Microorganism nucleic acid purification from host samples

• US 9,855,559 B2
• Filed: 12/21/2012
• Issued: 01/02/2018
• Est. Priority Date: 12/30/2011
• Status: Expired due to Fees

• Current Assignee: Abbott Molecular Incorporated (Abbott Laboratories)
• Original Assignee: Abbott Molecular Incorporated (Abbott Laboratories)
• Inventors: Marble, Herbert A., Laffler, Thomas
• Primary Examiner(s): Dauner, Joseph G.
• Application Number:
  US13/724,527
• Publication Number:
  US 20130184446A1
• Time in Patent Office: 1,838 Days
• Field of Search: None
• CPC Class Codes: B01L 2400/0415 electrical forces, e.g. electrokinetic
• CPC Class Codes: B01L 2400/0433 vibrational forces
• CPC Class Codes: B01L 2400/0445 Natural or forced convection
• CPC Class Codes: B01L 2400/086 using baffles or other fixed flow obstructions
• CPC Class Codes: B01L 3/502784 specially adapted for droplet or plug flow, e.g. digital microfluidics automatic analysis using a stream of discrete samples in a tube system G01N35/08
• CPC Class Codes: B01L 7/525 with physical movement of samples between temperature zones
• CPC Class Codes: B01L 7/54 using spatial temperature gradients
• CPC Class Codes: C07H 21/00 Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids
• CPC Class Codes: C12P 19/34 Polynucleotides, e.g. nucleic acids, oligoribonucleotides
• CPC Class Codes: C12Q 1/686 Polymerase chain reaction [PCR]
• CPC Class Codes: C12Q 2527/15 Gradients
• CPC Class Codes: C12Q 2563/159 Microreactors, e.g. emulsion PCR or sequencing, droplet PCR, microcapsules, i.e. non-liquid containers with a range of different permeability's for different reaction components
• CPC Class Codes: C12Q 2565/629 being a microfluidic device

Abstract

The present disclosure provides systems, devices, and methods for purifying microorganism nucleic acid from a host sample, such as a whole blood sample from a human. In certain embodiments, devices and systems with multiple filters are employed and provide for the selective removal of blood cells and host nucleic acids from a sample in order to enrich for microorganism nucleic acid.

Claims

1. A device comprising:

i) a first size-exclusion filter that;

excludes passage therethrough of monocytes, neutrophils, eosinophils, and basophils, and allows passage therethrough of erythrocytes, lymphocytes, and platelets;

ii) either;

a) a second size-exclusion filter that;

excludes passage therethrough of erythrocytes, lymphocytes, and platelets, and allows passage therethrough of microorganisms smaller than platelets;

or

b) both of the following;

I) a second size-exclusion filter that excludes passage therethrough of erythrocytes and lymphocytes, but allows passage therethrough of platelets and microorganisms smaller than platelets, and

II) a third size-exclusion filter that excludes passage therethrough of platelets, but allows passage therethrough of blood-borne microorganisms smaller than platelets;

iii) a shearing filter that mechanically shears said blood-borne microorganisms such that blood-borne microorganism nucleic acid is released wherein said shearing filter has a pore size of 0.05-0.25 μ

m; and

iv) a sample containment vessel comprising a proximal end and a distal end, wherein said first and second size exclusion filters, and said third size exclusion filter if present, and said shearing filter, are located inside said sample containment vessel such that fluid passing from said proximal end to said distal end of said sample containment vessel passes through said first size exclusion filter first, said second size exclusion filter second, and said third size exclusion filter third if present, wherein said distal end of said sample containment vessel is configured for collection or elution of a purified sample, and wherein said sample containment vessel comprises a purified sample at said distal end comprising said blood borne microorganism nucleic acid free of genomic human or animal nucleic acid.

2. The device of claim 1, further comprising v) an affinity capture filter comprising affinity binding molecules that bind human repetitive nucleic acid sequences, wherein said affinity capture filter is located inside said sample containment vessel distal to said shearing filter.

3. The device of claim 1, wherein said first size-exclusion filter has a pore size of 9-11 μ

m.

4. The device of claim 1, wherein the second size-exclusion filter of (ii) (a) has a pore size of 1-3 μ

m or wherein the second size-exclusion filter of (ii) (b) has a pore size of 3-7 μ

m and the third size-exclusion filter has a pore size of 1-3 μ

m.

