- Research article
- Open Access
Molecular identification of Mycobacterium bovis from cattle and human host in Mali: expanded genetic diversity
- Mamadou Diallo†1,
- Bassirou Diarra†2Email author,
- Moumine Sanogo2,
- Antieme C. G. Togo2,
- Anou M. Somboro2,
- Mariam H. Diallo2,
- Bréhima Traoré2,
- Mamoudou Maiga2,
- Younoussa Koné1,
- Karim Tounkara1,
- Yeya dit Sadio Sarro2,
- Bocar Baya2,
- Drissa Goita2,
- Hamadoun Kassambara2,
- Bindongo P. P. Dembélé2,
- Sophia Siddiqui3,
- Robert L. Murphy4,
- Sounkalo Dao2,
- Souleymane Diallo2,
- Anatole Tounkara^2 and
- Mamadou Niang1
© The Author(s). 2016
Received: 23 December 2015
Accepted: 12 July 2016
Published: 20 July 2016
Bovine tuberculosis (BTB) is a contagious, debilitating human and animal disease caused by Mycobacterium bovis, a member of the Mycobacterium tuberculosis complex. The study objective were to estimate the frequency of BTB, examine genetic diversity of the M. bovis population in cattle from five regions in Mali and to determine whether M. bovis is involved in active tuberculosis (TB) in humans. Samples from suspected lesions on cattle at the slaughterhouses were collected. Mycobacterial smear, culture confirmation, and spoligotyping were used for diagnosis and species identification. Mycobacterium DNA from TB patients was spoligotyped to identify M. bovis.
In total, 675 cattle have been examined for lesions in the five regions of Mali. Out of 675 cattle, 79 specimens presented lesions and then examined for the presence of M. bovis. Thus, 19 (24.1 %) were identified as M. bovis; eight (10.1 %) were non-tuberculous Mycobacterium (NTM). Nineteen spoligotype patterns were identified among 79 samples with five novel patterns. One case of M. bovis (spoligotype pattern SB0300) was identified among 67 TB patients.
This study estimates a relatively true proportion of BTB in the regions of Mali and reveals new spoligotype patterns.
Bovine tuberculosis (BTB) is a contagious, debilitating human and animal disease. It is caused by Mycobacterium bovis a member of the M. tuberculosis complex (MTBc), which also includes M. tuberculosis, M. africanum, M. microti, M. canettii, M. caprae, M. pinnipedii and the new discovered strain M.mungi . Cattle are considered as natural reservoir for M. bovis.
In Mali, West Africa, the total number of cattle is estimated to be more than 9,438,000, and the livestock sector occupies an important place in the development of the economy . In terms of the national economy, the livestock sector contribution to gross domestic product (GDP) is estimated to be 10 % and its contribution to export earnings was 40 billion CFA ($83 million United States of America Dollar: USD) in 1995, which represents 17.5 % of total exports, occupying third place after cotton and gold . The economic contributions from cattle have steadily declined in recent years, and were only 28 billion CFA ($58 million USD) in 1999 representing 7 % of total exports .
The monitoring of BTB is based partially on screening by tuberculin skin test of live animals and also on the testing of suspected lesions found at slaughterhouses. Bovine tuberculosis is a zoonotic disease caused by M. bovis, which is transmitted, from animals to humans by ingestion of raw milk, contaminated meat or aerosol . Mycobacterium bovis infection in humans often presents as extra pulmonary tuberculosis, especially in children . The possible role of M. bovis in human tuberculosis infection is not well known in Mali because tuberculosis in humans due to M. bovis is clinically indistinguishable from that of M. tuberculosis.
