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Aspergillus PCR formidable challenges and progress
Lena Klingspor1, Juergen Loeffler
1Karolinska Institute, Department of Laboratory Medicine, Division of Clinical Microbiology, Karolinska University Hospital, Stockholm, Sweden. lena.klingspor@ki.se
Abstract:
Invasive aspergillosis (IA) is an important cause of morbidity and mortality in immuno-compromised patients, with an incidence of 4-10%, and with a mortality rate of 80-90%, such as in allogeneic stem cell transplant recipients. Conventional diagnostic tests, like blood culture, are not useful in the diagnosis of Aspergillus spp. fungemia. Furthermore, non-culture based techniques that have been used in the past have lacked sensitivity and specificity in immunocompromised patients. New rapid methods which can detect IA early in the course of disease with high sensitivity and specificity are needed since treating these infections at an early stage is often essential for favourable outcomes. In this regard, the polymerase chain reaction (PCR) offers great promise for the rapid diagnosis of fungal infections, including detection of fungi that do not grow in blood cultures such as Aspergillus spp. At Karolinska University Hospital we have established a diagnostic assay, using a combination of a manual extraction and a robot for automated extraction of Candida and Aspergillus DNA, together with real-time PCR. To asses its clinical applicability, a large number of samples from patients with suspected invasive fungal infection have been analyzed with real time PCR. Data will be presented with focus on Aspergillus R-T PCR results in immunocompromised patients. A range of different PCR assays have been developed, targeting different gene regions and including a variety of amplicon detection methods. These molecular assays provide high potential in terms of sensitivity and specificity, but vary widely in their feasibility and have not, until now, been standardized. Despite this progress, there are certain questions to be addressed using these assays, such as the frequency of prospective sampling, as well as the number of positive results of a PCR assay required to initiate antifungal therapy. Furthermore, there are only a few standardized assays that are commercially available. This particular challenge will be addressed by the Working Group 'EAPCRI' (European Aspergillus PCR Initiative) under the auspices of ISHAM. Twenty-four centres have started to establish a European standard for Aspergillus-PCR. The principal goal of this initiative is to achieve a standard for PCR that can be incorporated into the next revision of the EORTC/MSG definitions for IA. Future prospective studies evaluating the potential benefits of early therapy based on R-T PCR in patients at high risk for IA infections are needed.
Insights
Rapid polymerase chain reaction (PCR) tests offer a promising solution for early detection of invasive aspergillosis (IA) in immunocompromised patients. This molecular method shows high potential for sensitive and specific diagnosis, improving patient outcomes.
Area of Science:
- Medical Mycology
- Infectious Diseases
- Molecular Diagnostics
Background:
- Invasive aspergillosis (IA) is a severe infection with high mortality (80-90%) in immunocompromised individuals, particularly stem cell transplant recipients.
- Conventional diagnostic methods like blood cultures lack utility for Aspergillus fungemia, and older non-culture techniques have insufficient sensitivity and specificity.
- Early diagnosis and treatment are crucial for improving outcomes in IA patients, necessitating advanced diagnostic tools.
Purpose of the Study:
- To evaluate the clinical applicability of a newly established diagnostic assay combining manual and automated DNA extraction with real-time PCR for detecting Aspergillus DNA.
- To present data on Aspergillus real-time PCR (R-T PCR) results in immunocompromised patients suspected of invasive fungal infections.
- To highlight the need for standardized molecular assays and address ongoing questions regarding their use in clinical practice.
Main Methods:
- Development and implementation of a diagnostic assay utilizing manual and robotic extraction for Candida and Aspergillus DNA.
- Application of real-time PCR (R-T PCR) for the detection of fungal DNA in patient samples.
- Analysis of a large number of samples from patients with suspected invasive fungal infections.
Main Results:
- Real-time PCR assays demonstrate high potential for sensitivity and specificity in detecting Aspergillus DNA.
- Various PCR assays targeting different gene regions and detection methods have been developed, showing variability in feasibility.
- Data on Aspergillus R-T PCR results in immunocompromised patients will be presented, focusing on clinical applicability.
Conclusions:
- Real-time PCR offers a promising rapid diagnostic method for invasive aspergillosis, addressing limitations of conventional tests.
- Standardization of PCR assays is critical, with initiatives like the European Aspergillus PCR Initiative (EAPCRI) working towards European standards.
- Further prospective studies are needed to evaluate the benefits of early antifungal therapy guided by R-T PCR results in high-risk patients.
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