Revisão Revisado por pares

Candida africana and its closest relatives

2010; Wiley; Volume: 54; Issue: 6 Linguagem: Inglês

10.1111/j.1439-0507.2010.01939.x

ISSN

1439-0507

Autores

Orazio Romeo, Giuseppe Criseo,

Tópico(s)

Plant Pathogens and Fungal Diseases

Resumo

MycosesVolume 54, Issue 6 p. 475-486 Review article Candida africana and its closest relatives Orazio Romeo, Orazio Romeo Department of Life Sciences “Marcello Malpighi”, Section of Microbiological, Genetic and Molecular Sciences, University of Messina, Messina, ItalySearch for more papers by this authorGiuseppe Criseo, Giuseppe Criseo Department of Life Sciences “Marcello Malpighi”, Section of Microbiological, Genetic and Molecular Sciences, University of Messina, Messina, ItalySearch for more papers by this author Orazio Romeo, Orazio Romeo Department of Life Sciences “Marcello Malpighi”, Section of Microbiological, Genetic and Molecular Sciences, University of Messina, Messina, ItalySearch for more papers by this authorGiuseppe Criseo, Giuseppe Criseo Department of Life Sciences “Marcello Malpighi”, Section of Microbiological, Genetic and Molecular Sciences, University of Messina, Messina, ItalySearch for more papers by this author First published: 11 October 2011 https://doi.org/10.1111/j.1439-0507.2010.01939.xCitations: 58 G. Criseo, Dipartimento di Scienze della Vita ‘Marcello Malpighi’, Sezione di Scienze Microbiologiche, Genetiche e Molecolari, Università degli studi di Messina, Salita Sperone 31, 98166 Messina, Italy.Tel.: +39 09 0676 5195. Fax: +39 09 039 2733.E-mail: [email protected] Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat Summary Candida africana is a recently described opportunistic yeast pathogen that has been linked to vaginal candidiasis. This yeast was first described, in 1995, as atypical chlamydospore-negative Candida albicans strain, and subsequently proposed as a new Candida species on the basis of morphological, biochemical and physiological characteristics clearly different from those of typical C. albicans isolates. Phylogenetic studies based on the comparison of ribosomal DNA sequences demonstrated that C. africana and C. albicans isolates are too closely related to draw any conclusions regarding the status of a new species. Therefore, on the basis of these studies, some authors considered C. africana as a biovar of C. albicans even if genetic differences may be found if additional regions of genomic DNA are sequenced. The taxonomic situation of C. africana and its phylogenetic relationship with other Candida species is still controversial and remains, at present, a matter of debate. Our goal is to review the current knowledge about C. africana and highlight the development of rapid and accurate tests for its discrimination from C. albicans, Candida dubliniensis and Candida stellatoidea. Furthermore, through the analysis of literature data, we have found that C. africana has a worldwide distribution and a considerable number of features making its study particularly interesting. References 1 Meyer SA, Payne RW, Yarrow D. Candida Berkhout. In: CP Kurtzman, JW Fell (eds), The Yeasts, A Taxonomic Study. Amsterdam: Elsevier, 1998: 454–573. 2 Pfaller MA, Diekema DJ. Epidemiology of invasive candidiasis: a persistent public health problem. Clin Microbiol Rev 2007; 20: 133–63. 3 Krcmery V, Barnes AJ. Non-albicans Candida spp. causing fungaemia: pathogenicity and antifungal resistance. J Hosp Infect 2002; 50: 243–60. 