- Short Report
- Open Access
Evaluation of the Xpert® MTB/RIF assay and microscopy for the diagnosis of Mycobacterium tuberculosis in Namibia
Infectious Diseases of Poverty volume 6, Article number: 13 (2017)
Tuberculosis (TB) kills approximately two million people and infects around nine million worldwide annually. Its proper management, especially in resource-limited settings, has been hindered by the lack of rapid and easy-to-use diagnostic tests. Sputum smear microscopy remains the cheapest, readily available diagnostic method but it only identifies less than half of the patients with a HIV/TB co-infection because the bacilli would have disseminated from the lungs to other areas of the body. The fully automated Xpert® MTB/RIF assay is a promising innovation for diagnosing TB and detecting resistance to rifampicin. This study aimed to evaluate the use of Xpert® MTB/RIF assay and microscopy in the diagnosis of Mycobacterium tuberculosis in Namibia, by determining the disease’s epidemiology and calculating the proportion of cases infected just with TB and those with a resistance to rifampicin among the total suspected cases of TB in the country.
This retrospective study analysed TB cases that were diagnosed using both the Xpert® MTB/RIF assay and microscopy. Data were collected from patient records from the Meditech laboratory information system of the Namibia Institute of Pathology for the time period of July 2012–April 2013. Data from 13 regions were collected.
The total number of specimens collected from patients with symptoms of pulmonary TB was 1 842. Of these, 594 (32.20%) were found to be positive for MTB by Xpert® MTB/RIF assay, out of which 443 (24.05%) were also found to be positive by microscopy. The remainder was negative. The male patients were more resistant to rifampicin when compared to the female patients.
Tuberculosis is widely distributed throughout Namibia, with slightly more males infected than females. Most TB patients are also co-infected with HIV. Both microscopy and Xpert® MTB/RIF assay are crucial for the diagnosis of TB in the country. Screening diagnostic efforts should focus on the sexually active HIV positive male population who could be the source of more RIF-resistant TB than females to prevent its spread.
Please see Additional file 1 for translations of the abstract into the five official working languages of the United Nations
Tuberculosis (TB), an infection that mainly affects the lungs, is caused by Mycobacterium tuberculosis (MTB). The infection can be diagnosed by sputum smear microscopy, chest radiography, culture-based testing, or nucleic acid amplification tests (NAATs) [1, 2]. Recently, new diagnostic techniques have been discovered, including interferon-gamma release assays and Xpert® MTB/RIF assay .
The elimination of TB requires improved detection and early treatment. Many people still die from TB due to delayed diagnosis and this contributes to the risk of TB transmission . Microscopy with Ziehl-Neelsen (ZN) staining is the most common and often the only laboratory technique used to diagnose TB in most developing countries [1, 5–8]. However, errors associated with microscopy lead to misdiagnoses . It is therefore vital to improve and possibly replace microscopy with simpler, more affordable, and more accurate diagnostic methods. Patients who are co-infected with HIV are often the ones whose smear results are negative, when in fact they actually have TB . This is because the bacilli would have disseminated from the lungs to other organs due to immunosuppression. If facilities are available, it would be best to use the gold standard of diagnosing pulmonary TB using culture-based testing in HIV positive patients .
GeneXpert is a system based on a NAAT that rapidly diagnoses and detects MTB and rifampicin (RIF) resistance in clinical specimens [4, 9, 11]. The World Health Organization endorsed it as the initial diagnostic test for individuals suspected of having multidrug-resistant TB (MDR-TB) or HIV-associated TB [7, 12, 13]. However, Xpert® MTB/RIF assay cannot completely eliminate the need for microscopy and culture, as the latter are essential for the detection of resistance to drugs other than RIF .
Namibia is the country with the fourth highest TB burden in the world. The incidence rate in 2015 was 651/100 000 . Cases of TB in Namibia are widely distributed throughout the country, however, the majority of cases are reported in the regions of Khomas, Ohangwena, Erongo, and Kavango [15, 16]. Currently, the public health reference diagnostic laboratory, the Namibia Institute of Pathology (NIP), uses ZN microscopy, Xpert® MTB/RIF assay, and, to a lesser extent, TB culture to diagnose TB.
The aim of the study was to evaluate the use of ZN microscopy and Xpert® MTB/RIF assay for the diagnosis of TB cases in Namibia. This was done by determining the disease’s epidemiology and calculating the proportion of TB positive cases and cases with resistance to RIF among the sputum samples stored at the NIP in Windhoek.
