]

Diazonium Blue B Test

This test uses the azo dye, diazonium blue B which differentially stains cells from species affiliated with the Division, Basidiomycota. For C. tropicalis, this test is negative.[6]

Parasexuality

C. tropicalis diploid cells of opposite mating type can mate to form tetraploid cells.[11] These cells may then undergo chromosome loss during long-term propagation in rich medium resulting in the eventual regeneration of diploid cells.[12] Such diploid cells are again mating competent thus completing a parasexual cycle. Opaque C. tropicalis cells can also form an architecturally complex sexual biofilm.[13]

Habitat and ecology

Candida species are very pervasive yeasts that are distributed worldwide geographically. They are more likely to be found in tropical climate where temperature and humidity will enhance the adaptability of C. tropicalis.[5] They can be found in food such as sauerkraut, molasses, miso, fruit, baker’s yeast and some fruits.[9] They are commonly found on plants and in the digestive system of mammals, especially in the gastrointestinal tract, and in the mucocutaneous membranes of humans.[3] C. tropicalis is considered as an osmotolerant yeast; microorganisms that are able to survive in high salt concentration and able to develop fungal persistence in saline environments.[7]

Storage and transportation

The selection of medium for sample growth is very important accounting for the pros and cons of each type of growth medium. Once decided on the medium, need to add 8 ug of fluconazole per mL to limit bacterial growth and contamination.[3] When the medium is ready, it is optional to add supplement to help and optimize specimen growth. After the growth, features examination including shape, size, bud arrangement, cell wall thickness, temperature of growth, pseudohyphae presence, arthroconidia presence, and capsule presence are all important to take into account.[3] If the species are grown using any type of the medium mentioned, the transportation of specimens for testing should be completed in less than two hours.[3] If there is any delay, the samples should be stored at 37 °C with the exception of contaminated specimens that need be stored in 4 °C.[3]

Pathogenicity

In tropical countries, C. tropicalis is one of the most common colonizer and pathogen causing human disease,[5] especially found on human skin, in the gastrointestinal tract and also in female genitourinary tract.[4] It can be transmitted between health-care workers and patients,[5] especially in environments such as hospitals.[5] C. tropicalis can survive for up to 24 hours therefore be cross-transmitted to a second hand with a probability of 69% and to a third hand with 38% probability.[5] It is the cause responsible for approximately half of the beyond-surface candida infections.[5] C. tropicalis is the second most virulent Candida species[7] that can significantly affect by spreading through the weakened immune system host and can occupy the gastrointestinal tract within 30 minutes of inoculation, all this resulting in increased mortality.[5][14][10] Impact of candidiasis, infections cause by C. tropicalis, have increased globally.[14] C. tropicalis is virulent due to its ability to produce biofilm, secrete lytic enzymes, adhere to epithelial and endothelial cells, and undergo transition of bud to hyphae.[15][10][7]

Biofilms are complex structures that are formed from the grouping of microorganisms on a local surface, either biotic or abiotic,[15] dependent on the ability of cellular adhesion to substrates.[7] For C. tropicalis to fully enter and cause infection in the host, it needs some helpers. First, once it is attached onto the host tissues, extracellular enzymes called the proteases will be produced to facilitate the penetration of the pathogen and allow it to interfere with the host defense system.[5] proteases will hydrolyze peptide bonds; secreted aspartic proteases (SAP) support C. tropicalis to be attached and penetrate deep into the tissues to affect the organs.[5] phospholipases will hydrolyze phospholipid; assist to break the epithelial cell membrane structure allowing the hyphal tip to enter into the cytoplasm.[5] Many conditions that contribute to C. tropicalis survival and colonization are: a) increase the use of antifungal regimen, b) increased number of immunocompromised patients, c) long-term use of catheters, and d) use of broad-spectrum antibiotics.[14] Although different tests are able to use for identification of species, each of the tests will have different limitations such as sensitivity, specificity, cost and equipment availability.[3]