4 Sobel JD. The emergence of non-albicans Candida species as causes of invasive candidiasis and candidemia. Curr Infect Dis Rep 2006; 8: 427–33. 5 Alcoba-Flórez J, Méndez-Álvarez S, Cano J, Guarro J, Pérez-Roth E, del Pilar Arévalo M. Phenotypic and molecular characterization of Candida nivariensis sp. nov., a possible new opportunistic fungus. J Clin Microbiol 2005; 43: 4107–11. 6 Correia A, Sampaio P, James S, Pais C. Candida bracarensis sp. nov., a novel anamorphic yeast species phenotypically similar to Candida glabrata. Int J Syst Evol Microbiol 2006; 56: 313–7. 7 Sullivan DJ, Westerneng TJ, Haynes KA, Bennett DE, Coleman DC. Candida dubliniensis sp. nov.: phenotypic and molecular characterization of a novel species associated with oral candidosis in HIV-infected individuals. Microbiology 1995; 141: 1507–21. 8 Tavanti A, Davidson AD, Gow NA, Maiden MC, Odds FC. Candida orthopsilosis and Candida metapsilosis spp. nov. to replace Candida parapsilosis groups II and III. J Clin Microbiol 2005; 43: 284–92. 9 Boerlin P, Boerlin-Petzold F, Durussel C et al. Cluster of oral atypical Candida albicans isolates in a group of human immunodeficiency virus-positive drug users. J Clin Microbiol 1995; 33: 1129–35. 10 McCullough M, Ross B, Reade P. Characterization of genetically distinct subgroup of Candida albicans strains isolated from oral cavities of patients infected with human immunodeficiency virus. J Clin Microbiol 1995; 33: 696–700. 11 Tietz HJ, Küssner A, Thanos M, De Andreade MP, Presber W, Schönian G. Phenotypic and genotypic characterization of unusual vaginal isolates of Candida albicans from Africa. J Clin Microbiol 1995; 33: 2462–5. 12 Pujol C, Renaud F, Mallié M, de Meeûs T, Bastide JM. Atypical strains of Candida albicans recovered from AIDS patients. J Med Vet Mycol 1997; 35: 115–21. 13 Al-Hedaithy SS, Fotedar R. Recovery and studies on chlamydospore-negative Candida albicans isolated from clinical specimens. Med Mycol 2002; 40: 301–16. 14 Odds FC, Nuffel LV, Dams G. Prevalence of Candida dubliniensis isolates in a yeast stock collection. J Clin Microbiol 1998; 36: 2869–73. 15 Gutiérrez J, Morales P, González MA, Quindós G. Candida dubliniensis, a new fungal pathogen. J Basic Microbiol 2002; 42: 207–27. 16 Loreto ES, Bolzan AR, Linares CE, Boff E, Santurio JM, Alves SH. Evaluation of 5 new media containing extracts of seeds applied to Candida dubliniensis screening. Diagn Microbiol Infect Dis 2006; 55: 191–3. 17 Khlif M, Sellami H, Sellami A et al. Candida dubliniensis: first identification in Sfax hospital, Tunisia. Mycoses 2009; 52: 171–5. 18 Jones CP, Martin DS. Identification of yeastlike organisms isolated from the vaginal tracts of pregnant and non-pregnant women. Am J Obstet Gynecol 1938; 35: 98–106. 19 Langeron M, Guerra P. Remarques sur le Candida stellatoidea (Jones et Martin 1938). Ann Parasitole Hum Comp 1939; 17: 257–60. 20 Meyer SA. DNA relatedness between physiologically similar strains and species of yeasts of medical and industrial importance. In: S Garrattini, S Paglialunga, NS Scrimshaw (eds), Investigation of Single Cell Protein. New York: Pergamon Press, 1979: 13–19. 21 Kamiyama A, Niimi M, Tokunaga M, Nakayama H. DNA homology between Candida albicans strains: evidence to justify the synonymous status of C. stellatoidea. Mycopathologia 1989; 107: 3–7. 22 Kwon-Chung KJ, Wickes BL, Merz WG. Association of electrophoretic karyotype of Candida stellatoidea with virulence for mice. Infect Immun 1988; 56: 1814–9. 