BioMed Research International

BioMed Research International / 2019 / Article

Research Article | Open Access

Volume 2019 |Article ID 5327287 |

Maryam Hakkour, Mohamed Mahmoud El Alem, Asmae Hmamouch, Abdelkebir Rhalem, Bouchra Delouane, Khalid Habbari, Hajiba Fellah, Abderrahim Sadak, Faiza Sebti, "Leishmaniasis in Northern Morocco: Predominance of Leishmania infantum Compared to Leishmania tropica", BioMed Research International, vol. 2019, Article ID 5327287, 14 pages, 2019.

Leishmaniasis in Northern Morocco: Predominance of Leishmania infantum Compared to Leishmania tropica

Academic Editor: Elena Pariani
Received24 Apr 2019
Revised17 Jun 2019
Accepted01 Jul 2019
Published08 Aug 2019


In Morocco, Leishmania infantum species is the main causative agents of visceral leishmaniasis (VL). However, cutaneous leishmaniasis (CL) due to L. infantum has been reported sporadically. Moreover, the recent geographical expansion of L. infantum in the Mediterranean subregion leads us to suggest whether the nonsporadic cases of CL due to this species are present. In this context, this review is written to establish a retrospective study of cutaneous and visceral leishmaniasis in northern Morocco between 1997 and 2018 and also to conduct a molecular study to identify the circulating species responsible for the recent cases of leishmaniases in this region. Data concerning leishmaniases cases were collected from the Epidemiology and Disease Control Directorate from 1997 to 2018. Human samples obtained from peripheral laboratories were examined using PCR-ITS1 method. The ITS1 products were subjected to digestion with the restriction endonuclease Mn1-I. Between 1997 and 2018, a total of 1,255 cases of cutaneous and visceral leishmaniasis were recorded in Tangier-Tetouan-Al Hoceima Region, i.e., 1.56% of the reported cases in Morocco (1,255/80,299). Concerning the geographical study covering the period 2007-2018, 79.5% (105/132) of the sectors were affected by leishmaniases. The molecular results showed that Humans were found to be infected with the L. infantum species with a high infection rate compared to L. tropica infection. Moreover, molecular characterization using ITS1 PCR-RFLP showed that the density of L. infantum was significantly higher (n = 68/81; 84%) than that of L. tropica (n = 13/81; 16%) (P-value 9.894e-10). While regarding visceral leishmaniasis, L. infantum was the only species responsible of this form. These findings of this study showed the emergence of L. infantum in Morocco and suggest that this species might be more prevalent than previously thought. Furthermore, the molecular determination of L. infantum will be helpful for control strategies by taking into consideration the reservoir of this species.

1. Introduction

Leishmaniasis is a parasitic disease that affects both humans and animals and is caused by flagellated protozoa belonging to the genus Leishmania [1]. These unicellular protozoa are usually transmitted by the bite of female phlebotomine sand flies (Diptera, Psychodidae) [2]. It is known that more than 20 species of Leishmania infect mammals. They are responsible for two forms of leishmaniasis depending on the location of parasites in mammalian tissues, namely, visceral and cutaneous forms. The outcome of the infection depends on the species responsible and the immune responses of the host [3].

Human cutaneous leishmaniasis (CL) is caused by most Leishmania species of the subgenus Leishmania. In Maghreb area, including Morocco, three major species responsible for this disease are Leishmania major, L. tropica, and L. infantum [4], the latter being more often associated with visceral leishmaniasis. The transmission is zoonotic for L. major with a wild animal reservoir [5], and rather anthroponotic for L. tropica. In fact, the isolation of this species (MON-102 and MON-113) from dog suggests that this mammal (dog) could be implicated as the secondary reservoir host in the life cycle of L. tropica. Nevertheless, the few sporadic cases viscerotropic do not confirm that the dog is the principal host and the life cycle is zoonotic [68]. In some parts of the Maghreb, L. Killicki has also been proven to be responsible for zoonotic CL, particularly in Tunisia [9]. Concerning L. infantum, studies carried out in Maghreb countries isolated this species from dog suggesting it as the reservoir of this disease [10].

Regarding visceral leishmaniasis (VL), Leishmania infantum is the single agent responsible for this human form in the Mediterranean basin [11, 12]. However, Ready et al. suggested that any parasite responsible for cutaneous leishmaniasis can visceralize [13] (e.g., Leishmania tropica, which causes CL cases, has been proven as the agent responsible for human VL and canine leishmaniasis (CanL) in Turkey [14].

In Morocco, the epidemiological situation of leishmaniasis as well as the distribution of Leishmania species varies. Two different eco-epidemiological entities have been known in the past: CL due to L. major also called wet or rural form and CL due to L. tropica also known as dry or urban form. However, for L. infantum, it was responsible for sporadic cases [4]. The recently published work revealed a new distribution of species by province. Indeed, many studies reported that CL cases in south-east of Morocco were caused essentially by L. major but L. tropica is also present [1517]. However, in the Southwestern, L. tropica is the only circulating species [1820]. In the center of the kingdom, L. tropica is being the only agent responsible for CL cases in some provinces [21, 22]. In others, this species was isolated beside few cases of L. infantum [23, 24]. Approaching north, limited cases of L. infantum have been also isolated with the presence of major cases of L. tropica [25].