Human diseases

Types of disease caused by C. tropicalis will vary depending on the location where the species colonizes. With an infection in the mucous membrane, subject will experience oropharyngeal candidiasis, angular cheilitis, balanoposthitis, oral thrush and vulvovaginal candidiasis.[14] Although provided with oral cavity defenses such as epithelial cells, saliva, salivary immunoglobin (IgA), lysozyme, lactoferrin, histidine-rich polypeptide and lactoperoxidase to suppress C. tropicalis’ overgrowth,[14] C. tropicalis is reported to secrete additional products that can preferably target onto T-cell deficient host.[14] C. tropicalis is a normal flora which is found on the skin and nails on approximately 10% of the patients.[5] Superficial and localized mucosal infections are mostly reported with a higher risk factor when combined with other diseases found in a patient.[5] Patients with C. tropicalis infections are also seen with denture, HIV infection or irradiation for malignancies.[5] 38% of AIDS patients with recurrent disease are more likely to get infected by C. tropicalis, getting oral thrush and oropharyngeal candidiasis.[5] Only filamentous growth of C. tropicalis have the ability to invade and colonize orally in the epithelium,[10] commonly seen in cancer patients and higher risk for someone who subsequently develops disseminated invasive disease.[5] Candiduria is referred to as urinary tract infections caused by C. tropicalis which are often presented as nosocomial infections.[5] Although up to 2% of patients are asymptomatic, those with diabetes mellitus and with leukemia are more likely to be infected.[5]

If an infection involves interdigital candidiasis, paronychia and diaper rash, subject is likely to have cutaneous candidiasis.[14] Otherwise, if an infection involves body fluid and internal organs damages, subject will experience pulmonary candidiasis, invasive and disseminated candidiasis, gastrointestinal candidiasis and candidemia.[14] C. tropicalis colonization is favoured in the gastrointestinal tract;[14] a common risk factor for individuals that are susceptible for invasive candidiasis development.[5] Candidemia is a worldwide bloodstream disease mainly affecting peripheral organs in humans.[5] Usually, candidemia caused by C. tropicalis are associated with cancer patients that have either leukemia or neutropenia.[15] According to the data obtained from 2010, frequency of candidemia is 12-25% in the US, 4.5-9% in Europe, 20-24% in Brazil and 20-60% in South Asia.[5] C. tropicalis can cause nosocomial fungal bloodstream infections along with C. glabrata and C. parapsilosis.[5] Mortality rate of invasive and disseminated infections caused by C. tropicalis is high, ranging from 40% to 70%.[5] Risk factors that contribute to the high rate are leukemia, anti-neoplastic chemotherapy, previous neutropenia, central venous catheters, long stay on intensive care and total parenteral nutrition.[5] Although children infections are not as common seen as in adults, leukemia, secondary neutropenia and bone marrow transplantation[14] are factors favouring C. tropicalis infections.[5] Another infection seen commonly in patients who have leukemia and secondary neutropenia, is chronic disseminated candidiasis (CDC) is another type of disseminated candida infection that mainly develops in the liver, spleen and kidney.[5]

Treatment and prevention

The most important and most essential step to prevent contact with the fungi species is by washing the hands.[4] There are several types of therapy for the different level of infections caused by C. tropicalis. Normally, antifungal agents are used to treat these infections.[4] Amphotericin B deoxycholate is the most common treatment antifungal agent used to treat Candida infections.[4] Topical antifungal agents are commonly taken in 3 forms: oral suspension, ointment and powder.[4] Oral suspension is mainly used to treat thrush whereas ointment is directly applied onto the infected section.[4] Nystatin is a type of antifungal agent used because it is not absorbed by the gastrointestinal tract.[4] These types of agents will function to lower candida species’ phospholipases activities.[14] Flucytosine (5FC) is another type of therapy treatment including 3 agents used; caspofungin, micafungin and anidulafungin.[5] Usage of caspofungin will efficiently target against oropharyngeal and oesophageal candidiasis and invasive candidiasis.[5] Micafungin, compared to amphotericin B, it is more efficient.[5] Anidulafungin results are similar to Caspofungin and Micafungin.[5] echinocandin are a type of non-competitive inhibitors of cell wall 1,3-b-D-glucan synthase complex mainly used to treat fungal infections.[5][4][7] Azoles are agents that can deplete ergosterol, the main component of the fungus cell wall membrane,[7] in order to inhibit fungal growth.[4] fluconazole is water-soluble, ready to be taken orally.[5] C. tropicalis can rapidly develop resistance towards fluconazole therefore it's not recommended to retreat fluconazole-treated patients with recurrent candidiasis.[14] Other azoles that are highly active against C. tropicalis are itraconazole, voriconazole, posaconazole, ravuconazole and isavuconazole.[5] Voriconazole is a new generation from fluconazole with a higher potential of broad spectrum activity.[4] All of the mentioned treatments and drug therapies can also be applied onto neonates and premature newborns taking into account the amount of recommended dose. Although there are several ways to treat the different types of C. tropicalis’ infections, the best way to improve treatments results is to improve host immune system.[14]

