Evaluation of the analytical performances of two diagnostic kits based on multiplex RT PCR for the detection and quantification of BKV and JCV in human samples using the Sentinat® 200 automated instrument

Evaluation of the analytical performances of two diagnostic kits based on multiplex RT PCR for the detection and quantification of BKV and JCV in human samples using the Sentinat® 200 automated instrument

M.A. De Lorenzis, C. Pultrone, S. Zonca, M. Gilardi, D. Rigamonti, I. Merli, M.L. Incandela, L. Spinelli

 

Background

Polyomaviruses are ubiquitous, species specific, members of the Polyomaviridae family Human Polyomavirus 1 (BKV) and Human Polyomavirus 2 (JCV) are the most commonly known viruses that can cause mild pathologies in childhood, and more serious disease states if reactivated or acquired by immunocompromised patients1 2 3 4. While BKV is mainly associated with nephropathies, JCV can cause progressive multifocal leukoencephalopathy. Both viruses are diagnosed by multiplex Real-Time PCR assays.
The aim of this work was to evaluate the analytical performances of STAT-NAT® SN 200 BKV and STAT-NAT® SN 200 JCV (Sentinel Diagnostics) kits for the detection and quantification, respectively, of BKV and JCV on different human matrices, using the fully automated system SENTiNAT® 200 (Sentinel Diagnostics).

 

 

Methods

Human plasma and urine samples were analyzed to evaluate the performances of STAT-NAT® SN 200 BKV kit and human plasma and blood samples were analyzed to evaluate the performances of STAT-NAT® SN 200 JVC kit to determine the analytical sensitivity (LoD, LoQ), linearity, precision and specificity on 22 pathogens, following the CLSI 5 (Clinical and Laboratory Standards Institute) guidelines.
DNA from samples was extracted using SENTiNAT® X 48 Pathomag Extraction kit (Sentinel Diagnostics). The extraction, PCR set up and amplification reaction were performed with SENTiNAT® 200 a fully automated, sample-to-result platform.

 

SENTiNAT 200 from sample to result

Results

For the STAT-NAT® SN 200 BKV and STAT-NAT® SN 200 JCV kits, the analytical sensitivity was evaluated by calculating the Limit of Detection (LoD) and the Limit of Quantitation (LoQ) using different concentrations of EDX (Exact Diagnostics, Bio Rad Laboratories).
Results showing a 95% probability of having a positive LoD and LoQ result were calculated on multiple sample replicates (Table A).

Table A. LoD and LoQ in different matrices (whole blood, plasma and urine)

Table A. LoD and LoQ in different matrices (whole blood, plasma and urine). The tested dilution range of BKV viral particles is from 1.5 x 102 IU/mL to 1 x 103 IU/mL, while for JCV it is from 1 x 102 IU/mL to 9 x 102 IU/mL.

 

Linearity of the STAT-NAT® SN 200 BKV kit was investigated using an 8 level panel of EDX BKV virus particles (Exact Diagnostics) The BKV assay presents a linear trend from a concentration of 1 x 102 to 1 x 108 IU/mL (Figure 1). As for BKV, also the linearity of the STAT-NAT® SN 200 JCV kit was investigated using an 8 level panel of EDX JCV (Exact Diagnostics) and the assay shows a linear trend from 1 x 102 to 1 x 108 IU/mL (Figure 2).

Figures 1 and 2. Linearity plots of BKV and JCV in plasma matrix. Linearity of STAT NAT ® SN 200 BKV and STAT NAT ® SN 200 JCV kits was investigated in the range from 1 x 10 2 to 1 x 10 8 IU/ mL

Figures 1 and 2. Linearity plots of BKV and JCV in plasma matrix. Linearity of STAT NAT ® SN 200 BKV and STAT NAT ® SN 200 JCV kits was investigated in the range from 1 x 10 2 to 1 x 10 8 IU/ mL

Figures 1 and 2. Linearity plots of BKV and JCV in plasma matrix. Linearity of STAT-NAT ® SN 200 BKV and STAT-NAT® SN 200 JCV kits was investigated in the range from 1 x 10 2 to 1 x 108 IU/ mL.

 

 

Pathogens BKV
Cross-reactivity
(Yes/No)
JCV
Cross-reactivity
(Yes/No)
Enterovirus NO NO
Adenovirus NO NO
Streptococcus pneumoniae NO NO
Herpes Simplex Virus 1 NO NO
Herpes Simplex Virus 2 NO NO
Varicella-Zoster virus NO NO
Epstein-Barr virus NO NO
Human herpes virus 8 NO NO
Human immunodeficiency virus 1 NO NO
Human immunodeficiency virus 2 NO NO
Cytomegalovirus NO NO
Staphylococcus aureus NO NO
Streptococcus pyogenes NO NO
Staphylococcus epidermidis NO NO
BK polyomavirus NO
Hepatitis B virus NO NO
Enterococcus faecalis NO NO
Klebsiella pneumoniae NO NO
Human betaherpesvirus 7 NO NO
JC polyomavirus NO
Parvovirus B19 NO NO
Toxoplasma gondii NO NO
Human herpes virus 6 NO NO


Table B. Evaluation of in vitro cross reactivity.
A panel of 22 pathogens was used for STAT-NAT® SN 200 BKV and STAT-NAT® SN 200 JCV kits.

 

Interfering substances Tested concentrations
Valganciclovir 10 µg/mL
Prednisone 22,2 µg/mL
Cidofovir 20 µg/mL
Cefotaxime 214 µg/mL
Mycophenolate mofetil 40 µg/mL
Vancomycin 50 µg/mL
Tacrolimus 100 ng/mL
Famotidine 200 µg/mL
Valacyclovir 100 µg/mL
Leflunomide 100 µg/mL
Triglycerides 500 mg/dL
Conjugated bilirubin 0,25 g/L
Unconjugated bilirubin 0,25 g/L
Albumin 58,7 g/L
Hemoglobin 0,25 g/L
Human genome 2 mg/L
Glucose 1000 mg/dL


Table C. Exogenous and endogenous interferents tested.
The results obtained show an irrelevant interfering effect of the endogenous or exogenous molecules on the analytical sensitivity of the kits.

 

 

 

CONCLUSIONS

 

The evaluated STAT-NAT® kits, used in combination with the SENTiNAT® 200 instrument, offer a complete, automated, sample to result solution for the simultaneous detection and quantification of BKV and JCV in different human matrices, providing sensitive, precise and reproducible results.

 

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REFERENCES
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3. Michelle Pinto, Simon Dobson BK and JC virus a review J Infect; 68 Suppl 1:S2-8. 2014.
4. Benedetta Assetta, Walter J Atwood The biology of JC polyomavirus Biol Chem 26; 398(8):839-855. 2017.
5. CLSI Evaluation of Detection Capability for Clinical Laboratory Measurement Procedures (EP17-A2); Evaluation of Linearity of Quantitative Measurement Procedures (EP06); Evaluation of Precision of Quantitative Measurement Procedures (EP05-A3); Molecular Diagnostics Methods for Infectious Diseases (MM03 Quantitative Molecular Methods for Infectious Diseases (MM06-A 2).