TestLine AdM096 EIA Adenovirus IgM Instructions

TestLine AdM096 EIA Adenovirus IgM

Document Records

Intended Purpose

The immunoenzymatic assay is intended for the diagnosis of adenovirus infections using IgM antibodies in human serum or plasma in the general population. The semi-quantitative manual assay is designed for professional use in a laboratory.

Introduction

Adenoviruses are human and animal pathogens characterised by significant indifference to the  environment. Acute adenoviral infections have an incubation period of 5–7 days. They spread via droplets or the faucal-oral route. Reinfections are common. The presence of IgG antibodies prevents a more serious course of infection. The viruses attack mainly the mucosa of the respiratory and digestive tract, but may affect also the conjunctiva and the cornea. They accumulate in epithelial  cells and regional lymph nodes. The infection most often leads to respiratory tract affection  (pharyngitis, tonsillitis, laryngitis, bronchitis, bronchiolitis or pneumonia). Adenoviruses caused pharyngoconjunctival fevers in the summer (the virus originates from swimming pool water) and keratoconjunctivitis epidemic. The intestinal form of adenovirus infections occurs mainly in children under one year of age.
Acute infection can be detected by isolation of the virus or serologically. Serological tests are particularly important as they are able to detect the acute phase of infection and can be used in extensive epidemiological investigations. CFR and ELISA detect predominantly antibodies targeting genus- specific antigenic determinants on the heron component of the capsid. The recommended tests for the detection of antibodies specific for individual serotypes are the hemagglutination inhibition test and the virus neutralization test. Seroconversion with at least a 4-fold increase in antibody titer is required for the confirmation of the infection due to the ubiquity of adenoviruses and numerous cross-reactions between related serotypes. IgG antibodies are predominantly detected in serological tests.

Test Principle

The kit is intended for detection of specific IgM antibodies in a sample by means of a sandwich type of the EIA method (i.e. a solid phase coated with specific antigen – antibody from the analyzed sample – labelled antibody). The labelled antibody (conjugate) is an animal immunoglobulin fraction to human IgM conjugated with horseradish peroxidase. Peroxidase activity is determined in the test by a substrate containing TMB. Positivity is indicated when blue colour appears; after stopping solution has been added, blue changes to yellow. The yellow colour intensity is measured by a photometer at 450 nm, and it is proportional to the concentration of specific IgM antibodies in the sample.
Antigen Used
Native antigen

Materials Provided

| Microtiter Plate 1 pc coated with antigen, 12 x 8 wells in bag with desiccant
---|---
| Negative Control 1 × 2 ml Solution containing no specific human antibodies, ready to use
| CUT-OFF 1 × 3 ml Solution containing specific human antibodies in cutoff concentration, ready to use
| Positive Control 1 × 2 ml Solution containing specific human antibodies, ready to use
| Conjugate 1 × 15 ml Solution containing peroxidase labelled animal immunoglobulin to human IgM, ready to use
|  Sample Diluent 11 1 × 105 ml Buffer with protein stabilizers and IgG/RF sorbent, ready to use
| TMB-Complete 2 1 × 15 ml Chromogenic substrate solution containing TMB/H2O2, ready to use
| Wash Solution 1 × 75 ml 20× concentrated buffer
| Stop Solution 1 × 15 ml Acid solution, ready to use
| Instructions for use 1 pc

Other Material Required for Test Performance

Single and multichannel pipettes
Disposable tips Microplate washer Timer  Incubator (37 °C)Microplate reader

Storage and Stability

Store the kit at +2°C to +8°C. Do not freeze. If the kit is stored as described, the labelled expiration date is valid. The expiration date is indicated on the package. The opened kit should be used within three months.

Sample Preparation and Storage
Samples listed in the intended use may be used for the examination. The following human body liquids can be used for testing: serum and citrate plasma. Anticoagulants in the plasma (except for citrate) as well as bacterially contaminated, hemolytic or chilies samples can affect the test results.
A coagulating blood collection tube is recommended for serum collection. A citrated plasma  collection bag is recommended for plasma collection. Other types of plasma (EDTA, heparin) maybe used but they are not recommended since anticoagulants may affect the test result.
Follow the manufacturer’s instructions when using commercial or other specially modified samples.
Clinical samples collected within standard medical procedures into standardized tubes are ready for immediate use. Centrifugation or other separations are not required.
The examined samples can be stored at +2°C to +8°C for a maximum of 1 week.

