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An outbreak investigation of visceral leishmaniasis among residents of Dharan town, eastern Nepal, evidence for urban transmission of Leishmania donovani
© Uranw et al.; licensee BioMed Central Ltd. 2013
Received: 15 June 2012
Accepted: 14 January 2013
Published: 18 January 2013
Visceral leishmaniasis (VL) is a predominantly rural disease, common in the low lands of eastern Nepal. Since 1997 VL cases have also been reported among residents of the city of Dharan. Our main research objective was to find out whether there had been local transmission of VL inside the city.
We conducted an outbreak investigation including a case–control study; cases were all urban residents treated for VL between 2000 and 2008 at BP Koirala Institute of Health Sciences, a university hospital in the city. For each case, we selected four random controls, with no history of previous VL; frequency-matched for age. Cases and controls were subjected to a structured interview on the main exposures of interest and potential confounders; a binominal multilevel model was used to analyze the data. We also collected entomological data from all neighborhoods of the city.
We enrolled 115 VL patients and 448 controls. Cases were strongly clustered, 70% residing in 3 out of 19 neighborhoods. We found a strong association with socio-economic status, the poorest being most at risk. Housing was a risk factor independent from socio-economic status, most at risk were those living in thatched houses without windows. ‘Sleeping upstairs’ and ‘sleeping on a bed’ were strongly protective, OR of 0.08 and 0.25 respectively; proximity to a case was a strong risk factor (OR 3.79). Sand flies were captured in all neighborhoods; in collections from several neighborhoods presence of L. donovani could be demonstrated by PCR.
The evidence found in this study is consistent with transmission of anthroponotic VL within the city. The vector P. argentipes and the parasite L. donovani have both been identified inside the town. These findings are highly relevant for policy makers; in VL endemic areas appropriate surveillance and disease control measures must be adopted not only in rural areas but in urban areas as well.
Visceral leishmaniasis (VL), is a vector-borne parasitic disease, common in Nepal’s plains known as Terai lowlands. Kala-azar (KA), the name used for VL in South Asia, is a significant public health problem in the country. Twelve districts in the eastern and central Terai regions, bordering the Indian state of Bihar, are endemic. In the Indian subcontinent, VL is mainly caused by Leishmania donovani and its transmission is assumed anthroponotic through the bite of the sand fly species Phlebotomus argentipes . Nepal’s border with the highly endemic state of Bihar, home to 85% of India’s VL cases, makes Nepal a key partner in the regional VL elimination program .
VL is known as a disease that predominantly affects the rural poor [3–7]. Outbreaks have been reported in several rural villages  but VL is also spreading into areas that were previously non-endemic [9, 10]. Since 1997 VL cases have also been reported among urban residents in the town of Dharan. Many of those were treated at B.P. Koirala Institute of Health Sciences (BPKIHS), the only hospital facility in the town. A survey conducted in July 2006 showed an average VL incidence rate of 2.05% per year (for 2004–2006) in certain neighbourhoods of Dharan . Dharan is located on the foothills of the Mahabharata range, at the ecological transition zone between the sub-tropical forest of the plains and the mountains. The residents of Dharan town use this forest as their source of firewood and fodder. The historic town centre is surrounded by suburban residential areas of recent legal settlers as well as slum areas, where displaced people have moved in at high speed over the past ten years - during the civil conflict- seeking safety and job opportunities. Those recent immigrants could of course have been infected with L. donovani outside Dharan town, but there is a definite concern about the possibility of local transmission of L. donovani in the urban/suburban area for several reasons. The sand fly vector was observed in peripheral neighbourhoods of Dharan town in previous studies [12, 13]. Dharan town is also known to host a community of intravenous-drug users (IDUs), which might act as a catalyser for VL transmission. The HIV infection rate in IDUs in Nepal is estimated at 14-39%, compared to approximately 0.5% in the general population [14, 15]. Sharing of needles by IDUs could shift the mode of transmission of VL  and was the basis for previous outbreaks in Europe .
To study the possibility of urban transmission of VL in Dharan town we conducted a case–control study and collected entomological data from all neighbourhoods of the town.
Study area and population
Study design and case definitions
This study was designed as an outbreak investigation including a case–control study; we selected four controls for each case. For ethical reasons, we included only individuals aged above 5 years. All study subjects had been residents of Dharan town for at least 2 years at time of diagnosis (cases) or at time of enrolment (controls). Cases (fever ≥ 2 weeks duration with clinical splenomegaly) were those with parasitologically confirmed VL registered at BPKIHS between January 2000 and December 2008 were enrolled in the study. Controls were individuals randomly selected from the town population who had not suffered from VL in the past and did not present with fever and/or splenomegaly on the day of survey. Controls were frequency-matched for age to cases.
