In 2005 a cluster of 53 HIV-infected patients with extensively drug-resistant tuberculosis (XDR-TB) was detected in the Msinga sub-district, the catchment area for the Church of Scotland Hospital (CoSH) in Tugela Ferry, in KwaZulu-Natal province (KZN), South Africa. KZN is divided into 11 healthcare districts. We sought to determine the distribution of XDR TB cases in the province in relation to population density.
In this cross-sectional study, the KZN tuberculosis laboratory database was analysed. Results of all patients with a sputum culture positive for Mycobacterium tuberculosis from January 2006 to June 2007 were included. Drug-susceptibility test results for isoniazid, rifampicin, ethambutol, streptomycin, kanamycin and ofloxacin were available for all patients as well as the location of the hospital where their clinical diagnosis was made.
In total, 20858 patients attending one of 73 hospitals or their adjacent clinics had cultures positive for M. tuberculosis. Of these, 4170 (20%) were MDR-TB cases. Four hundred and forty three (11%) of the MDR tuberculosis cases displayed the XDR tuberculosis susceptibility profile. Only 1429 (34%) of the MDR-TB patients were seen at the provincial referral hospital for treatment. The proportion of XDR-TB amongst culture-confirmed cases was highest in the Msinga sub-district (19.6%), followed by the remaining part of the Umzinyati district (5.9%) and the other 10 districts (1.1%). The number of hospitals with at least one XDR-TB case increased from 18 (25%) to 58 (80%) during the study period.
XDR-TB is present throughout KZN. More than 65% of all diagnosed MDR-TB cases, including XDR-TB patients, were left untreated and likely remained in the community as a source of infection.
Citation: Moodley P, Shah NS, Tayob N, Connolly C, Zetola N, Gandhi N, et al. (2011) Spread of Extensively Drug-Resistant Tuberculosis in KwaZulu-Natal Province, South Africa. PLoS ONE 6(5): e17513. doi:10.1371/journal.pone.0017513
Editor: Georges Snounou, Université Pierre et Marie Curie, France
Received: November 1, 2010; Accepted: February 3, 2011; Published: May 31, 2011
Copyright: © 2011 Moodley et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: Drs. Shah and Gandhi are recipients of a Doris Duke Charitable Foundation, Clinical Scientist Development Award. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Multidrug-resistant (MDR) tuberculosis, including its extensively resistant (XDR) form has become a threat to the success of tuberculosis control programs. MDR tuberculosis is now a global epidemic with over 511000 estimated cases in 2007 .
All 53 were HIV infected. They sought healthcare at the Church of Scotland Hospital (CoSH) in Tugela Ferry whose catchment area is the Msinga sub-district. This raised the question as to whether this was nosocomial transmission in CoSH, an isolated outbreak in the Msinga community, or a widespread epidemic involving other districts of KwaZulu-Natal Province. The first indication that this was not an isolated nosocomial outbreak in CoSH came from the observation that 30 of the 53 patients were identified through a survey amongst outpatients suspected of having tuberculosis. Fourteen of the 30 had no prior history of hospitalization . While there was evidence of nosocomial and community transmission, the question remained as to how extensive the latter was. Since there was no obvious reason why community spread should be restricted to the Msinga sub-district, we hypothesised that XDR tuberculosis was present throughout KwaZulu-Natal Province.
This was a cross-sectional study, examining the culture and drug susceptibility database of the provincial tuberculosis laboratory in KwaZulu-Natal Province.
KwaZulu-Natal Province has a population of 9.7 million (2003 census)  and is divided in 11 health districts (Fig. 1). According to the provincial register, the incidence of tuberculosis in 2006 was 780 per 100,000 population. The HIV sero-prevalence among antenatal attendees was 38% in 2006 .
KwaZulu-Natal Province has 74 public hospitals, with varying numbers of affiliated clinics. Hospitals were grouped according to the district in which they are located. At the time of this study, King George V Hospital (KGV) was the single MDR and XDR tuberculosis referral hospital for patients in KwaZulu-Natal Province. Patients confirmed as being infected with a MDR/XDR strain of M. tuberculosis at one of the public hospitals or clinics, were referred to King George V Hospital for further management.
TB culture and drug-susceptibility testing
The South African national guidelines for diagnosis of tuberculosis allow culture and drug-susceptibility testing to be performed only on specimens from patients with a clinical diagnosis of tuberculosis who failed to respond to first-line therapy, who interrupted treatment, who had a previous diagnosis of tuberculosis or had repeatedly negative smear microscopy results. Adherence to these guidelines depends on accessibility to diagnostic facilities. Of note, after the report of XDR tuberculosis in 2005 , providers at CoSH in the Msinga sub-district started to send specimens from all patients suspected of tuberculosis for culture and drug-susceptibility testing.