Preparation of Reagents

Dilute the Wash Solution 1:20 (1 part of solution and 19 parts of distilled water); e.g. 75 ml of the concentrated Wash Solution + 1425 ml of distilled water.
Salt crystals might develop in the bottle with the concentrated Wash Solution. Prior to use, it is necessary to dissolve the crystals by warming the bottle in a water bath. The diluted Wash Solution is stable at +2°C to +8°C for one week.
The Controls (positive, negative and CUT-OFF) are ready to use, do not dilute further!
The Conjugate is ready to use, do not dilute further!
TMB-Complete is a one-component chromogenic substrate solution ready to use, do not dilute further!

Interchangeability of reagents
The Sample Diluent, TMB-Complete and the Avidity Solution are interchangeable in EIA kits of TestLine Clinical Diagnostics s.r.o., provided they have the identical numeric marking (e.g. Sample Diluent 2, Sample Diluent 3, etc.). The Stop Solution and the Wash Solution are universal in all kits.

Preparation of Samples

Mix gently the Sample Diluent prior to use.
Dilution of sera and plasma samples Dilute well mixed samples 1:101 with the Sample Diluent:
E.g.: 10 µl of sample + 1 ml of the Sample Diluent Mix well and incubate 10 minutes at room temperature.

Assay Procedure

Allow all reagents to come to room temperature and mix well. If you do not use a whole microplate,  return unnecessary strips into the bag with desiccant. Seal the bag tightly and store at +2°C to +8°C.Keep dry!

1. Dispense the controls and the diluted samples according to the working schedule.
   • Leave A1 well empty (blank).
   • Pipette 100 µl of the Negative Control into 1 well.
   • Pipette 100 µl of CUT-OFF into 2 wells.
   • Pipette 100 µl of the Positive Control into 1 well.
   • Pipette 100 µl of the diluted samples (see Chapter Preparation of Samples) into the other wells.
2. Cover the microplate with the lid and incubate at 37°C for 30 minutes.
3. Aspirate the content of the wells and wash 5× with the working strength Wash Solution. Fill the wells up to the edge. Finally, tap the inverted microplate thoroughly on an absorbent paper to remove solution remnants.
4. Pipette 100 µl of the Conjugate into all wells except A1 well.
5. Cover the microplate with the lid and incubate at 37°C for 30 minutes.
6. Aspirate the content of the wells and wash 5× with the working strength Wash Solution. Fill the wells up to the edge. Finally, tap the inverted microplate thoroughly on an absorbent paper to remove solution remnants.
7. Pipette 100 µl of TMB-Complete into all wells. Avoid contamination – see Chapter Procedural Notes.
8. Cover the microplate with the lid and incubate at 37°C for 30 minutes. Keep out of light.
9. Stop the reaction by adding 100 µl of the Stop Solution in the same order and intervals as the substrate was added.
10. Read the colour intensity in wells against blank (A1 well) using photometer set to 450 nm. The absorbance should be read within 30 minutes after stopping the reaction.

Working Schedule

Quality Control

Test is valid if:
The absorbance of blank is lower than 0.150.
BLANK < 0.150
The absorbance of the Negative Control is lower than half of the mean absorbance of CUT‒OFF.

The mean absorbance of CUT-OFF is within a range of 0.150 – 0.900.

0.150 < < 0.900

The absorbance of the Positive Control is higher than the mean absorbance of CUT-OFF

Results Interpretation

Calculation of Index of Positivity (IP)
Divide the absorbance of a tested sample by the mean absorbance of CUT-OFF measured in the same test run:

Interpretation of the test results is described in the table (Table 1).

Table 1 Interpretation of test results

Examination of borderline samples, i.e. samples with Index of Positivity from 0.9 to 1.1, should be repeated from a new sample collected after 2 to 6 weeks regarding to the disease specifics.
Serological finding can be interpreted only in the context of results of other laboratory tests and  patient clinical picture.

Analytical performance

Specificity and Sensitivity

Specificity was determined in the panel of negative samples. Sensitivity was determined in the panel of positive samples. The number of samples tested and the results obtained are described in the table (Table 2).

Trueness (bias)

Trueness is the closeness of agreement between the average value obtained from a large number of measurement results and the reference value. Its measure is bias. The nature of the method does not allow quantitative determination of bias (and thus the trueness). The trueness of the method is  ensured by clinical parameters such as sensitivity and specificity, comparison with the reference method and batch continuity. The obtained results are described in the table (Table 2).

