review article

Status of Leishmaniasis in North India: A Review

Naveen Samuel Singh*, Doris Phillips Singh

Sandfly Research Laboratory, Lucknow Christian College, India

*Corresponding author: Naveen Samuel Singh, Sandfly Research Laboratory, Lucknow Christian College, India. Tel: +919415101589; Email: naveendoris@rediffmail.com

Received Date: 25 May, 2018; Accepted Date: 24 July, 2018; Published Date: 31 July, 2018

Citation: Singh NS, Singh DP (2018) Status of Leishmaniasis in North India: A Review. J Trop Med Health: JTMH-126. DOI: 10.29011/JTMH-126.000026

1.                   Abstract

More than 1,00,000 people are affected every year by Visceral Leishmaniasis (VL) in India. VL is a chronic and fatal disease caused by Leishmania donovani parasites, which are transmitted by infected female sand flies, Phlebotomus argentipes. VL is a serious public health concern and is endemic in Brazil, southern and central parts of Europe, eastern and central division of Bangladesh, southern region of Nepal, Sudan, north-eastern regions of India and south-east Asia. It is mostly endemic in countries that are least developed in the world. Ninety percent of total cases of the world are reported from India, Bangladesh and Sudan. Several districts of the state Bihar show the occurrence of VL which is 40-50% of the world cases and 90% of the cases in India. Conversely, information on epidemiology of kala-azar in India and other affected countries except few developed countries, remain scanty due to inadequate studies about the various risk factors associated with VL. The present review on the status of Leishmaniasis in North-India contributes to the study of the number of cases, deaths, prevalence, incidence caused by VL, spatial distribution, basic epidemiologic features, the vector biology, transmission of the parasite, hosts and some major risk factors viz. climatic, natural calamities, the physical and biotic, the socio-economic conditions, the environmental factors, vegetation, urbanization, domestic animals and the living standard.

This study based on the 5 major states in North India suggests that the maximum number of cases, deaths incidence and prevalence of VL have been observed in Bihar, Jharkhand and West Bengal with a decreasing trend in the years 2010-2017 but on the contrary the Post Kala-Azar Dermal Leishmaniasis (PKDL) cases exhibit an increasing trend during the same period of study with total elimination in Uttar Pradesh and Uttarakhand by 2017. The study suggests that the control measures have been effective in suppressing/eradicating VL but it also leaves a suspicion that apart from P. argentipus some other flies may also be playing the role as vectors in spreading the disease. To improve the control measures to decrease transmission of Leishmania donovani and consequently the frequency of leishmaniasis and to achieve the goal of total eradication of VL from India in near future, a better understanding of the biology underlying transmission and disease with the major risk factors is the pressing need.

2.                   Keywords: Control Measures; Endemic; India; Incidence; Leishmaniasis; Phlebotomine; Risk Factors

1.                   Introduction

Visceral leishmaniasis is a chronic and potentially fatal parasitic disease of the viscera which affects the organs due to the infection by Leishmania donovani. The worldwide incidence is estimated to be between 1,46,700 and 2,82,800 cases (appro. 0.5 and 2.5 million respectively) per year [1]. Sixty-six countries in the world have been reported confirmed kala-azar cases [2,3]. The spatial distribution of leishmaniasis also seems to expand in the Southern parts of Europe [4,5], and in the Central Europe where the first cases of autochthonous origin are recently reported [6].

It is important to note that this disease was not endemic in the past in this region [7-9]. But it is mainly reported from six countries namely Bangladesh, Brazil, Ethiopia, India, South Sudan and Sudan [10] (NVBDCP-website) and 90% of these occur in India, Nepal, Bangladesh and Sudan [3] while it has also reported that north eastern region of India, southern region of Nepal and eastern and central division of Bangladesh harbor an estimated 67% of the global VL disease burden (NVBDCP-website). Visceral Leishmaniasis, also known as Kala-Azar (KA) in the Indian subcontinent which is prone to the occurrences of chronic Visceral Leishmaniasis (VL) or Kala-azar and is one of the major causes of morbidity and mortality creating a significant impediment to human development. Geographical distribution of the disease is endemic in the states of Bihar, West Bengal, Uttar Pradesh, Jharkhand, Delhi, Gujarat, Madhya Pradesh and Kerala in India. 90% of the disease has mainly affected the children below 9-15 years of age and has been causing 50% death incidents annually in India [11]. The reports of Kala-azar cases occurring in Bihar state in India, which is 40% to 50%, of the world cases and is severely affected states, and account to 90% of the total recorded cases in India. The disease affects mainly poor, rural communities; appro. 80% of all cases in the region are reported from the state of Bihar in India [12]. Furthermore, reports of Kala azar cases occurring in Bihar state in India which is 40%-50% of the world cases accounts to 90% of the total recorded cases in India. At present, it is a severe public health problem in Indian subcontinent, especially in the Bihar state [13]. Visceral leishmaniasis affects the internal organs principally spleen, liver, and bone marrow. It is estimated that more than 90% visceral leishmaniasis infected people are concentrated in lower and middle gangetic plains in India.