Drug-susceptibility test results were generated by the 1% proportional method using Middlebrook 7H10 agar plates . In KwaZulu-Natal Province, routine susceptibility testing for M.tuberculosis includes the following drugs: isoniazid, rifampicin, ethambutol, streptomycin, kanamycin and ofloxacin.
Data Source and Data Management
The drug-susceptibility profile of all M.tuberculosis isolates from sputum, obtained from patients between 1 January 2006 and 30 June 2007 at the centralised TB laboratory in KwaZulu-Natal Province, were analysed. Specimens from patients attending private hospitals are not sent to this laboratory and therefore such patients are excluded from this analysis.
If a patient had multiple isolates during the study period, those with identical susceptibility profiles were regarded as a single isolate. For patients with multiple isolates with varying susceptibility profiles, only the most resistant isolate was selected. If specimens from patients were received from more than one hospital, then the most resistant isolate was used for analysis and attributed to the hospital of first contact. Patients with missing drug susceptibility data and/or hospital location were excluded from this analysis. Numbers of MDR patients referred to KGV Hospital were compared with the number of patients that were diagnosed to ascertain referral and treatment rates. Data were not available on clinical symptoms, tuberculosis treatment outcome, new vs. re-treatment cases or HIV status.
MDR tuberculosis was defined as resistance to isoniazid and rifampin, with or without resistance to additional anti-tuberculosis drugs. XDR tuberculosis was defined as MDR tuberculosis with additional resistance to kanamycin and ofloxacin. The term MDR tuberculosis includes XDR tuberculosis cases, unless specified otherwise.
MDR and XDR tuberculosis proportion was calculated as number of cases per 100 culture confirmed cases. The denominator to calculate the number of culture confirmed tuberculosis cases was obtained from the KZN laboratory database. Population data from the health statistics report of 2003 were used for the calculation of incidence . No accurate population data were available for the study period. The incidence rates in two groups are compared using an incidence rate ratio and the p-value is calculated by assuming that under H0 the number of cases in group 1 follows a binomial distribution with N = total number of cases in both groups, and p = person-time in group1/total person-time in both groups.
After excluding the Umzinyati district, the remaining districts were separated into two groups which have distinctly different proportions of XDR cases. These groups were found by sequentially pooling the districts and using Fisher's Exact test to determine if the proportion of XDR cases were not significantly different across the districts within each group.
A generalized linear model (GLM) for the binomial family with a log-link was fitted to the data to estimate the risk ratios comparing the risk of XDR tuberculosis in different geographical regions.
The data analysis was conducted using R version 2.11.0, The R Foundation for Statistical Computing and STATA® 11.0, StataCorp College Station, Texas.
The study was approved by the Biomedical Research Ethics Committee at the University of KwaZulu-Natal (#BCA274/09). As these samples were collected for routine clinical care, patients were not asked to give informed consent at the time of the clinical encounters. For the intentions of this study, there was no requirement for informed consent since all data used were previously collected during the course of routine medical care and did not pose any additional risks to the patients.
During the study period, M.tuberculosis was cultured from 20858 patients in KwaZulu-Natal Province. Of these, 4170 (20%) were infected with MDR tuberculosis isolates. Four hundred and forty three (11% of the MDR tuberculosis cases) displayed the XDR tuberculosis susceptibility profile. Overall, 1429 (34%) of the MDR tuberculosis cases were referred to KGV Hospital for further management. This included 212 (48%) of all XDR tuberculosis cases in the province during the study period.
The incidence of culture confirmed cases of tuberculosis in the province was 144.6 per 100.000 person-years. However, this varied widely between districts (Table 1). The highest incidence was found in eThekwini (236.6/100.000 person-yrs) and the lowest in Amajuba (20.4/100.000 person-yrs). The incidence of culture confirmed MDR and XDR tuberculosis in the province was 28.9 and 3.1/100.000 person-years respectively (Table 1). The highest incidence of both MDR (77.2/100.000 person-years) and XDR (34.1/100.000 person years) tuberculosis was found in Umzinyati district, which includes the Msinga sub-district. When the cases found in the Msinga sub-district were removed from those in the remainder of the district, the MDR incidence dropped to a level comparable with other districts. However, the XDR incidence remained at 5.0 versus 1.5/100.000 person years, significantly higher (Incidence rate ratio: 3.36, p-value<0.0001).