Study design and setting
This was a retrospective study that analyzed MTB cases diagnosed using both the Xpert® MTB/RIF assay (Cepheid, Sunnyvale, CA, USA) and microscopy. Data were collected from patient records that were retrieved from the Meditech laboratory information system of the NIP for the period of July 2012–April 2013. The records came from all 13 regions of Namibia, but excluded data from private hospitals and clinics. The specimens were tested for acid-fast bacilli using microscopy and Xpert® MTB/RIF assay within three days of being received by the laboratory. The total number of specimens collected from patients with symptoms of pulmonary TB was 1 842.
The data extracted included: HIV status based on the Determine™ HIV-1/2 test (Alere, Milan, Italy), laboratory number, age, sex, positive and negative results from microscopy and Xpert® MTB/RIF assay testing, and the patient’s region as indicated by the given residential address. Data were entered and sorted using Microsoft Excel before being analyzed using IBM SPSS version 21.0 (SPSS Inc., Chicago, Illinois, USA). If the p-value was less than 0.05, this was considered as significant.
Cases were categorized as either sputum smear-positive or sputum smear-negative. They were also categorized as either Xpert® MTB/RIF assay positive or Xpert® MTB/RIF assay negative, based on the assay results. Out of the 1 842 specimens tested, 594 (32.20%) were found to be positive for MTB by Xpert® MTB/RIF assay, and of those 443 (24.05%) were also found to be positive by microscopy. The remainder was negative.
Table 1 summarizes the numbers of MTB cases detected by microscopy in the 13 regions of Namibia with regard to sex. Khomas had the highest number of MTB cases, followed by Oshana and Ohangwena. The lowest numbers of cases were recorded in Zambezi and Omaheke. The specific regions where fifteen women resided were not indicated in the data set and hence were missing. We also compared the results from the smear microscopy by sex. Microscopy detected that there were slightly more males with MTB than females. The P-value obtained using the chi-square test was 0.489, indicating that there was no significant association between smear microscopy and sex.
The majority of the patients belonged to the age groups of 20–40 years and 41–60 years. In the age group of above 60 years, there was a lower number of MTB cases, but the lowest number of MTB cases was recorded among the age group of below 20 years (see Table 2). Data on the age of four patients were not available because it was missing from the data set. Of the total 249 MTB-positive males, 190 (76.3%) tested positive for MTB using both methods and the rest tested positive by Xpert® MTB/RIF assay only. Out of the females, 238 (95.2%) tested positive for MTB using both methods, with an extra 12 testing positive using Xpert® MTB/RIF assay only.
Of the total positive MTB cases, 341 (57.4%) patients also tested positive for HIV and 137 (23.1%) tested negative for HIV. The HIV status of the remaining 116 (19.5%) patients was unknown (see Table 3). Patients in the age groups of 20–40 years and 41–60 years were found to be the most co-infected with MTB/HIV (45.7% and 49.0% HIV, respectively). Only 18 (5.3%) of the total HIV-positive patients belonged to the age group of above 60 years. There were no HIV-positive patients among the age group of below 20 years.
Table 4 summarizes the distribution of HIV in MTB-infected patients, by sex. A higher percentage of HIV-positive males (63.9%) as compared to females (52.8%) was recorded.
The number of MTB cases and RIF-resistant cases diagnosed using the Xpert® MTB/RIF assay with regard to sex is presented in Table 5. From the total of 594 MTB-positive patients, 27.9% were resistant to RIF and 72.1% were sensitive to it. More males were found to be resistant to RIF as compared to the females, with the difference statistically significant (P = 0.023).
A total of 594 specimens tested positive for MTB using the Xpert® MTB/RIF assay, and of these 443 (74.6%) also tested positive using smear microscopy. These data indicate that smear microscopy detected TB in fewer patients than Xpert® MTB/RIF assay. Smear microscopy might miss specimens with low bacilli/ml, as direct smear microscopy needs at least 5 000 bacilli/ml of sputum for direct microscopy to show a positive result [1, 11].
In the current study, there were slightly more females with stronger smear-positivity than males and the difference was not statistically significant. Although culture-based testing is the gold standard for TB diagnosis, it needs high-safety settings and facilities that are expensive to maintain, and this means that most low- and middle- income countries cannot afford to do this kind of testing. For this reason, sputum smear microscopy remains the main and often only diagnostic tool for MTB [6–8, 17, 18]. Tuberculosis culture for drug-susceptibility testing is not routinely performed in Namibia . Culture-based testing is also quite time-consuming, requiring more than eight weeks for results to become available. However, the Xpert® MTB/RIF assay gives accurate results in a shorter time period of less than 2 h and being cheaper than culture is therefore more appropriate for use in low- and middle-income countries . That being said, it cannot completely replace culture-based testing, as it only detects RIF resistance and does not provide drug resistance profiles for other TB drugs. Namibia needs to scale up its facilities for culture-based testing so that specimens that are found to be RIF-resistant are further tested for MDR-TB and extensively drug-resistant (XDR) TB. This will assist in guiding treatment regimens for patients who might have MDR-TB or XDR TB.
