key: cord-0705306-zx7w2ymw
authors: Gunson, R.N.; Collins, T.C.; Carman, W.F.
title: Real-time RT-PCR detection of 12 respiratory viral infections in four triplex reactions
date: 2005-05-31
journal: J Clin Virol
DOI: 10.1016/j.jcv.2004.11.025
sha: 4722ba9e08882f95803f25913a13366aba053de4
doc_id: 705306
cord_uid: zx7w2ymw

nan

Traditional viral culture, usually in combination with direct immunofluoresence (DIF), is the gold standard for the laboratory diagnosis of viral respiratory infection. However, these methods are insensitive, laborious, have prolonged turnaround times, and cannot detect all recognised viral respiratory pathogens. PCR is more sensitive and specific than traditional methods and can be used to detect fastidious viruses. Real-time PCR is at least as sensitive as nested gel-based PCR protocols and offers increased rapidity (results available within the working day). The use of specific labelled probes ensures easy interpretation when used in a multiplex format. We describe four triplex TaqMan TM -based RT-PCR methods adapted from published methods and further developed in-house for the diagnosis of 12 viral respiratory pathogens.

Primers and probes for each triplex are described in full (Table 1) . Real-time RT-PCR assays for human metapneumovirus (hMPV) (Mackay et al., 2003) , RSV A and B (van Elden et al., 2003) , and coronavirus 229E and OC43 (van Elden et al., 2004) were published previously. Although the primers for the detection of influenza A and influenza B, rhinovirus, and parainfluenza 1 and 2 were from previously published methods (Bredius et al., 2004; Templeton et al., 2004) , TaqMan TM probes for these pathogens were adapted from the original molecular beacons. In-house realtime RT-PCR methods were developed for coronavirus NL63 and parainfluenza 3 using Beacon designer 2.0 (Premier Biosoft International) and Primer Express (Applied Biosystems). Conserved target regions were identified using BLAST (www.ncbi.nlm.nih.gov/blast). Regions within the 1a and haemagluttinin genes were chosen for coronavirus NL63 and parainfluenza 3, respectively. The primers and probes were shown to detect all submitted NL63 and parainfluenza 3 sequences. No interfering secondary structures were observed using the mfold algorithm (www.bioinfo.rpi.edu).

All real-time RT-PCR assays were developed for use on the ABI 7500 real-time PCR system. For multiplex real-time PCR, ABI recommend that probes are labelled with the dyes FAM and VIC, as they are distinguishable from each other because they have different emission wavelength maxima (518 nm and 554 nm). We chose CY5 as the third dye as its emission wavelength maxima is far removed from both FAM and VIC (670 nm). No cross-talk was observed.

Respiratory controls and samples were extracted using the Qiagen blood minikit on the Biorobot 9604 using standard protocols. Amplification was carried out in a 25 l reaction volume using the Invitrogen superscript III One step q-RT-PCR system containing 10 l of extracted sample. Primers and probes were added to each PCR reaction at the concentration shown (Table 1) for 15 min at 50 • C. Platinum taq polymerase was activated 95 • C for 2 min and 40 cycles of PCR performed at 95 • C for 8 s and 60 • C for 34 s using an ABI 7500 SDS. Total reaction time per triplex reaction was approximately 75 min.

All real-time PCR assays were previously assessed in their original single target or duplex formats using panels of known culture and DIF or nested PCR positive and negative samples. All of the real-time RT-PCR assays were more sensitive than traditional or nested RT-PCR methods (data not shown). All real-time RT-PCR assays (except coronavirus NL63 and parainfluenza 2) were also assessed using quality control molecular diagnostics (QCMD) respiratory panel (Forde et al., in press) . Each real-time RT-PCR test detected the appropriate target at the appropriate end point dilution.

Four multiplex real-time RT-PCR assays were developed for the simultaneous detection of 1. influenza A, influenza B, and hMPV; 2. RSV A, RSV B, and rhinovirus; 3. parainfluenza 1, 2, and 3; 4. coronavirus 229E, OC43, and NL63.

Each triplex real-time RT-PCR assay was initially assessed using positive controls and compared to the previous duplicate or single target format. Triplex assays were then compared to panels of tissue culture and DIF and/or nested RT-PCR positive samples (where available). To determine whether mixed infections would reduce triplex sensitivity end point dilutions of each viral target were tested in both a single target and a pooled target (containing 10 different viral targets at the same endpoint dilution) format.

Positive control samples for influenza A, influenza B, and hMPV were tested in triplicate wells using the triplex assay in parallel with the previous duplex or single target format (Table 2 ). There was no significant loss of sensitivity (as observed by cycle threshold (Ct)) between methods. The triplex assay was then tested on 11 influenza A positive samples. The triplex assay detected all the previous positive samples. The endpoint dilution of both the single target controls and pooled format controls were detected by the triplex assay showing that "mixed infections" would not reduce the sensitivity of this assay. 

Positive samples for RSV A, RSV B, and rhinovirus were tested in a triplex format in triplicate and compared to duplex or single target format (Table 3) . No loss in sensitivity was observed for RSV A and RSV B. The sensitivity of the rhinovirus real-time RT-PCR improved when incorporated in the triplex assay (as shown by a reduction in the Ct). This increase in sensitivity was sample specific (only occurred with the positive control) as no reduction in Ct was observed when the testing the rhinovirus positive samples. The triplex assay was then assessed on 42 RSV positive samples (NPA samples positive by DIF and nested gel-based PCR) and 11 rhinovirus positive samples. The triplex assay detected all previously positive samples. The endpoint dilution of both the single target controls for RSV A, RSV B, and rhinovirus and pooled format controls (containing 10 viral targets) were detected by the triplex assay showing that "mixed infections" would not reduce the sensitivity of this assay.

Positive control samples for parainflueza 1, 2, and 3 were tested in a triplex format, either with the new PF3 assay or the original test. The introduction of the new PF3 assay had no effect on the sensitivity of the PF1 and PF2 RT-PCR assays (Table 4 ). However, the new PF3 RT-PCR was more sensitive than the previous method. The new triplex assay was then compared to the published method on 19 DIF PF3 positive samples. The new method detected one additional sample (19 versus 18). The endpoint dilution of both the single target controls and pooled format controls were detected by the triplex assay showing that "mixed infections" would not reduce the sensitivity of this assay.

Positive samples for coronavirus 229E, OC43, and NL63 were tested in a triplex format and in the duplex or single target format (Table 5) . No significant changes in Ct were observed. The endpoint dilution of both the single target controls and pooled format controls were detected by the triplex assay showing that "mixed infections" would not reduce the sensitivity of this assay.

Prospective study of respiratory viral infections in pediatric hemopoietic stem cell transplantation patients

Molecular assays for detection of human metapneumovirus

Rapid and sensitive method using multiplex real-time PCR for diagnosis of infections by influenza A and influenza B viruses, respiratory syncytial virus, and parainfluenza viruses 1, 2, 3, and 4

Frequent detection of human coronaviruses in clinical specimens from patients with respiratory tract infection by use of a novel real-time reverse-transcriptase polymerase chain reaction

Applicability of a real-time quantitative PCR assay for diagnosis of respiratory syncytial virus infection in immunocompromised adults

We have shown these triplex real-time RT-PCR assays to be at least as sensitive our previous RT-PCR assays. The rapidity, stability, and ease of use of these triplex real-time RT-PCR assays results in improved turn-around-times (12 pathogens within the working day), easier interpretation, and increased cost effectiveness. The implementation of these assays will no doubt improve patient management, infection control procedures, and the effectiveness of surveillance systems.