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Andrew M. Borman Adrien Szekely Chistopher J. Linton Michael D. Palmer Phillipa Brown Elizabeth M. Johnson 《Journal of clinical microbiology》2013,51(3):967-972
Candida africana was previously proposed as a new species within the Candida albicans species complex, together with C. albicans and C. dubliniensis, although further phylogenetic analyses better support its status as an unusual variant within C. albicans. Here we show that C. africana can be distinguished from C. albicans and C. dubliniensis by pyrosequencing of a short region of ITS2, and we have evaluated its occurrence in clinical samples by pyrosequencing all presumptive isolates of C. albicans submitted to the Mycology Reference Laboratory over a 9-month period. The C. albicans complex constituted 826/1,839 (44.9%) of yeast isolates received over the study period and included 783 isolates of C. albicans, 28 isolates of C. dubliniensis, and 15 isolates of C. africana. In agreement with previous reports, C. africana was isolated exclusively from genital specimens, in women in the 18-to-35-year age group. Indeed, C. africana constituted 15/251 (6%) of “C. albicans” isolates from female genital specimens during the study period. C. africana isolates were germ tube positive, grew significantly more slowly than C. albicans and C. dubliniensis on conventional mycological media, could be distinguished from the other members of the C. albicans complex by appearance on chromogenic agar, and were incapable of forming chlamydospores. Here we present the detailed evaluation of epidemiological, phenotypic, and clinical features and antifungal susceptibility profiles of United Kingdom isolates of C. africana. Furthermore, we demonstrate that C. africana is significantly less pathogenic than C. albicans and C. dubliniensis in the Galleria mellonella insect systemic infection model. 相似文献
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994.
Julie Caron Alain Mangé Bernard Guillot Jérôme Solassol 《Journal of cancer research and clinical oncology》2009,135(9):1257-1264
Purpose There is no available tumor marker that can detect primary melanoma. Proteomics analysis has been proposed as a novel tool
that would lead to the discovery of potential new tumor markers.
Methods We developed a serum proteomic fingerprinting approach coupled with a classification method to determine whether proteomic
profiling could discriminate between melanoma and healthy volunteers. A total of 108 serum samples from 30 early-stage [American
Joint Committee on Cancer (AJCC) stage I or II] and 30 advanced-stage (AJCC stage III or IV) melanoma patients and 48 healthy
volunteers were analyzed by surface-enhanced laser desorption/ionization time-of-flight mass spectrometry (SELDI-TOF-MS) utilizing
protein chip technology and artificial neural networks.
Results In a first step, a multiprotein classifier was built using a training set of 30 pathologically confirmed melanoma and 24 healthy
volunteer serum samples, resulting in good classification accuracy for correct diagnosis and stage classification assignment.
Subsequently, our multiprotein classifier was tested in an independent validation set of 30 melanoma and 24 non-cancer serum
samples patients, maintained in a good diagnostic accuracy of 98.1% (sensitivity 96.7%, specificity 100%), and 100% stage
I/II classification assignment.
Conclusions Although results remain to be confirmed in larger collective patient cohorts, we could demonstrate the usefulness of proteomic
profiling as a sensitive and specific assay to detect melanoma, including non-metastatic melanoma, from the serum.
J. Caron and A. Mangé contributed equally to this work. 相似文献
995.
C. Thirion‐Delalande J. Guillot H. E. Jensen F. L. Crespeau F. Bernex 《Transboundary and Emerging Diseases》2005,52(3):121-124
A 6‐year‐old female pony died after 2 days of prostration. Clinical signs included hyperthermia and abnormal pulmonary auscultation sounds. Necropsy revealed diffuse severe necrohaemorrhagic colitis and splenitis, multiple visceral ecchymoses, petechial haemorrhages in the brain and lungs. Microscopical examination showed acute necrohaemorrhagic colitis, encephalitis, pneumonia and splenitis associated with fibrinoid vasculitis, thrombosis and fungal hyphae within and around vessels. Immunohistologically, concomitant aspergillosis (caused by Aspergillus fumigatus) and mucormycosis (causde by Absidia corymbifera) were identified in the colonic and pulmonary lesions, whereas pure mucormycosis was observed in cerebral and splenic lesions. Dual mycotic infections are very rarely described, and the present case emphasizes the need of immunohistochemistry in order to obtain a clear‐cut diagnosis of mixed fungal infections. 相似文献
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