Literature DB >> 15124867

Molecular typing of Cryptococcus neoformans by PCR fingerprinting, in comparison with serotyping and Fourier transform infrared-spectroscopy-based phenotyping.

K Lemmer1, D Naumann, B Raddatz, K Tintelnot.   

Abstract

Molecular typing by PCR fingerprinting using the single primer (GACA)4 was performed with 110 isolates of Cryptococcus neoformans. Seventy clinical isolates of C. neoformans var. neoformans from Germany (n = 52) and Africa (n = 18) were included. Of these, serotype A (C. neoformans var. grubii) accounted for 47 isolates, serotype D for 12 and serotype AD for 11. Fourier transform infrared (FT-IR) spectroscopy was evaluated for its discriminatory power in phenotyping. Molecular types, defined by different PCR fingerprinting patterns, were compared to serotypes, and both sets of results were compared with the results of analysis by FT-IR spectroscopy. PCR fingerprinting revealed genotypic diversity within each serotype; it showed three different genotypes (designated VNA1-VNA3) within serotype A, two within serotype D (VND1 and VND2), and three within serotype AD (VNAD1-VNAD3). The nomenclature of molecular types within C. n. var. neoformans, as seen in publications to date, is not uniform. In this study, the name assigned to each genotype was based on the 98.6% concordance of genotypes with serotypes, a correspondence that facilitates interlaboratory comparison. This nomenclature is tentatively recommended as a standard. FT-IR spectroscopy combined with hierarchical cluster analysis successfully distinguished C n. var. neoformans from C. n. var. gattii. For C. n. var. neoformans, FT-IR confirmed three distinct genotypes within serotype A and was able to distinguish isolates derived from particular patients as well as isolates differing at the sub-genotype level. Within C. n. var. gattii, the serotypes B and C did not correlate with the four genotypes VGI-VGIV. However, these serotypes could clearly be separated by FT-IR spectroscopy. The molecular profiles were reproducible, and were more stable and more discriminating than serotyping. In connection with a standardized nomenclature, PCR fingerprinting can be a beneficial tool for global epidemiological studies. FT-IR spectroscopy adds an additional level of resolution.

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Year:  2004        PMID: 15124867     DOI: 10.1080/13693780310001624565

Source DB:  PubMed          Journal:  Med Mycol        ISSN: 1369-3786            Impact factor:   4.076


  5 in total

1.  Opportunistic Cryptococcal Antigenemia in the HAART Era at HIV Epidemic Settings of Northwest Ethiopia.

Authors:  Markos Negash; Tadelo Wondmagegn; Fitsumbrhan Tajebe
Journal:  Can J Infect Dis Med Microbiol       Date:  2020-09-07       Impact factor: 2.471

2.  Cryptococcus gattii meningoencephalitis in an immunocompetent person 13 months after exposure.

Authors:  A Georgi; M Schneemann; K Tintelnot; R C Calligaris-Maibach; S Meyer; R Weber; P P Bosshard
Journal:  Infection       Date:  2009-04-23       Impact factor: 3.553

3.  MALDI-TOF MS enables the rapid identification of the major molecular types within the Cryptococcus neoformans/C. gattii species complex.

Authors:  Carolina Firacative; Luciana Trilles; Wieland Meyer
Journal:  PLoS One       Date:  2012-05-29       Impact factor: 3.240

4.  Identification and Characterization of VNI/VNII and Novel VNII/VNIV Hybrids and Impact of Hybridization on Virulence and Antifungal Susceptibility Within the C. neoformans/C. gattii Species Complex.

Authors:  Mojgan Aminnejad; Massimo Cogliati; Shuyao Duan; Michael Arabatzis; Kathrin Tintelnot; Elizabeth Castañeda; Marcia Lazéra; Aristea Velegraki; David Ellis; Tania C Sorrell; Wieland Meyer
Journal:  PLoS One       Date:  2016-10-20       Impact factor: 3.240

Review 5.  Global Molecular Epidemiology of Cryptococcus neoformans and Cryptococcus gattii: An Atlas of the Molecular Types.

Authors:  Massimo Cogliati
Journal:  Scientifica (Cairo)       Date:  2013-01-09
  5 in total

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