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Pathology Research International
Volume 2015, Article ID 438749, 4 pages
http://dx.doi.org/10.1155/2015/438749
Research Article

Leishmaniasis in Central Morocco: Seasonal Fluctuations of Phlebotomine Sand Fly in Aichoun Locality, from Sefrou Province

1Analysis and Modelisation of Continental Ecosystems Laboratory, Faculty of Sciences Dhar El Mehraz, Sidi Mohamed Ben Abdellah University, 30000 Fes, Morocco
2Laboratory of Medical Entomology, National Institute of Hygiene, 27 Avenue Ibn Battuta, Agdal, 11400 Rabat, Morocco
3Regional Diagnostic Laboratory Epidemiological and Environmental Health, Regional Health Directorate, EL Ghassani Hospital, 30000 Fes, Morocco
4National Reference Laboratory of Leishmaniasis, National Institute of Hygiene, 27 Avenue Ibn Battuta, Agdal, 11400 Rabat, Morocco

Received 27 August 2014; Accepted 9 January 2015

Academic Editor: Shahid Pervez

Copyright © 2015 Fatima Zahra Talbi et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Cutaneous leishmaniases (CL) are endemic in Morocco. They are common in the human population in different localities such as Aichoun in Sefrou province, Morocco. This study was carried out in Aichoun locality from April to October 2012 in order to study the spatiotemporal trends of the main Leishmania phlebotomine vectors in this focus. Overall, 1171 sand flies, belonging to four species, were collected by sticky traps. Phlebotomus sergenti was the predominant species (78.4%) followed by Ph. perniciosus (10.5%), Ph. papatasi (7.94%), and Ph. longicuspis (3.16%). Sandflies were active during 6 months (May–October). Ph. sergenti, Ph. perniciosus, and Ph. papatasi displayed a bimodal distribution with a first peak in July and a second peak in September, while Ph. longicuspis showed a monophasic trend with a peak in August. The high abundance and the lengthy period of activity of Ph. sergenti and Ph. perniciosus, vectors of L. tropica and L. infantum, respectively, are a cause for concern as they indicate the high potential risk of Leishmania transmission in the studied areas.

1. Introduction

Cutaneous Leishmaniasis (CL) is an increasingly public health problem in Morocco. Three forms are present: anthroponotic leishmaniasis caused by Leishmania tropica and zoonotic leishmaniasis caused by L. major and less frequently by Leishmania infantum [1]. The parasites are transmitted by phlebotomine sand flies, namely, Phlebotomus sergenti for ACL and Ph. papatasi and phlebotomines from Larrousius subgenus for L. major and L. infantum, respectively, for ZCL [2]. The main reservoir host for L. major is considered to be the rodent Meriones shawi [1].

CL caused by L. tropica is the most widespread in semiarid areas in central and south-western Morocco. This disease was reported for the first time in Azilal province in 1989 [3], then in other focus in central and southern areas of the country such as Guelmim, Agadir, Essaouira [4], and Taza [5]. CL due to L. infantum was reported in Taounate province in 1996, within an active focus of visceral leishmaniasis [6]. L. infantum is also responsible for widespread visceral leishmaniasis in the north-eastern slope of the Rif Mountains when dog is the main domestic reservoir of the parasite [7].

Each year, we witness the emergence of new foci, extending the disease distribution and increasing its total impact. In 2011 and 2012, the Ministry of Health recorded, respectively, 4426 and 2990 cases with 4.92% and 7.19% in the region of Fes-Boulmane [8, 9]. The region of Fes-Boulmane recorded the first outbreak of CL in 2001 with 1600 cases in the province of Moulay Yacoub alone [10, 11]. The outbreak was rapidly stopped by insecticides use, but the disease has persisted since that under endemic and epidemic forms in other provinces of the region with more than 100 cases each year despite a strong monitoring plan.

The control of the disease is mainly based on case detection and treatment of human cases and on vector control. This is based essentially on environmental management including promotion of improved solid waste disposal practices. The use of bed nets and local residual indoor spraying with synthetic pyrethroids are often applied in newly emerged epidemic foci. Nevertheless, few data are available on the vector Ph. sergenti, especially seasonal fluctuations of its abundance. This information is essential for the success of vector control. In this context, we have conducted this study for the first time in a village belonging to the region of Sefrou province in center of Morocco.