References

  1. ^ Mastromarino, Paola; Vitali, Beatrice; Mosca, Luciana (2013). "Bacterial vaginosis: a review on clinical trials with probiotics" (PDF). New Microbiologica. 36 (3): 229–238. PMID 23912864.
  2. ^ Chai LY, Denning DW, Warn P (2010). "Candida tropicalis in human disease". Crit. Rev. Microbiol. 36 (4): 282–98. doi:10.3109/1040841X.2010.489506. PMID 20883082. S2CID 36366177.
  3. ^ a b c d e f g h i j k l m n Murray, P. R.; Baron, E. J.; Jorgensen, J. H.; Pfaller, M. A.; Yolken, R. H. (2003). Manual of Clinical Microbiology. Washington, US: ASM Press. ISBN 978-1555812553.
  4. ^ a b c d e f g h i j k l m n o Wilson, C. B.; Nizet, V.; Maldonado, Y.; Remington, J. S.; Klein, J. O. (2015). Remington and Klein's Infectious diseases of the Fetus and Newborn Infant. Philadelphia, US: Saunders. ISBN 9780323241472.
  5. ^ a b c d e f g h i j k l m n o p q r s t u v w x y z aa ab ac ad ae af ag Chai, L. Y.; Denning, D. W.; Warn, P. (2010). "Candida tropicalis in human disease". Crit. Rev. Microbiol. 26 (4): 282–98. doi:10.3109/1040841X.2010.489506. PMID 20883082. S2CID 36366177.
  6. ^ a b c d e f g h i j k l Kurtzman, C. P.; Fell, J. W. (1998). The yeasts: A Taxonomic Study. New York, US: Elsevier Science. ISBN 978-0444813121.
  7. ^ a b c d e f g h i Zuza-Alves, D. L.; Silva-Rocha, W. P.; Chaves, G. M. (2017). "An update on Candida tropicalis based on basic and clinical approaches". Frontiers in Microbiology. 8: 1927. doi:10.3389/fmicb.2017.01927. PMC 5645804. PMID 29081766.
  8. ^ a b c d e f g h i j Rippon, J. W. (1988). Medical Mycology: The Pathogenic Fungi and The Pathogenic Actinomycetes. Philadelphia, US: Saunders. ISBN 978-0721624440.
  9. ^ a b c d Barnett, J. A.; Payne, R. W.; Yarrow, D. (1991). Yeasts: Characteristics and identification. Cambridge, UK: Cambridge University Press. ISBN 978-0521350563.
  10. ^ a b c d e Silva, S.; Negri, M.; Henriques, M.; Oliveira, R.; Williams, D. W.; Azeredo, J. (2011). "Candida glabrata, Candida parapsilosis and Candida tropicalis: biology, epidemiology, pathogenicity and antifungal resistance". FEMS Microbiology Reviews. 36 (2): 288–305. doi:10.1111/j.1574-6976.2011.00278.x. PMID 21569057.
  11. ^ Porman AM, Alby K, Hirakawa MP, Bennett RJ. Discovery of a phenotypic switch regulating sexual mating in the opportunistic fungal pathogen Candida tropicalis. Proceedings of the National Academy of Sciences USA 2011 Dec 27;108(52):21158-63. doi: 10.1073/pnas.1112076109.
  12. ^ Seervai RN, Jones SK Jr, Hirakawa MP, Porman AM, Bennett RJ. Parasexuality and ploidy change in Candida tropicalis. Eukaryot Cell. 2013 Dec;12(12):1629-40. doi: 10.1128/EC.00128-13. PMID 24123269
  13. ^ Jones SK Jr, Hirakawa MP, Bennett RJ. Sexual biofilm formation in Candida tropicalis opaque cells. Mol Microbiol. 2014 Apr;92(2):383-98. doi: 10.1111/mmi.12565. PMID 24612417
  14. ^ a b c d e f g h i j k l m Kothavade, R. J.; Kura, M. M.; Valand, A. G.; Panthaki, M. H. (2010). "Candida tropicalis: its prevalence, pathogenicity and increasing resistance to fluconazole". Journal of Medical Microbiology. 59 (8): 873–80. doi:10.1099/jmm.0.013227-0. PMID 20413622.
  15. ^ a b c Sardi, J. C. O.; Scorzoni, L.; Bernardi, T.; Fusco-Almeida, A. M.; Mendes Giannini, M. J. S. (2013). "Candida species: current epidemiology, pathogenicity, biofilm formation, natural antifungal products and new therapeutic options". Journal of Medical Microbiology. 62 (Pt 1): 10–24. doi:10.1099/jmm.0.045054-0. PMID 23180477.
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Candida tropicalis: Brief Summary ( 英語 )

