Replication Stable and RNase Resistant Chimeras of Pestivirus with Insertion in 3' Nontranslated Region (3'NTR)

Abstract

The invention relates to the field of nucleic acid amplification, particularly to quality control materials for use in viral RNA assays. It specifically relates to the construction of a recombinant Pestivirus by the identification of a region in the 3′NTR of the viral RNA genome where additional sequence elements can be stably inserted. Chimeric Pestivirus with sequence insertions in the 3′ nontranslated region (3′NTR) of the viral RNA genome were stable in replication and capable of forming infectious, RNase resistant virus particles. This chimeric Pestivirus with a 3′NTR insertion can be utilized as a quality control material in analytical assays for RNA targets, including external, internal controls, quantitative standards in PCR and NAT nucleic acid assays.

Description

BACKGROUND OF THE INVENTION[0001]An RNA virus has RNA (ribonucleic acid) as its genetic material, and infects host cells from bacteria, plants or animals, such as livestock and humans. The major criteria of how RNA viruses are classified are the sense and organization of the viral genome that determines the mode of viral RNA replication, including whether the viral RNA genome has positive (message) or negative sense, whether it is single or double stranded, and whether it is non-segmented or segmented.[0002]Regulatory agencies often require that assays for detection of nucleic acids utilize quality control materials, including standards, calibrators and controls (Molecular Diagnostic Methods for Infectious Diseases; Approved Guideline, 2nd ed., Clinical and Laboratory Standards Institute, vol 26 (8), 2006). Quality control materials insure optimum performance and reliability of test results, including nucleic acid test (NAT) assays. Laboratories are required to demonstrate that assa...

AI Technical Summary

Benefits of technology

[0023]This invention provides RNA viral chimeras with insertions in the 3′NTR as quality control material, including use as controls, standards and calibrators in RNA viral analytical NAT assays.

Problems solved by technology

While PCR and other NAT techniques can test both DNA and RNA, there are technical challenges especially with quality control for RNA assays: 1) RNA is generally more labile than DNA, presenting additional technical difficulties for analytical RNA assays as compared to DNA assays.

It may not be combined, however, with the test sample to be used as an internal control or quantitative standard, because it would cause a false positive signal.

3) The use of materials potentially infectious for humans is not desirable in a diagnostic kit due to safety concerns and shipping regulations.

4) Internal Quality Standards (IQS) like Internal Controls (IC) and internal Quantification or Quantitation standards (QS) materials often can not be obtained from naturally occurring sources.

While it is known to transcribe RNA sequences from recombinant DNA sequences, it is difficult to package and protect these RNA transcript sequences from degradation by RNases.

Armored RNA also is utilized as a high titer HCV surrogate material, since it is not possible to grow all different HCV subtypes in culture.

Armored RNA has several disadvantages for use as a quality control material in analytical assays.

In this case the result could be a false negative blood screening result for HIV resulting in the transfusion of HIV positive CD4 blood cells to several recipients.

If the chimeric viral RNA replicates improperly, spontaneous sequence changes, such as deletions or frameshifts, may occur during replication in the RNA sequence of the virus chimera to form useless sequence revertants or pseudo-revertants.

The ultimate genomic sequence of the revertant virus is unpredictable and may exclude part or parts of the applied insert.

Unstable chimeric RNA virus, therefore, is usually not useful as a quality control material in an analytical RNA assay.

Rice et al., therefore, did not construct a replication competent BVDV chimera with insertion within the 3′NTR that was genetically stable and could be grown in culture.

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