Antifungal susceptibility patterns of opportunistic fungi in the genera verruconis and ochroconis

Antimicrobial Agents and Chemotherapy

Volumn 58, Issue 6, 2014, Pages 3285-3292

  Seyedmousavi, S ^a,b   Samerpitak, K ^c,d,e   Rijs, A J M M ^a   Melchers, W J G ^a   Mouton, J W ^a   Verweij, P E ^a   De Hoog, G S ^{d,e,f,g,h,i,j}  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^b MAZANDARAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^c KHON KAEN UNIVERSITY   (Thailand)

^d CBS KNAW FUNGAL BIODIVERSITY CENTRE   (Netherlands)

^e UNIVERSITY OF AMSTERDAM   (Netherlands)

^f PEKING UNIVERSITY HEALTH SCIENCE CENTER   (China)

^g SUN YAT SEN UNIVERSITY   (China)

^h SECOND MILITARY MEDICAL UNIVERSITY   (China)

ⁱ FEDERAL UNIVERSITY OF PARANÁ   (Brazil)

^j KING ABDULAZIZ UNIVERSITY   (Saudi Arabia)

more..

Author keywords

[No Author keywords available]

Indexed keywords

AMPHOTERICIN B; ANIDULAFUNGIN; CASPOFUNGIN; ECHINOCANDIN; FLUCONAZOLE; FLUCYTOSINE; INTERNAL TRANSCRIBED SPACER; ITRACONAZOLE; POSACONAZOLE; RIBOSOME DNA; VORICONAZOLE; ANTIFUNGAL AGENT; FUNGAL DNA; RIBOSOMAL SPACER DNA;

ANTIFUNGAL SUSCEPTIBILITY; ARTICLE; BROTH DILUTION; FILAMENTOUS FUNGUS; FUNGUS IDENTIFICATION; GEOMETRY; HEAT TOLERANCE; IN VITRO STUDY; MINIMUM INHIBITORY CONCENTRATION; NONHUMAN; NUCLEOTIDE SEQUENCE; OCHROCONIS; PHYLOGENY; PRIORITY JOURNAL; VERRUCONIS; ASCOMYCETES; DEUTEROMYCETES; DRUG EFFECTS; GENETICS; MICROBIAL SENSITIVITY TEST; MICROBIOLOGY; MYCOSIS;

ANTIFUNGAL AGENTS; ASCOMYCOTA; DNA, FUNGAL; DNA, RIBOSOMAL; DNA, RIBOSOMAL SPACER; MICROBIAL SENSITIVITY TESTS; MITOSPORIC FUNGI; MYCOSES;

EID: 84901280176     PISSN: 00664804     EISSN: 10986596     Source Type: Journal    
DOI: 10.1128/AAC.00002-14     Document Type: Article

References (59)