Precision: Repeatability – Intra-assay (within run)

The precision is defined as the closeness of agreement between measured values obtained by replicate measurements on the same object under specified conditions. The Intra-assay repeatability is expressed as agreement level among sample replicates within a run of the assay (in one batch). The obtained results are described in the table (Table 2).

Precision: Reproducibility – Inter-assay (between-run)

Reproducibility is a measure of precision under a defined set of conditions which include the intraassay, expressed as agreement level among sample replicates within runs of the assay in one batch. The obtained results are described in the table (Table 2).

Accuracy

Accuracy is defined as the closeness of agreement between the measured value and the reference value. It is expressed as an achievable measure of the combined uncertainty. The obtained results are described in the table (Table 2).

Analytical sensitivity – limits of detection and quantitation

The analytical sensitivity is the maximum binary dilution of CUT-OFF or international standard samples, respectively, giving absorbance significantly different from the background. The value is expressed as an index of positivity and/or a concentration in units. This value is a minimum limit of detection and quantification. The obtained results are described in the table (Table 2).

Measuring Range

The measuring range of the kit lies between values where the lower limit is determined by the  analytical sensitivity value and the upper limit depends on the measuring capability of the equipment used.

Linearity

The linearity is the ability of the method to obtain final values proportional (directly or after mathematical transformation) to the concentration of analyte in the sample; it is expressed as the range in which the method provides linear results. The obtained results are described in the table(Table 2).

Hook effect

Hook effect is an immunological phenomenon that causes falsely low results in the presence of an excess amount of analyte. Its presence is detected by serial dilution of a highly positive sample (Table 2).

Comparison with the reference method

Comparison with the reference method was performed. The results of both methods are comparable, considering the differences of both methods and completely meeting the requirements if the agreement in the classification of the samples is at least 90% (Table 2).

Table 2 Analytical Performance

N/A – not applicable

Interference

Two samples (one negative plasma pool and one positive plasma pool) were spiked with potentially interfering substances. Results of interference testing are shown in the table (Table 3).

Table 3 Interference Results

**Interfering substance| The result was not affected up to concentration:**
---|---
Bilirubin| 0.4 mg/ml
Triacylglycerol’s| 20 mg/ml
Hemoglobin| 5 mg/ml
Biotin| 3500 ng/ml

Cross-reactivity

The assay was evaluated for potential cross-reactivity using samples positive for selected pathogens and factors. Results of testing are shown in the table (Table 4)

Table 4 Results of Cross-Reacting Pathogens or Factors

Clinical Performance

Diagnostic specificity and diagnostic sensitivity

Diagnostic specificity was determined in the panel of negative samples. Diagnostic sensitivity was determined in the panel of positive samples. The number of samples tested and the results obtained are shown in the table (Table 5).

Positive and negative predictive value

A positive predictive value is probability that a person is actually affected by infection if the result was positive. A negative predictive value is probability that a person is actually healthy if the result was negative. The results obtained are shown in the table (Table 5).

Likelihood ratio of the kit

The likelihood ratio of the kit for a positive test is the ratio of probability that an individual from affected  population is diagnosed as positive by the test and probability that a healthy individual is misdiagnosed as positive.
The likelihood ratio of the kit for a negative test is the ratio of probability that an individual from affected population is misdiagnosed as negative by the test and probability that a healthy individual is diagnosed as negative. The results obtained are shown in the table (Table 5).

Expected values in population

Expected values in population are established based on the value results in a file of samples declared as negative and a file of samples declared as positive for the presence of specific antibodies. The results obtained are shown in the table (Table 5).

Table 5 Clinical performance

Safety Precautions

The kit is intended for in vitro diagnostic use only.
The sera used for controls were tested and found to be negative for HIV 1 and HIV 2, HBsAg, HCV, TPHA. In spite of this fact, they still need to be handled as potentially infectious materials.
Some reagents contain the toxic component sodium aside or gentamicin, but in very low concentrations. Avoid contact with skin.
The Stop Solution contains diluted acid solution. Avoid contact with eyes and skin. It is necessary to observe the local safety rules and regulations.

First aid

In case of contact with eyes, flush with copious amount of water and seek medical assistance. In case of contact with skin and clothing, remove all the contaminated clothes. Wash the skin with soap and plenty of running water. In case of contact with solutions containing plasma or clinical samples, disinfect the skin. In case of accidental ingestion, flush the mouth with drinking water and seek medical assistance.

Remnants disposal

All the materials used for performing the test must be treated as potentially infectious due to the contact with biological materials. Therefore they need to be disposed together with biological waste.