Nevertheless, epidemiological data on leishmaniases are missing in the northern region. So, in order to give a general overview of the new distribution of CL species in Morocco, it is essential to carry out molecular investigations in the Northern provinces which have never been started and which remain until nowadays unknown.

The purpose of this study is to establish epidemiological data on leishmaniasis in seven provinces located in the extreme north of Morocco during the 21-year period 1997-2018 and to characterize the parasite species responsible for recent cases of leishmaniasis.

2. Material and Methods

2.1. Study Area

This study was established in Tangier-Tetouan-Al Hoceima Region belonging to the northwestern section (35° 46′ 00′′ N, 5° 48′ 00′′ W) and concerns Al Hoceima, Chefchaouen, Larache, Tangier-Assilah, Tetouan, M’diq-Fnidq, and Fahs-Anjra Provinces. This region is bordered to the north by the Strait of Gibraltar and the Mediterranean Sea, to the west by the Atlantic Ocean, to the south-west by the Rabat-Sale-Kenitra Region, to the south by the Fes-Meknes Region, and to the east by the Oriental Region (Figure 1). Climatically, this region is characterized by a Mediterranean climate [26]. Moreover, in terms of tourism, its exceptional location with its two maritime facades and its roots in history and cultural diversity predispose it to occupy a favorite place as a tourist destination.

The Tangier-Tetouan-Al Hoceima Region extends over a surface of 17,262 km2 (2.43% of the national territory) and has a total of 3,556,729 inhabitants with a density of 206 inhabitants per km2 [27].

2.2. Diagnosis
2.2.1. Microscopic Confirmation

The molecular characterization has concerned all smears received in the National Reference Laboratory for Leishmaniasis (NRLL) at the National Institute of Hygiene (NIH-Rabat, Morocco) between 2016 and 2017 (89/119). The remaining cases were not received and others were defective. These smears were sent by the peripheral laboratories in order to confirm and control their positivity. Only confirmed positive cases were included in this study.

Concerning 2018, the number of smears received was not representative compared to the number declared. As a result, these cases were excluded from the molecular study.

2.2.2. DNA Extraction

The DNA extraction was performed with the Qiagen Blood and Tissue kit (Hilden, Germany) respecting the usage protocol provided by the manufacturer with minor modifications (Proteinase K was incubated for 1H at a temperature of 56°C) [28].

2.2.3. ITS1 PCR-RFLP Analysis

The internal transcribed spacer (ITS1) region was amplified using the pairs of primers LITSR (5′-TGATACCACTTATCGCACTT-3′) and L5.8S (5′-CTGGATCATTTTCCGATG-3′). ITS1-PCR products were digested with the restriction endonuclease Mn1-I [8, 25, 29, 30]. Reference strains of Leishmania tropica (MHOM/MA/2010/LCTIOK-4), Leishmania infantum (MHOM/MA/1998/LVTA), and Leishmania major (MHOM/MA/2009/LCER19-09) were used as positive controls.

2.3. Data Collection

In 1997-2018, a total of 1,255 leishmaniases cases were the subject of an epidemiological study. Data on human cases were obtained from the Epidemiology and Disease Control Directorate [31]. The data are the result of passive surveillance based on the notifications recorded by the medical staff of the provincial laboratories of Tangier-Tetouan-Al Hoceima Region who reported each case to the Epidemiology Department of the Ministry of Health. The database contains all patient data, including sex, age, and place of residence.

The study area is known to be moderately affected by CL and highly affected by VL as well. In fact, in Morocco, the provinces considered to be strongly affected by CL recorded a total of between 10,500 and 1,000 cases during this period (such as Errachidia Province, Zagora Province, and Chichaoua Province). Provinces classified as moderately affected recorded a total between 1,000 and 100 (such as Beni Mellal Province, Settat Province, and Driouch Province). Provinces with fewer than 100 cases are considered to be slightly affected (such as Guercif Province, Agadir Province, and Tiznit Province) [32]. About visceral form, the provinces noted more than 100 cases are considered highly infected. Provinces with 100-10 cases are known to be moderately affected. Provinces registering less than 10 cases are poorly affected.

Concerning the geographical study, all data about autochthonous patients presenting the clinical symptoms of leishmaniasis during 2007-2018 were collected from health centers and infrastructure services of ambulatory actions provincial of the study provinces.

2.4. Statistical Analysis

Statistical analysis was performed using software R version 3.3.3.

3. Results

3.1. Molecular Diagnosis

A total of 89 slides were analyzed by ITS1 PCR-RFLP. This total is distributed over the seven Provinces: 38 CL slides in Larache Province, 21 CL/5VL slides in Al Hoceima Province, 10 CL / 1VL slides in Tetouan Province, 5 CL slides in Chefchaouen, 3 CL slides in Fahs-Anjra, 2 CL / 2VL slides in Tangier-Assilah, and 2 CL slides in Mdiq-Fnidq (Table 1).