In many resource-limited settings, the diagnosis of tuberculosis is based only on smear microscopy which cannot differentiate Mycobacterium species or the different strains of MTBc. Bovine tuberculosis cannot be specifically diagnosed without confirmation using additional microbiological methods. New molecular methods such Mycobacterial Interspersed Repetitive Units (MIRU), Variable Number of Tandem Repeats (VNTR) and restriction fragment length polymorphism (IS6110 RFLP) techniques  can determine the importance and factors influencing the transmission of BTB among cattle. Among these methods, spoligotyping technique is most often used for molecular typing of Mycobacterium strains . This technique has the advantage to confirm the diagnosis of tuberculosis and also to classify subspecies of Mycobacterium tuberculosis complex (MTBc) . Because of this method, M. bovis was isolated in countries where mycobacterial isolates from humans were fully typed .
In Mali, there has been an increase in the number and variety of cattle, and as well as in the number of tuberculin skin test-positive cases. Several studies on M. bovis population focused only in the capital city of Bamako have been performed excluding other regions of Mali [8, 9]. The goal of this study was first to estimate the apparent prevalence of BTB, second to examine the genetic diversity of strains of M. bovis obtained in five distinct regions of Mali from infected cattle, using spoligotyping technique. Lastly, we examined whether M. bovis is involved in active TB in the human host.
Slaughterhouses and specimens collection
The regions of Ségou, Mopti, Sikasso, Kayes and Bamako were selected for this study. These five regions are home to more than 80 % of the livestock of Mali . In each region there is a slaughterhouse maintained by a trained veterinarian.
We conducted this study from January 2008 to December 2010. During that period, 675 cattle were examined for the presence of lesions in the regions of Kayes (75), Sikasso (160), Ségou (80), Mopti (140) and Bamako (220). At the slaughterhouses, specimen collection was based on suspicion of bovine tuberculosis lesions after slaughtering by meat inspection . Suspected lesions were lymph nodes and or necrotic nodules. They were size different and were containing yellow, green or tan pus. Tissue specimens were collected from affected organs such as lymph nodes, lungs, chest, and liver as described by Cosins . Upon collection, tissue specimens were transported on ice to the Central Veterinary Laboratory of Bamako (Laboratoire Central Vétérinaire de Bamako) and kept at −80 °C before testing. Each specimen was uniquely identified by collection date, sample number and region of origin.
Specimens processing, smear microscopy and culture
All the laboratory work was performed in the BSL-3 facility within the Human Immunodeficiency Virus and Tuberculosis (HIV-TB) Research and Training Center (SEREFO Laboratories) at the University of Sciences, Techniques and Technologies of Bamako (USTTB).
Tissue specimens were washed with sterile saline solution (Remel Inc., Lenexa, KS 66215, USA). Specimens were then cut into small pieces using the Tissue Grinder (Precision Disposable Tissue Grinder, Covidien, Mansfield, MD, USA). Thereafter, specimens were digested and decontaminated using the standard N-Acetyl-L-Cysteine/4 % NaOH solution (Alpha Tec System. Inc., Vancouver, USA), concentrated by high speed centrifugation (4500 rpm or 3000 g, Eppendorf centrifuge) and inoculated on both liquid (Mycobacterium Growth Incubator Tube, BBL™ MGIT™ Becton Dickinson, Sparks MD, USA), and solid (Middlebrook 7H11 Agar and Selective 7H11 Agar) media. Simultaneously, an aliquot of concentrated specimen was prepared for Auramine-Rhodamine staining (BBL™ Becton Dickinson, Sparks MD, USA) for microscopic examination (Olympus, Olympus Corporation, Tokyo, Japan).
Identification of mycobacterial isolates
Positive cultures were confirmed by smear using Kinyoun (Remel Inc. Lenexa, KS 66215, US) stain acid fast method. The mycobacterial infection of specimens was based on a combination of the initial fluorescent acid-fast microscopy result, colonial morphology of growth in culture, and confirmation by Kinyoun staining. Suspected tuberculosis cases were confirmed by spoligotyping technique.
In order to test whether there is transmission of M. bovis in human hosts, we examined the spoligotyping results for 67 new human TB cases screened at the University Teaching Hospital of Point G and the six-TB care units located in the health referral centers of Bamako between 2006 and 2010 from SEREFO database.