由wikipedia EN提供

Candida tropicalis is a species of yeast in the genus Candida. It is a common pathogen in neutropenic hosts, in whom it may spread through the bloodstream to peripheral organs. For invasive disease, treatments include amphotericin B, echinocandins, or extended-spectrum triazole antifungals.

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Candida tropicalis ( 西班牙、卡斯蒂利亞西班牙語 )

由wikipedia ES提供

Candida tropicalis es una levadura del género Candida, puede causar enfermedad en humanos (candidiasis), especialmente virulentas en pacientes inmunodeprimidos. El género Candida incluye aproximadamente 150 especies identificadas, el principal patógeno es Candida albicans que causa alrededor del 50% del total de candidiasis, candida tropicalis es más infrecuente, originando alrededor del 15% del total de infecciones producidas por levaduras del género Candida. Esta especie se presenta sobre todo en países tropicales, pero su prevalencia tiende a aumentar en todo el mundo, puede ser resistente a algunos medicamentos utilizados habitualmente en el tratamiento de la candidiasis, como el fluconazol.[2][3]

Referencias

  1. Berkhout, De Schimmelgesl. Monilia, Oidium, Oospora en Torula, Disset. Ultrecht: 44 (1923)
  2. Candida tropicalis in human disease. Crit Rev Microbiol. 2010 Nov;36(4):282-98. doi: 10.3109/1040841X.2010.489506.
  3. Rajendra Kothavade et al.Candida tropicalis: its prevalence, pathogenicity and increasing resistance to fluconazole. J Med Microbiol. 2010 Aug;59(Pt 8):873-80. doi: 10.1099/jmm.0.013227-0. Epub 2010 Apr 22.
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Candida tropicalis: Brief Summary ( 西班牙、卡斯蒂利亞西班牙語 )

由wikipedia ES提供

Candida tropicalis es una levadura del género Candida, puede causar enfermedad en humanos (candidiasis), especialmente virulentas en pacientes inmunodeprimidos. El género Candida incluye aproximadamente 150 especies identificadas, el principal patógeno es Candida albicans que causa alrededor del 50% del total de candidiasis, candida tropicalis es más infrecuente, originando alrededor del 15% del total de infecciones producidas por levaduras del género Candida. Esta especie se presenta sobre todo en países tropicales, pero su prevalencia tiende a aumentar en todo el mundo, puede ser resistente a algunos medicamentos utilizados habitualmente en el tratamiento de la candidiasis, como el fluconazol.​​

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Candida tropicalis ( 波蘭語 )

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C tropicalis YC466.png

Candida tropicalis (Castell.) Berkhout — gatunek grzybów należący do rzędu drożdżakowców (Saccharomycetales)[1].

Systematyka i nazewnictwo

Pozycja w klasyfikacji według Index Fungorum: Candida, Incertae sedis, Saccharomycetales, Saccharomycetidae, Saccharomycetes, Saccharomycotina, Ascomycota, Fungi[1].

Po raz pierwszy takson ten zdiagnozował w 1910 r. Aldo Castellani nadając mu nazwę Oidium tropicale. Obecną, uznaną przez Index Fungorum nazwę nadał mu w 1923 r. C. M. Berkhout, przenosząc go do rodzaju Candida[1].

Ma ok. 100 synonimów nazwy naukowej[2].

