Molecular typing of Australian Scedosporium isolates showing genetic variability and numerous S-aurantialcum
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Delhaes, Laurence
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Westmead Hosp, Inst Clin Pathol & Med Res, Ctr Infect Dis & Microbiol, Mol Mycol Res Lab, Westmead, NSW 2145, AustraliaWestmead Hosp, Inst Clin Pathol & Med Res, Ctr Infect Dis & Microbiol, Mol Mycol Res Lab, Westmead, NSW 2145, Australia
Delhaes, Laurence
[1
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Harun, Azian
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Westmead Hosp, Inst Clin Pathol & Med Res, Ctr Infect Dis & Microbiol, Mol Mycol Res Lab, Westmead, NSW 2145, Australia
Univ Sydney, Sydney, NSW 2006, AustraliaWestmead Hosp, Inst Clin Pathol & Med Res, Ctr Infect Dis & Microbiol, Mol Mycol Res Lab, Westmead, NSW 2145, Australia
Harun, Azian
[1
,2
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Chen, Sharon C. A.
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Westmead Hosp, Inst Clin Pathol & Med Res, Ctr Infect Dis & Microbiol, Mol Mycol Res Lab, Westmead, NSW 2145, AustraliaWestmead Hosp, Inst Clin Pathol & Med Res, Ctr Infect Dis & Microbiol, Mol Mycol Res Lab, Westmead, NSW 2145, Australia
Chen, Sharon C. A.
[1
]
Nguyen, Quoc
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St Vincents Hosp, Westmead, NSW, AustraliaWestmead Hosp, Inst Clin Pathol & Med Res, Ctr Infect Dis & Microbiol, Mol Mycol Res Lab, Westmead, NSW 2145, Australia
Nguyen, Quoc
[3
]
Slavin, Monica
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Alfred Hosp, Melbourne, Vic, AustraliaWestmead Hosp, Inst Clin Pathol & Med Res, Ctr Infect Dis & Microbiol, Mol Mycol Res Lab, Westmead, NSW 2145, Australia
Slavin, Monica
[4
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Heath, Christopher H.
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Royal Perth Hosp, Perth, WA, Australia
Univ Western Australia, Perth, WA 6009, AustraliaWestmead Hosp, Inst Clin Pathol & Med Res, Ctr Infect Dis & Microbiol, Mol Mycol Res Lab, Westmead, NSW 2145, Australia
Heath, Christopher H.
[5
,6
]
Maszewska, Krystyna
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Westmead Hosp, Inst Clin Pathol & Med Res, Ctr Infect Dis & Microbiol, Mol Mycol Res Lab, Westmead, NSW 2145, AustraliaWestmead Hosp, Inst Clin Pathol & Med Res, Ctr Infect Dis & Microbiol, Mol Mycol Res Lab, Westmead, NSW 2145, Australia
Maszewska, Krystyna
[1
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Halliday, Catriona
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Westmead Hosp, Inst Clin Pathol & Med Res, Ctr Infect Dis & Microbiol, Mol Mycol Res Lab, Westmead, NSW 2145, AustraliaWestmead Hosp, Inst Clin Pathol & Med Res, Ctr Infect Dis & Microbiol, Mol Mycol Res Lab, Westmead, NSW 2145, Australia
Halliday, Catriona
[1
]
Robert, Vincent
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Cent Bur Schimmelcultures, Utrecht, NetherlandsWestmead Hosp, Inst Clin Pathol & Med Res, Ctr Infect Dis & Microbiol, Mol Mycol Res Lab, Westmead, NSW 2145, Australia
Robert, Vincent
[7
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Sorrell, Tania C.
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Westmead Hosp, Inst Clin Pathol & Med Res, Ctr Infect Dis & Microbiol, Mol Mycol Res Lab, Westmead, NSW 2145, Australia
Univ Sydney, Sydney, NSW 2006, AustraliaWestmead Hosp, Inst Clin Pathol & Med Res, Ctr Infect Dis & Microbiol, Mol Mycol Res Lab, Westmead, NSW 2145, Australia
Sorrell, Tania C.
[1
,2
]
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Meyer, Wieland
[1
,2
]
机构:
[1] Westmead Hosp, Inst Clin Pathol & Med Res, Ctr Infect Dis & Microbiol, Mol Mycol Res Lab, Westmead, NSW 2145, Australia
[2] Univ Sydney, Sydney, NSW 2006, Australia
[3] St Vincents Hosp, Westmead, NSW, Australia
[4] Alfred Hosp, Melbourne, Vic, Australia
[5] Royal Perth Hosp, Perth, WA, Australia
[6] Univ Western Australia, Perth, WA 6009, Australia
One hundred clinical isolates from a prospective nationwide study of scedosporiosis in Australia (2003-2005) and 46 additional isolates were genotyped by internal transcribed spacer-restriction fragment length polymorphism (ITS-RFLP) analysis, ITS sequencing, and M13 PCR finger-printing. ITS-RFLP and PCR fingerprinting identified 3 distinct genetic groups. The first group corresponded to Scedosporium prolificans (n = 83), and the other 2 comprised isolates previously identified as S. apiospermum: one of these corresponded to S. apicispermum (n = 33) and the other to the newly described species S. aurantiacum (n = 30). Intraspecies variation was highest for S. apiospermum (58%), followed by S. prolificans (45%) and S. aurantiacum (28%) as determined by PCR fingerprinting. ITS sequence variation of 2.2% was observed among S. apiospermum isolates. No correlation was found between genotype of strains and their geographic origin, body site from which they were cultured, or colonization versus invasive disease. Twelve S. prolificans isolates from 2 suspected case clusters were examined by amplified fragment length polymorphism analysis. No specific clusters were confirmed.