全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

An IMS/ATP Assay for the Detection of Mycobacterium tuberculosis in Urine

DOI: 10.1155/2012/292605

Full-Text   Cite this paper   Add to My Lib

Abstract:

Background. Although sputum smears are the gold standard for diagnosis of tuberculosis, sensitivity in HIV/TB coinfection cases is low, indicating a need for alternative methods. Urine is being increasingly evaluated. Materials and Methods. A novel method for detecting Mycobacterium tuberculosis (MTB) in synthetic urine using a combined IMS/ATP assay was evaluated. Preliminary work established standard ATP conditions and the sensitivity and specificity of the MTB antibody. Eighty-four blinded samples in four replicate assays were evaluated for the presence of MTB using labeled immunomagnetic beads for capture. Beads were separated, washed, and resuspended in broth and added to a microtiter plate. Bioluminescent output was measured and signal-to-noise ratios were calculated. All samples were plated on Middlebrook 7H10 agar or trypticase soy agar to determine limit of detection and recoveries. Results and Conclusions. MTB was distinguished from common bacteriuria isolates and other nontarget bacteria by its ATP results. IMS/ATP successfully detected 19 of 28 samples of MTB in synthetic urine with a limit of detection of 104?CFU/ml. Sensitivity and specificity were 67.9% and 82.1%, respectively. This assay offers a possible rapid screening method for HIV-positive patients with suspected coinfection to improve MTB diagnosis. 1. Introduction There are over 8 million new cases of tuberculosis (TB) annually, with increasing incidence in areas where HIV is prevalent [1]. In 2009, there were 9.4 million new TB cases, with 1.1 million among HIV-positive individuals [2]. Sputum smear microscopy remains the standard for diagnosis. However, sensitivity varies even among HIV-negative patients, with an average sensitivity of less than 60%, and is as low as 20% for patients with HIV/TB coinfection [3]. This is further complicated by an inability to produce sputum among HIV-positive individuals [4–6]. In addition to smear-negative pulmonary TB, HIV-positive individuals tend to have abnormal chest X-rays and clinical presentations, so diagnosis and treatment are often delayed [3, 6, 7]. Furthermore, the sputum procedure is limited in diagnosing extrapulmonary infection, which is more common among patients in this group [3, 8, 9]. The impact of smear-negative disease on diagnostics is significant; even nucleic acid amplification tests such as the Gen-Probe MTD and Roche Amplicor MTB, which have sensitivities greater than 95% in smear-positive cases, have reduced sensitivities of 40–77% in smear-negative cases [3, 10]. Extrapulmonary TB and disseminated disease are more

