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Use of a suspension array for rapid identification of the varieties and genotypes of the Cryptococcus neoformans
1Division of Marine Biology and Fisheries, Rosenstiel School of Marine and Atmospheric Science, University of Miami, Miami, FL 33149, USA. mdiaz@rsmas.miami.edu
Abstract:
Cryptococcus neoformans is an encapsulated fungal pathogen known to cause severe disease in immunocompromised patients. The disease, cryptococcosis, is mostly acquired by inhalation and can result in a chronic meningoencephalitis, which can be fatal. Here, we describe a molecular method to identify the varieties and genotypic groups within the C. neoformans species complex from culture-based assays. The method employs a novel flow cytometer with a dual laser system that allows the simultaneous detection of different target sequences in a multiplex and high-throughput format. The assay uses a liquid suspension hybridization format with specific oligonucleotide probes that are covalently bound to the surface of fluorescent color-coded microspheres. Biotinylated target amplicons, which hybridized to their complementary probe sequences, are quantified by the addition of the conjugate, streptavidin R-phycoerythrin. In this study we developed and validated eight probes derived from sequence analysis of the intergenic spacer region of the rRNA gene region. The assay proved to be specific and sensitive, allowed discrimination of a 1-bp mismatch with no apparent cross-reactivity, and detected 10(1) to 10(3) genome copies. The described protocol, which can be used directly with yeast cells or isolated DNA, can be undertaken in less than 1 h following PCR amplification and permits identification of species in a multiplex format. In addition to a multiplex capability, the assay allows the simultaneous detection of target sequences in a single reaction. The accuracy, speed, flexibility, and sensitivity of this technology are a few of the advantages that will make this assay useful for the diagnosis of human cryptococcal infections and other pathogenic diseases.
Insights
A new molecular method accurately identifies Cryptococcus neoformans varieties and groups using flow cytometry. This rapid, multiplex assay aids in diagnosing cryptococcosis and other fungal infections.
Area of Science:
- Medical Mycology
- Molecular Diagnostics
- Infectious Diseases
Background:
- Cryptococcus neoformans causes severe cryptococcosis, particularly in immunocompromised individuals.
- Inhalation is the primary route of infection, often leading to fatal meningoencephalitis.
- Accurate identification of C. neoformans varieties and genotypes is crucial for effective treatment.
Purpose of the Study:
- To develop and validate a novel molecular method for identifying C. neoformans varieties and genotypic groups.
- To enable simultaneous detection of multiple target sequences in a high-throughput format.
- To provide a rapid and accurate diagnostic tool for cryptococcal infections.
Main Methods:
- Utilized a novel dual-laser flow cytometer for simultaneous detection.
- Employed liquid suspension hybridization with fluorescent color-coded microspheres and specific oligonucleotide probes.
- Developed and validated eight probes targeting the rRNA gene intergenic spacer region.
- Quantified biotinylated target amplicons using streptavidin R-phycoerythrin conjugate.
Main Results:
- The assay demonstrated high specificity and sensitivity, detecting 10(1) to 10(3) genome copies.
- Achieved discrimination of single-base mismatches with no cross-reactivity.
- Enabled multiplex identification of species in under 1 hour post-PCR amplification.
- Protocol adaptable for direct use with yeast cells or isolated DNA.
Conclusions:
- The developed flow cytometry-based assay offers an accurate, rapid, and sensitive method for identifying C. neoformans.
- This multiplex assay facilitates the simultaneous detection of various target sequences.
- The technology holds significant potential for diagnosing human cryptococcal infections and other pathogenic diseases.
