Methods and compositions for direct chemical lysis

Patent metadata

Field	Value
Publication number	US-10323267-B2
Application number	US-201615067428-A
Country	US
Kind code	B2
Filing date	Mar 11, 2016
Priority date	Sep 3, 2009
Publication date	Jun 18, 2019
Grant date	Jun 18, 2019

Abstract

A direct chemical lysis composition includes an assay compatible buffer composition and an assay compatible surfactant. When combined with a specimen storage composition, such compositions prevent undesired modifications to nucleic acid and proteins lysed from cells in the biological sample. Assays of samples from such compositions do not require expensive and time-consuming steps such as centrifugation and prolonged high temperature processing. The direct chemical lysis composition of the present invention permits direct nucleic acid extraction from the cells in the biological sample without the need to decant off the transport media or otherwise exchange the transport media with assay compatible buffers. There is no need to combine the sample with proteinase K or another enzyme to extract nucleic acids from the cells. A method for lysing cells to obtain target nucleic acid for assay and a kit for combining the direct chemical lysis composition with a sample are also contemplated.

First claim

The invention claimed is:

1. A method for analyzing sample stored in a specimen storage composition comprising:
combining the sample and the specimen storage composition with a direct chemical lysis composition consisting essentially of a) an assay compatible buffer composition consisting of a buffer component and a metal salt component; and b) an assay compatible non-ionic surfactant, wherein the sample combined with the specimen storage composition is a liquid-based cytology sample or a formalin-fixed, paraffin embedded sample;
removing at least a portion of the sample from the specimen storage composition, wherein the removed portion remains combined with the specimen storage composition and the direct chemical lysis composition;
incubating the removed portion of the sample at a temperature that is at least 80° C. for a time sufficient to lyse at least a portion of the cells in the removed portion of the sample which remains combined with the specimen storage composition and the direct chemical lysis composition;
extracting an assay target from the incubated and lyzed sample comprising the specimen storage composition and the direct chemical lysis composition;
assaying the target.

2. The method of claim 1 wherein the target is a target nucleic acid and the assay is an amplification assay for the target nucleic acid.

3. The method of claim 2 wherein the target nucleic acid is DNA.

4. The method of claim 2 wherein the target nucleic acid is RNA.

5. The method of claim 1 wherein the sample is a blood sample.

6. The method of claim 1 wherein the sample is cells selected from the group consisting of vaginal cells, cervical cells, endocervical cells, anal cells, exfoliated cells, oral cells, throat cells and peritoneal cells.

7. The method of claim 6 wherein the cells are collected by a swab, brush, broom, or biopsy.

8. The method of claim 1 wherein the specimen storage composition has at least one constituent selected from the group consisting of formaldehyde, formic acid, methanol, ethanol, buffered formalin, and EDTA.

9. The method of claim 8 wherein the specimen storage composition comprises buffered formalin.

10. The method of claim 1 wherein the pH of the direct chemical lysis composition is in the range of about 6.6 to about 10.

11. The method of claim 1 where the metal salt is NaCl and the concentration of NaCl in the direct chemical lysis composition is about 0.01 M or greater.

12. The method of claim 11 wherein the buffer component concentration is in the range of about 0.2 M to about 2M.

13. The method of claim 12 wherein the NaCl concentration is in the range of about 0.01 M to about 1 M.

14. The method of claim 1 wherein the concentration of the non-ionic surfactant is in the range of about 0.01 to about 2 percent (v/v).

15. The method of claim 12 wherein the buffer component is the acid salt of tris(hydroxymethyl)amino methane and the buffer concentration is about 0.75 M, the NaCl concentration is about 0.19 M and the non-ionic surfactant is a polyethylene glycol octylphenyl ether wherein the polyethylene glycol octylphenyl ether concentration is about 0.75 percent (v/v).

16. The method of claim 1 wherein the step of extracting is performed by a manual process.

17. The method of claim 2 wherein the amplifying step is performed by a manual process.

18. The method of claim 2 wherein the extracting and amplifying steps are performed in an automated process.

19. The method of claim 1 wherein the target is a protein and the assay is a detection assay for the protein.

20. The method of claim 19 wherein the protein is a biomarker.

21. The method of claim 20 wherein the biomarker is selected from the group consisting of antibodies and antigens.

22. The method of claim 19 wherein the assay is an Enzyme Linked Immunosorbent Assay (ELISA).

23. The method of claim 1 wherein the specimen storage composition has at least one constituent selected from the group consisting of: polypeptides, polyaminoacids, and polysaccharides.

Assignees

• Becton Dickinson Co

Inventors

• Yang Feng
• Wang Sha-Sha
• Vaughan Laurence Michael
• Porter Michael
• Rose Elaine

Classifications

• C12Q1/708

  for papilloma · CPC title

• C12Q1/6806 Primary

  Preparing nucleic acids for analysis, e.g. for polymerase chain reaction [PCR] assay (C12Q1/6804 takes precedence) · CPC title

• G01N33/56983

  Viruses · CPC title

• C12N1/06

  Lysis of microorganisms · CPC title

• G01N2333/025

  Papovaviridae, e.g. papillomavirus, polyomavirus, SV40, BK virus, JC virus · CPC title