References

[1]  J. B. Eastwood, C. M. Corbishley, and J. M. Grange, “Tuberculosis and the kidney,” Journal of the American Society of Nephrology, vol. 12, no. 6, pp. 1307–1314, 2001.
[2]  World Health Organization, Global Tuberculosis Control: Fact Sheet, World Health Organization, Geneva, Switzerland, 2010.
[3]  M. D. Perkins and J. Cunningham, “Facing the crisis: improving the diagnosis of tuberculosis in the HIV era,” Journal of Infectious Diseases, vol. 196, supplement 1, pp. S15–S27, 2007.
[4]  J. Peter, C. Green, M. Hoelscher, P. Mwaba, A. Zumla, and K. Dheda, “Urine for the diagnosis of tuberculosis: current approaches, clinical applicability, and new developments,” Current Opinion in Pulmonary Medicine, vol. 16, no. 3, pp. 262–270, 2010.
[5]  M. Shah, N. A. Martinson, R. E. Chaisson, D. J. Martin, E. Variava, and S. E. Dorman, “Quantitative analysis of a urine-based assay for detection of lipoarabinomannan in patients with tuberculosis,” Journal of Clinical Microbiology, vol. 48, no. 8, pp. 2972–2974, 2010.
[6]  G. Torrea, P. van de Perre, M. Ouedraogo et al., “PCR-based detection of the Mycobacterium tuberculosis complex in urine of HIV-infected and uninfected pulmonary and extrapulmonary tuberculosis patients in Burkina Faso,” Journal of Medical Microbiology, vol. 54, no. 1, pp. 39–44, 2005.
[7]  H. Getahun, M. Harrington, R. O'Brien, and P. Nunn, “Diagnosis of smear-negative pulmonary tuberculosis in people with HIV infection or AIDS in resource-constrained settings: informing urgent policy changes,” The Lancet, vol. 369, no. 9578, pp. 2042–2049, 2007.
[8]  M. P. Golden and H. R. Vikram, “Extrapulmonary tuberculosis: An overview,” American Family Physician, vol. 72, no. 9, pp. 1761–1768, 2005.
[9]  K. Gopinath and S. Singh, “Urine as an adjunct specimen for the diagnosis of active pulmonary tuberculosis,” International Journal of Infectious Diseases, vol. 13, no. 3, pp. 374–379, 2009.
[10]  D. V. Havlir and P. F. Barnes, “Tuberculosis in patients with human immunodeficiency virus infection,” The New England Journal of Medicine, vol. 340, no. 5, p. 367, 1999.
[11]  E. Mortier, J. Pouchot, L. Girard, Y. Boussougant, and P. Vinceneux, “Assessment of urine analysis for the diagnosis of tuberculosis,” British Medical Journal, vol. 312, no. 7022, pp. 27–28, 1996.
[12]  A. Aceti, S. Zanetti, M. S. Mura et al., “Identification of HIV patients with active pulmonary tuberculosis using urine based polymerase chain reaction assay,” Thorax, vol. 54, no. 2, pp. 145–146, 1999.
[13]  C. C. Boehme, P. Nabeta, D. Hillemann et al., “Rapid molecular detection of tuberculosis and rifampin resistance,” The New England Journal of Medicine, vol. 363, no. 11, pp. 1005–1015, 2010.
[14]  V. Choudhry and R. Saxena, “Detection of Mycobacterium tuberculosis antigens in urinary proteins of tuberculosis patients,” European Journal of Clinical Microbiology and Infectious Diseases, vol. 21, no. 1, pp. 1–5, 2002.
[15]  S. K. Chadha and R. P. Sahi, “Urinary tract involvement in pulmonary tuberculosis,” Indian Journal of Tuberculosis, vol. 18, no. 2, pp. 54–57, 1971.
[16]  V. K. Challu, B. Mahadev, R. Rajalakshmi, and K. Chaudhuri, “Recovery of tubercle bacilli from urine of pulmonary tuberculosis patients and its comparison with the corresponding sputum isolates,” Indian Journal of Tuberculosis, vol. 36, no. 2, pp. 107–111, 1989.
[17]  N. Selvakumar, A. M. Reetha, S. P. Vanajakumar, et al., “Mycobacteriuria in pulmonary tuberculosis patients in Madras, South India,” Indian Journal of Tuberculosis, vol. 40, pp. 43–45, 1993.
[18]  J. Syed, “Tuberculosis diagnostic pipeline,” TAG 2010 Pipeline Report, HIV i-Base HIV Treatment Bulletin, 2010, http://i-base.info/htb/13614.
[19]  Stop TB Partnership, “TB diagnostics pipeline,” 2007, TB Diagnostics Working Group, http://www.stoptb.org/.
[20]  World Health Organization, “TB diagnostics and laboratory strengthening,” 2011, http://www.who.int/tb/laboratory/en/.