BPKIHS drains a substantial proportion of VL cases from the eastern region and all cases from Dharan. We exploited the patient database of BPKIHS to identify and recruit VL cases. This patient register, which has clinical and epidemiological information of all admitted VL patients since 1997, is well maintained and has been monitored by external clinical monitors on a regular basis as several patient cohorts were entered into clinical studies [18–20].
Based on the reported numbers of VL cases, we expected to be able to enrol at least 110 cases. In that case a ratio of 4 controls for each case would be sufficient to detect an odds ratio of 2 with a power of 80% at a significance level of 5% for a factor to which 15% of controls are exposed.
The study was conducted between September and November 2009. We collected clinical and epidemiological information from the BPKIHS hospital patient records and through interviews. We compiled the list of all VL patients who gave ‘Dharan municipality’ as their residence at the time of admission. We then traced those persons at their homes. Controls were selected randomly from the updated 2007/8 voting register of Dharan municipality using a random-number table. This register was based on a census of all citizens carried out in 2007/8 in preparation of the elections and included all recent settlers at that time. All households are listed in the voting register by ward and household number, name and age of family members’ ≥ 16 years is enumerated. To allow for inclusion of the children in the group of controls in the same proportion as cases, we replaced the randomly selected adult voter by a child in 1 out of every 6 controls. In such case instead of interviewing the adult voter, we enrolled randomly one of all the under 16 years old present in that household. If there were no children in the household sampled, a child was selected from the house of the nearest neighbor.
After obtaining individual written informed consent, the field workers conducted structured interviews. The questionnaire contains detailed questions on individual and household level variables. Individual-level variables included among others sex, marital status, literacy, employment status, intravenous drug use, migration status and regular forest visit. Household variables included among others proximity to previous VL cases, socioeconomic status and housing characteristics. Houses were subdivided into ‘thatched houses without windows’ ‘thatched houses with windows’ and ‘brick houses’. Cases were asked to report their status vis-à-vis the different variables at the time of their illness; for controls the status at time of interview was recorded. In case of children, we interviewed parents or guardians.
Responses with regard to actual household income were unreliable. Therefore, socio-economic status was assessed for the household, based on a previously validated asset index . Included in the asset index are ownership of: radio (s), CD player (s), television (s), video or DVD player (s), mobile phone (s), non-mobile phone (s), refrigerator (s), iron (s), sewing machine (s), watch (s), chair(s), sofa(s), table(s), cupboard(s), bicycle(s), motorcycle or scooter (s), and animal draw cart (s). Also included was type of toilet facilities, fuel used for cooking, number of sleeping rooms and availability of electricity. The asset index was converted into assets scores, using principal component analysis. Based on the assets scores, households were divided into four socio-economic layers.
All households enrolled were georeferenced, so were the boundaries of the study area. A map was created using Arcview GIS 9.2 (ESRI, Redlands, USA). We created an individual 50 meter radius buffer around each VL case household; any control living within any of those buffer zones was considered to be contact of a case. A case was considered as a contact if at any time before the diagnosis another case had occurred in the same house or in another house within a 50 meter radius.
Ethical approval for the study was obtained from the Institutional Ethical Review Board of the B.P. Koirala Institute of Health Sciences, Dharan, Nepal. The use of patient’s medical records in this study was part of the approved study protocol.
We captured sand flies in 10 randomly selected households in each of the 19 wards, thus a total of 190 houses in Dharan town were sampled. Collections took place at the 19 locations; one day in each location from October 3–23, 2009 during the second annual peak for P. argentipes density . Sand flies were captured overnight using CDC light traps in each household, supplemented by mouth aspiration for 15 minutes the following morning to catch resting sand flies . This was performed by trained insect collectors and supervised by an entomologist. After collection, flies were brought to the entomology laboratory at BPKIHS and examined under a binocular dissecting microscope; female P. argentipes were morphologically identified and separated from other insects. Female P. argentipes were pooled by household in a cryotube with 80% alcohol.