23 Kwon-Chung KJ, Hicks JB, Lipke PN. Evidence that Candida stellatoidea type-II is a mutant of Candida albicans that does not express sucrose-inhibitable alpha-glucosidase. Infect Immun 1990; 58: 2804–8. 24 Kwon-Chung KJ, Riggsby WS, Uphoff RA et al. Genetic differences between type I and type II Candida stellatoidea. Infect Immun 1989; 57: 527–32. 25 Tietz HJ, Hopp M, Schmalreck A, Sterry W, Czaika V. Candida africana sp. nov., a new human pathogen or a variant of Candida albicans? Mycoses 2001; 44: 437–45. 26 Alonso-Vargas R, Elorduy L, Eraso E et al. Isolation of Candida africana, probable atypical strains of Candida albicans, from a patients with vaginitis. Med Mycol 2008; 46: 167–70. 27 Romeo O, Criseo G. Morphological, biochemical and molecular characterisation of the first Italian Candida africana isolate. Mycoses 2009; 52: 454–7. 28 Romeo O, Criseo G. Molecular epidemiology of Candida albicans and its closely related yeasts Candida dubliniensis and Candida africana. J Clin Microbiol 2009; 47: 212–4. 29 Odds FC, Bougnoux ME, Shaw DJ et al. Molecular phylogenetics of Candida albicans. Eukaryot Cell 2007; 6: 1041–52. 30 Asakura K, Iwaguchi S, Homma M, Sukai T, Higashide K, Tanaka K. Electrophoretic karyotypes of clinically isolated yeasts of Candida albicans and C. glabrata. J Gen Microbiol 1991; 137: 2531–8. 31 Sullivan DJ, Moran GP, Coleman DC. Candida dubliniensis: ten years on. FEMS Microbiol Lett 2005; 253: 9–17. 32 Czaika VA, Czaika GK, Schmalreck AF, Tietz HJ. Empfindlichkeitsmuster der neuen spezies Candida africana. Mykologie Forum, pp. 13–18, Ausgabe 3/2003. 33 Romeo O, De Leo F, Criseo G. Adherence ability of Candida africana: a comparative study with Candida albicans and Candida dubliniensis. Mycoses 2010 (in press). 34 Okawa Y, Miyauchi M, Takahashi S, Kobayashi H. Comparison of pathogenicity of various Candida albicans and C. stellatoidea strains. Biol Pharm Bull 2007; 30: 1870–3. 35 Thanos M, Schonian G, Meyer W et al. Rapid identification of Candida species by DNA fingerprinting with PCR. J Clin Microbiol 1996; 34: 615–21. 36 Tintelnot K, Haase G, Seibold M et al. Evaluation of phenotypic markers for selection and identification of Candida dubliniensis. J Clin Microbiol 2000; 38: 1599–608. 37 Pinjon E, Sullivan D, Salkin I, Shanley D, Coleman D. Simple, inexpensive, reliable method for differentiation of Candida dubliniensis from Candida albicans. J Clin Microbiol 1998; 36: 2093–5. 38 Jacobsen MD, Boekhout T, Odds FC. Multilocus sequence typing confirms synonymy but highlights differences between Candida albicans and Candida stellatoidea. FEMS Yeast Res 2008; 8: 764–70. 39 Borman AM, Linton C, Miles SJ, Johnson EM. Molecular identification of pathogenic fungi. J Antimicrob Chemother 2008; 61: i7–12. 40 Eraso E, Moragues MD, Villar-Vidal M et al. Evaluation of the new chromogenic medium Candida ID 2 for isolation and identification of Candida albicans and other medically important Candida species. J Clin Microbiol 2006; 44: 3340–5. 41 Al-Hedaithy SS, Fotedar R. Identification of chlamydospore-negative Candida albicans using CHROMagar Candida medium. Mycoses 2003; 46: 96–103. 42 Schoofs A, Odds FC, Colebunders R, Leven M, Goosens H. Use of specialized isolation media for recognition and identification of Candida dubliniensis isolates from VIH infected patients. Eur J Clin Infect Dis 1997; 16: 296–300. 