Charakterystyka

C. tropicalis jest, po C. albicans, drugim najbardziej wirulentnym grzybem z rodzaju Candida i, podobnie jak inne Candida, u człowieka i zwierząt może powodować zakażenia oportunistyczne[3], a szczególnie wirulentny jest wobec pacjentów cierpiących na białaczki czy podobne choroby[4]. Przebieg zakażenia i objawy są zbliżone do tych w przypadku zakażenia C. albicans i obejmują: zapalenie opon mózgowo-rdzeniowych, zapalenie wsierdzia, ostrą, ogólnoustrojową drożdżycę (w tym pochwy), odmiedniczkowe zapalenie nerek, zapalenie przełyku i pochwy u człowieka, a zapalenie sutków czy poronienia grzybiczne u zwierząt[3].

Według analizy rRNA małej podjednostki rybosomu (18S), C. tropicalis razem z innymi przedstawicielami rodzaju Candida (C. albicans, C. parapsilosis i C. viswanathii) tworzy silnie wyodrębnioną od innych patogennych grzybów grupę[5].

Morfologia

Hodowane na stałej pożywce YPD komórki C. tropicalis są okrągłe lub owalne o wielkości 3,5–7 na 5,5–10 μm. Hodowane przez trzy dni w temperaturze 25 °C na podłożu z mąki kukurydzianej z dodatkiem detergentu Tween 80 tworzą blastokonidia, pojedyncze lub w małych grupach, zebrane wzdłuż osi długiej pseudostrzępki. Czasami obecne są prawdziwe strzępki, a rzadko obserwuje się tworzenie chlamydospor w kształcie wydłużonych kropel[4].

Kolonie na płytkach YPD są okrągłe, w kolorze kremowym, przy brzegach czasami pomarszczone lub ze strzępkami grzybni[4].

Występowanie

Candida tropicalis został wyizolowany z wielu różnych zwierząt ciepłokrwistych i człowieka z różnych części ciała, takich jak jelita, pochwa, jama ustna, co wskazuje, że mikroorganizmy te są komensalami tych miejsc. W przypadku człowieka, wyniki te są trudne do jednoznacznej interpretacji, gdyż w większości wypadków materiał pochodził od pacjentów, a więc od wypadków klinicznych. Ze stanowisk naturalnych izolowany rzadko, ale stwierdzono jego obecność na wszystkich kontynentach, a także np. na wyspach Pacyfiku, co wskazuje, że C. tropicalis to gatunek kosmopolityczny[3].

Zastosowanie przemysłowe i naukowe

C. tropicalis znalazł zastosowanie w produkcji poliestrów, poliamidów, ksylitolu i etanolu[6]. Gatunek ten może także znaleźć zastosowanie w produkcji przemysłowej szeregu innych związków (m.in. różnych kwasów organicznych, alkoholi) na drodze fermentacji odpowiednich substratów[7].

W nauce organizm ten jest modelem w badaniach biogenezy peroksysomów i ekspresji białek peroksysomalnych[6].

Przypisy

  1. a b c Index Fungorum (ang.). [dostęp 2013-11-12].
  2. Species Fungorum (ang.). [dostęp 2015-12-16].
  3. a b c C. Davis. CMI Descriptions of pathogenic fungi and bacteria No. 871. „Mycopathologia”. 96 (3), s. 171–196, 1986. CAB International Mycological Institute. DOI: 10.1007/BF00437384.
  4. a b c Davise H. Larone: Medically Important Fungi: A Guide to Identification. American Society Microbiology, 2002, s. 119. ISBN 978-1-55581-172-3.
  5. SM. Barns, DJ. Lane, ML. Sogin, C. Bibeau i inni. Evolutionary relationships among pathogenic Candida species and relatives.. „J Bacteriol”. 173 (7), s. 2250-5, Apr 1991. PMID: 2007550.
  6. a b Candida tropicalis (ID 12494) Genome Project Result (ang.). W: NCBI Entrez Genome Project [on-line]. National Center for Biotechnology. [dostęp 2010-11-04].
  7. George G. Khachatourians: Food Biotechnology: Microorganisms. New York: Wiley-Interscience, 1995, s. 316–320. ISBN 978-0-471-18570-3.
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Candida tropicalis: Brief Summary ( 波蘭語 )

由wikipedia POL提供
C tropicalis YC466.png

Candida tropicalis (Castell.) Berkhout — gatunek grzybów należący do rzędu drożdżakowców (Saccharomycetales).