ProvinceSectorUrban/RuralCutaneous formVisceral formTotal
L. infantumL. tropicaL. infantum

LaracheBen saidR20-2
Od KhalkhalR10-1
Larache CenterU20-2
Od hartiR10-1
Souk ToulbaR20-2
Ksar KbirU20-2
Souk L’qollaR10-1
Bni AroussR20-2
Al ManarR10-1
Ksar BjirR10-1
Bni GarfetR11-2

Al HoceimaAjdirU01-1
Ait Youssef OualiR10-1
Bni BouayachR30-3
Arbaa TaourirtR10-1
Bni AbdellahR10-1
Al Hoceima CenterU10-1
Arbaa TaourirtR10-1
Douar AssammarR--11
Ait zianeR--11

Bni HsenR01-1

Chefchaouen CenterU01-1

Fahs AnjraAnjraR10-1
Khmis AnjraR10-1



R: rural, U: urban.

The results of this molecular characterization show the coexistence of L. infantum and L. tropica responsible of cutaneous form with a predominance of L. infantum species (P-value 9.894e-10) while L. infantum is the only species responsible of visceral form (Figure 2) (Table 2).

ProvincesL. infantumL. tropicaTotalP-value

Al Hoceima192210.00020∗
Fahs Anjra303-

P< 0.001.

The distribution of Leishmania species is directly associated with the presence of sandflies species. Figure 3 summarizes the results of molecular identification in association with the repartition of sandflies species [33] according to their bioclimatic stage preferences (

3.2. Epidemiology of Leishmaniasis in Tangier-Tetouan-Al Hoceima Region
3.2.1. Temporal Distribution of VL and CL Cases in Tangier-Tetouan-Al Hoceima Region

According to the Moroccan Ministry of Health, between 1997 and 2018, among the total declared (1,255) of VL and CL cases, 44.2% (n=555/1,255) have been noted as VL cases in this region.

Approximately half of the total VL cases (300/555 = 54.05%) were registered in Chefchaouen Province with an average incidence of 2.86. In Al Hoceima Province, an average incidence of 2.07 per year of cases were noted (29.73% (n=165/555)) (Figure 4). As for them, Tetouan Province, Larache Province, Mdiq-Fnidq Province, Tangier-Assila Province, and Fahs Anjra Province have registered, respectively 7.20% (n=40/555), 6.49% (n=36/555), 1.44% (n=8/555), 0.72% (n=4/555), and 0.36% (n=2/555) of cases.

About CL cases, a total of 700 cases were recorded and distributed as follows: 32.14% (n=225/700) in Larache Province, 28.86% (n=202/700) in Al Hoceima Province, 23.28% (n=163/700) in Chefchaouen Province, 10.86% (n=76/700) in Tetouan Province, 2.43% (n=17/700) in Tangier-Assila, 1.57% (n=11/700) in Fahs-Anjra Province, and 0.85% (n=6/700) in Mdiq-Fnidq Province (Figure 4).

3.2.2. Geographical Study of Leishmaniasis Cases in Tangier-Tetouan-Al Hoceima Region

The geographical study showed that 79.5% (105/132) of the sectors were affected by leishmaniasis in this study area between 2007 and 2018.

Regarding visceral leishmaniasis, a percentage of 52.3 (69/132) sectors were affected during this period (Figure 5). Figure 6 shows a plot number of affected sectors by VL in each province per year with the majority of cases 80% (n = 28/35) noted in Al Hoceima Province. In brief, the spatial distribution of cases during the study period in this region has shown a remarkable spatial extension of VL within these provinces. In fact, there is not a concentration and a prioritization of the sectors on the other. Furthermore, it is important to note that these sectors are not regularly affected. Indeed, some sectors have been touched once or twice during this period and others have been affected yearly but distributed in different localities of the sector.

Concerning the distribution of cutaneous form, a total of 86 sectors were affected in this region with 65.15% (86/132) (Figure 7). The highest number of affected sectors were observed in Larache Province 100% (n= 19/19) followed by Al Hoceima Province with 77.14% (n= 27/35) of affected sector. About Chefchaouen Province, 58.82% (n= 20/34) of the sectors have been touched. Figure 8 shows the number of affected sectors by CL in each province per year.

3.2.3. Repartition of CL and VL in Relation to Age and Sex

This study was performed to show the most infected population in this region. The statistical study about the distribution of leishmaniasis according to sex has shown there is not a significant difference between genders (Pearson Chi-square test: χ2 = 0.22314, df= 1, P = 0.6367) with a slight predominance of leishmaniasis in males (51.23% vs. 48.76% for females; sex-ratio M/F= 1.05). About age group, 49.86% were children under 11 years old. The difference was statistically significant regarding the other age group (Pearson Chi-square test: χ2= 300.82, df= 5, P<2.2e-16) (Figure 9).