43 Sivakumar VG, Shankar P, Nalina K, Menon T. Use of CHROMagar in the differentiation of common species of Candida. Mycopathologia 2009; 167: 47–49. 44 Saunte DM, Klingspor L, Jalal S, Arnau J, Arendrup MC. Four cases of Candida albicans infections with isolates developing pink colonies on CHROMagar Candida plates. Mycoses 2005; 48: 378–81. 45 Forche A, Schönian G, Gräser Y, Vilgalys R, Mitchell TG. Genetic structure of typical and atypical populations of Candida albicans from Africa. Fungal Genet Biol 1999; 28: 107–25. 46 Ciardo DE, Schär G, Böttger EC, Altwegg M, Bosshard PP. Internal transcribed spacer sequencing versus biochemical profiling for identification of medically important yeasts. J Clin Microbiol 2006; 44: 77–84. 47 Graf B, Trost A, Eucker J, Göbel UB, Adam T. Rapid and simple differentation of C. dubliniensis from C. albicans. Diagn Microbiol Infect Dis 2004; 48: 149–51. 48 Romeo O, Criseo G. First molecular method for discriminating between Candida africana, Candida albicans and Candida dubliniensis by using hwp1 gene. Diagn Microbiol Infect Dis 2008; 62: 230–3. 49 Sampaio P, Nogueira E, Loureiro AS, Delgado-Silva Y, Correia A, Pais C. Increased number of glutamine repeats in the C-terminal of Candida albicans Rlm1p enhances the resistance to stress agents. Antonie Van Leeuwenhoek 2009; 96: 395–404. 50 Tavanti A, Davidson AD, Fordyce MJ et al. Population structure and properties of Candida albicans, as determined by multilocus sequence typing. J Clin Microbiol 2005; 43: 5601–13. 51 de Andrade MP, Schönian G, Forche A et al. Assessment of genetic relatedness of vaginal isolates of Candida albicans from different geographical origins. Int J Med Microbiol 2000; 290: 97–104. 52 Ells R, Kock JL, Pohl CH. Candida albicans or Candida dubliniensis? Mycoses 2009 (in press). 53 Magee BB, D’Souza TM, Magee PT. Strain and species identification by restriction fragment polymorphisms in the ribosomal DNA repeat of Candida species. J Bacteriol 1987; 169: 1639–43. 54 McCullough MJ, Clemons KV, Stevens DA. Molecular and phenotypic characterization of genotypic Candida albicans subgroups and comparison with Candida dubliniensis and Candida stellatoidea. J Clin Microbiol 1999; 37: 417–21. 55 Biswas SK, Yokoyama K, Wang L, Nishimura K, Miyaji M. Typing of Candida albicans isolates by sequence analysis of the cytochrome b gene and differentiation from Candida stellatoidea. J Clin Microbiol 2001; 39: 1600–3. 56 Biswas SK, Yokoyama K, Wang L, Nishimura K, Miyaji M. Identification of Candida dubliniensis based on the specific amplification of mitochondrial cytochrome b gene. Nippon Ishinkin Gakkai Zasshi 2001; 42: 95–98. 57 Cindamporn A, Nakagawa Y, Homma M, Chibana H, Doi M, Tanaka K. Analysis of the chromosomal localization of the repetitive sequences (RPSs) in Candida albicans. Microbiology 1995; 141: 469–76. 58 Kanbe T, Kurimoto K, Hattori H, Iwata T, Kikuchi A. Rapid identification of Candida albicans and its related species Candida stellatoidea and Candida dubliniensis by a single PCR amplification using primers specific for the repetitive sequence (RPS) of Candida albicans. J Dermatol Sci 2005; 40: 43–50. 59 Hattori H, Tanaka R, Chibana H et al. Improvement of the repetitive sequence-based identification and genotyping of Candida albicans using ALT-specific primers. Jpn J Infect Dis 2009; 62: 215–9. 60 Iwata T, Hattori H, Chibana H et al. Genotyping of Candida albicans on the basis of polymorphisms of ALT repeats in the repetitive sequence (RPS). J Dermatol Sci 2006; 41: 43–54. 