We applied polymerase chain reaction (PCR) technique as described by Bhattarai . The molecular analysis was done by extracting DNA from sandflies by using the QIAmp DNA minikit (Qiagen, Germany), as per the manufacturer’s instruction. Firstly, a sand fly specific cytochrome b PCR was applied to verify the quality of the DNA present in each pool. Secondly, Leishmania specific PCR was used to detect Leishmania infection. The PCR positive samples were further sequenced in 3730 DNA Analyzer (Applied Bio systems, Foster City, CA, USA) in order to confirm that the amplified DNA corresponded well to the Leishmania donovani species.
Data was double entered in a Microsoft Access database independently by two data entry clerks and the two files were compared after the completion of data entry. In case of discrepancies, corrections were made after reviewing the original questionnaire forms.
For data analysis, we used binominal multilevel model in Stata /IC V10.1 (Stata Corp., College Station, Tx, USA) with ‘ward’ (neighborhood) as random effect. Observed associations were assessed through multilevel logistic regression. All variables with a P-value ≤ 0.10 in univariate analysis were included in the multivariate logistic regression model. Variables for the final model were selected using the backward elimination strategy. The probability of removal was set at P = 0.05. We tested for biologically plausible interactions between factors retained. To test for interactions between ward and various factors, we fitted random slopes for all factors retained and used likelihood ratio testing to assess whether the model with random slope fits the data significantly better than the model without; probability for removal was set at 0.05.
Characteristics of visceral leishmaniasis cases and controls
OR † (95% CI) ‡
Median (Inter quartile range)
31 (18 – 42)
36 (26 – 50)
0.65 (0.40 – 1.05)
0.55 (0.34 – 0.91)
0.78 (0.38 – 1.59)
Others (Budhist, Christian, Muslim)
0.65 (0.31 – 1.41)
Factors associated with VL in a ‘univariate’ model with ‘ward’ as random effect
95% CI ‡
(n = 115)
(n = 448)
0.35 – 1.31
0.40 – 1.05
0.34 – 0.91
0.38 – 1.59
0.31 – 1.41
Large households (> 5 person)
1.46 – 3.93
Intravenous Drug use
0.69 – 7.66
Proximity to other VL cases within 50 m
3.69 – 11.82
Regular forest visit
3.49 – 10.61
Daily wage earner (vs fixed employment)
1.78 – 5.02
History of migration
1.08 – 2.83
Bed net use ever
0.62 – 1.81
Sleeping on a bed (vs on the floor)
0.03 – 0.24
0.01 – 0.21
0.70 – 2.19
0.01 – 0.82
0.52 – 1.44
0.31 – 1.22
Type of house
Thatched house, no windows
Thatched house with windows
0.13 – 0.60
0.02 – 0.12
Socio economic status (by asset score level)
Level 1 (poorest)
0.11 - 0.42
0.03 - 0.23
Level 4 (least poor)
0.001 - 0.08
The asset-index clearly distinguishes between the poorest (1st quartile) from the richest (4th quartile). Of all cases, 76% belonged to the poorest quartile and only 1% to the richest quartile of the study population. With the poorest quartile as referent we found odds ratios of 0.22, 0.09 and 0.01 for the second poorest, the second richest and the richest quartile respectively.
Factors associated with VL in a ‘multivariate’ model with ‘ward’ as random effect
95% CI ‡
Proximity to other VL cases ( within 50 m)
1.86 – 7.71
Regular forest visit
2.15 – 8.40
Large households size (>5 person)
1.84 – 6.83
Sleeping on a bed (vs on the floor)
0.08 – 0.78
0.01 – 0.64
0.46 – 2.46
Type of house
Thatched house, no windows
Thatched house with windows
0.15 – 0.84
0.09 – 0.73
Socio economic status (by asset score level)
Level 1 (poorest)
0.20 – 0.95
0.08 – 0.81
Level 4 (least poor)
0.004 – 0.38
Altogether 592 sandflies (female P. argentipes) were captured from 121 out of 190 households in Dharan town. These sand flies were pooled by household, resulting in 121 pools each containing 1–22 female Phlebotomus argentipes. All pools were found to be PCR positive for the cytochrome b gene, indicating the presence of good quality of DNA in these samples. Out of these 121 pools, 13 were found to be positive for L. donovani and originated from 6 wards (1, 5, 15, 16, 18 & 19); none of them was from the two worst affected wards (14 and 17). An important observation we made during our study is the inadequate coverage (≤ 70%) of the insecticide residual spraying (IRS), with exception of the three wards worst affected with VL (14, 15 & 17) where IRS coverage was ≥ 90%.