1.1                Biology of the Vector

Phlebotomine sand flies are well-known to transmit leishmaniasis, bacteria and viruses which affect humans and animals and have been endemic in India since ancient times [14,15]. The sandflies carry the parasite from reservoirs to humans. Reservoirs for the parasite are mostly rodents and large domestic and wild mammals. Humans are ‘accidental hosts’ when they invade the reservoir and vector’s ecosystem [16]. They are small bloodsucking insects of which there are about 700 species of six genera of the female Phlebotomus, suspected or proven vectors transmitting the parasites from animal-to-animal, animal-to-man and man-to-man' considered to be the disease vectors [2]. The promastigote forms of Leishmania donovani parasites enter the human host through the proboscis when the sand fly bites and sucks the blood from an infected person or animal [17]. The parasite survives and multiplies within phago-lysosomes of macrophages as intracellular amastigotes inside the human host (Figure-1).

Leishmaniasis is an emerging vector borne disease in India. Knowing the activity of sand flies is important in the influential period of maximum risk of Leishmania transmission and for the successful achievement of control programs, Phlebotomus argentipes make up a very small proportion of sand flies and ill-considered proactive interference may disturb this balance in favor of this species and other species as potential vectors. The conditions that favor epidemics of kala-azar are rural areas more than 600 meters above sea level, heavy annual rainfall, mean humidity above 70%, a temperature range of 15°C to 38°C with a diurnal variation of more than 7°C, abundant vegetation, subsoil water and alluvial soil. Deforestation, which is a consequence of increasing agriculture, cattle and urbanization, plays an important role in the ecologic niche changes to thou­sands of phlebotomine species [18]. Few information on epidemiology of kala-azar in India and other affected countries, are available due to inadequate studies about the various risk factors associated with this disease [19,20] and also on the relation­ship between anthroponotic transmission and the increas­ing cases of VL due to possible urbanization in Uttaranchal. It is important to focus on VL education and policies at an early stage with the aim of encouraging protective measures. Therefore, a review to investigate the presence of Phlebotomus argentipes in environments altered by man is a requirement for the better control of VL in endemic areas. Hence, the purpose of this paper is to review the various risk factors including climatic changes (temperature and humidity and speed of the wind), natural calamities, the physical factors (geographical barriers and habitat availability), the biotic factors (distribution and abundance of vertebrate hosts), the socio-economic conditions (poor nutrition affecting immunity), the environmental factors, the other risk factors including cooking of food on wood fire, rearing of domestic animals, certain vegetation, forests, livelihood and urbanization coupled with deforestation etc. and to discuss their contributions in further understanding of the epidemiology and control of VL in India.

1.2                Rationale and Design of the Study

Globally, the number of vector-borne infections in humans and animals increases rapidly, meanwhile causing almost one third of all cases of emerging infectious diseases [21]. In the Old World, sandfly species of the genus Phlebotomus serve as vectors for sandfly borne pathogens such as Leishmania, Bartonella and several other viruses (for eg. Phlebovirus, Vesiculovirus and Orbivirus), [22]. Sandfly-borne diseases and in particular visceral leishmaniasis are a main public health concern [23] and for its prevention and control, it demands more attention in science and policy [24]. While the spatial distribution of leishmaniasis seems to expand in southern parts of Europe [4,5] the presence of sandflies as vectors is mainly regulated by the species’ climatic requirements on temperature and humidity or soil moisture respectively [25-28]. Temperature and humidity are the main factors impacting the altitudinal structure of sandfly occurrences [29]. Temperature directly affects insect population dynamics through modification of developmental rates, reproduction and mortality. Weather can also affect insect populations indirectly via alteration of the abundance, distribution and physiology of the host trees. It is known that sandflies react very sensitively to the wind speed and prefer breeding sites sheltered from wind [30-33]. Few reports from India are available on the role of various ecological parameters like air, temperature, rainfall, wind speed, relative humidity, soil moisture, temperature, pH, and organic carbon [34] are known to influence the ovipositor of gravid female sand flies as well as the survival and development of the larvae [35] Beyond that, high wind speed decreases or even excludes flight activity [30,36]. For the purpose of inferring geographic distribution for sandflies, the advantages of ecological niche models have been demonstrated on the example of Lutzomyia species (Lutzomyia spp.) in the New World [37]. For the first time, Peterson & Shaw, (2003) [38] integrated climate change scenarios in order to project future distribution of Lutzomyia spp. in Brazil. Recently, range expansions for sandflies of the genus Lutzomyia have also been projected for North America in the face of climate change [39]. In addition, no study monitoring the promising urbanization process of Phlebotomus argentipes has been performed. Deforestation, which is a consequence of increasing agriculture, cattle and urbanization, plays an important role in the ecologic niche changes to thou­sands of phlebotomine species [18]. In spite of a lot of efforts done for the eradication of VL in the VL prone areas viz. Bihar or Jharkhand the disease seems not to be under control [40]. Hence it was decided by the authors to study the status of Leishmaniasis in North India to reason out the particular causes as to why full eradication of VL has not yet reached.