4. Discussion

The region of Tangier-tetouan-Al hoceima, made up of seven provinces (Tangier-Assilah, Fahs-Anjra, Tetouan, Larache, Chefchaouen, Al Hoceima, and Mdiaq-Fnidq), is known to be among the moderately affected regions by leishmaniasis especially the cutaneous form. During the period 1997-2018, 1.56% of the reported cases of leishmaniases in Morocco were registered in this region (n= 1,255/80,299). Concerning clinical types, the cutaneous form represented 0.90% (n= 700/78,001) of the reported leishmaniasis cases in Morocco, whereas the visceral form accounted for 24.15% (n= 555/2,298) [32].

In order to properly intervene in the fight against leishmaniasis in this region, a persistent follow-up of this pathology is indispensable, in particular the visceral form, which is considered as a deadly form and which continues to record a rather large number of cases. The measures of control of this disease should take into account rapid diagnosis in suspected clinical cases and treatment of confirmed positive cases, vector control measures, improvement of hygiene conditions, and the zoonotic cycle of this form. Unfortunately, the results showed that these interventions are not yet taken into consideration.

Regarding the molecular characterization, the identification of DNA from CL slides showed that L. infantum and L. tropica circulate together in this region with a predominance of L. infantum (n = 68/81; 84%) (P-value = 6.026e-06), while L. infantum was the only causal species of VL. On the other hand, the distribution of these parasites showed that L. infantum was the only circulating species in Chefchaouen, Tangier-Assilah, and Fahs-Anjra provinces, while in Larache, Al Hoceima, and Tetouan, the predominance of L. infantum beside L. tropica was registered. Indeed, this is the first identification of this species as the main causative agent of human cutaneous form of leishmaniasis in this region.

The dominance of L. infantum is no longer surprising. In fact, this species starts to have a wide extension throughout the world, including several Mediterranean countries, in particular Southern Europe, such as the famous foci in Abruzzi (Italy) [34], and Cukurova region (Turkey) [35]. Also several other epidemiological studies were performed in North Africa such as Tunisia and Algeria [36, 37].

In Morocco this species was responsible for sporadic cases in the north of the country [4]. Indeed, the molecular survey of leishmaniasis in Taza Province showed the existence of many cases of CL due to L. infantum [23]. The same results were observed in another study realized in Ouazzane and Sid Kacem Provinces [25]. Going further, exactly to the south of the country, a sporadic case of CL due to L. infantum in Ouarzazate Province was declared [38].

The presence of L. infantum in this region at a high rate could be explained firstly by the dominance of VL due to L. infantum in this area. On the other hand, our study area belongs to humid, subhumid, and semiarid climate located at an altitude of between 0 and 573m. Indeed, Rioux et al. in 1984 showed that the repartition of different sandflies species is mostly related to the bioclimatic areas [39]. In addition, Laqraa et al. in 2015 provided an updated distribution of leishmaniasis vectors in Morocco according to their bioclimatic and altitudinal preferences [33]. This update showed an abundance of sandfly species known to be vectors of VL and CL in this region. These species include Phlebotomus perniciosus, which dominates in the humid, subhumid and semiarid zones at high altitudes and Phlebotomus longicuspis which is preponderant in semiarid stages at low altitudes [33, 40]. This may explain the abundance of this Leishmania species in the north part of the country, which is characterized by this type of climate.

The epidemiological study established during the surveyed period showed that peaks in the number of human CL cases were recorded in three provinces (Larache, Al Hoceima, and Chefchaouen). The number of cases continues to increase in the provinces of Larache and Al Hoceima, while a remarkable decrease is known in Chefchaouen Province. Moreover, Tetouan Province has recorded a lower number. However, the epidemiological situation of the visceral form showed an important geographical extension, especially in Chefchaouen and Al Hoceima Provinces. Several factors can explain the increase of the number cases until 2010. Among these factors, the active screening is carried out following the introduction of a response action plan between 2010 and 2016. In addition, this increase can be explained also by the neighbourship of these provinces with several provinces already known to be foci of CL and VL such as Ouazzane [25], Sidi Kacem [25], Taounate [41], and Taza [23]. Also, the population activities and shifting could also cause this increase [42]. Moreover, the majority of these cities are located on a mountainous area that is surrounded by old unrestored fissured walls, with a nearby spring that provide daytime resting places for sandflies.

Furthermore, most cases have been reported in rural and periurban areas. In fact, the provinces of Chefchaouen, Al Hoceima, and Larache, which recorded the maximum number of cases, have a relatively low rate of urbanization (respectively, 12.5%, 32.5%, and 52.5%) [26]. According to the WHO, the urbanization rate is indicated as a key factor in the increase of leishmaniasis [43]. The transmission of leishmaniasis generally occurs in rural areas [44], in which it could be related to human behavior through human-animal coexistence and the accumulation of animal waste near homes [45]. Boussaa et al. have confirmed that this factor has a huge influence on vector populations and consequently on the epidemiology of the disease. The abundance of sandflies appears to decrease with increasing urbanization and some potential vector species may disappear [46]. In addition, movement population from rural neighboring foci to periurban areas may increase leishmaniasis cases which are due to the poor quality of life and socioeconomic status [47, 48]. These factors constitute favorable conditions for the propagation of reservoir hosts and vectors and consequently for the spread of leishmaniasis [47].