This is the first study to describe urban transmission of VL in Nepal, VL still being largely considered a disease of the rural poor. VL in Dharan town has a strongly clustered distribution reflected in an intra-class correlation for ward of 50.5%; worst affected were the more peripheral wards (Figure 1B). These are wards with new settlements of recent migrants where the poorest segments of the population reside and which lack adequate infrastructure, sanitation and housing. They are typically a rural–urban interface as most residents depend on daily manual labor for their livelihood (unpublished data), and therefore VL cases might have been easily exposed to L. donovani infection elsewhere. However the results of our study are more consistent with local urban transmission. We demonstrated the presence of Phlebotomine sand flies in all the Dharan wards as was observed in earlier studies [12, 13] and we were able to confirm infection with L. donovani in some of the flies captured.
The final multilevel model showed a very strong association between VL and certain housing factors, those living in a thatched houses without windows having 3–4 times higher odds of kala-azar. Sleeping on a bed and upstairs were protective (OR 0.25, 95% CI 0.08-0.78 and OR 0.08, 95% CI 0.01 - 0.64 respectively). Proximity to previous VL cases was a strong risk factor for VL (OR 3.79, 95% CI 1.86 – 7.71). These associations are all consistent with local transmission. Regular forest visits was also associated though, with an odds ratio of 4.25 (95% CI 2.15 – 8.40), which would point at transmission outside the city.
The entomological data provide further evidence in support of local transmission of VL inside the city. P. argentipes sand flies were captured in all 19 wards of the town; in 13 out of 121 pools of sand flies captured, the presence of L. donovani infection could be confirmed. The fact that no L. donovani infected sand flies were captured in the two wards worst affected (wards 14 and 17) could be explained by the low yield of entomological sampling in these wards linked to recent Indoor Residual Spraying (IRS) in response to the VL outbreak. The 13 L. donovani positive pools did originate from 6 neighboring wards where IRS coverage had been substantially lower (wards 1, 5, 16, 18 & 19, IRS coverage 10-70%), however the absolute numbers of infected sandflies captured were low and random variation may have played a role. Since our study was retrospective, entomology data reflect the situation in 2009, rather than the situation at the time the VL cases were diagnosed. Our findings suggest that IRS has been highly effective in reducing vector abundance. To prevent further outbreaks of VL a scaling up to fully cover all wards could be recommended.
This study has one major limitation, it was a retrospective study looking back at cases occurring over a period of more than 10 years. Cases occurred from 2000 to 2008, but cases and controls were interviewed in 2009. For cases we asked for the conditions as they were at the time of their illness, for controls this was not possible so their answers reflect conditions in 2009. Conditions may have changed over this period and there is likely to be a recall bias among some of the cases interviewed; the entomological data also reflect the situation in 2009. We did perform a sensitivity analysis including only cases from 2005 onward but did not find any major differences in results (data not shown). Despite the limitations mentioned we did find strong indications in favor of urban transmission of anthroponotic VL. This may have important implications for VL control not only for Dharan but also for other cities in VL endemic regions on the Indian subcontinent.
A spatial analysis conducted in 1,744 cases reported from 1991 to 2000 in the city of Teresina, Brazil showed the highest incidence rate of VL in neighbourhoods with a rural–urban interface, located in the city’s peripheral areas and occupied by low-income populations . A rapid disorganized increase in population associated with an increase in the number of VL cases in the city was also observed in another study . The establishment of new residential colonies in the town and an increased migration from known endemic areas were also identified as the source of VL transmission into virgin areas in Shimla, India .
With a very high likelihood the outbreak of VL observed in Dharan can be attributed to transmission within the town. The vector P. argentipes and the parasite L. donovani have been identified inside the town. Vector control activities (IRS) appear to have been effective in controlling the outbreak. However the vector is still present in all wards, in particular in those wards that did not have a very high IRS coverage. Ensuring adequate IRS coverage in all wards of the town is recommended. These findings also have implications for other urban areas on the Indian subcontinent. In endemic areas, surveillance for VL needs to be in place not just in rural areas but in cities as well.
The authors are indebted to the residents of Dharan town for their active participation in the study.
We thank field workers, Bhesh Raj Katwal, Rajan Neupaney, Tika Ram Khatri, Anil Chaudhary and Shrawan Chaudhary for their contribution in data collection and collectors, Sashi Chaudhary, Manish Karna, Satya Narayan Bhagat, and Kailash Chaudhary for their help in capturing insects. We thank the KalaDrug-R molecular biology laboratory, BPKIHS for sand fly analysis.