Keeping in view the above facts it was important to reason out the discrepancies in the number of incidence /deaths in the five main critical states (Bihar, Jharkhand, West Bengal, Uttar Pradesh and Uttarakhand) known for the occurrence of the VL, was chosen to explore the status of Leishmaniasis in India, the following factors have been taken into consideration-

·                     Studies on the prevalence and incidence and the effect of climate on Visceral Leishmaniasis transmission in India.

·                     Studies on the risk factors of visceral leishmaniasis in the study areas.

2.                   Results and Discussion

2.1                Prevalence and Incidence and the Effect of Climate on VL Transmission

The report of deaths due to kala azar from 2010-2017 in the five main states of India shows the highest number of incidences in Bihar (23084) and least in Uttarakhand in almost every year [13]. Max deaths in Bihar and 0 in Uttarakhand and Uttar Pradesh. Jharkhand is on the second number and West Bengal on the third. We also observe a decline in the no. of cases and deaths from 2010 to 2017 in Bihar. More of less the same situation is found in all the five states. If we see the total no. of cases in the North India (in these five states, we observe a decreasing trend in both cases and deaths with a slight discrepancy in the total no. of cases in 2011 (Table-1). Whereas a gradual decrease in the number of cases of kala-azar has been reported from 2010-2017 (Figure-2) suggesting that effective control measures have been taken to prevent the occurrence of VL.

An increasing trend is observed in cases of skin presentation of Kala-azar called ‘Post Kala-azar Dermal Leishmaniasis’ (PKDL) in the three main critical states i.e. Jharkhand, Bihar and West Bengal. Uttarakhand and Uttar Pradesh show a promising status of elimination of this disease. PKDL is first characterized by discoloration of the skin and later distinct, clear and evident manifests as lesions. These lesions are reservoirs for the parasite. A person with lesions can therefore become infectious if bitten by a sand fly, leaving a source of infection within the community (Table 2).

On the other hand, Data from Jharkhand, Bihar, West Bengal, Uttar Pradesh and Uttara Khand shows that the number of deaths due to kala-azar since 2010 is decreasing gradually which was very high in 2010 due to several geo-climatic factors (Figure-3a and 3b).

This suggests that efforts are been done by the WHO and other agencies like NVBDCP, Ministry of Health and Family Welfare, Government of India to eliminate VL to much extent and a vision is clearly seen about the total eradication of kala-azar in the coming few years [40]. But the rise in PKDL cases also indicates that the infection is circulating within the affected communities, and may be due to relapses of VL/PKDL and therefore better surveillance system, effective and accessible treatment and reporting system is urgently needed. Leishmaniasis is climate-sensitive and affects its epidemiology in several ways; changes in temperature, rainfall and humidity can have strong effects on vectors and reservoir hosts by altering their distribution and influencing their survival and population sizes. Small fluctuations in temperature can have a profound effect on the developmental cycle of Leishmania promastigote in sandflies, allowing transmission of the parasite in areas not previously endemic for the disease. The Visceral Leishmaniasis vector (sandfly) abundance has been found in the months between June and September; with P. argentipes most active abundance when the temperature range was between 27.5°C and 31°C [41]. The impact of temperature on sandfly populations is rapid and the distribution, vegetation condition and synoptic temperature to an overall accuracy. The northeastern regions of India, southern region of Nepal and eastern and central divisions of Bangladesh in South-East Asia are prone to endemic regions of VL transmission. Climate change and extreme weather events affect plants and animals and the direct impact of anthropogenic climate change has been documented on every continent, in every ocean, and in most major taxonomic groups [42].

The VL status in North India after this review confirms that longevity and survival of vector populations of Kala-azar is significantly determined by the geographically controlled factors viz. the climate (temperature, relative humidity and rainfall), soil types and soil moisture [43]. These have been progressively affecting the vegetation growth and density, and then the conditions on the surrounding environment. Introduction of new technique -Geographical Information Systems (GIS) and remote sensing is a strong step in stratifying a region into different areas of transmission risk, thereby providing a guideline to mapping the areas under the risk of visceral leishmaniasis transmission in India [44]. The distribution of phlebotomine sandflies varies highly within its range, depending on local environmental factors, such as precipitation and temperature, physical factors, such as geographical barriers, habitat availability and biotic factors such as the distribution and abundance of vertebrate hosts [45]. Natural calamities drought, famine and flood can lead to massive displacement and migration of people to areas with transmission of Leishmania, and poor nutrition could compromise their immunity [46]. The clinical manifestations are dependent both on the infecting species of Leishmania and the immune response of the host. In the last two decades VL has been recognized as an opportunistic disease in the immune-compromised, particularly in patients infested with human immunodeficiency virus (HIV) [47].