Molecular strain typing for genetic diversity study within M. bovis
All Kinyoun-positive colonial growth suggestive of M. bovis underwent molecular strain typing. Spoligotyping technique was performed using a commercially available kit (Isogen Life Science, Netherlands) by following the manufacturer’s instructions to amplify the whole direct repeat region (DR) within the M. tuberculosis genome. The amplified biotin labeled PCR product was then hybridized to 43 ordered synthetic DNA oligonucleotide spacers bound to a nylon membrane. After hybridization, the membrane was developed by incubating with a streptavidin peroxidase conjugate, which binds to the biotin label on the PCR product. Next, the membrane was washed and incubated with Enhanced Chemiluminescent (ECL) Detection Reagents. This reaction results in the emission of light, and is detected by exposing a light sensitive film to the membrane. Comparison and naming of the patterns were done through global M. bovis database (http://www.mbovis.org).
The proportion of each strain type with 95 % confidence interval (CI) and their geographical region were compared using the χ 2 test or Fisher’s exact test. The study included all the suspected cases which were seen at each slaughterhouse during our visit. A descriptive analysis was performed by evaluating the number of isolates determined to be M. bovis cases by spoligotyping technique. Thereafter similar spoligotypes were grouped in a same cluster. The relationship of clusters to geographical origin of animal was also evaluated. At the same these patters were compared to the M.bovis case which was isolated from human during one of our previous study on human tuberculosis.
Tissue sample number, region of provenance and prevalence using liquid media technique
Number of examined cattle
Number of cattle with lesions
Percentage of cattle with lesion
Number of positive M. bovis
Percentage of positive (microscopy)
Percentage of positive (liquid media culture)
1/11 (9.1 %)
1/11 (9.1 %)
4/12 (33.3 %)
4/12 (33.3 %)
0/10 (0 %)
1/10 (10 %)
5/19 (26.3 %)
7/27 (25.9 %)
8/27 (29.6 %)
16/79 (20.25 %)
19/79 (24.05 %)
Proportion of infection per region
Number of examined cattle (%)
Number of Positive (M. bovis) by microscopy and (%)
Number of Positive (M. bovis) by liquid media culture (%)
1/75 (1.33 %)
1/75 (1.33 %)
4/160 (2.5 %)
4/160 (2.5 %)
0/80 (0 %)
1/80 (1.25 %)
4/140 (2.86 %)
5/140 (3.57 %)
7/220 (3.18 %)
8/220 (3.63 %)
16/675 (2.37 %)
19/675 (2.81 %)
Culture results of tissue specimens from Malian cattle. Specimens were digested, decontaminated, centrifuged at high speed and inoculated onto two types of media
Tissue specimens culture results
Positive (M. bovis)
Contaminated with other bacteria
Spoligotype patterns revealed during the study in Mali and their frequency
Kayes, Bamako, Ségou, Mopti
Among the 67 specimens obtained from individual human subjects infected with pulmonary tuberculosis, only one had confirmed M. bovis. This case was also a pulmonary tuberculosis infection. In comparison to the spoligotypes from cattle, the spoligotype pattern obtained from human host was similar to the pattern observed in the cattle M. bovis pattern SB0300. Both lack the spacers 6 and 30 (Table 4). The patient with the SB0300 spoligotype pattern of M. bovis had developed active tuberculosis with characteristic symptoms including weight loss, cough and fever. The serological testing for HIV was negative.
Results of the smear microscopy from tissue pellets
Sixty-three percent of specimens from tuberculosis lesions were culture-positive. This proportion is similar to the frequency observed in Chad, which was 65 % as reported by Diguimbaye-Djaibé & al. in 2006 . The smear positivity was only one fifth (20.3 %) of the specimens, which was low and confirms the lack of sensitivity of smear microscopy for tuberculosis diagnosis in this setting.