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Candida tropicalis ( 葡萄牙語 )

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Candida tropicalis é uma espécie de fungo pertencente ao gênero Candida e a ordem Saccharomycetales. Ao lado de outro membros do gênero, é oportunista, causadora da candidíase.

A Candida tropicalis é por vezes usada como modelo em pesquisas genéticas e medicinais.

Referências

  1. Berkhout, De Schimmelgesl. Monilia, Oidium, Oospora en Torula, Disset. Ultrecht: 44 (1923)
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Candida tropicalis: Brief Summary ( 葡萄牙語 )

由wikipedia PT提供

Candida tropicalis é uma espécie de fungo pertencente ao gênero Candida e a ordem Saccharomycetales. Ao lado de outro membros do gênero, é oportunista, causadora da candidíase.

A Candida tropicalis é por vezes usada como modelo em pesquisas genéticas e medicinais.

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Candida tropicalis ( Szl )

由wikipedia SZL提供

Candida tropicalis je grzib[44], co go nojprzōd ôpisoł Castell., a terŏźnõ nazwã doł mu Christine Marie Berkhout 1923. Candida tropicalis nŏleży do zorty Candida, rzyndu Saccharomycetales, klasy Saccharomycetes, grōmady Ascomycota i krōlestwa grzibōw.[62][63] Żŏdne podgatōnki niy sōm wymianowane we Catalogue of Life.[62]