1. Samerpitak K, Van der Linde E, Choi HJ, Gerrits van den Ende AHG, Machouart M, Gueidan C, de Hoog GS. 2014. Taxonomy of Ochroconis, genus including opportunistic pathogens on humans and animals. Fungal Divers. 65:89-126. http://dx.doi.org/10.1007/s13225-013-0253-6.
2. de Hoog GS, Guarro J, Gene J, Figueras MJ. 2009. Atlas of clinical fungi: the ultimate benchtool for diagnostics. A pilot version of the 3rd ed. Centraalbureau voor Schimmelcultures, KNAW Fungal Biodiversity Centre, Utrecht, The Netherlands.
3. Silveira F, Nucci M. 2001. Emergence of black moulds in fungal disease: epidemiology and therapy. Curr. Opin. Infect. Dis. 14:679-684. http://dx.doi.org/10.1097/00001432-200112000-00003.
4. Qureshi ZA, Kwak EJ, Nguyen MH, Silveira FP. 2012. Ochroconis gallopava: a dematiaceous mold causing infections in transplant recipients. Clin. Transplant. 26:E17-E23. http://dx.doi.org/10.1111/j.1399-0012.2011.01528.x.
5. Cardeau-Desangles I, Fabre A, Cointault O, Guitard J, Esposito L, Iriart X, Berry A, Valentin A, Cassaing S, Kamar N. 2013. Disseminated Ochroconis gallopava infection in a heart transplant patient. Transpl. Infect. Dis. 15:E115-E118. http://dx.doi.org/10.1111/tid.12084.
6. Shoham S, Pic-Aluas L, Taylor J, Cortez K, Rinaldi MG, Shea Y, Walsh TJ. 2008. Transplant-Associated Ochroconis gallopava infections. Transpl. Infect. Dis. 10:442-448. http://dx.doi.org/10.1111/j.1399-3062.2008.00327.x.
7. Georg LK, Bierer BW, Cooke WB. 1964. Encephalitis in turkey poults due to a new fungus species. Sabouraudia 3:239-244. http://dx.doi.org/10.1080/ 00362176485190401.
8. Blalock HG, Georg LK, Derieux WT. 1973. Encephalitis in turkey poults due to Dactylaria (Diplorhinotrichum) gallopava-A case report and its experimental reproduction. Avian Dis. 17:197-204. http://dx.doi.org/10.2307/1588939.
9. Ranck FM, Jr, Georg LK, Wallace DH. 1974. Dactylariosis-A newly recognized fungus disease of chickens. Avian Dis. 18:4-20. http://dx.doi.org/10. 2307/1589237.
10. Randall CJ, Owen DM, Kirkpatrick KS. 1981. Encephalitis in broiler chickens caused by a hyphomycete resembling Dactylaria gallopava. Avian Pathol. 10:31-41. http://dx.doi.org/10.1080/03079458108418456.
11. Shane SM, Markovits J, Snider TG, Harrington KS. 1985. Encephalitis attributed to dactylariosis in Japanese quail chicks (Coturnix coturnix japonica). Avian Dis. 29:822-828. http://dx.doi.org/10.2307/1590673.
12. Karesh WB, Russell R, Gribble D. 1987. Dactylaria gallopava encephalitis in two grey-winged trumpeters (Psophia crepitans). Avian Dis. 31:685-688. http://dx.doi.org/10.2307/1590762.
13. Salkin IF, Dixon DM, Kemna ME, Danneman PJ, Griffith JW. 1990. Fatal encephalitis caused by Dactylaria constricta var. gallopava in a snowy owl chick (Nyctea scandiaca). J. Clin. Microbiol. 28:2845-2847.
14. Connole MD. 1990. Review of animal mycoses in Australia. Mycopathologia 111:133-164. http://dx.doi.org/10.1007/BF02282798.
15. Mohapatra N. 1993. Fungal encephalitis in poultry. Poult. Advis. 26:61-62.
16. Singh K, Flood J, Welsh RD, Wyckoff JH, Snider TA, Sutton DA. 2006. Fatal systemic phaeohyphomycosis caused by Ochroconis gallopavum in a dog (Canis familaris). Vet. Pathol. 43:988-992. http://dx.doi.org/10.1354/vp.43-6-988.