The frequency of BTB varies from one geographical zone to another depending on the population density of cattle. An example is Tanzania, where the prevalence of BTB (by using a single tuberculin skin test) was 14 % in the Southern Highlands , and 0.2 % in the Lake Victoria zone . This difference was explained partially by the density and number of cattle in the region.
Tuberculosis in cattle has been demonstrated to be prevalent in sedentary breeding style, where cattle are used for milk production as these conditions allow better transmission of M. bovis infection between animals [14, 15]. In Mali, the prevalence of tuberculin-skin test positive cattle in Sikasso and Ségou was respectively 20 % and 64.3 % in different herds,1 % and 2.8 % in individual cattle, and the same observation was seen in the suburban area of Bamako in 2003 [14, 16].
We further found that 10.1 % of specimens were infected with non-tuberculous mycobacteria (NTM) and 29.1 % with bacteria or yeast. Almost one third (36.7 %) of the specimens was culture negative, a proportion higher than what was seen in Chad (27.3 %) . The isolation of NTM from tissue samples may represent true infections, co-infections or colonization. However, we do not know from our data the importance and infectiousness of those isolates. In view of the lack of pasteurization of milk, these data do suggest that, cattle may be one source of NTM transmission.
Our study was limited to the south of the country, and the cattle were from the urban areas of each region. The transmission profiles in rural areas of the regions may be different if we were able to include cattle from these areas. Thus, a cross sectional with larger sample size and sampling combining slaughterhouses, rural and urban areas from all the country may reveal the true country profile of M.bovis strains circulating in Mali. Another limitation was that our focus was mainly for identification of M.bovis and we didn’t focus on identifying other mycobacteria species. Despite these limitations, the study revealed that the Bamako region has the highest frequency of BTB and showed a wide variety of M. bovis strains (SB2262, SB2263, SB2264, and SB0300). Only the SB0300 was previously reported . This frequency is higher than the one reported by Sidibé in 2003 .
Such high prevalence and diversity in Bamako, the capital city of Mali, may be due to the semi-intensive breeding style used in this region to improve milk and meat production. The high demand for meat in the capital city of Bamako increases the different varieties of cattle, the biggest market for livestock in Mali . These data are in line with previous studies that showed that imported cattle are sensitive to different types of diseases in general and bovine tuberculosis in particular . Another explanation may be the high number of tissue samples collected from Bamako region in comparison to the other regions (27/79), although this difference was not significant (p = 0.47). Bamako was followed by the Mopti region, which has the highest number of cattle in Mali and is an excellent geographical breeding zone because of its diverse climate . We discovered a wide variation in M. bovis strains with five new spoligotype patterns identified. However, the particular distribution of the spoligotype SB0944 in Sikasso has to be investigated further. In fact, this region in the south of the country has received funding to breed the N’dama race, which is Trypano- tolerant . In addition, all the strains observed in Sikasso had the spacer 6 which was absent in all strains studied so far in Mali . This may explain the clustering of this spoligotype in Sikasso and we believe that strain was imported through the intense breeding related to this N’dama project. We also have identified seven cattle infected with M. bovis that are lacking the spacers 6 and 21. This is the first time those spoligotypes have been observed in Mali. In the previous study done in the Bamako abattoir, Muller & al. , have identified spoligotypes lacking spacer 6 in Bamako. We observed that five cattle were infected with strains of M. bovis lacking simultaneously the spacers 6 and 21, which may indicate that the genome is flexible enough to allow creation of new spoligotypes that in turn helps to increase the antigenic repertoire within M. bovis. The cluster number six was the most prevalent and was seen in four regions out of five .