2.2                The Associated Risk Factors

Socio-economic conditions in North-India, such as poor housing and domestic sanitary conditions (such as a lack of waste management or presence of open sewerage) may increase sandfly breeding and resting sites, as well as their access to humans. Sandflies are attracted to crowded housing as these provide a good source of blood-meals. Another group of factors are related to housing conditions. Studies have shown that when walls, roofs, and floors are not made of durable materials, cracks can be formed, becoming a shelter or a gateway for vectors into the households [48]. While in endemic sites thatched, mud plastered roof tops of households with crack and crevices on it as well as on walls may serve as effective day-resting habitats for these nocturnal feeder species, mainly tiled, dry, non-porous roof tops without any cracks/crevices in endemic foci cannot be a resting habitat for the adult population. Again loose, wet solid with rich organic debris, on house floors in endemic sites not only serve as a very good resting habitat/food source for thriving and probation of immature stages of vector sandfly, but also act as resting habitat of newly emerged adult population. Damp floors or ‘dampness in the home’ were risk factors in the study by [49]. The use of bed nets was found to be protective in some studies therefore decrease the incidence of VL [49-51]. Lack of cleanliness because of illiteracy is also a cause for sand fly propagation and the parasite transmission. In a study highest numbers of the VL cases were found living in the house which were huts (36%) and kachha (mud) houses (30%) and 65% of VL cases having less than 40,000 incomes per year [52]. Thus, poverty could be the major determinant for the transmission of visceral leishmaniasis in the Jharkhand and Bihar. The occurrence of granaries inside the houses was found to be extensively associated with visceral leishmaniasis because they are usually kept inside the houses. Perhaps, better housing and improved living conditions in diseased areas of Jharkhand, Bihar and West Bengal could decrease the transmission of the disease by eliminating conditions suitable for the breeding of sand flies inside the houses. VL was reported curable in highly endemic village of West Bengal only by improving the housing conditions. High rates of infection indicated that transmission persisted in this community. Factors associated with infection included residing in homes with mud walls [53,54], dampness in homes, proximity to bodies of water, livestock ownership, sleeping dressed or under a bed net, or in a cot were associated with a lower risk. Poor housing conditions were associated with a higher risk, while personal protection measures against vectors were effective [49]. Studies investigating risk factors for visceral leishmaniasis (VL) on the Indian Subcontinent have shown contradictory results related to the role of domestic animals. In some studies, having animals in or around the house was a risk factor, in others it was protective [53]. Due to rearing of animals the dampness of the floor increases which is significantly associated with altered risk of VL [50]. Sleeping near the domestic animals and improper drainage system was significantly associated with visceral leishmaniasis. But [55] confirms that keeping animals inside the house is not a risk factor for VL in Bihar, India rather improving housing conditions and personal protection efforts for the poor has the potential to reduce VL incidence. On social grounds, human behavior, such as sleeping outside or on the ground may increase the risk for leishmaniasis. Starvation due to diets lacking protein-energy, iron, vitamin A and zinc increase the risk that an infection will progress to kala-azar [56]. In Bihar, low casts (Musahars) due to poverty are unable to take the treatment [57,58].

Some studies have also found that using wood as a cooking fuel was a risk factor arguing that it would increase exposure when it is used in open environments [48]. Other studies have however identified this as protective arguing that probably the smoke drives away the vectors [59]. Environmental factors also affect the occurrence of visceral leishmaniasis. The presence of vegetation plays a significant association with VL in univariate analysis. Presence of banana trees around the house was extensively associated with visceral leishmaniasis [60]. The village areas of Jharkhand and Bihar are usually surrounded by the high density of vegetation such as banana trees, seasonal crops, bamboo trees and herbs. Hence, they are more prone to dermal/cutaneous leishmaniasis. Bamboo trees (Bambusa arundinacea) in the pre-domestic areas are most significant factors, because these trees provide shade and consequently engineer dark and humid weather condition in the neighborhood areas of the house locations, and also creating suitable quiescent sites for Visceral Leishmaniasis vector population. The large amount of VL vector profusion is occurring in the months of July to September, and hence, it is suitable season for development of VL vectors, because, during these months starts the rainy season and the plants, such as Amaranthus spinosa (Amaranthaccae), Musa sapientum, and Croton sparciflorous are growing well and become very rich sources of breeding habitats, and thus, it attracts P. argentipes [54,61,62].

