Abstract
In characterizing a pathogen, priority is often given to the assessment of antibiotic susceptibility (Chapter 8); indeed, this feature can be clinically more important than identification itself. However, in some contexts the need is primarily for quantitative data, i.e. information on the number of cells/virions per unit volume in the specimen — and on the changes which occur in this parameter; such information can be used, for example:
-
To monitor the progression of viral infection by measurement of viral load in serial specimens.
-
To evaluate the efficacy of chemotherapy by direct observation of its effect on virus/cell numbers.
-
To test the efficacy of new antiviral agents.
-
In chronic hepatitis C: to assess the probable response to therapy with IFN-α (interferon-α) — a long-term response commonly being associated with lowlevel viraemia (e.g. Yamada et al, 1995) and with certain genotypes of the hepatitis C virus.
-
To assess infectiousness; for example, in hepatitis B, high-level viraemia is associated with ready transmission of virus via needle-stick accidents etc. — transmission in low-level viraemia is more likely via large volumes of blood (e.g. transfusion).
-
To assess the gut concentration of Oxalobacter formigenes in the context of cystic fibrosis/hyperoxaluria (see later).
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
References
Allen M, Gauthier J, desLauriers M et al (1999) Two sensitive PCR-based methods for detection of hepatitis B virus variants associated with reduced susceptibility to lamivudine. Journal of Clinical Microbiology 37: 3338–3347.
Chan AB and Fox JD (1999) NASBA and other transcription-based amplification methods for research and diagnostic microbiology. Reviews in Medical Microbiology 10: 185196.
Collins ML, Zayati C, Detmer JJ et al (1995) Preparation and characterization of RNA standards for use in quantitative branched DNA hybridization assays. Analytical Biochemistry 226: 120–129.
Detmer J, Lagier R, Flynn J et al (1996) Accurate quantification of hepatitis C virus (HCV) RNA from all HCV genotypes by using branched-DNA technology. Journal of Clinical Microbiology 34: 901–907.
Hawkins A, Davidson F and Simmonds P (1997) Comparison of plasma virus loads among individuals infected with hepatitis C virus (HCV) genotypes 1, 2 and 3 by Quantiplex
HCV RNA assay versions 1 and 2, Roche Monitor assay, and an in-house limiting dilution method. Journal of Clinical Microbiology 35: 187–192.
Hellyer TJ, desJardin LE, Hehman GL et al (1999) Quantitative analysis of mRNA as a marker for viability of Mycobacterium tuberculosis. Journal of Clinical Microbiology 37: 290–295.
Hendricks DA, Stowe BJ, Hoo BS et al (1995) Quantitation of HBV DNA in human serum using a branched DNA (bDNA) signal amplification assay. American Journal of Clinical Pathology 104: 537–546.
Jacob S, Baudy D, Jones E et al (1997) Comparison of quantitative HCV RNA assays in chronic hepatitis C. American Journal of Clinical Pathology 107: 362–367.
Kapke GF, Watson G, Sheffler S et al (1997) Comparison of the Quantiplex branched DNA (bDNA) assay and the Abbott Genostics solution hybridization assay for quantification of hepatitis B viral DNA. Journal of Viral Hepatitis 4: 67–75.
Lai VCH, Guan R, Wood ML et al (1999) Nucleic acid-based cross-linking assay for detection and quantification of hepatitis B virus DNA. Journal of Clinical Microbiology 37: 161–164.
Sidhu H, Holmes RP, Allison MJ and Peck AB (1999) Direct quantification of the enteric bacterium Oxalobacter formigenes in human fecal samples by quantitative competitive-template PCR. Journal of Clinical Microbiology 37: 1503–1509.
Yamada G, Takatani M, Kishi F et al (1995) Efficacy of interferon alpha in chronic hepatitis C patients depends primarily on hepatitis C virus RNA level. Hepatology 22: 1351–1354.
Zaaijer HL, ter Borg F, Cuypers HTM et al (1994) Comparison of methods for detection of hepatitis B virus DNA. Journal of Clinical Microbiology 32: 2088–2091.
Zheng X, Kolbert CP, Varga-Delmore P et al (1999) Direct mecA detection from blood culture bottles by branched-DNA signal amplification. Journal of Clinical Microbiology 37: 4192–4193.
Rights and permissions
Copyright information
© 2000 Springer Science+Business Media Dordrecht
About this chapter
Cite this chapter
Singleton, P. (2000). Quantification of Pathogens. In: DNA Methods in Clinical Microbiology. Springer, Dordrecht. https://doi.org/10.1007/978-94-017-1286-6_9
Download citation
DOI: https://doi.org/10.1007/978-94-017-1286-6_9
Publisher Name: Springer, Dordrecht
Print ISBN: 978-90-481-5456-2
Online ISBN: 978-94-017-1286-6
eBook Packages: Springer Book Archive