All our examined specimens showed an absence of spacer 30 (Fig. 2), which confirmed the results obtained in 2007 by Muller et al. . However, Muller found the presence of the spacer 30 among seven strains out of 20 from Bamako abattoir . Taken together, M. bovis strains from Cameroun, Nigeria, Chad and Mali examined by spoligotyping technique showed similar spoligotype patterns that lacked the spacer 30 . This may suggest that strains from those countries are phylogenetically similar . The reason may be a specific deletion within a chromosomal DNA (Af 1) . The shortest sequence through the Direct Repeat region was observed in the SBXXXX Mopti. In addition to known missing spacers, there are the spacers 4, 5, 22 and 23 which were also missing. The deletion of those spacers which are contiguous may have a rich AT content which is prone for deletion. During this study, M. caprae, which is known to be associated tuberculosis infection in sheep and goats, was not observed .
The use of spoligotyping for accurate diagnosis is important for assessing the fight against this zoonosis . In this study, spoligotyping was used as a diagnostic and confirmatory tool, but also yielded important insight into the epidemiology and characteristic of M. bovis in Mali and revealed that more spoligotyping patterns are emerging. Another important impact of this study concerns the neighbor countries of Mali, since a large percentage of meat from cattle in Mali is consumed in those countries, and the mobility of livestock in the vast region of Sahel which could potentially lead to further transmission of BTB .
In this study, we identified one case of M. bovis infection in humans for a crude estimated prevalence of 1.5 % (1 out 67). This zoonotic TB was found in several countries in Africa with a median of 2.8 % (range 0–37.7 %). Our prevalence falls in that range and below the prevalence observed in Ethiopia, Nigeria and Tanzania [12, 21, 22]. We assume that the proportion of human cases of M. bovis depends on the efficacy of disease control such as regular milk pasteurization, and slaughterhouse meat inspection [10, 23]. In Mali, little is known about the transmission of M. bovis to, or between humans. Mycobacterium bovis can be easily transmitted through ingestion of unpasteurized milk, or undercooked meat and can cause pulmonary tuberculosis mainly in children [5, 12] among workers from farms and slaughterhouses . Although we have not performed a proper study on risk factors analysis, but we may speculate that those means are the common route of M. bovis among our patient.
M. bovis is present in Mali and accounts for approximately one quarter of suspected lesions from infected cattle in the tested regions. Our approach by the use of spoligotyping is a logical step for a better understanding of different mycobacterial species circulating in the country. In order to further characterize the frequency of BTB in Mali and to estimate human transmission rates of NTM as well as BTB, more extensive testing is necessary. The presence of confirmed M. bovis in one Malian subject suggests that there may be a lack of effective disease control which includes regular milk pasteurization and slaughterhouse meat inspection.
BTB, bovine tuberculosis; DR, direct repeat; ECL, enhanced chemiluminescent; GDP, Growth Domestic Product; HIV, human immunodeficiency virus; IS6110 RFLP, restriction fragment length polymorphism; MIRU, Mycobacterial Interspersed Repetitive Units; MTBc, Mycobacterium tuberculosis complex; NTM, non-tuberculous mycobacteria; TB, tuberculosis; USD, Dollar of United States of America; USTTB, University of Sciences, Techniques and Technologies of Bamako; VNTR, variable number of tandem repeats
The authors express special thanks to all the slaughterhouses technicians of the different regions, for their collaboration during the study period, and also to all the staff of the Laboratoire Central Vétérinaire de Bamako. They also express our special thanks to Prof. Ousmane Koita for his assistance and guidance in this manuscript, thanks to Janice A Washington for her assistance with the manuscript, to Dansine Diarra for making the map of Mali, to Bakary Konaté and Oumar Mangané for their assistance and help for samples collection and transportation, and Michael Polis from the intramural program of the US National Institute of Allergy and Infectious Diseases, National Institutes of Health.
This study was funded by World Bank through Programme Maladie Infectieuse (PMI PMI-23/LCV) and le programme d’appui aux services agricoles et aux organisations paysannes (PASAOP) and by the Division of Clinical Research (DCR) of NIAID/NIH. This work was also partially supported by NIH grants 5D43TW007995 and 5UM1AI69471.
