A simple high-volume culture technique-Good substitute for polymerase chain reaction for the detection of Aspergillus species in bronchoalveolar lavage samples.


Journal

Mycoses
ISSN: 1439-0507
Titre abrégé: Mycoses
Pays: Germany
ID NLM: 8805008

Informations de publication

Date de publication:
Jan 2022
Historique:
revised: 16 06 2021
received: 30 04 2021
accepted: 22 06 2021
pubmed: 29 6 2021
medline: 7 1 2022
entrez: 28 6 2021
Statut: ppublish

Résumé

Aspergillus species is the most common agent of invasive pulmonary fungal disease. Culture-based diagnosis considered as gold standard is limited by the fungal load in samples. Detection of Aspergillus by polymerase chain reaction (PCR) has been included as a diagnostic criterion by European Organisation for Research and Treatment of Cancer (EORTC). Most routine laboratories lack facilities for molecular diagnosis. Better yield using high-volume culture (HVC) technique has been reported. Studies have not compared HVC and PCR for detection of Aspergillus species in respiratory samples from patients with suspected invasive pulmonary Aspergillosis (IPA) not on antifungal therapy. This pilot study compared HVC and PCR for the detection of Aspergillus species in respiratory samples from treatment naïve patients. Bronchoalveolar lavage (BAL) samples from 30 patients with clinical suspicion of IPA were evaluated. Direct microscopy, culture both conventional (CC) and HVC and qualitative Pan Aspergillus PCR were performed. Latent class model was used for statistical analysis. Sensitivity of HVC (100%) was better compared with CC (60%) and comparable to that of PCR (100%). Specificities of CC, HVC and PCR were 100%, 100% and 25%, respectively. High-volume culture is a simple cost-effective technique with a high sensitivity and specificity. It can be easily introduced in routine microbiology laboratories. In centres with the availability of infrastructure for molecular analysis, Aspergillus PCR with other mycological techniques can be used for better diagnosis and management of patients with IPA.

Sections du résumé

BACKGROUND BACKGROUND
Aspergillus species is the most common agent of invasive pulmonary fungal disease. Culture-based diagnosis considered as gold standard is limited by the fungal load in samples. Detection of Aspergillus by polymerase chain reaction (PCR) has been included as a diagnostic criterion by European Organisation for Research and Treatment of Cancer (EORTC). Most routine laboratories lack facilities for molecular diagnosis. Better yield using high-volume culture (HVC) technique has been reported. Studies have not compared HVC and PCR for detection of Aspergillus species in respiratory samples from patients with suspected invasive pulmonary Aspergillosis (IPA) not on antifungal therapy.
OBJECTIVE OBJECTIVE
This pilot study compared HVC and PCR for the detection of Aspergillus species in respiratory samples from treatment naïve patients.
METHODS METHODS
Bronchoalveolar lavage (BAL) samples from 30 patients with clinical suspicion of IPA were evaluated. Direct microscopy, culture both conventional (CC) and HVC and qualitative Pan Aspergillus PCR were performed. Latent class model was used for statistical analysis.
RESULTS RESULTS
Sensitivity of HVC (100%) was better compared with CC (60%) and comparable to that of PCR (100%). Specificities of CC, HVC and PCR were 100%, 100% and 25%, respectively.
CONCLUSION CONCLUSIONS
High-volume culture is a simple cost-effective technique with a high sensitivity and specificity. It can be easily introduced in routine microbiology laboratories. In centres with the availability of infrastructure for molecular analysis, Aspergillus PCR with other mycological techniques can be used for better diagnosis and management of patients with IPA.

Identifiants

pubmed: 34181777
doi: 10.1111/myc.13347
doi:

Substances chimiques

DNA, Fungal 0

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

24-29

Informations de copyright

© 2021 Wiley-VCH GmbH.

Références

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Auteurs

Haritha Subhagan (H)

Department of Microbiology, St. John's Medical College Hospital, Bengaluru, Karnataka, India.

Jayanthi Savio (J)

Department of Microbiology, St. John's Medical College Hospital, Bengaluru, Karnataka, India.

Priyadarshini Padaki (P)

Department of Microbiology, St. John's Medical College Hospital, Bengaluru, Karnataka, India.

Sweta Srivastava (S)

Department of Transfusion Medicine and Immuno Hematology, St. John's Medical College Hospital, Bengaluru, Karnataka, India.

Pavana Thomas (P)

Department of Transfusion Medicine and Immuno Hematology, St. John's Medical College Hospital, Bengaluru, Karnataka, India.

Rajeshwari Veerappan (R)

Department of Microbiology, St. John's Medical College Hospital, Bengaluru, Karnataka, India.

Priya Ramachandran (P)

Department of Pulmonary Medicine, St. John's Medical College Hospital, Bengaluru, Karnataka, India.

John Michael Raj Ashok (J)

Department of Biostatistics, St. John's Medical College Hospital, Bengaluru, Karnataka, India.

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