Crop vegetation types have also been correlated with Kala-azar transmission in India. During summers (March-June) and rainy season (July- October) there is increasing trend of irrigation as well as water areas, with edible shrubs and plants, alluvial soil types, dark coloured alkaline in nature (pH 7.2-8.5), calcareous with chief inorganic constituents of silicon, iron and aluminum. This type of soil enhances its capability of retaining water as well as successful growth and abundance of edible shrubs, plants or agricultural crops. Public health measures such as case detection and treatment, the control of sand flies, the conjunction elimination of infected stray dogs and health education can be effective in controlling the disease [63]. These results will be useful for further improvement in the VL control programs for intervention strategies in respect of various socioeconomic and the environmental factors that affect the occurrence of visceral leishmaniasis. Intensive and constant monitoring of sandflies on the edge of the forest and in intermediate areas is recom­mended to detect local patterns and periods of higher vector abundance, which will allow for better preventive anti-vector intervention [64]. Using the results of this investigation, health workers in such areas may be better able to control and prevent leishmaniasis.

Epidemics of both cutaneous and visceral leishmaniasis are often associated with migration and the movement of non-immune people into areas with existing transmission cycles. Occupational exposure as well as widespread deforestation remains important factors. The incidence of leishmaniasis can be affected by changes in urbanization and the human incursion into forested areas. One frequent factor is the human settlements close to a primary forest. When the ecological environments are disturbed, humans are more likely to be exposed to reservoirs and vectors increasing the risk for Acute Cutaneous Leishmaniasis (ACL) [65]. A deeper understanding of both sand fly and host biology and behavior is therefore essential to ensuring effectiveness of vector interventions and avoiding unintended counterproductive (hindrance) consequences etc. at an early age at the domestic or sylvatic areas with the aim of encouraging the use of protective measures that reduce vector exposure [66]. Efforts have been constantly made for the elimination of Kala-azar from the Indian Sub-continent; but the goal has not been yet achieved [67,68]. The above discussed risk factors (viz. climate, environmental conditions such as vegetation, temperature, humidity, rain, wind speed, natural calamities, socio-economic conditions, poverty, livelihood and deforestation due to urbanization) suggest that elimination of kala-azar can be achieved in near future if we take up these risk factors into consideration with the elimination programmes with renewed vigor, effective drugs, diagnostics, better insecticides, modern surveillance techniques, absence of animal reservoir in the Indian subcontinent, services of health workers, awareness programs, education and prevention policies and strict supervision and support from the Government agencies.

3.                   Acknowledgements

Authors are extremely thankful to Primary Health Centers of Jharkhand, Bihar, West Bengal, Uttarakhand and Uttar Pradesh for their help in data survey. We want to thank the local Gram Pradhans (Village Heads) for helping and introducing us to the localities. Authors are also thankful to the Manager and the Principal, Lucknow Christian College for providing necessary facilities.


Figure 1: Life cycle of Leishmania spp.in Phlebotomus spp. & Humans.




Figure 2: Number of cases of Kala-azar since 2010. Source: http://nvbdcp.gov.in/ka-cd.html.




Figure 3a: Number of Deaths due to Kala-azar since 2010. Source: http://nvbdcp.gov.in/ka-cd.html.




Figure 3b: Post-Kala-azar Dermal Leishmaniasis (PKDL) situation in India since 2012. Source: http://nvbdcp.gov.in/ka-cd.html.

Year

Cases & Deaths

Bihar

West Bengal

Uttar Pradesh

Jharkhand

Uttarakhand

Total

2010

Cases

23084

1482

14

4305

1

28886

Deaths

95

4

0

5

0

104

2011

Cases

25222

1962

11

5960

0

33155

Deaths

76

0

1

3

0

80

2012

Cases

16036

995

5

3535

7

20578

Deaths

27

0

0

1

1

29

2013

Cases

10730

595

11

2515

0

13851

Deaths

17

2

1

0

0

20

2014

Cases

7615

668

11

937

4

9235

Deaths

10

1

0

0

0

11

2015

Cases

6517

576

131

1262

3

8489

Deaths

5

0

0

0

0

5

2016

Cases

4773

179

107

1185

2

6246

Deaths

0

0

0

0

0

0

2017

Cases

3519

109

92

1184

2

4906

Deaths

0

0

0

0

-

0

Table 1: Kala-Azar Cases and Deaths in India (2010 to 2017). (Data source: NVBDCP, Ministry of Health & Family Welfare, Government of India.)


 

S. No.

States Affected

Number of Cases

2012

2013

2014

2015

2016

2017

1.

Bihar

113

122

119

247

542

477

2.

Jharkhand

234

304

81

153

873

1069

3.

West Bengal

82

73

221

225

240

115

4.

Uttar Pradesh

0

0

0

0

2

0

5.

Uttra khand

1

0

1

0

1

0

Total

430

499

422

655

1658

1661



Table 2: Post-Kala-azar Dermal Leishmaniasis (PKDL) situation in India since 2012. (As per the reports received from states up to October 2017).

1.       WHO (1998) Life in the 21st century: A vision for all. World Health Report 1998. Geneva: World Health Organization.