Przipisy

  1. Nowak.-Waszcz. & Pietka (1983), In: Acta microbiol. pol. 32(1):84
  2. J.M. Baker, Salkin, Pincus & D'Amatao (1981), In: Mycotaxon 13(1):115
  3. Furukawa, Matsuyoshi, Monoda & Yamada (1977), In: J. Ferment. Technol., Osaka 55:356
  4. E.K. Novák & Vitéz (1964), In: Zentbl. Bakt. ParasitKde, Abt. I 193:127
  5. E.K. Novák & Zsolt (1961), In: Acta bot. hung. 7:133
  6. Cif. (1960), In: Manuale di Micologia Medica, Edn 2 2:252
  7. Yamaguchi{?} (1954), In: J. agric. Chem. Soc. Japan 28:415
  8. Kobay.{?} (1953), In: Rep. Wood Saccharification Discussion Ctee (Japan) 2:88
  9. Cif. & Redaelli (1943), In: Atti Ist. bot. Univ. Lab. crittog. Pavia, Ser. 5 3:48
  10. C.W. Dodge & M. Moore (1936), In: Ann. Mo. bot. Gdn 23:142
  11. C.W. Dodge & M. Moore (1936), In: Ann. Mo. bot. Gdn 23:140
  12. C.W. Dodge (1935), In: Medical mycology. Fungous diseases of men and other mammals:269
  13. C.W. Dodge (1935), In: Medical mycology. Fungous diseases of men and other mammals:255
  14. 14,0 14,1 14,2 14,3 14,4 14,5 14,6 14,7 14,8 14,9 CABI databases. [dostymp 24 stycznia 2013].
  15. Ciferri & Redaelli (1935), In: Arch. Mikrobiol. 6:35
  16. Redaelli & Cif. (1935), In: Arch. Mikrobiol. 6:46
  17. 17,0 17,1 17,2 C.W. Dodge (1935), In: Medical mycology. Fungous diseases of men and other mammals:258
  18. C.W. Dodge (1935), In: Medical mycology. Fungous diseases of men and other mammals:243
  19. 19,0 19,1 19,2 C.W. Dodge (1935), In: Medical mycology. Fungous diseases of men and other mammals:264
  20. C.W. Dodge (1935), In: Medical mycology. Fungous diseases of men and other mammals:256
  21. C.W. Dodge (1935), In: Medical mycology. Fungous diseases of men and other mammals:260
  22. C.W. Dodge (1935), In: Medical mycology. Fungous diseases of men and other mammals:280
  23. C.W. Dodge (1935), In: Medical mycology. Fungous diseases of men and other mammals:268
  24. C.W. Dodge (1935), In: Medical mycology. Fungous diseases of men and other mammals:277
  25. 25,0 25,1 25,2 C.W. Dodge (1935), In: Medical mycology. Fungous diseases of men and other mammals:254
  26. C.W. Dodge (1935), In: Medical mycology. Fungous diseases of men and other mammals:176
  27. C.W. Dodge (1935), In: Medical mycology. Fungous diseases of men and other mammals:291
  28. Nann. (1934), In: Repertorio sistematico dei miceti dell'uemo e degli animale Siena 4:327
  29. Nann. (1934), In: Repertorio sistematico dei miceti dell'uemo e degli animale Siena 4:394
  30. F.P. Almeida (1933), In: Anais Fac. Med. Univ. S. Paulo 9:76
  31. F.P. Almeida (1933), In: Anais Fac. Med. Univ. S. Paulo 9:77
  32. Khoury (1932), In: C. r. Seanc. Soc. Biol. 111:419
  33. Vivoli, Avell. & Barbier (1932), In: 7a. Reunion Soc. Argentina Patol. Region Norte:239
  34. Langeron & Talice (1932), In: Annls Parasit. hum. comp. 10:68
  35. Lodder (1932), In: Zentbl. Bakt. ParasitKde, Abt. II 86:227–253
  36. 36,0 36,1 36,2 36,3 36,4 36,5 Basgal (1931), In: Contrib. Estud. Blastom. Pulmon.:49
  37. 37,0 37,1 37,2 37,3 37,4 37,5 37,6 M. Ota (1927), In: Jap. J. Derm. Urol. 27:178
  38. M. Ota (1927), In: Jap. J. Derm. Urol. 27:175
  39. Brumpt (1927), In: Précis Parasitol. hum.:1241
  40. M. Ota (1927), In: Jap. J. Derm. Urol. 27:169
  41. 41,0 41,1 Mattlet (1926), In: Ann. Soc. belg. Méd. trop. 6:16–20
  42. Pollacci & Nann. (1926), In: Miceti. pat. Uomo. Anim., fasc. 5:no. 44
  43. Mattlet (1926), In: Ann. Soc. belg. Méd. trop. 6:26
  44. 44,0 44,1 Berkhout (1923), In: De Schimmelgesl. Monilia, Oidium, Oospora en Torula, Disset. Ultrecht:44
  45. Berkhout (1923), In: Schimmelgesl. Monilia:42
  46. Macfie (1921), In: Ann. trop. Med. Parasit. 15:274
  47. Castellani & Chalmers (1919), In: Man. trop. med., 3rd Edn (London):1087
  48. 48,0 48,1 48,2 Castell. & Chalm. (1913), In: Manual of tropical medicine, Edn 2 (London):827
  49. 49,0 49,1 Castell. (1913), In: Archs Parasit. 16(1):186
  50. Castell. & Chalm. (1913), In: Manual of tropical medicine, Edn 2 (London):828
  51. 51,0 51,1 Castell. & Chalm. (1913), In: Manual of tropical medicine, Edn 2 (London):826
  52. Castell. & Chalm. (1913), In: Manual of tropical medicine, Edn 2 (London):829
  53. Castell. & Chalm. (1913), In: Manual of tropical medicine, Edn 2 (London):825
  54. Castell. & Chalm. (1913), In: Manual of tropical medicine, Edn 2 (London):824
  55. 55,0 55,1 Castell. (1912), In: Lancet 1(1):15
  56. 56,0 56,1 56,2 Castell. (1912), In: British Medical Journal 2:1210
  57. Vuill. (1911), In: Bull. trimest. Soc. mycol. Fr. 27(2):140
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  61. Lindner (1844), In: Handb. Allgem. mykol. (Stuttgart) 1:120
  62. 62,0 62,1 Bisby F.A., Roskov Y.R., Orrell T.M., Nicolson D., Paglinawan L.E., Bailly N., Kirk P.M., Bourgoin T., Baillargeon G., Ouvrard D. (red.): Species 2000 & ITIS Catalogue of Life: 2019 Annual Checklist.. Species 2000: Naturalis, Leiden, the Netherlands., 2019. [dostymp 24 września 2012].
  63. Saccharomycetes. Offord L.C. & Kirk P.M., 2010-11-23
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Candida tropicalis: Brief Summary ( Szl )

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Candida tropicalis je grzib, co go nojprzōd ôpisoł Castell., a terŏźnõ nazwã doł mu Christine Marie Berkhout 1923. Candida tropicalis nŏleży do zorty Candida, rzyndu Saccharomycetales, klasy Saccharomycetes, grōmady Ascomycota i krōlestwa grzibōw. Żŏdne podgatōnki niy sōm wymianowane we Catalogue of Life.

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