Availability of data and materials
All the data supporting our findings can be found (including information found in any supplementary files) within the manuscript.
MD conceived and developed the protocol. BD, MN, SDa, SDi, RLM, SS, YK, BK, OM, KT, helped in the protocol development. MN, SS, SDi, and RLM, led the study. BD, MS, MHD, BT, MM, AMS, ACGT, YSS, DG, BB, HK, BPPD, were instrumental in data generation and laboratory assays. BD, MD, BT, YSS, SDi. and MN collated, reviewed and interpreted data and contributed to the writing of the manuscript. MD, YK, BK, OM, KT, reviewed and selected cattle for the study. YSS did all statistical analysis and figures. BD and MD wrote the first draft. SS, SDa, SDi, RLM, and MC reviewed the drafts. SS, SDi, SDa, MN, RLM, and AT provided administrative and scientific oversight for this work. All authors had access to the data, read and approved the final manuscript.
Dr Mamadou Diallo is a senior researcher at the laboratoire central veterinaire (Bamako, Mali), his research is aimed at understanding the zoonotic diseases.
Dr Bassirou Diarra is a senior scientist at SEREFO, specialist of tropical medicine; head of BSL-3 laboratory and his work is related to Human TB.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
The protocol for spoligotyping of M. tuberculosis DNA was approved by the Ethical committees of Northwestern University of Chicago, IL, USA, and the USTTB, Mali. The study performed on human subjects was approved by the “Comite d’éthique de la Faculté de Médecine, de pharmacie et d’odontostomatologie” of the University of sciences, techniques and technologies of Bamako and the institutional review board (IRB) of the National Institute of Allergy and Infectious Diseases, National Institutes of Health (NIAID/NIH), USA. The protocol for the cattle study was also approved by the ethic committee of the “laboratoire central vétérinaire de Bamako”, Mali.
Before collecting tissue samples, verbal consent was obtained from the livestock owners for samples to be taken and used.
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- Alexander KA, et al. Novel Mycobacterium tuberculosis complex pathogen, M. mungi. Emerg Infect Dis. 2010;16(8):1296–9.View ArticlePubMedPubMed CentralGoogle Scholar
- Ministère de l'élevage et de la Pêche RM. Direction Nationale de l'appui au Monde Rural, Rapport d'activité 2000. 2000.Google Scholar
- Ministère de l'Economie et des Finances RM. Direction Nationale de la Statistique, Rapport d'activités 1997. 1997.Google Scholar
- Ministère de l'élevage et de la Pêche RM. Politique Nationale de Développement de l'élevage au Mali, Rapport d'activité 2003. 2003.Google Scholar
- Dankner WM, Davis CE. Mycobacterium bovis as a significant cause of tuberculosis in children residing along the United States-Mexico border in the Baja California region. Pediatrics. 2000;105, E79.View ArticlePubMedGoogle Scholar
- Barnes PF, Cave MD. Molecular epidemiology of tuberculosis. N Eng J Med. 2003;349:1149–56.View ArticleGoogle Scholar
- Kamerbeek J, et al. Simultaneous detection and strain differentiation of Mycobacterium tuberculosis for diagnosis and epidemiology. J Clin Microbiol. 1997;35(4):907–14.PubMedPubMed CentralGoogle Scholar
- Muller B, Steiner B, Bonfoh B, Fane A, Smith NH, Zinsstag J. Molecular characterization of M. bovis isolated from cattle slaughtered at the Bamako abattoir in Mali. BMC Vet Res. 2008;4:26.View ArticlePubMedPubMed CentralGoogle Scholar
