Nucleic acid amplification controls
View Patent ↗The present invention discloses positive control material for nucleic acid amplification based detection of microorganisms in biological samples. The control material comprises purified microorganism that is rendered non-infectious but is amenable to nucleic acid amplification. Also disclosed is a process for making and using the control material.
1. A method for producing a positive control for the detection of microorganisms which comprises
(a) purifying microorganisms from a source; (b) exposing the purified microorganism to an aldehyde at a temperature of 2-8° C. such that one or more surface proteins are irreversibly modified while leaving the nuclear components substantially intact, and the purified microorganism is thereby rendered non-pathogenic and is capable of nucleic acid amplification; and (c) suspending the microorganism in a liquid matrix comprising a biological fluid or a synthetic biological fluid,
wherein the composition is useful as a positive internal control for nucleic acid amplification detection tests.
2. The method of claim 1 , wherein the aldehyde is selected from the group consisting of formaldehyde, acetaldehyde, propionaldehyde, n-butyraldehyde, benzaldehyde, p-nitrobenzaldehyde, p-tolualdehyde, salicylaldehyde, phenylacetaldehyde.
3. The method of claim 1 , wherein the aldehyde comprises two or more reactive functional groups.
4. The method of claim 3 , wherein the aldehyde is paraformaldehyde.
5. The method of claim 4 , wherein paraformaldehyde is used at a concentration of no more than 5%.
6. The method of claim 1 , wherein the microorganism is a virus.
7. The method claim 6 , wherein the virus is chosen from the group consisting of human immunodeficiency virus, hepatitis C virus, hepatitis B virus, cytomegalovirus, human lymphotrophic virus, Epstein-Barr virus, parvovirus, herpes simplex virus, human herpes virus 8 and hepatitis A virus.
8. The method of claim 1 , wherein the microorganism is an intracellular parasite.
9. The method of claim 8 , wherein the parasite is chosen from the group consisting of Chlamydia trachomatis, Chlamydia psittaci, Rickettsia prowazeki, Rickettsia typhi, Rickettsia rickettsi, Rickettsia sibtncus, Rickettsia conori, Rickettsia australis, Rickettsia akari, Rickettsia tsutsugamushi, Coxiella bumeti and Rochalimaea quintana.