61 Scherer S, Stevens DA. Application of DNA typing methods to epidemiology and taxonomy of Candida species. J Clin Microbiol 1987; 25: 675–9. 62 Boucher H, Mercure S, Montplaisir S, Lemay G. A novel group I intron in Candida dubliniensis is homologous to a Candida albicans intron. Gene 1996; 180: 189–96. 63 Clemons KV, Shankland GS, Richardson MD, Stevens DA. Epidemiologic study by DNA typing of Candida albicans outbreak in heroin addicts. J Clin Microbiol 1991; 29: 205–7. 64 Tamura M, Watanabe K, Mikami Y, Yazawa K, Nishimura K. Molecular characterization of new clinical isolates of Candida albicans and C. dubliniensis in Japan: analysis reveals a new genotype of C. albicans with group I intron. J Clin Microbiol 2001; 39: 4309–15. 65 Botterel F, Desterke C, Costa C, Bretagne S. Analysis of microsatellite markers of Candida albicans used for rapid typing. J Clin Microbiol 2001; 39: 4076–81. 66 Costa JM, Eloy O, Botterel F, Janbon G, Bretagne S. Use of microsatellite markers and gene dosage to quantify gene copy numbers in Candida albicans. J Clin Microbiol 2005; 43: 1387–9. 67 Sampaio P, Gusmao L, Correia A et al. New microsatellite multiplex PCR for Candida albicans strain typing reveals microevolutionary changes. J Clin Microbiol 2005; 43: 3869–76. 68 Eloy O, Marque S, Botterel F et al. Uniform distribution of three Candida albicans microsatellite markers in two French ICU populations supports a lack of nosocomial cross-contamination. BMC Infect Dis 2006; 6: 162. 69 Garcia-Hermoso D, Cabaret O, Lecellier G et al. Comparison of microsatellite length polymorphism and multilocus sequence typing for DNA-based typing of Candida albicans. J Clin Microbiol 2007; 45: 3958–63. 70 Sampaio P, Gusmão L, Alves C, Pina-Vaz C, Amorim A, Pais C. Highly polymorphic microsatellite for identification of Candida albicans strains. J Clin Microbiol 2003; 41: 552–7. 71 Watanabe Y, Irie K, Matsumoto K. Yeast RLM1 encodes a serum response factor-like protein that may function downstream of the Mpk1 (Slt2) mitogen-activated protein kinase pathway. Mol Cell Biol 1995; 15: 5740–9. 72 Nobile CJ, Nett JE, Andes DR, Mitchell AP. Function of Candida albicans adhesin Hwp1 in biofilm formation. Eukaryot Cell 2006; 5: 1604–10. 73 Nobile CJ, Schneider HA, Nett JE et al. Complementary adhesin function in C. albicans biofilm formation. Curr Biol 2008; 18: 1017–24. 74 Staab JF, Bradway SD, Fidel PL, Sundstrom P. Adhesive and mammalian transglutaminase substrate properties of Candida albicans Hwp1. Science 1999; 283: 1535–8. 75 Sundstrom P. Adhesion in Candida spp. Cell Microbiol 2002; 4: 461–9. 76 Iwaguchi SI, Sato M, Magee BB, Magee PT, Makimura K, Suzuki T. Extensive chromosome translocation in a clinical isolate showing the distinctive carbohydrate assimilation profile from a candidiasis patient. Yeast 2001; 18: 1035–46. 77 Forche A, Alby K, Schaefer D, Johnson AD, Berman J, Bennett RJ. The parasexual cycle in Candida albicans provides an alternative pathway to meiosis for the formation of recombinant strains. PLoS Biol 2008; 6: e110. 78 Jackson AP, Gamble JA, Yeomans T et al. Comparative genomics of the fungal pathogens Candida dubliniensis and Candida albicans. Genome Res 2009; 19: 2231–44. 79 Kottelat M. Systematic studies and biodiversity: the need for a pragmatic approach. J Nat Hist 1955; 29: 565–9. Citing Literature Volume54, Issue6November 2011Pages 475-486 ReferencesRelatedInformation

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