According to the clinical study of leishmaniasis in Tangier-Tetouan-Al Hoceima Region, the repartition of CL and VL in relation to age showed that no age group was spared from leishmaniasis with the dominance of children under 9 years old. This dominance could be explained by the weak immune system and consequently the inability to fight the Leishmania infection. In addition, this may be due also to the habits of children who often play near breeding sites which make them prone to insect bites [49]. Moreover, this study also shows a predominance of men with leishmaniasis; this dominance could be explained essentially by the rural character of the provinces where people’s activities depend closely to the breeding generally practiced by men.

In addition, the predominance of this cutaneous form due to L. infantum prompts us to know whether an immune suppression of the patients with this form can lead to relapses and develop a visceral form of leishmaniasis. Indeed this species proved to be an important opportunistic agent with high rates of relapse and death in patients with acquired immunodeficiency [50]. Moreover, the emergence of an anthroponotic cycle of HIV/VL coinfections by sharing contaminated syringes among intravenous drug users has been reported [51]. Additionally, it is important to note that the provisional number of cumulative cases of HIV-AIDS in Morocco was 12,545 in 2016 according to the Ministry of Health [52].

Molecular identification of circulating species of Leishmania and knowledge of temporal and spatial distribution of leishmaniasis cases are essential in order to understand epidemiology of the diseases [53].

In fact, the transmission cycle of L. infantum is zoonotic; dogs have been implicated as the main reservoir hosts of this species. In Morocco, both the MON-1 and MON-24 zymodemes have been isolated from dogs [10, 54]. However, data on density of dogs and their positivity for L. infantum in this region are missing. Furthermore, it is important to mention that rodents may also transmit this parasite of which L. infantum has been isolated from rodents belonging to the species Rattus norvegicus in Greece and Brazil [55, 56].

Interestingly, the identification of L. infantum species causing human cutaneous form in this region will play a major role in helping and guiding the national leishmaniasis control program by preventing and taking into consideration the zoonotic character.

5. Conclusion

The present study concerns both cutaneous and visceral leishmaniasis prevalence in northern Morocco. Our results showed that two Leishmania species (L. infantum and L. tropica) are present in the northern region of Morocco with a predominance of L. infantum. These findings are consistent with studies which have shown that L. infantum is the main agent responsible for VL and CL cases in the Mediterranean subregion.

The identification of circulating zoonotic L. infantum species in this region is of great importance since it allows the determination of transmission cycles. In fact, these funding will allow us to monitor the health of human and animal with thinking about “One health” as the potential of closer cooperation between human and animal health.


CL:Cutaneous leishmaniasis
VL:Visceral leishmaniasis
NRLL:National Reference Laboratory of Leishmaniasis-Rabat
NIH:National Institute of Hygiene-Morocco.

Data Availability

The data used to support the findings of this study are included within the article.

Conflicts of Interest

The authors declare that they have no competing interests.


The authors would like to thank the delegates, animators, and physicians of the provinces studied in this paper for providing all the necessary information on the samples and the study area. Also, they send big thanks to MOUNTAJ Sara (PhD student) and MHIYAOUI Hassan (PhD student) from laboratory of Applied Geosciences Engineering (GAIA), Faculty of Sciences Aïn Chock-Casablanca, for their contribution in carrying out studies of GIS.