The proportion of MDR cases among culture confirmed patients with tuberculosis varied per district from 14.2% in eThekwini to 45.6% in uMkhanyakude. Umzinyati district that includes the Msinga sub-district, ranked third highest with 36.2% (Table 2).
The proportion of XDR tuberculosis cases in the Umzinyati district was 16%; this figure ranged from 0.3% to 2.0% in the other 10 districts (Table 2). The proportion of XDR tuberculosis in the Msinga sub-district was 19.6% vs 5.9% in the remaining part of the Umzinyati district. This last figure is approximately 3 times higher than in the district with the second highest proportion (Table 2).
When Umzinyati was excluded, the ten remaining districts formed two distinct groups based on the proportion of XDR cases (Table 3). Group 1 had an average proportion of XDR of 1.9% (range 1.9 to 2.0) while in group 2 the average was 0.8% (range 0.3 to 1.4). Compared with the Umzinyati district (without Msinga sub-district), this translated to a Risk Ratio of 0.33 (95% CI 0.21–0.51) and 0.14 (95% CI: 0.09–0.22) respectively (p<0.0001). All 3 districts in group 1 are adjacent to each other and located southwest of Umzinyati. The 7 districts of group 2 are in the north of the province and along the coast (Figure 1).
On the 1st of January 2006, patients infected with XDR tuberculosis had been detected in 16 (22%) hospitals, which increased to 58 (78%) by the end of June 2007. The geographical distribution of this increasing number of hospitals over time is shown in figure 2.
We report on the temporal spread of XDR tuberculosis in KwaZulu-Natal, the province of South Africa from which the first report on XDR tuberculosis emerged . The data show that in January 2006, XDR patients were detected in 16 hospitals located in five provincial districts. By the end of the 18-month study period, this figure extended to 58 hospitals involving all 11 districts.
The reported incidence of tuberculosis in 2006 in KZN was 780/100,000 . We found the incidence of culture-confirmed disease to be 145/100,000. This highlights the fact that over 80% of reported cases of tuberculosis are not culture-confirmed and, by default, also lack drug susceptibility test results. Although this may be in keeping with the policy on diagnosis of tuberculosis in South Africa, it is a matter of concern since a significant proportion of patients with MDR/XDR tuberculosis are likely to die before it is realized that drug susceptibility tests are needed to guide their treatment. An additional concern is that more than 65% of MDR (including XDR) cases of culture-confirmed tuberculosis did not reach the referral centre and therefore remained untreated. These large groups of undiagnosed and diagnosed-but-not-referred cases of drug-resistant tuberculosis form a contingent of patients whose disease is inappropriately managed. They also represent a pool of potential transmitters of drug-resistant tuberculosis in the community or in hospitals.
The last drug resistance survey in South Africa in 2001/2002 found that the MDR tuberculosis prevalence in KwaZulu-Natal was 1.7% among new patients and 7.7% among retreatment patients. This was similar to other provinces . Second-line drug susceptibility testing was not performed in this survey and therefore the proportion of XDR cases is unknown. However, XDR was already present in KwaZulu-Natal Province in 2001 . We show an overall increase in the proportion of culture-confirmed MDR to 20% (Table 1). However, this figure cannot be compared with those found during the 2001/02 survey. The reported prevalence in 2001/02 is based on active case finding in randomly chosen areas in the province and reflects the situation amongst all patients with tuberculosis. Our figures represent only the proportion amongst culture-confirmed cases in the province and are therefore a gross underestimation of the total number of MDR cases in KZN. Despite this underestimation, we show a doubling of MDR cases over the 5-year period from 2001/02 to 2006.
The proportion of culture-confirmed XDR tuberculosis in the Umzinyati district was more than seven times higher than that in the rest of the province. Although this was largely attributable to the high prevalence in the Msinga sub-district where all suspected cases are cultured, the observation that the remaining part of the Umzinyati district with culture practices comparable to the other districts also had a higher proportion of XDR cases than the rest of the province (Table 3) alludes to circumstances in that district that may have facilitated the emergence of XDR tuberculosis.
The data also show that the presence of XDR tuberculosis is not restricted to the Umzinyati district. Although the proportion of XDR amongst culture-confirmed cases is lower in the other districts (Table 2), this might not reflect the real situation. Patients with tuberculosis from the Msinga sub-district obtained a diagnosis through culture and drug susceptibility testing on first presentation. As a result, a diagnosis of drug-resistant tuberculosis was already made even if patients died in the ensuing weeks. In the rest of the province, cultures were done when there was no response to treatment. As many patients with XDR tuberculosis die within weeks from first presentation , a significant number of patients in other parts of the province may have remained undiagnosed.