- Cousins DV. Mycobacterium bovis infection and control in domestic livestock. Rev Sci Tech. 2001;20:71–85.PubMedGoogle Scholar
- Cosivi O, et al. Zoonotic tuberculosis due to Mycobacterium bovis in developing countries. Emerg Infect Dis. 1998;4:59–70.View ArticlePubMedPubMed CentralGoogle Scholar
- Diguimbaye-Djaibe C, et al. Mycobacterium bovis isolates from tuberculous lesions in Chadian zebu carcasses. Emerg Infect Dis. 2006;12:769–71.View ArticlePubMedPubMed CentralGoogle Scholar
- Kazwala RR, et al. Isolation of Mycobacterium bovis from human cases of cervical adenitis in Tanzania: a cause for concern? Int J Tuberc Lung Dis. 2001;5:87–91.PubMedGoogle Scholar
- Jiwa SF, et al. Bovine tuberculosis in the Lake Victoria zone of Tanzania and its possible consequences for human health in the HIV/AIDS era. Vet Res Commun. 1997;21:533–9.View ArticlePubMedGoogle Scholar
- Sidibe SS NAD, Fane A, Doumbia RM, Sidibe CK, Kante S, Mangane O, Konate B, Kone AZ, Maiga MS, Fofana M. Tuberculose bovine au Mali: Résultats d'une enquête épidémiologiques dans les élevages laitiers de la zone périurbaine du district de Bamako. Revue Elev Med Vet Pays Trop. 2003;56:115–20.Google Scholar
- Cosivi O, et al. Epidemiology of Mycobacterium bovis infection in animals and humans, with particular reference to Africa. Rev Sci Tech. 1995;14:733–46.PubMedGoogle Scholar
- Mamadou, D. Etude de la prévalence de la tuberculose bovine au Mali et caractérisation des souches de mycobactéries isolées, étude pilote. Rapport de projet PMI-23/LCV 2011.Google Scholar
- International Livestock Research institute (ILRI). http://agtr.ilri.cgiar.org/index.php?option=.
- Müller B, Hilty M, Berg S, Garcia-Pelayo MC, Dale J, Boschiroli ML, Cadmus S, Ngandolo BN, Godreuil S, Diguimbaye-Djaibé C, et al. African 1, an epidemiologically important clonal complex of Mycobacterium bovis dominant in Mali, Nigeria, Cameroon, and Chad. J Bacteriol. 2009;191:1951–60.View ArticlePubMedPubMed CentralGoogle Scholar
- Aranaz A, Liebana E, Gomez-Mampaso E, Galan JC, Cousins D, Ortega A, Blazquez J, Baquero F, Mateos A, Suarez G, Dominguez L. Mycobacterium tuberculosis subsp. caprae subsp. nov.: a taxonomic study of a new member of the Mycobacterium tuberculosis complex isolated from goats in Spain. Int J Syst Bacteriol. 1999;49:1263–73.View ArticlePubMedGoogle Scholar
- Mazurek GH, et al. Chromosomal DNA fingerprint patterns produced with IS6110 as strain-specific markers for epidemiologic study of tuberculosis. J Clin Microbiol. 1991;29:2030–3.PubMedPubMed CentralGoogle Scholar
- Alemayehu R, Girmay M, Gobena A. Bovine tuberculosis is more prevalent in cattle owned by farmers with active tuberculosis in Central Ethiopia. Vet J. 2008;178:119–25.View ArticleGoogle Scholar
- Mawak J, Gomwalk N, Bello C, Kandakai-Olukemi Y. Human pulmonary infections with bovine and environment (atypical) mycobacteria in Jos, Nigeria. Ghana Med J. 2006;40:132–6.PubMedPubMed CentralGoogle Scholar
- Ayele WY, Neil SD, Zinsstad J, Weiss MG, Pavlik I. Bovine tuberculosis: an old disease but a new threat to Africa. Int J Tuberc Lung Dis. 2004;8:924–37.PubMedGoogle Scholar
- Daborn CJ, Grange JM, Kazwala RR. The bovine tuberculosis cycle--an African perspective. Soc Appl Bacteriol Symp Ser. 1996;25:27S–32.View ArticlePubMedGoogle Scholar