17. Padhye AA, Amster RL, Browning M, Ewing EP. 1994. Fatal encephalitis caused by Ochroconis gallopava in a domestic cat. J. Med. Vet. Mycol. Res. 32:141-145. http://dx.doi.org/10.1080/02681219480000191.
18. Hatai K, Kubota SS. 1989. A visceral mycosis in cultured masu salmon (Oncorhynchus masou) caused by a species of Ochroconis. J. Wildl. Dis. 25:83-88. http://dx.doi.org/10.7589/0090-3558-25.1.83.
19. VanSteenhouse JL, Padhye AA, Ajello L. 1988. Subcutaneous phaeohyphomycosis caused by Scolecobasidium humicola in a cat. Mycopathologia 102:123-127. http://dx.doi.org/10.1007/BF00437449.
20. Ge YP, Lv GX, Shen YN, Li M, Deng SW, De Hoog S, Samerpitak K, Liu WD. 2012. First report of subcutaneous phaeohyphomycosis caused by Ochroconis tshawytschae in an immunocompetent patient. Med. Mycol. 50:637-640. http://dx.doi.org/10.3109/13693786.2011.653834.
21. Lewis RE. 2011. Current concepts in antifungal pharmacology. Mayo Clin. Proc. 86:805-817. http://dx.doi.org/10.4065/mcp.2011.0247.
22. Tamura K, Peterson D, Peterson N, Stecher G, Nei M, Kumar S. 2011. MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. Mol. Biol. Evol. 28:2731-2739. http://dx.doi.org/10.1093/molbev/msr121.
23. Dereeper A, Guignon V, Blanc G, Audic S, Buffet S, Chevenet F, Dufayard JF, Guindon S, Lefort V, Lescot M, Claverie JM, Gascuel O. 2008. Phylogeny.fr: robust phylogenetic analysis for the non-specialist. Nucleic Acids Res. 36:W465-W469. http://dx.doi.org/10.1093/nar/gkn180.
24. CLSI. 2008. Reference method for broth dilution antifungal susceptibility testing of filamentous fungi; approved standard, 2nd ed. CLSI document M38-A2, vol 28, no 16. Clinical and Laboratory Standards Institute, Wayne, PA.
25. de Hoog GS, Vicente VA, Najafzadeh MJ, Harrak MJ, Badali H, Seyedmousavi S. 2011. Waterborne Exophiala species causing disease in cold-blooded animals. Persoonia 27:46-72. http://dx.doi.org/10.3767/003158511X614258.
26. Sudhadham M, Prakitsin S, Sivichai S, Chaiyarat R, Dorrestein GM, Menken SB, de Hoog GS. 2008. The neurotropic black yeast Exophiala dermatitidis has a possible origin in the tropical rain forest. Stud. Mycol. 61:145-155. http://dx.doi.org/10.3114/sim.2008.61.15.
27. Horré R, de Hoog GS. 1999. Primary cerebral infections by melanized fungi: a review. Stud. Mycol. 43:176-193.
28. Vicente VA, Orelis-Ribeiro R, Najafzadeh MJ, Sun J, Guerra RS, Miesch S, Ostrensky A, Meis JF, Klaassen CH, de Hoog GS, Boeger WA. 2012. Black yeast-like fungi associated with lethargic crab disease (LCD) in the mangrove-land crab, Ucides cordatus (Ocypodidae). Vet. Microbiol. 158: 109-122. http://dx.doi.org/ 10.1016/j.vetmic.2012.01.031.
29. Seyedmousavi S, Guillot J, de Hoog GS. 2013. Phaeohyphomycoses, emerging opportunistic diseases in animals. Clin. Microbiol. Rev. 26:19-35. http://dx.doi.org/10.1128/CMR.00065-12.
30. Mayer N, Bastani B. 2009. A case of pulmonary cavitary lesion due to Dactylaria constricta var. gallopava in a renal transplant patient. Nephrology 14:262. http://dx.doi.org/10.1111/j.1440-1797.2009.01107.x.
