Abstract

BackgroundRoutine culture-based diagnosis of Pseudomonas aeruginosa lung infection in Cystic Fibrosis (CF) patients can be hampered by the phenotypic variability of the microorganism, including its transition to a Viable But Non-Culturable (VBNC) state. The aim of this study was to validate an ecfX-targeting qPCR protocol developed to detect all viable P. aeruginosa bacteria and to identify VBNC forms in CF sputum samples.MethodsThe study involved 115 P. aeruginosa strains of different origins and 10 non-P. aeruginosa strains and 88 CF sputum samples, 41 Culture-Positive (CP) and 47 Culture-Negative (CN). Spiking assays were performed using scalar dilutions of a mixture of live and dead P. aeruginosa ATCC 9027 and a pooled P. aeruginosa-free sputum batch. Total DNA from sputum samples was extracted by a commercial kit, whereas a crude extract was obtained from the broth cultures. Extracellular DNA (eDNA) interference was evaluated by comparing the qPCR counts obtained from DNase-treated and untreated aliquots of the same samples. The statistical significance of the results was assessed by the Wilcoxon test and Student’s t test.ResultsThe newly-developed qPCR protocol identified 96.6% of the P. aeruginosa isolates; no amplification was obtained with strains belonging to different species. Spiking assays supported protocol reliability, since counts always matched the amount of live bacteria, thus excluding the interference of dead cells and eDNA. The protocol sensitivity threshold was 70 cells/ml of the original sample. Moreover, qPCR detected P. aeruginosa in 9/47 CN samples and showed higher bacterial counts compared with the culture method in 10/41 CP samples.ConclusionsOur findings demonstrate the reliability of the newly-developed qPCR protocol and further highlight the need for harnessing a non-culture approach to achieve an accurate microbiological diagnosis of P. aeruginosa CF lung infection and a greater understanding of its evolution.

Highlights

  • Routine culture-based diagnosis of Pseudomonas aeruginosa lung infection in Cystic Fibrosis (CF) patients can be hampered by the phenotypic variability of the microorganism, including its transition to a Viable But Non-Culturable (VBNC) state

  • We Mangiaterra et al BMC Infectious Diseases (2018) 18:701 report the diagnostic performance of a newly-developed qPCR protocol targeting ecfX, which proved capable of detecting all viable P. aeruginosa subpopulations, including VBNC forms, and showed the specificity, sensitivity, ease of use, and cost-effectiveness required for routine microbiological use

  • Primer pair sensitivity and specificity The primer pair targeting ecfX was tested by standard PCR assays on 115 P. aeruginosa strains of different origins

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Summary

Introduction

Routine culture-based diagnosis of Pseudomonas aeruginosa lung infection in Cystic Fibrosis (CF) patients can be hampered by the phenotypic variability of the microorganism, including its transition to a Viable But Non-Culturable (VBNC) state. The aim of this study was to validate an ecfX-targeting qPCR protocol developed to detect all viable P. aeruginosa bacteria and to identify VBNC forms in CF sputum samples. Routine culture-based diagnosis of P. aeruginosa lung infection may fail to detect these bacterial populations in CF patients, providing false negative results or underestimating bacterial abundance [5]. We Mangiaterra et al BMC Infectious Diseases (2018) 18:701 report the diagnostic performance of a newly-developed qPCR protocol targeting ecfX, which proved capable of detecting all viable P. aeruginosa subpopulations, including VBNC forms, and showed the specificity, sensitivity, ease of use, and cost-effectiveness required for routine microbiological use

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