Expired kit disposal
Disassemble the kit and dispose the components as biological material. Discard the packaging material as required by local regulations.

Procedural Notes

In order to obtain reliable results, it is necessary to strictly follow the Instructions for Use. Always use clean preferably disposable tips and glassware.
Microtiter Plate – in order to prevent water condensation on the surface of the microplate, always allow the bag with the microplate to warm up to room temperature before opening.
Wash Solution – use high quality distilled water for preparing the working strength Wash Solution.
Washing procedure – keep to the prescribed number of wash cycles and fill the wells to the upper edge. The soak time (i.e. interval between two different wash cycles during which the wells stay filled up with the Wash Solution) should be approx. 30-60 seconds.
TMB-Complete – the vessel used for multichannel pipetting should not be used for other reagents.
Do not return the surplus TMB-Complete from the pipetting vessel into the vial.
Non-reproducible results might be caused by improper methodology as following:

• * insufficient mixing of reagents and samples before use

  • improper replacement of vial caps

  • using the same tip for pipetting different reagents

  • reagent exposure to excessive temperature; bacterial or chemical contamination

  • insufficient washing or filling of the wells (the wells should be filled to the upper edge),
    improper aspiration of Wash Solution remnants

  • contamination of the well edges with Conjugate or samples

  • using reagents from different kit lots

  • contact of reagents with oxidants, heavy metals and their salts

Technical limitation of samples
Materials of a human origin from donor population listed in the intended use were used for  manufacture and development of the kit. Kits are intended for use in general population, unless otherwise stated.
When using samples from other specific populations (comorbid, immunocompromised, pregnant, pediatric population), the risk of a specific effect on the result of the applied test due to e.g.
interference or cross-reactivity should be considered in the context of expert knowledge and current scientific knowledge.

Other notes
The kit might be used for sequential examinations. When preparing working strength solutions, use only the amount of reagents needed for the analysis.
The kit might be used in all types of automatic EIA analyzers. If necessary, TestLine Clinical Diagnostics s.r.o. can offer a certified modification of the Instructions for Use for the specific type of analyzer.

The producer cannot guarantee that the kit will function properly if the assay procedure instructions are not strictly adhered to.

References

1. Bednar M et al., Lékařská microbiology: bacteriology, virology, parasitology (1. Vidani), Praha: Marvel, 1996. 558 s. s. 416–419. ISBN 8023802976.26

2. Harmon MW, Drake S, Kasel JA, Detection of Adenovirus by Enzyme-Linked Immunosorbent
   Assay. Journal of Clinical Microbiology, Mar. 1979; 9(3), p. 342-346.

3. Lynch JP, Fishbein M, Echevarria M, Adenovirus. Seminars in Respiratory and Critical Care Medicine, 2011; 32(4), p. 494-511.

4. Thiele GM, Okano M, Purtily DT, Enzyme-linked immunosorbent assay (ELISA) for detecting antibodies in sera of patients with adenovirus infection. Journal of Virologic Methods, Mar. 1989; 23(3), p. 321-332.

IFU Symbols

| Temperature limitation
---|---

| Keep dry

| Expiry date

| Lot number

| Manufactured by

| Consult instructions

| Catalogue number

| Number of tests

| In vitro diagnostic medical device

Summary of EIA Adenovirus IgM Protocol

| Dilute samples

serum/plasma 1:101 (10 µl + 1 ml)

2|

| Incubate at room temperature for 10 min
3| | Pipette Controls and diluted samples – 100 µl Blank = empty well
4| | Incubate at 37°C for 30 min
5|

| Aspirate and wash the wells 5×
6|

| Pipette Conjugate – 100 μl Blank = empty well
7|

| Incubate at 37°C for 30 min
8|

| Aspirate and wash the wells 5×
9|

| Pipette Substrate (TMB-Complete) – 100 µl Including blank
10|

| Incubate at 37°C for 30 min
11|

| Pipette Stop Solution – 100 µl Including blank
12|

| Read colour intensity at 450 nm

Instruction for use

EIA Adenovirus IgM

AdM096

96

Kit for professional use

TestLine Clinical Diagnostics s.r.o. Kfiiikova 68, 612 00 Brno, Czech Republic
Tel.: +420 541 248 311 FAX: +420 541 243 390
E-mail: [email protected]
www.testlinecd.cz
www.testlinecd.com

Read User Manual Online (PDF format)

Download This Manual (PDF format)

Download this manual  >>