  1. J. Dedet, “Leishmanies, leishmanioses. Biologie, clinique et thérapeutique,” Encyclopédie Médico-Chirurgicale Maladies Infectieuses, vol. 8, no. 506, pp. 10-11, 2001. View at: Google Scholar
  2. R. Killick-Kendrick, “The biology and control of phlebotomine sand flies,” Clinics in Dermatology, vol. 17, no. 3, pp. 279–289, 1999. View at: Publisher Site | Google Scholar
  3. M. T. M. Roberts, “Current understandings on the immunology of leishmaniasis and recent developments in prevention and treatment,” British Medical Bulletin, vol. 75-76, no. 1, pp. 115–130, 2005. View at: Publisher Site | Google Scholar
  4. M. Rhajaoui, “Human leishmaniases in Morocco: a nosogeographical diversity,” Pathologie Biologie, vol. 59, no. 4, pp. 226–229, 2011. View at: Publisher Site | Google Scholar
  5. J. Rioux, F. Petter, O. Akalay, G. Lanotte, A. Ouazzani, M. Seguignes et al., “Meriones shawi (Duvernoy 1842) (Rodentia, Gerbillidae), reservoir de Leishmania major Yakimoff et Schokhor, 1914 (Kinetoplastida, Trypanosomatidae) dans le Sud marocain,” Comptes Rendus de l'Académie des Sciences, vol. 294, pp. 515–517, 1982. View at: Google Scholar
  6. F. Pratlong, J. Rioux, J. Dereure et al., “Leishmania tropica au Maroc. IV — Diversité isozymique intrafocale,” Annales de Parasitologie Humaine et Comparée, vol. 66, no. 3, pp. 100–104, 1991. View at: Publisher Site | Google Scholar
  7. M. Lemrani, R. Nejjar, and F. Pratlong, “A new Leishmania tropica zymodeme—causative agent of canine visceral leishmaniasis in Northern Morocco,” Annals of Tropical Medicine and Parasitology, vol. 96, no. 6, pp. 637-638, 2002. View at: Publisher Site | Google Scholar
  8. J. Derreure, A. Saddiki, and A. Martini, “Leishmania tropica au Maroc. Rôle du vecteur de P.sergenti. A propos de 89 isolats,” Annales de Parasitologie Humaine et Comparée, vol. 66, no. 3, pp. 96–99, 1991. View at: Google Scholar
  9. K. Jaouadi, J. Depaquit, N. Haouas et al., “Twenty-four new human cases of cutaneous leishmaniasis due to Leishmania killicki in Metlaoui, southwestern Tunisia: probable role of Phlebotomus sergenti in the transmission,” Acta Tropica, vol. 122, no. 3, pp. 276–283, 2012. View at: Publisher Site | Google Scholar
  10. R. Benikhlef, Z. Harrat, M. Toudjine, A. Djerbouh, S. Bendali-Braham, and M. Belkaid, “Detection of Leishmania infantum MON-24 in the dog,” Medecine Tropicale: Revue du Corps de Santé Colonial, vol. 64, no. 4, pp. 381–383, 2004. View at: Google Scholar
  11. F. Pratlong, P. Lami, C. Ravel, Y. Balard, J. Dereure, G. Serres et al., “Geographical distribution and epidemiological features of Old World Leishmania infantum and Leishmania donovani foci, based on the isoenzyme analysis of 2277 strains,” Parasitology, vol. 140, pp. 423–434, 2013. View at: Google Scholar
  12. M. Mniouil, H. Fellah, F. Amarir et al., “Epidemiological characteristics of visceral leishmaniasis in Morocco (1990–2014): an update,” Acta Tropica, vol. 170, pp. 169–177, 2017. View at: Publisher Site | Google Scholar
  13. P. D. Ready, “Epidemiology of visceral leishmaniasis,” Journal of Clinical Epidemiology, vol. 6, no. 1, pp. 147–154, 2014. View at: Publisher Site | Google Scholar
  14. S. O. Toz, G. Culha, F. Y. Zeyrek et al., “A real-time ITS1-PCR based method in the diagnosis and species identification of leishmania parasite from human and dog clinical samples in Turkey,” PLOS Neglected Tropical Diseases, vol. 7, no. 5, 2013. View at: Google Scholar
  15. M. Ait Kbaich, I. Mhaidi, A. Ezzahidi et al., “New epidemiological pattern of cutaneous leishmaniasis in two pre-Saharan arid provinces, southern Morocco,” Acta Tropica, vol. 173, pp. 11–16, 2017. View at: Publisher Site | Google Scholar
  16. E. A. Mohamed Mahmoud, S. Faiza, M. Lemine et al., “Geographical distribution and new situation of leishmania species after the control of cutaneous leishmaniasis foci in errachidia province, Morocco, in 2014,” BioMed Research International, vol. 2016, Article ID 8642373, 7 pages, 2016. View at: Publisher Site | Google Scholar
  17. A. Hmamouch, M. M. El Alem, M. Hakkour et al., “Circulating species of Leishmania at microclimate area of Boulemane Province, Morocco: impact of environmental and human factors,” Parasites & Vectors, vol. 10, no. 1, 2017. View at: Publisher Site | Google Scholar
  18. M. M. El Alem, M. Hakkour, A. Hmamouch et al., “Risk factors and prediction analysis of cutaneous leishmaniasis due to Leishmania tropica in Southwestern Morocco,” Infection, Genetics and Evolution, vol. 61, pp. 84–91, 2018. View at: Publisher Site | Google Scholar