Whole genome sequencing data on a limited number of randomly chosen XDR isolates from KwaZulu-Natal Province suggest that one XDR strain has spread throughout the province . This needs confirmation by sequencing of a larger number of isolates. The observation that the proportion of XDR cases in the Umzinyati district (even without Msinga) is higher than that in the other districts suggests that this may be the source of such clonal spread. This is supported by the observation that the three districts in the southwest of the province had a higher proportion of XDR patients as compared to the other districts. Like the communities of Umzinyati, people from these districts use Pietermaritzburg as their main shopping and cultural centre. The other districts use Durban and Empangeni for that purpose. The observed temporal increase of XDR throughout the province during the study period also supports the possibility of clonal spread. However, this is a retrospective study and no concrete conclusions can be made regarding the true nature of the acquisition and spread of TB in this group of patients.
Since there is not, as yet, effective treatment for XDR tuberculosis, tuberculosis control programmes need to include more effective strategies to curb its spread. A rapid and efficient implementation of the new national guidelines for the initiation of anti-retroviral treatment at a CD4 count of 350/mm3 as opposed to 200/mm3 would assist in decreasing the size of the susceptible population . In addition, the infection prevention strategies to limit transmission in health care facilities as well as in the community need to be implemented and evaluated. Without this, the implementation of the new policy of combined care for patients with active tuberculosis and HIV infected patients without tuberculosis is likely to promote further spread of tuberculosis. The development of a rapid diagnostic test that is able to detect the presence of M. tuberculosis and its susceptibility to first-line and second-line drugs within a couple of hours should have the highest priority. Such a test will be able to identify MDR and XDR cases much earlier and facilitate more efficient management of this disease and earlier implementation of strategies to prevent transmission of drug-resistant tuberculosis.
Conceived and designed the experiments: PM NSS NG GF AWS. Performed the experiments: PM AWS. Analyzed the data: PM CC NT NZ. Contributed reagents/materials/analysis tools: PM CC NT NZ. Wrote the paper: PM NSS NT CC NZ NG GF AWS.
- 1. World Health Organization (2009) Global tuberculosis control - epidemiology, strategy, financing: WHO report 2009. Geneva, Switzerland; Report No: WHO/HTM/TB/2009.411.
- 2. Gandhi NR, Moll A, Sturm AW, Pawinski R, Govender T, et al. (2006) Extensively drug-resistant tuberculosis as a cause of death in patients co-infected with tuberculosis and HIV in a rural area of South Africa. Lancet 368: 1575–1580.
- 3. Statistical Release P0302 (2003) Statistics South Africa. Available: http://www.statssa.gov.za/publications/P0302/P03022003.pdf. Accessed 2011 Mar 20.
- 4. Department of Health South Africa (2007) National HIV and Syphilis Prevalence Survey in South Africa, 2006 Report. Available: http://www.doh.gov.za/docs/reports/2007/hiv/part1.pdf. Accessed 2011 March 20.
- 5. Hacek D (1992) Modified Proportion Agar Dilution Test for slowly growing Mycobacteria. In: Isenberg HD, editor. Clinical Microbiology Procedures Handbook. pp. 5.13.1–15. AMS: volume 1.
- 6. Weyer K, Lancaster J, Brand J, van der Walt M, Levin J (2003) Survey of Tuberculosis Drug Resistance in South Africa 2001–2002. Medical Research Council Unit for TB Epidemiology and Interventions Branch, Pretoria.
- 7. Pillay M, Sturm AW (2007) Evolution of the extensively drug-resistant F15/LAM4/KZN strain of Mycobacterium tuberculosis in KwaZulu-Natal, South Africa. Clin Infect Dis 45: 1409–1414.
- 8. Ioerger TR, Koo S, No EG, Chen X, Larsen MH, et al. (2009) Genome Analysis of multi- and extensively-drug resistant tuberculosis from KwaZulu-Natal, South Africa. PLoS One 4(11): e7778.
- 9. Harrison D (2009) Report: An Overview of Health and Health care in South Africa 1994–2010: Priorities, Progress and Prospects for New Gains. Available: http://www.doh.gov.za/docs/reports/2010/overview1994-2010.pdf. Accessed 2011 Mar 20.