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Rapid Virological Diagnosis of Central Nervous System Infections by Use of a Multiplex Reverse Transcription-PCR DNA Microarray Viktoriya Morozova

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Page 1: Rapid virological diagnosis of central nervous system infections 22

Rapid Virological Diagnosis of

Central Nervous System Infections

by Use of a Multiplex Reverse Transcription-PCR

DNA Microarray

Viktoriya Morozova

Page 2: Rapid virological diagnosis of central nervous system infections 22

Preliminary evaluation of the analytical and clinical performances multiplex RT-PCR DNA microarray, the Clart Enthepex kit.

Aim of the study

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This kit has been developed to determine in a fast way the agent(s) responsible for the illness (Herpesvirus or Enterovirus), thus allowing the establishment of the most effective clinical treatment in each case.

CLART® ENTHERPEX kit

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This kit is based on viral genome-specific fragment amplification by multiplex PCR and its subsequent detection via hybridization with a microorganism-specific binding probe on low-density microarrays. 

Clart Entherpex kit

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allows simultaneous detection and identification of the eight human herpesviruses and enteroviruses.

Coxsackivirus

HHV-8

Clart Entherpex kit

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HSV-Herpes Simplex virus

VZV-Varicella Zoster virus

CMV- Cytomegalovirus

EBV-Epstein-Barr virus

HHV-6, HHV-7, HHV-8 -human herpesvirus

HEVs – human enteroviruses

Viruses

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Evaluation

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Since neither QCMD panels nor known clinical samples containing HHV-7 or HHV-8 were available, the performances of the DNA microarray regarding the detection of both these viruses have not been evaluated.

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4 proficiency samples for each of HSV-1, HSV-2, VZV, CMV, EBV, HHV-6 and HEVs with concentrations ranging from 10² to 10⁵ copies/ml were selected and independently tested 4 times each in order to assess the specificity, the sensitivity, and reproducibility of the DNA microarray.

Phase 1

Page 10: Rapid virological diagnosis of central nervous system infections 22

Limit of detection of less than 500 copies/ml for all of the 6 herpesviruses tested.

HEVs- the low viral loads corresponding to

280 and 390 genome copies/ml were not detected

HEVs – the viral load corresponding to 1480 genome copies/ml was detected in 3 out 4 analyses (75%)

Results

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The analytical sensitivities of the test corresponding to the copy number of each one of the viruses that can be detected in 100% of the analyses performed were :

HHV-6 between 500 to 1,000 copies/ml

HSV-1, HSV-2, VZV, and EBV >2,000 copies/ml

Results

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Results

Page 13: Rapid virological diagnosis of central nervous system infections 22

The manufacturer's claims regarding the analytical sensitivities of the assay are:

10 copies for VZV, HHV-7, and HSV-1

100 copies for HSV-2, CMV, EBV, HHV-6, HHV-8, and the coxsackieviruses

1,000 copies for the echoviruses and the polioviruses

per PCR mixture containing 5 μl of DNA/RNA extract. 

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Retrospective analysis of 78 CSF samples obtained from patients hospitalized for suspected neurological virus infections from 2002 to 2009

Phase 2

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28 samples previously tested positive for herpesviruses (7 HSV-1, 2 HSV-2, 8 VZV, 1 CMV, 4 EBV, 6 HHV-6) and negative for HEV

30 samples previously positively tested for HEV and negative for herpesviruses.

20 samples previously tested negative for both HEVs and herpesviruses.

Phase 2 continued….

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27 of the 28 herpesvirus-positive CSF samples were detected (96%)

30 of the 30 HEV-positive CSF samples were detected (100%)

Were detected 11 (37%) HHV-7 and HEV mixed infections among the 30 pediatric aseptic meningitis cases initially related to HEVs

Phase 2. Results

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Results

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Results

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Conclusion

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High sensitivity allowing the detection of minimum quantities of DNA.

High specificity, when using a sequence corresponding to a highly preserved region within the viral genome and binding probes specific to each human herpes and enterovirus type. 

Fast. Allowing the laboratory to provide the answer to the clinician in a single work day

Simultaneous detection of multiple DNA & RNA viruses present in a single sample

Pros

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Limited automation (requires numerous handlings)

Kit cannot be used without a microarray reader piloted by specific software provided by the manufactures, thus limiting the implementation of the kit

Risk of contamination during handling amplicons

Cons

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Due to the small number of CSF specimens tested, further studies are needed to better characterize the performances of this test before its use in routine patient care.

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The end