  19. A. Fatima, S. Faiza, F. Hajiba et al., “Epidemiological characteristics of a new focus of cutaneous leishmaniasis caused by Leishmania tropica in Settat, Morocco,” Acta Tropica, vol. 150, pp. 116–121, 2015. View at: Publisher Site | Google Scholar
  20. M. Rhajaoui, F. Sebti, H. Fellah et al., “Identification of the causative agent of cutaneous leishmaniasis in Chichaoua province, Morocco,” Parasite, vol. 19, no. 1, pp. 81–84, 2012. View at: Publisher Site | Google Scholar
  21. H. Arroub, S. Hamdi, M. Ajaoud, K. Habbari, and M. Lemrani, “Epidemiologic study and molecular detection of Leishmania and sand fly species responsible of cutaneous leishmaniasis in Foum Jamâa (Azilal, Atlas of Morocco),” Acta Tropica, vol. 127, no. 1, pp. 1–5, 2013. View at: Publisher Site | Google Scholar
  22. S. Faiza, H. Asmae, A. Fatima et al., “Molecular epidemiological study of cutaneous leishmaniasis in Beni Mellal and Fquih Ben Saleh provinces in Morocco,” Acta Tropica, vol. 149, pp. 106–112, 2015. View at: Publisher Site | Google Scholar
  23. M. Hakkour, A. Hmamouch, M. M. El Alem et al., “New epidemiological aspects of visceral and cutaneous leishmaniasis in Taza, Morocco,” Parasites & Vectors, vol. 9, no. 1, 2016. View at: Publisher Site | Google Scholar
  24. H. Asmae, A. Fatima, F. Hajiba et al., “Coexistence of Leishmania tropica and Leishmania infantum in Sefrou province, Morocco,” Acta Tropica, vol. 130, no. 1, pp. 94–99, 2014. View at: Publisher Site | Google Scholar
  25. H. El Miri, C. Faraj, O. Himmi et al., “Cutaneous leishmaniasis in Ouazzane and Sidi Kacem provinces, Morocco (1997-2012),” Bulletin de la Société de Pathologie Exotique, vol. 109, no. 5, pp. 376–380, 2016. View at: Publisher Site | Google Scholar
  26. HCP, Monographie de la région Tanger-Tétouan-Al Hoceima, 2015, file:///C:/Users/Admin/Downloads/MONOGRAPHIE DE LA REGION DE TANGER TETOUAN_fr (3).pdf.
  27. HCP, Vue d’ensemble de la Région Tanger-Tétouan-Al Hoceima, Haut Commissariat au Plan, 2017
  28. M. A. Mahdy, H. M. Al-Mekhlafi, A. M. Al-Mekhlafi et al., “Molecular characterization of leishmania species isolated from cutaneous leishmaniasis in Yemen,” PLoS ONE, vol. 5, no. 9, Article ID e12879, pp. 1–4, 2010. View at: Publisher Site | Google Scholar
  29. A. Al-Jawabreh, L. Schnur, A. Nasereddin, J. Schwenkenbecher, Z. Abdeen, F. Barghuthy et al., “The recentemergence of Leishmania tropica in Jericho (Ariha) and its environs, a classicalfocus of Leishmania major,” Tropical Medicine & International Health, vol. 9, pp. 1–5, 2004. View at: Google Scholar
  30. G. Schönian, A. Nasereddin, N. Dinse et al., “PCR diagnosis and characterization of Leishmania in local and imported clinical samples,” Diagnostic Microbiology and Infectious Disease, vol. 47, no. 1, pp. 349–358, 2003. View at: Publisher Site | Google Scholar
  31. DELM, Programme de Lutte contre les Leishmanioses, 2000.
  32. MMH MM of H, Santé en chiffres (edition 2017 en cours), 2016
  33. E. Laqraa, M. Elkohli, E. Adlaoui, and C. Faraj, “Les phlébotomes du Maroc,” Bulletin de l'Institut National d'Hygiène, vol. 3, p. 4, 2015. View at: Google Scholar
  34. M. Gramiccia, L. Gradoni, and E. Pozio, “Leishmania infantum sensu lato as an agent of cutaneous leishmaniasis in Abruzzi region (Italy),” Transactions of the Royal Society of Tropical Medicine and Hygiene, vol. 81, no. 2, pp. 235–237, 1987. View at: Publisher Site | Google Scholar
  35. J. Votýpka, O. E. Kasap, P. Volf, P. Kodym, and B. Alten, “Risk factors for cutaneous leishmaniasis in Cukurova region, Turkey,” Transactions of the Royal Society of Tropical Medicine and Hygiene, vol. 106, no. 3, pp. 186–190, 2012. View at: Publisher Site | Google Scholar
  36. M. BenSaid, S. Guerbouj, F. Saghrouni, A. Fathallah-Mili, and I. Guizani, “Occurrence of Leishmania infantum cutaneous leishmaniasis in central Tunisia,” Transactions of the Royal Society of Tropical Medicine and Hygiene, vol. 100, no. 6, pp. 521–526, 2006. View at: Publisher Site | Google Scholar
  37. K. Aoun and A. Bouratbine, “Cutaneous leishmaniasis in North Africa: a review,” Parasite, vol. 21, pp. 14–23, 2014. View at: Publisher Site | Google Scholar
  38. A. El Hamouchi, R. Ejghal, M. Hida, and M. Lemrani, “Intraspecific genetic variability in a population of Moroccan Leishmania infantum revealed by PCR-RFLP of kDNA minicircles,” Acta Tropica, vol. 169, pp. 142–149, 2017. View at: Publisher Site | Google Scholar