The work was financially supported by the Belgian Development Cooperation (FA3, 2008–2013), Strategic project 3.04: Support to the Visceral Leishmaniasis elimination initiative in the Indian subcontinent. The funding source had no role in the study design; data collection and analysis, interpretation of results, or preparation of the manuscript for publication. The author’s work was independent of the funders (the funding source had no involvement).
- World Health Organisation: Control of the leishmaniasis. World Health Organ Tech Rep Ser. 2010, 949: 186-Google Scholar
- World Health Organisation/TDR: Press release for the Elimination of Kala-azar from endemic countries in the South-East Asia region. Health Ministers Sign Memorandum of Understanding. 2005, Geneva/New Delhi: WHO, [document on the internet]. Available from: http://www.who.int/tdrold/publications/tdrnews/news75/leish_elimination.htm. (accessed on 17 May 2011)Google Scholar
- Bista MB: National overview of Kala-azar in Nepal. Kala-azar in Nepal: principals, practices and public health perspectives. Edited by: Bastola S, Karki P, Rijal S, Gautam A. 1998, Kathmandu, Nepal: EDCD/BPKIHS/WHO, 1-5.Google Scholar
- Bern C, Joshi AB, Jha SN, Das ML, Hightower AW, Thakur GD, Bista MB: Factors associated with visceral leishmaniasis in Nepal: bed-net use is strongly protective. AmJTrop Med Hyg. 2000, 63 (3–4): 184-188.Google Scholar
- Rijal S, Boelaert M, Regmi S, Karki BMS, Jacquet D, Singh R, Chance ML, Chappuis F, Hommel M, Desjeux P, Van der Stuyft P, Le Ray D, Koirala S: Evaluation of a urinary antigen-based latex agglutination test in the diagnosis of kala-azar in eastern Nepal. Trop Med Int Health. 2004, 9 (6): 724-729. 10.1111/j.1365-3156.2004.01251.x.View ArticlePubMedGoogle Scholar
- Joshi A, Narain JP, Prasittisuk C, Bhatia R, Hashim G, Jorge A, Banjara M, Kroeger A: Can visceral leishmaniasis be eliminated?. J Vector Borne Dis. 2008, 45 (2): 105-111.PubMedGoogle Scholar
- Boelaert M, Meheus F, Sanchez A, Singh SP, Vanlerberghe V, Picado A, Meessen B, Sundar S: The poorest of the poor: a poverty appraisal of households affected by visceral leishmaniasis in Bihar, India. Trop Med Int Health. 2009, 14 (6): 639-644. 10.1111/j.1365-3156.2009.02279.x.View ArticlePubMedGoogle Scholar
- Schenkel K, Rijal S, Koirala S, Vanlerberghe V, Van der Stuyft P, Gramiccia M, Boelaert M: Visceral leishmaniasis in south-eastern Nepal: A cross-sectional survey on Leishmania donovani infection and its risk factors. Trop Med Int Health. 2006, 11 (12): 1792-1799. 10.1111/j.1365-3156.2006.01735.x.View ArticlePubMedGoogle Scholar
- World Health Organization: Urbanization: an increasing risk factor for leishmaniasis. Wkly Epidemiol Rec. 2002, 44: 365-370.Google Scholar
- Barnett PG, Singh SP, Bern C, Hightower AW, Sundar S: Virgin soil: the spread of visceral leishmaniasis into Uttar Pradesh, India. AmJTrop Med Hyg. 2005, 73 (4): 720-725.Google Scholar
- Rijal S, Uranw S, Chappuis F, Picado A, Khanal B, Paudel IS, Andersen EW, Meheus F, Ostyn B, Das ML, Davies C, Boelaert M: Epidemiology of Leishmania donovani infection in high-transmission foci in Nepal. Trop Med Int Health. 2010, 15 (Suppl.2): 21-28.View ArticlePubMedGoogle Scholar
- Bhattarai NR, Das ML, Rijal S, Van der Auwera G, Picado A, Khanal B, Roy L, Speybroeck N, Berkvens D, Davies CR, Coosemans M, Boelaert M, Dujardin JC: Natural infection of Phlebotomus argentipes with Leishmania and other trypanosomatid in a visceral leishmaniasis endemic region of Nepal. Trans R Soc Trop Med Hyg. 2009, 103 (11): 1087-1092. 10.1016/j.trstmh.2009.03.008.View ArticlePubMedGoogle Scholar