[21]  E. Liandris, M. Gazouli, M. Andreadou, L. A. Sechi, V. Rosu, and J. Ikonomopolous, “Detection of pathogenic mycobacteria based on functionalized quantum dots coupled with immunomagnetic separation,” PLoS One, vol. 6, no. 5, Article ID e20026, 2011.
[22]  G. H. Mazurek, V. Reddy, D. Murphy, and T. Ansari, “Detection of Mycobacterium tuberculosis in cerebrospinal fluid following immunomagnetic enrichment,” Journal of Clinical Microbiology, vol. 34, no. 2, pp. 450–453, 1996.
[23]  A. N. Sharpe, “Separation and concentration of samples,” in Detecting Pathogens in Food, T. A. McMeekin, Ed., pp. 52–68, CRC Press, Boca Raton, Fla, USA, 2003.
[24]  K. A. Stevens and L. A. Jaykus, “Bacterial separation and concentration from complex sample matrices: a review,” Critical Reviews in Microbiology, vol. 30, no. 1, pp. 7–24, 2004.
[25]  R. B. Schifman, M. Wieden, J. Brooker, et al., “Bacteriuria screening by direct bioluminescence assay of ATP,” Antimicrobial Agents and Chemotherapy, vol. 20, no. 4, pp. 644–648, 1984.
[26]  W. D. Welch, L. Thompson, M. Layman, and P. M. Southern Jr., “Evaluation of two bioluminescence-measuring instruments, the turner design and lumac systems, for the rapid screening of urine specimens,” Journal of Clinical Microbiology, vol. 20, no. 6, pp. 1165–1170, 1984.
[27]  D. S. Askgaard, A. Gottschau, K. Knudsen, and J. Bennedsen, “Firefly luciferase assay of adenosine triphosphate as a tool of quantitation of the viability of BCG vaccines,” Biologicals, vol. 23, no. 1, pp. 55–60, 1995.
[28]  L. E. Nilsson, S. E. Hoffner, and S. Ansehn, “Rapid susceptibility testing of Mycobacterium tuberculosis by bioluminescence assay of mycobacterial ATP,” Antimicrobial Agents and Chemotherapy, vol. 32, no. 8, pp. 1208–1212, 1988.
[29]  R. N. Bushon, A. M. Brady, C. A. Likirdopulos, and J. V. Cireddu, “Rapid detection of Escherichia coli and enterococci in recreational water using an immunomagnetic separation/adenosine triphosphate technique,” Journal of Applied Microbiology, vol. 106, no. 2, pp. 432–441, 2009.
[30]  D. M. Hunter, S. D. Leskinen, S. Maga?a, S. M. Schlemmer, and D. V. Lim, “Dead-end ultrafiltration concentration and IMS/ATP-bioluminescence detection of Escherichia coli O157:H7 in recreational water and produce wash,” Journal of Microbiological Methods, vol. 87, no. 3, pp. 338–342, 2011.
[31]  J. Lee and R. A. Deininger, “Detection of E. coli in beach water within 1 hour using immunomagnetic separation and ATP bioluminescence,” Luminescence, vol. 19, no. 1, pp. 31–36, 2004.
[32]  A. Dalhoff, W. Stubbings, and S. Schubert, “Comparative in vitro activities of the novel antibacterial finafloxacin against selected Gram-positive and Gram-negative bacteria tested in Mueller-Hinton broth and synthetic urine,” Antimicrobial Agents and Chemotherapy, vol. 55, no. 4, pp. 1814–1818, 2011.
[33]  L. L. Swaim, R. C. Johnson, Y. Zhou, C. Sandlin, and J. R. Barr, “Quantification of organophosphorus nerve agent metabolites using a reduced-volume, high-throughput sample processing format and liquid chromatography-tandem mass spectrometry,” Journal of Analytical Toxicology, vol. 32, no. 9, pp. 774–777, 2008.
[34]  P. Uppuluri, H. Dinakaran, D. P. Thomas, A. K. Chaturvedi, and J. L. Lopez-Ribot, “Characteristics of Candida albicans biofilms grown in a synthetic urine medium,” Journal of Clinical Microbiology, vol. 47, no. 12, pp. 4078–4083, 2009.
[35]  MedlinePlus, 2011, Urine pH. MedlinePlus, a service of the U.S. National Library of Medicine through the National Institutes of Health, http://www.nlm.nih.gov/medlineplus/ency/article/003583.htm.
[36]  V. M. Bapat, A. M. Bal, R. S. Bhuta, and D. R. Salvi, “Mycobacteriuria—whether a forerunner of manifest tuberculosis?” Journal of Association of Physicians of India, vol. 54, pp. 588–590, 2006.
[37]  C. H. Collins, J. M. Grange, and M. D. Yates, Organization and Practice in Tuberculosis Bacteriology, Butterworths, London, UK, 1985.
[38]  C. B. Inderlied, C. A. Kemper, and L. E. M. Bermudez, “The Mycobacterium avium complex,” Clinical Microbiology Reviews, vol. 6, no. 3, pp. 266–310, 1993.

Full-Text

comments powered by Disqus

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133