  39. J. Rioux, P. Rispail, G. Lanotte, and J. Lepart, “Relations Phlébotomes-bioclimats en écologie des leishmanioses Corollaires épidémiologiques. L'exemple du Maroc,” Bulletin de la Société Botanique de France. Actualités Botaniques, vol. 131, no. 2–4, pp. 549–557, 2014. View at: Publisher Site | Google Scholar
  40. J. Rioux, “Eco-épidémiologie des leishmanioses au Maroc. Bilan de 30 ans de coopération. Direction de lEpidémiologie et de Lutte contre les Maladies,” Bulletin Epidémiologique, vol. 37, pp. 2–10, 1999. View at: Google Scholar
  41. J. Rioux, J. Mahjour, M. Gallego, J. Dereure, J. Périères, A. Laamrani et al., “Leishmaniose cutanée humaine à Leishmania infantum MON-24 au Maroc,” Bulletin de la Société Française de Parasitologie, vol. 14, no. 2, pp. 179–183, 1996. View at: Google Scholar
  42. WHO, Report on Global Surveillance of Epidemic-prone Infectious Diseases – Leishmaniasis, 2000
  43. WHO, “Urbanization: An increasing risk factor for Leishmaniasis,” The Weekly Epidemiological Record, vol. 77, pp. 365–372, 2002. View at: Google Scholar
  44. WHO, Leishmaniasis, 2017,
  45. W. d. Nunes, S. R. Araújo, and C. M. Calheiros, “Epidemiological profile of leishmaniasis at a reference service in the state of Alagoas, Brazil, from January 2000 to september 2008,” The Brazilian Journal of Infectious Diseases, vol. 14, no. 4, pp. 342–345, 2010. View at: Publisher Site | Google Scholar
  46. S. Boussaa, B. Pesson, and A. Boumezzough, “Phlebotomine sandflies (Diptera: Psychodidae) of Marrakech city, Morocco,” Annals of Tropical Medicine and Parasitology, vol. 101, no. 8, pp. 715–724, 2007. View at: Publisher Site | Google Scholar
  47. R. Reithinger, M. Mohsen, and T. Leslie, “Risk factors for anthroponotic cutaneous leishmaniasis at the household level in Kabul, Afghanistan,” PLOS Neglected Tropical Diseases, vol. 4, no. 3, Article ID e639, 2010. View at: Publisher Site | Google Scholar
  48. M. A. Ghatee, I. Sharifi, A. A. Haghdoost et al., “Spatial correlations of population and ecological factors with distribution of visceral leishmaniasis cases in southwestern Iran,” Journal of Vector Borne Diseases, vol. 50, no. 3, pp. 179–187, 2013. View at: Google Scholar
  49. H. Arroub, A. Alaoui, M. Lemrani, and K. Habbari, “Cutaneous leishmaniasis in foum jamâa (Azilal, Morocco): micro-environmental and socio-economical risk factors,” Journal of Agriculture and Social Sciences, vol. 8, pp. 6–10, 2012. View at: Google Scholar
  50. J. Alvar, P. Aparicio, A. Aseffa et al., “The relationship between leishmaniasis and AIDS: the second 10 years,” Clinical Microbiology Reviews, vol. 21, no. 2, pp. 334–359, 2008. View at: Publisher Site | Google Scholar
  51. I. Cruz, M. A. Morales, I. Noguer, A. Rodríguez, and J. Alvar, “Leishmania in discarded syringes from intravenous drug users,” The Lancet, vol. 359, no. 9312, pp. 1124-1125, 2002. View at: Publisher Site | Google Scholar
  52. DELM, Bulletin d’Epidémiologie et de Santé Publique, 2017,
  53. G. Schönian, L. Schnur, M. El Fari et al., “Genetic heterogeneity in the species Leishmania tropica revealed by different PCR-based methods,” Transactions of the Royal Society of Tropical Medicine and Hygiene, vol. 95, no. 2, pp. 217–224, 2001. View at: Publisher Site | Google Scholar
  54. J. Rioux, G. Lanotte, F. Petter, J. Dereure, O. Akalay, F. Pratlong et al., “Les Leishmanioses cutanées du bassin Méditerranéen occidental. De lidentification enzymatique à lanalyse éco-épidémiologique. Lexemple de trois, foyers , tunisien, marocain et français. IMEEE,” Montpellier Applications éco-épidémiologiques, pp. 365–395, 1986. View at: Google Scholar
  55. Y. Özbel, I. Balcioglu, M. Ölgen, F. Simsek, S. Töz, H. Ertabaklar et al., “Spatial distribution of phlebotomine sand flies in the Aydin Mountains and surroundings: the main focus of cutaneous Papadogiannakis E, Spanakos G, Kontos V, Menounos PG, Tegos N, Vakalis N. Molecular detection of Leishmania infantum in wild rodents (Ratt),” Zoonoses Public Health, vol. 57, pp. e23–e25, 2010. View at: Google Scholar
  56. F. O. Lara-Silva, R. A. Barata, É. M. Michalsky et al., “Rattus norvegicus (Rodentia: Muridae) Infected by Leishmania (Leishmania) infantum (syn. Le. chagasi) in Brazil,” BioMed Research International, vol. 2014, Article ID 592986, 7 pages, 2014. View at: Publisher Site | Google Scholar

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