2.       WHO (1990) Control of the Leishmaniasis. Report of a World Health Organization Expert Committee. World Health Organ Tech Rep Ser 793: 1-158.

3.       WHO (1995) Bridging the gap: World Health Report Geneva: World Health Organization.

4.       Maroli M, Rossi L, Baldelli R, Capelli G, Ferroglio E, et al. (2008) The northward spread of leishmaniasis in Italy: evidence from retrospective and ongoing studies on the canine reservoir and phlebotomine vectors. Trop Med Int Health 13: 256-264.

5.       Morosetti G, Bongiorno G, Beran B, Scalone A, Moser J, et. al. (2009) Risk assessment for canine leishmaniasis spreading in the north of Italy. Geospatial Health 4: 115-127.

6.       Silva GAR, Boechat TO, Ferry FRA, Pinto JFC, Azevedo, et al. (2014) First case of autochthonous human visceral leishmaniasis in the ban Center of Rio de Janeiro: Case report. Rev Inst Med Trop Sao Paulo 56: 81-84.

7.       Bogdan C, Schonian G, Banuls AL, Hide M, Pratlong F, et.al. (2001) Visceral leishmaniasis in a German child who had never entered a known endemic area: Case report and review of the literature. Clin Infect Dis 32: 302-306.

8.       Koehler K, Stechele M, Hetzel U, Domingo M, Schonian G, et al. (2002) Cutaneous leishmaniosis in a horse in southern Germany caused by Leishmania infantum. Vet Parasitol 109: 9-17.

9.       Müller N, Welle M, Lobsiger L, Stoffel MH, Boghenbor KK, et al. (2009) Occurrence of Leishmania sp. in cutaneous lesions of horses in Central Europe. Vet Parasitol 166: 346-351.

10.    Killick-Kendrick R (1999) The biology and control of phlebotomine sand flies. Clin Dermatol 17: 279-289.

11.    Sharma U, Redhu NS, Mathur P, Singh S (2007) Re-emergence of visceral Leishmaniasis in Gujarat, India. J Vect Borne Dis 44: 230-232.

12.    Joshi A, Narain JP, Prasittisuk C, Bhatia R, Hashim G, et al (2008) Can Visceral Leishmaniasis be eliminated from Asia ? Vector Borne Diseases 45: 105-111.

13.    NVBDCP (2017) NVBDCP Ministry of Health & Family Welfare, Government of India, 2010-2017.

14.    Thakur CP (1992) Treatment of kala-azar in India. National Med J of India 5: 203-205.

15.    Sundar S and Murray HW (1995) Gamma interferon in the treatment of kala-azar and other forms of Leishmaniasis. The J. of the Asso of Physicians of India 43: 348-350.

16.    Desjeux P (2004) Leishmanias: Current situation and new perspectives. Comp Immunol Microbiol Infect Dis 27: 305-318.

17.    Swaminath CS and Supa Kankunti S (1942) Transmission of Indian kala-azar to man by the bite of Phlebotomus. argentipes, Annandale & Brunetti. The Indian J of Med Res 30: 473-477.

18.    Lainson R, Rangel EF (2005) Lutzomyia longipalpis and the eco-epidemiology of American visceral leishmaniasis, with particular reference to Brazil- A Review. Mem Inst Oswaldo Cruz 100: 811-827.

19.    Belo VS, Werneck GL, Barbosa DS, Simões TC, Nascimento BWL, et al. (2013) Factors associated with visceral leishmaniasis in the Americas: a systematic review and meta-analysis. PLoS Neg Trop Dis 7: e2182.

20.    Belo VS, Struchiner CJ, Werneck GL, Barbosa DS, de Oliveira RB, et al. (2013) A systematic review and meta-analysis of the factors associated with Leishmania infantum infection in dogs in Brazil. Veterinary parasitology 195: 1-13.

21.    Jones KE, Patel NG, Levy MA, Storegard A, Balk D, et al (2008) Global trends in emerging infectious diseases. Nature 451: 990-993.

22.    Lindgren E, Naucke TJ (2006) Leishmaniasis: Influences of climate and climate change: Epidemiology, ecology and adaption measures. In: Climate change and adaptation strategies for human health. Darmstadt: Springer. Menne, B., Ebi, K.L., Eds. Pp. 131-156.

23.    Camargo LB, Langoni H (2006) Impact of leishmaniasis on public health. J Venom Anim Toxins Trop Dis 12: 527-548.

24.    Dujardin JC, Campino L, Cañavate C, Dete JP, Gradoni L, et al. (2008) Spread of vector-borne diseases and neglect of leishmaniasis, Europe. Emerg Infect Dis 14: 1013-1018.

25.    Aspöck H, Gerersdorfer T, Formayer H, Walochnik J (2008) Sandflies and sandfly-borne infections of humans in Central Europe in the light of climate change. Wien Klin Wochen 120: 24-29.