31. Wong JS, Schousboe MI, Metcalf SS, Endre ZH, Hegarty JM, Maze MJ, Keith ER, Seaward LM, Podmore RG. 2010. Ochroconis gallopava peritonitis in a cardiac transplant patient on continuous ambulatory peritoneal dialysis. Transpl. Infect. Dis. 12:455-458. http://dx.doi.org/10.1111/j.1399-3062.2010.00523.x.
32. Odabasi Z, Paetznick VL, Rodriguez JR, Chen E, Ostrosky-Zeichner L. 2004. In vitro activity of anidulafungin against selected clinically important mold isolates. Antimicrob. Agents Chemother. 48:1912-1915. http://dx.doi.org/10.1128/ AAC.48.5.1912-1915.2004.
33. Dodds Ashley ES, Varkey JB, Krishna G, Vickery D, Ma L, Yu X, Malavade D, Goodwin M, Perfect JR, Power E. 2009. Pharmacokinetics of posaconazole administered orally or by nasogastric tube in healthy volunteers. Antimicrob. Agents Chemother. 53:2960-2964. http://dx.doi.org/10.1128/AAC.01178-08.
34. Meriden Z, Marr KA, Lederman HM, Illei PB, Villa K, Riedel S, Carroll KC, Zhang SX. 2012. Ochroconis gallopava infection in a patient with chronic granulomatous disease: case report and review of the literature. Med. Mycol. 50:883-889. http://dx.doi.org/10.3109/13693786.2012.681075.
35. Jenney A, Maslen M, Bergin P, Tang SK, Esmore D, Fuller A. 1998. Pulmonary infection due to Ochroconis gallopavum treated successfully after orthotopic heart transplantation. Clin. Infect. Dis. 26:236-237. http://dx.doi.org/10.1086/517075.
36. Wang TK, Chiu W, Chim S, Chan TM, Wong SS, Ho PL. 2003. Disseminated Ochroconis gallopavum infection in a renal transplant recipient: the first reported case and a review of the literature. Clin. Nephrol. 60:415-423. http://dx.doi.org/10.5414/CNP60415.
37. Kralovic SM, Rhodes JC. 1995. Phaeohyphomycosis caused by Dactylaria (human dactylariosis): report of a case with review of the literature. J. Infect. 31:107-113. http://dx.doi.org/10.1016/S0163-4453(95)92060-9.
38. Ruping MJ, Albermann N, Ebinger F, Burckhardt I, Beisel C, Muller C, Vehreschild JJ, Kochanek M, Fatkenheuer G, Bangard C, Ullmann AJ, Herr W, Kolbe K, Hallek M, Cornely OA. 2008. Posaconazole concentrations in the central nervous system. J. Antimicrob. Chemother. 62: 1468-1470. http://dx.doi.org/10. 1093/jac/dkn409.
39. Fothergill AW, Rinaldi MG, Sutton DA. 2009. Antifungal susceptibility testing of Exophiala spp.: a head-to-head comparison of amphotericin B, itraconazole, posaconazole and voriconazole. Med. Mycol. 47:41-43. http://dx.doi.org/10.1080/13693780802512451.
40. Al-Abdely HM, Najvar LK, Bocanegra R, Graybill Jr. 2005. Antifungal therapy of experimental cerebral phaeohyphomycosis due to Cladophialophora bantiana. Antimicrob. Agents Chemother. 49:1701-1707. http://dx.doi.org/10.1128/ AAC.49.5.1701-1707.2005.
41. Calvo E, Pastor FJ, Rodriguez MM, Mayayo E, Salas V, Guarro J. 2010. Murine modelofadisseminatedinfectionbythenovelfungusFonsecaeamonophoraand successful treatment with posaconazole. Antimicrob. Agents Chemother. 54: 919-923. http://dx.doi.org/10.1128/AAC.01284-09.
42. Graybill JR, Najvar LK, Johnson E, Bocanegra R, Loebenberg D. 2004. Posaconazole therapy of disseminated phaeohyphomycosis in a murine model. Antimicrob. Agents Chemother. 48:2288-2291. http://dx.doi.org/10.1128/AAC.48.6. 2288-2291.2004.