5. The device of claim 1, wherein said sample containment vessel has a tube-type shape.

6. A system comprising:

i) a first size-exclusion filter that;

excludes passage therethrough of monocytes, neutrophils, eosinophils, and basophils, and allows passage therethrough of erythrocytes, lymphocytes, and platelets;

ii) either;

a) a second size-exclusion filter that;

excludes passage therethrough of erythrocytes, lymphocytes, and platelets, and allows passage therethrough of microorganisms smaller than platelets;

or

b) both of the following;

I) a second size-exclusion filter that excludes passage therethrough of erythrocytes and lymphocytes, but allows passage therethrough of platelets and microorganisms smaller than platelets, and

II) a third size-exclusion filter that excludes passage therethrough of platelets, but allows passage therethrough of blood-borne microorganisms smaller than platelets;

iii) a shearing filter that mechanically shears said blood-borne microorganisms such that blood-borne microorganism nucleic acid is released wherein said shearing filter has a pore size of 0.05-0.25 μ

m; and

iv) a sample containment vessel comprising a proximal end and a distal end, wherein said first and second size exclusion filters, and said third size exclusion filter if present, and said shearing filter, are located inside said sample containment vessel such that fluid passing from said proximal end to said distal end of said sample containment vessel passes through said first size exclusion filter first, said second size exclusion filter second, and said third size exclusion filter third if present, wherein said distal end of said sample containment vessel is configured for collection or elution of a purified sample, and wherein said sample containment vessel comprises a purified sample at said distal end comprising said blood borne microorganism nucleic acid free of genomic human or animal nucleic acid.

7. The system of claim 6, further comprising v) an affinity capture filter comprising affinity binding molecules that bind human repetitive nucleic acid sequences, wherein said affinity capture filter is located inside said sample containment vessel distal to said shearing filter.

8. The system of claim 6, wherein said first size-exclusion filter has a pore size of 9-11 μ

m.

9. The system of claim 6, wherein the second size-exclusion filter of (ii) (a) has a pore size of 1-3 μ

m or wherein the second size-exclusion filter of (ii) (b) has a pore size of 3-7 μ

m and the third size-exclusion filter has a pore size of 1-3 μ

m.

10. The system of claim 6, wherein said sample containment vessel has a tube-type shape.

11. A device, comprising:

i) a first upper size-exclusion filter with a pore size of 10-20 μ

m;

ii) either;

a) a second size-exclusion filter with a pore size of 1-3 μ

m distal to said first upper size exclusion filter;

or

b) both of the following;

I) a second size-exclusion filter with a pore size of 3-7 μ

m distal to said first upper size exclusion filter; and

II) a third size-exclusion filter with a pore size of 1-3 μ

m distal to said second size exclusion filter;

iii) a shearing filter with a pore size of 0.05-0.25 μ

m distal to said second or to said third size exclusion filter;

iv) an affinity capture filter comprising affinity binding molecules that bind human repetitive nucleic acid sequences distal to said shearing filter;

v) a sample containment vessel comprising a proximal end and a distal end, wherein said first and second size exclusion filters, and said third size exclusion filter if present, said shearing filter, and said affinity capture filter are located inside said sample containment vessel wherein said distal end of said sample containment vessel is configured for collection or elution of a purified sample, and wherein said sample containment vessel comprises a purified sample at said distal end comprising said blood borne microorganism nucleic acid free of genomic human or animal nucleic acid.

13. The device of claim 11, wherein said device does not contain a chemical lytic agent.

12. A system, comprising:

i) a first upper size-exclusion filter with a pore size of 10-20 μ

m;

ii) either;

a) a second size-exclusion filter with a pore size of 1-3 μ

m distal to said first upper size exclusion filter;

or

b) both of the following;

I) a second size-exclusion filter with a pore size of 3-7 μ

m distal to said first upper size exclusion filter; and

II) a third size-exclusion filter with a pore size of 1-3 μ

m distal to said second size exclusion filter;

iii) a shearing filter with a pore size of 0.05-0.25 μ

m distal to said second or to said third size exclusion filter;

iv) an affinity capture filter comprising affinity binding molecules that bind human repetitive nucleic acid sequences distal to said shearing filter;

v) a sample containment vessel comprising a proximal end and a distal end, wherein said first and second size exclusion filters, and said third size exclusion filter if present, said shearing filter, and said affinity capture filter are located inside said sample containment vessel wherein said distal end of said sample containment vessel is configured for collection or elution of a purified sample, and wherein said sample containment vessel comprises a purified sample at said distal end comprising said blood borne microorganism nucleic acid free of genomic human or animal nucleic acid.

14. The system of claim 12, wherein said system does not contain a chemical lytic agent.