This study found that MTB infection is distributed throughout Namibia, with males slightly more infected than females. Khomas was the region with the highest number of MTB cases, whereas Zambezi and Omaheke had the lowest numbers of MTB cases (each). This is similar to findings from a previous study, which also showed that TB was distributed all over Namibia with the highest number of cases reported in Khomas and Okavango . Khomas had the highest number of MTB cases possibly because of its central location, which includes the densely populated capital city Windhoek, where there is also a high HIV prevalence. HIV predisposes patients to TB. This region is receiving information on MTB testing awareness from different health-related stakeholders, which likely resulted in more people with TB getting tested once they suspected that they had TB symptoms. Zambezi and Omaheke recorded fewer MTB-positive patients probably due to their remote locations. Those who could be TB positive rarely have the information that could make them question or suspect that they are TB positive.
This study found that the age group with the highest MTB infection were those aged between 20 and 40 years (44.8%). The age group of below 20 years had the least amount of people with MTB infection (2.7%). The low infection rate in the younger age group could possibly be explained by this age group’s literacy, which allows them to effectively receive educational information on MTB prevention from schools and the media.
The study found a high MTB/HIV co-infection rate of 57.4% emphasizing the need for proactive and rapid screening of MTB/HIV co-infected patients. The number of patients with MTB/HIV in the age groups of 20–40 years was found to be high because the age group is considered a sexually active age group, with members having an increased risk of contracting HIV through unsafe sex . Most of the HIV-positive patients in our study belonged to that age group.
Xpert® MTB/RIF assay is an important initial diagnostic test for patients suspected of having MDR-TB and those with a MTB/HIV co-infection . An association between sex and sensitivity to RIF was noted. A smaller number of females was infected with a RIF-resistant strain than males possibly because females better adhere to drug taking than males. Fewer females than males are known to take alcohol or drugs in Namibia which often contributes to poor drug adherence. However, there could also be other reasons for this such as TB transmission mechanisms, primary versus secondary drug resistance, different co-infections, and different health-seeking behaviors. For instance men tend to socialize in crowded places than females such that they are likely to get community-acquired resistant strains. Further investigations are therefore needed. In 2014, only 137 cases of MDR-TB have been reported, indicating that drug susceptibility testing is improving in Namibia .
Tuberculosis is widely distributed throughout Namibia, with more males infected than females. Males have more resistance to RIF than females. Tuberculosis infection was mainly common in the age group of 20–40 years. A large proportion of MTB patients were also infected with HIV. Microscopy and Xpert® MTB/RIF assay are both crucial MTB diagnostic tools in areas of high HIV incidence. Screening diagnostic efforts should focus on the sexually active male HIV positive population who could be the source of more RIF-resistant TB than females to prevent its spread.
Nucleic acid amplification test
Namibia Institute of Pathology
- XDR TB:
Extensively drug-resistant TB
Palomino JC. Nonconventional and new methods in the diagnosis of tuberculosis: feasibility and applicability in the field. Eur Resp J. 2005;26(2):339–50.
Banada PP, Koshy R, Alland D. Detection of Mycobacterium tuberculosis in blood by use of the Xpert MTB/RIF assay. J Clin Microbiol. 2013;51(7):2317–22.
Dorman SE. New diagnostic test for tuberculosis: bench, bedside and beyond. Clin Infect Dis. 2010;50 Suppl 3:S173–7.
Piatek SA, van Cleeff M, Alexander H, Coggin LW, Rehr M, van Kampen S, et al. GeneXpert for TB diagnosis: planned and purposeful implementation. Glob Health Sci Pract. 2013;1(1):18–23.
Van Rie A, Fitzgerald D, Kabuya G, Van Deun A, Tabala M, Jarret N, et al. Sputum smear microscopy: evaluation of impact of training, microscope distribution, and use of external quality assessment. Guidelines for resource-poor settings. J Clin Microbiol. 2008;46(3):897–901.
Nour EMM, Saeed EMA, Zaki AZSA, Saeed ENS. Specificity of sputum smear compare to culture diagnosis of pulmonary tuberculosis. World J Med Sci. 2011;6(3):121–5.
Lawn DS, Nicol PM. Xpert MTB/RIF assay: development, evaluation and implementation of a new rapid molecular diagnostic for tuberculosis and rifampicin resistance. Future Microbiol. 2011;6(9):1067–82.