43. Marine M, Pastor FJ, Guarro J. 2009. Combined antifungal therapy in a murine model of disseminated infection by Cladophialophora bantiana. Med. Mycol. 47:45-49. http://dx.doi.org/10.1080/13693780802526840.
44. Negroni R, Helou SH, Petri N, Robles AM, Arechavala A, Bianchi MH. 2004. Case study: posaconazole treatment of disseminated phaeohyphomycosis due to Exophiala spinifera. Clin. Infect. Dis. 38:e15-e20. http://dx.doi.org/10.1086/ 380840.
45. Al-Abdely HM, Alkhunaizi AM, Al-Tawfiq JA, Hassounah M, Rinaldi MG, Sutton DA. 2005. Successful therapy of cerebral phaeohyphomycosis due to Ramichloridium mackenziei with the new triazole posaconazole. Med. Mycol. 43: 91-95. http://dx.doi.org/10.1080/13693780400011104.
46. Seyedmousavi S, Mouton JW, Verweij PE, Bruggemann RJ. 2013. Therapeutic drug monitoring of voriconazole and posaconazole for invasive aspergillosis. Expert Rev. Anti Infect. Ther. 11:931-941. http://dx.doi.org/10.1586/14787210. 2013.826989.
47. Yarita K, Sano A, Samerpitak K, Kamei K, de Hoog GS, Nishimura K. 2010. Ochroconis calidifluminalis, a sibling of the neurotropic pathogen O. gallopava, isolated from hot spring. Mycopathologia 170:21-30. http://dx.doi.org/10.1007/ s11046-010-9292-7.
48. Sides EH, Benson JD, Padhye AA. 1991. Phaeohyphomycotic brain abscess due to Ochroconis gallopavum in a patient with malignant lymphoma of a large cell type. J. Med. Vet. Mycol. 29:317-322.
49. Terreni AA, DiSalvo AF, Baker AS, Jr, Crymes WB, Morris PR, Dowda H, Jr. 1990. Disseminated Dactylaria gallopava infection in a diabetic patient with chronic lymphocytic leukemia of the T-cell type. Am. J. Clin. Pathol. 94:104-107.
50. Horré R, de Hoog GS, Kluczny C, Marklein G, Schaal KP. 1999. rDNA diversity and physiology of Ochroconis and Scolecobasidium species reported from humans and other vertebrates. Stud. Mycol. 43:194-205.
51. Doty MS, Slater DW. 1946. A new species of Heterobasidium tshawytschae pathogenic on young chinook salmon. Amer. Midl. Naturalist 36:663-665.
52. Ge YP, Lv GX, Shen YN, Li M, Deng SW, de Hoog S, Samerpitak K, Liu WD. 2012. First report of subcutaneous phaeohyphomycosis caused by Ochroconis tshawytschae in an immunocompetent patient. Med. Mycol. 50:637-640. http://dx.doi.org/10.3109/13693786.2011.653834.
53. Wada S, Nakamura K, Hatai K. 1995. First case of Ochroconis humicola infection in marine cultured fish in Japan. Fish Pathol. 30:125-126.
54. de Hoog GS, von Arx JA. 1973. Revision of Scolecobasidium and Pleurophragmium. Kavaka 1:55-60.
55. Fassatiová O. 1967. Ceská Mykol. 21:87.
56. de Hoog GS. 1985. Taxonomy of the Dactylaria complex, IV. Dactylaria, Neta, Subulispora and Scolecobasidium. Stud. Mycol. 26:1-60.
57. Zachariah S, Sankaran KV, Leelavathy KM. 1981. A new species of Septonema from Indian soil. Mycologia 73:208-210.
58. Graniti A. 1962. Scolecobasidium anellii n. sp., agenti di annerimenti superficiali di stalattiti. Giorn. Bot. Ital. 69:360-365.
59. Martin-Sanchez PM, Nováková A, Bastian F, Alabouvette C, Saiz-Jimenez C. 2012. Two new species of the genus Ochroconis, O. lascauxensis and O. anomala isolated from black stains in Lascaux Cave, France. Fungal Biol. 116:574-589. http://dx.doi.org/10.1016/j.funbio.2012.02.006.