- Picado A, Das ML, Kumar V, Kesari S, Dinesh DS Roy L, Rijal S, Das P, Rowland M, Sundar S, Coosemans M, Boelaert M, Davies CR: Effect of Village-wide use of long-lasting insecticidal nets on Visceral Leishmaniasis vector in India and Nepal: A cluster Randomized Trial. PLoS Negl Trop Dis. 2010, 49 (1): e587-View ArticleGoogle Scholar
- Peak J, Rana S, Rai LB: Asian Harm Reduction Network and Family Health International Report. HIV and injecting drug use in selected sites of Terai, Nepal. 2001, 13-15.Google Scholar
- Government of Nepal, Ministry of Health and Population: Report of USAID/National centre for AIDS and STDs control in Nepal. National health profile of Nepal. 2004, 1-5.Google Scholar
- Desjeux P: Human leishmaniasis: epidemiology and public health aspects. World Health Stat Q. 1992, 45 (2–3): 267-275.PubMedGoogle Scholar
- Molina R, Gradoni L, Alvar J: HIV and the Transmission of Leishmania. Ann Trop Med Parasitol. 2003, 97 (Suppl. 1): S29-S45.View ArticleGoogle Scholar
- Boelaert M, Rijal S, Regmi S, Singh R, Karki B, Jacquet D, Chappuis F, Campino L, Desjeux P, Le Ray D, Koirala S, Van der Stuyft P: A comparative study of the effectiveness of diagnostic tests for visceral leishmaniasis. AmJTrop Med Hyg. 2004, 70 (1): 72-77.Google Scholar
- Rijal S, Yardley V, Chappuis F, Decuypere S, Khanal B, Singh R, Boelaert M, De Doncker S, Croft S, Dujardin JC: Antimonial treatment of visceral leishmaniasis: are current in vitro susceptibility assays adequate for prognosis of in vivo therapy outcome?. Microbes Infect. 2007, 9 (4): 529-535. 10.1016/j.micinf.2007.01.009.View ArticlePubMedGoogle Scholar
- Rijal S, Bhandari S, Koirala S, Singh R, Khanal B, Loutan L, Dujardin JC, Boelaert M, Chappuis F: Clinical risk factors for therapeutic failure in Kala-azar patients treated with pentavalent antimonial in Nepal. Trans R Soc Trop Med Hyg. 2010, 104 (3): 225-229. 10.1016/j.trstmh.2009.08.002.View ArticlePubMedGoogle Scholar
- Picado A, Das ML, Kumar V, Dinesh DS, Rijal S, Singh SP, Das P, Coosemans M, Boelaert M, Davies C: Phlebotomus argentipes seasonal pattern in India and Nepal. J Med Entomol. 2010, 47 (2): 283-286. 10.1603/ME09175.View ArticlePubMedGoogle Scholar
- Dinesh DS, Das P, Picado A, Davies C, Speybroeck N, Boelaert M, Coosemans M: The efficacy of indoor CDC light traps for collecting the sand fly Phlebotomus argentipes, vector of Leishmania donovani. Med Vet Entomolol. 2008, 22 (2): 120-123. 10.1111/j.1365-2915.2008.00724.x.View ArticleGoogle Scholar
- Cerbino Neto J, Loureiro Werneck G, Henrique Nery Costa C: Factors associated with the incidence of urban visceral leishmaniasis: an ecological study in Teresina, Piaui State, Brazil. Cad Saude Publica. 2009, 25 (7): 1543-1551. 10.1590/S0102-311X2009000700012.View ArticlePubMedGoogle Scholar
- Albuquerque PL, Silva Júnior GB, Freire CC, Oliveira SB, Almeida DM, Silva HF, Cavalcante Mdo S, Sousa Ade Q: Urbanization of visceral leishmaniasis (Kala-azar) in Fortaleza, Ceará, Brazil. Pan Am J Public Health. 2009, 26 (4): 330-333. 10.1590/S1020-49892009001000007.View ArticleGoogle Scholar
- Raina S, Mahesh DM, Kaul R, Satindera KS, Gupta D, Sharma A, Thakur S: A new focus of visceral leishmaniasis in the Himalayas, India. J Vector Borne Dis. 2009, 46 (4): 303-306.PubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2334/13/21/prepub
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