26.    Cross ER, Hyams KC (1996) The potential effect of global warming on the geographic and seasonal distribution of Phlebotomus papatasi in Southwest Asia. Environ Health Perspect 104: 724-727.

27.    Gebre-Michael T, Malone JB, Balkew M, Ali A, Berhe N, et al. (2004) Mapping the potential distribution of Phlebotomus martini and P. orientalis (Diptera: Psychodidae), vectors of kala-azar in East Africa by use of geographic information systems. Acta Trop 90: 73-86.

28.    Oshagi MA, Ravasan NM, Javadian E, Rassi Y, Sadraei J, et al. (2009) Application of predictive degree day model for field development of sandfly vectors of visceral leishmaniasis in northwest of Iran. J Vector Borne Dis 46: 247-255.

29.    Aransay AM, Testa JM, Morillas-Marquez F, Lucientes J, Ready PD (2004) Distribution of sandfly species in relation to canine leishmaniasis from the Ebro Valley to Valencia, northeastern Spain. Parasitol Res 94: 416-420.

30.    Killick-Kendrick R, Wilkes TJ, Bailly M, Bailly I, Righton LA (1986) Preliminary field observations on the flight speed of a phlebotomine sandfly. Trans R Soc Trop Med Hyg 80: 138-142.

31.    Ximenes M, Castellon EG, Souza M, Lara Menezes AA, Queiroz JW, et al. (2006) Effect of abiotic factors on seasonal population dynamics of Lutzomyia longipalpis (Diptera: Psychodidae) in northeastern Brazil. J Med Entomol 43: 990-995.

32.    Galvez R, Descalzo MA, Miro G, Jimenez MI, Martin O, et al (2010) Seasonal trends and spatial relations between environmental/meteorological factors and leishmaniosis sand fly vector abundances in Central Spain. Acta Trop 115: 95-102.

33.    Orshan L, Szekely D, Khalfa Z, Bitton S (2010) Distribution and seasonality of Phlebotomus sand flies in cutaneous leishmaniasis foci, Judean Desert, Israel. J Med Entomol 47: 319-328.

34.    Ghosh K, Mukhopadhyay J, Desai MM, Senroy S, Bhattacharya A (1999) Population ecology of Phlebotomus argentipes (Diptera: Psychodidae) in West Bengal, India. J Med Entomol 36: 588-594.

35.    Sivagnaname N, Amalraj DD (1997) Breeding habitats of vector sand flies and their control in India. J Commun Dis 29: 153-159.

36.    Sawalha SS, Shtayeh MS, Khanfar HM, Warburg A, Abdeen ZA (2003) Phlebotomine sand flies (Dipteria, Psychodidae) of the Palestinian West Bank: Potential vectors of leishmaniasis. J Med Entomol 40: 321-328.

37.    Peterson AT, Pereira RS, Neves VF (2004) Using epidemiological survey data to infer geographic distributions of leishmaniasis vector species. Rev Soc Bras Med Trop 37: 10-14.

38.    Peterson AT, Shaw J (2003) Lutzomyia vectors for cutaneous leishmaniasis in Southern Brazil: ecological niche models, predicted geographic distributions, and climate change effects. Int J Parasitol 33: 919-931.

39.    Gonzales C, Wang O, Strutz SE, Gonza´les-Salazar C, Sanchez-Cordero V, et al. (2010) Climate change and risk of leishmaniasis in North America: predictions from ecological niche models of vector and reservoir species. PLoS Negl Trop Dis 4: e585.

40.    Thakur CP (2016) Is elimination of kala-azar feasible by 2017? Ind. J Med Res 144: 789-802.

41.    Bhunia GS, Kumar V, Kumar AJ, Das P, Kesari S (2010) The use of remote sensing in the identification of the eco-environmental factors associated with the risk of human visceral leishmaniasis (kala-azar) on the Gangetic plain, in north-eastern India. Annals of Trop Med and Parasit 104: 35-53.

42.    Parmesan C (2006) Ecological and evolutionary responses to recent climate change. Ann Rev Ecol Evol Syst 37: 637-669.

43.    Fischer D, Moeller P, Thomas SM, Naucke TJ, Beierkuhnlein C (2011) Combining Climatic Projections and Dispersal Ability: A Method for Estimating the Responses of Sandfly Vector Species to Climate Change. PLoS Negl Trop Dis 5: e1407.

44.    Palaniyandi M, Anand PH, Maniyosai R (2014) Climate, Landscape and the Environments of Visceral Leishmaniasis Transmission in India, Using Remote Sensing and GIS. J Geophys Remote Sensing 3: 122.

45.    Singh NS, Phillips-Singh D (2009) Seasonal occurrence of Phlebotominae sandflies (Phlebotominae: Diptera) and it’s correlation with kala-azar in eastern Uttar Pradesh, India. The Southeast Asian J of Trop Med and Public Health 40: 458-462.