Walusimbi S, Bwabga F, De Costa A, Haile M, Joba M, Hoffner S. Meta-analysis to compare the accuracy of GeneXpert, MODS and the WHO 2007 algorithm for the diagnosis of smear negative pulmonary tuberculosis. BMC Infect Dis. 2013;13:507–20.
Weyer K, Mirzayev F, Migliori GB, Van Gemert W, D'Ambrosio L, Zignol M, et al. Rapid molecular TB diagnosis: evidence, policy making and global implementation of Xpert MTB/RIF. Eur Respir J. 2013;42(1):252–71.
Uddin MN, Chowdhury MR, Ahmed S, Rahman MT, Khatum R, van Leth FR, et al. Comparison of direct versus concentrated smear microscopy in detection of pulmonary tuberculosis. BMC Res Notes. 2013;6:291.
Zeka AN, Tasbakan S, Cavusoglu C. Evaluation of the GeneXpert MTB/RIF pulmonary and extrapulmonary specimens and detection of rifampin resistance in assay for rapid diagnosis of tuberculosis. J Clin Microbiol. 2011;49(12):4138–41.
Raj A, Singh N, Mehta PK. Gene Xpert MTB/RIF assay: a new hope for extrapulmonary tuberculosis. IOSR J Pharm. 2012;2(1):083–9.
Abed Al-Darraji HA, Abd Razak HA, Ng KP, Altice FI, Kamarulzaman A. The diagnostic performance of a single GeneXpert MTB/RIF assay in an intensified Tuberculosis case finding survey among HIV-infected prisoners in Malaysia. PLoS One. 2013;8(9):e73717.
WHO. TB Diagnostics and Laboratory Services. 2009. Available at http://www.who.int/tb/dots/lab.pdf. Accessed 12 Dec 2016.
Ministry of Health and Social Services. National Tuberculosis and Leprosy Programme Summary Report 2014–15. Republic of Namibia: MOHSS; 2016.
Namibia Ministry of Health and Social Services. National Guidelines for the Managementof Tuberculosis. 2011. http://www.who.int/hiv/pub/guidelines/namibia_tb.pdf. Accessed 12 Dec 2016.
Swai FH, Mugusi FM, Mbwambo JK. Sputum smear negative pulmonary tuberculosis: sensitivity and specificity of diagnostic algorithm. BMC Res Notes. 2011;4:476–82.
Pinyopornpanish K, Chaiwarith R, Pantip C, Keawvichit R, Wongworapat K, Khamnoi P, et al. Comparison of Xpert MTB/RIF assay and the conventional sputum microscopy in detecting Mycobacterium tuberculosis in Northern Thailand. Tuberc Res Treat. 2015;2015:1–6.
Ricks PM, Mavhunga F, Modi S, Indongo R, Zezai A, Lambert LA, et al. Characteristics of multidrug-resistant tuberculosis in Namibia. BMC Infect Dis. 2012;29(12):385.
Iram S, Zeenat A, Hussain S, Yusuf NW, Askam M. Rapid diagnosis of tuberculosis using Xpert MTB/RIF assay- Report from a developing country. Pak J Med Sci. 2015;1:105–10.
Mavenyengwa RT, Mukesi M, Chipare I, Shoombe E. Prevalence of human immunodeficiency virus, syphilis, hepatitis B and C in blood donations in Namibia. BMC Public Health. 2015;14:424–31.
We would like to thank NIP for giving us access to the data for this study. We would also like to thank Mrs. E. Shipiki (Chief Technologist at the Tuberculosis department, NIP) for assisting with the data collection process.
Availability of data and materials
The datasets generated during and/or analysed during the current study available from the corresponding author on reasonable request.
RTM conceived the research idea, supervised the work, conducted the data analysis, and participated in the write-up of the paper. ES contributed to the retrieval of the data and the write-up of the paper. IM contributed to the study design, data analysis, and the write-up. All authors read and approved the final paper for publication.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
The permission to conduct this study was obtained from the ethics committee of the NIP, as well as from the Ministry of Health and Social Services Research Ethics Committee. There is no way to trace patients’ identities from the results generated in this study.
Additional file 1:
Multilingual abstracts in the five official working languages of the United Nations. (PDF 783 kb)
Rights and permissions
Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
About this article
Cite this article
Mavenyengwa, R.T., Shaduka, E. & Maposa, I. Evaluation of the Xpert® MTB/RIF assay and microscopy for the diagnosis of Mycobacterium tuberculosis in Namibia. Infect Dis Poverty 6, 13 (2017). https://doi.org/10.1186/s40249-016-0213-y
- Xpert® MTB/RIF assay
- Diagnostic tests