46.    WHO (2018) Leishmaniasis, Fact sheet.

47.    Choi CM, Lerner EA (2001) Leishmaniasis as an emerging infection. J Investigative Dermatology Symp. Proceedings 6: 175-182.

48.    Yadon ZE, Rodrigues LC, Davies CR, Quigley MA (2003) Indoor and peridomestic transmission of American cutaneous leishmaniasis in north western Argentina: a retrospective case-control study. Am J Trop Med Hyg 68: 519-526.

49.    Saha S, Ramachandran R, Hutin YJF, Mohan D, Gupte MD (2009) Visceral leishmaniasis is preventable in a highly endemic village in West Bengal, India. Transactions of The Royal Soc of Trop Med Hygiene 103: 737-742.

50.    Bern C, Joshi AB, Jha SN, Das ML, Hightower A, et al. (2000) Factors associated with visceral leishmaniasis in Nepal: bed-net use is strongly protective. Am J Trop Med Hyg 63: 184-188.

51.    Bern C, Hightower AW, Chawdhury R, Ali M, Amann J, et al. (2005) Risk factors for Kalaazar in Bangladesh Emerg. Infect Dis 11: 655-662.

52.    Thakur CP (2000) Socio-economics of Visceral Leishmaniasis in Bihar (India). Trans R. Soc Trop Med Hyg 94: 156-157.

53.    Schenkel K, Rijal S, Koirala S, Koirala S, Vanlerberghe V, et al. (2006) Visceral leishmaniasis in southeastern Nepal: a cross-sectional survey on Leishmania donovani infection and its risk factors. Trop Med and Int Health 11: 1792-1799.

54.    Ranjan A, Sur D, Singh VP, Siddique NA, Manna B, et al. (2005) Risk factors for Indian kala-azar. American Journal of Tropical Medicine and Hygiene 73: 74-78.

55.    Singh SP, Hasker E, Picado A, Gidwani K, Malaviya P, et al. (2010) Risk factors for visceral leishmaniasis in India: further evidence on the role of domestic animals. Trop Med and Inter Health 15: 29-35.

56.    Boelaert M, Meheus F, Sanchez A, Singh SP, Vanlerberghe V, et al. (2009) The poorest of the poor: a poverty appraisal of households affected by visceral leishmaniasis in Bihar, India. Trop Med Int Health 14: 639-644.

57.    Pascual Martinez F, Picado A, Roddy P, Palma P (2012) Low castes have poor access to visceral leishmaniasis treatment in Bihar, India. Trop Med Int Health 17: 666-673.

58.    Picado A, Roddy P, Palma P (2012) Low castes have poor access to visceral leishmaniasis treatment in Bihar, India. Trop Med Int Health 17: 666-673.

59.    Armijos RX, Weigel MM, Izurieta R, Racines J, Zurita C, et al. (1997) The epidemiology of cutaneous leishmaniasis in subtropical Ecuador. Tropical Med Int Health 2: 140-152.

60.    Sudhakar S, Srinivas T, Palit A, Kar SK, Battacharya SK (2006) Mapping of risk prone areas of kala-azar (Visceral leishmaniasis) in parts of Bihar state, India: an RS and GIS approach. J. Vect. Borne Dis 43: 115-22.

61.    Dinesh DS, Dhima RC (1991) Plant source of fructose to sandflies, particularly Phlebotomous argentipes in nature. J of Commu Dis 23: 160-161.

62.    Dhiman RC, Sen AB (1991) Epidemiology of Kala-azar in rural Bihar (India) using village as a component unit of study. Indian J Med Res 93: 155-160.

63.    Singh NS, Phillips-Singh D (2010) Relative abundance of Phlebotominae sand flies with emphasis on vectors of kala-azar. Asian Paci J Trop Med 3: 270-271.

64.    Salomón OD, Quintana MG, Bruno MR, Quiriconi RV, Cabral V (2009) Visceral leishmaniasis in border areas: clustered distribu­tion of phlebotomine sandflies in Clorinda, Argentina. Mem Inst Oswaldo Cruz 104: 801-804.

65.    Desjeux P (2001) The increase in risk factors for leishmaniasis worldwide. Trans R Soc Trop Med Hyg 95: 239-243.

66.    Pouche DM, Grant WE, Wang HH (2016) Visceral Leishmaniasis on the Indian Subcontinent: Modeling the dynamic relationship between vector control schemes and vector life cycles. PLOS Neglected Tropical Diseases 10: e0004868.

67.    Singh OP, Hasker E, Boelaert M, Sundar S (2016) Elimination of visceral leishmaniasis on the Indian subcontinent. The Lancet infectious diseases 16: e304-e309.

68.    NVBDCP (2018) National Kala-azar Elimination Programme-2018 National Vector Borne Disease Control Programme (NVBDCP 2010-17), Directorate of Health Services, Ministry of Health and Family Welfare, New Delhi, India.


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