This study also allows a better understanding of the dynamics of the transmission of leishmaniasis in the area of Aichoun and, therefore, contributes to the future design of surveillance strategies.

2. Materials and Methods

2.1. Study Area and Environment

The entomological study was conducted in the locality of Aichoun (33°39′N, 04°38′W) situated in the northwest of the Moroccan Middle Atlas, a part of the province of Sefrou that belongs to the territory pastoral village of Tazouta with a cold semiarid climate. The mean altitude is 750 m. The average annual rainfall is 400 mm, the main minimum of the coldest month is 2°C, and maximum of the hottest month is 40°C.

The locality of Aichoun is characterized by the presence of cowsheds, caves, and accumulation of animal waste that creates an environment favorable to the biological cycle of sand flies. The vegetation is characterized by a covering more or less degraded because of overgrazing and overexploitation for domestic uses (Tetraclinis articulata, Pistacia lentiscus, Olea oleaster, Olea europaea, and Juniperus phoenicea).

2.2. Sand Fly Collection and Identification

Sand flies were collected bimonthly during their optimum development period in Morocco, between May and October. Five collecting sites were chosen in Aichoun locality. Collections were performed by using sticky papers (21 × 27,3 cm) coated with castor oil. We used 40 traps in each trapping campaign. The traps were installed in different habitats during the day and were removed the next day. Collected sand flies were transferred in glass tubes containing a solution of ethanol at 70° . After sex determination, all sand flies collected were identified by examining the morphology of the pharyngeal armature and spermathecae of female flies and the external genitalia of males using the morphological key [12, 13]. Morphological differentiation of the two sympatric species Ph. longicuspis and Ph. perniciosus was made according to description of Berchi et al. [14].

3. Results

3.1. Taxonomic Inventory of Sand Flies

This study has established a faunal inventory of Aichoun revealing the presence of four species belonging to the genus Phlebotomus. The sex ratio indicated that more males were collected; the male/female ratio was 7.54.

The collections accounted for 1171 sand fly specimens. Ph. sergenti was the predominant and the most frequently collected species with 918 individuals (78.4%). In second place comes Ph. perniciosus Newstead with 123 (10.50%) followed by Ph. papatasi Scopoli with 93 individuals (7.94%). Ph. longicuspis Nitzulescu was represented by 3.16% (Table 1).

Table 1: Sandflies collected in Aichoun locality, 2012.

3.2. Seasonal Fluctuations of Sand Flies Species

Seasonal activity of sand flies extended from May to the end of October, with variation in the monthly evolution according to species. Ph. sergenti, Ph. Perniciosus, and Ph. papatasi displayed a bimodal distribution with a first peak in July, where Ph. sergenti dominates (29.46%), and a second peak in September with 13.83%, while Ph. longicuspis showed a monophasic trend with a slight peak in August (1.11%) (Figure 1).

Figure 1: Seasonal variation of sand flies collected in Aichoun by sticky paper traps.

4. Discussion

Over the last years, incidence of L. tropica CL has continuously increased in the province of Sefrou [15]. Between 1997 and 2011, 1242 cases were declared [16]. The majority of cases were reported mainly in El Menzel, Sefrou, Aghbalou, Tazouta, Sidi Lahcen, and Ain Chegag communes [17].

Ph. sergenti is confirmed as vector of L. tropica in northern Africa, Middle East, and Central Asia [18, 19], the same in Morocco [4]. It dominates in arid and semiarid areas [20]. In this study area, Ph. sergenti was largely widespread; it was present throughout the whole period of our surveys, showing a biphasic course evolution with two peaks in July and September, respectively. Its activity period was investigated in Taza, a semiarid area in northern Morocco, where it was collected from June to November showing two density peaks [21]. Ph. sergenti was the dominant species compared to other species, which confirms the results obtained in 2011 [22] and with a maximum activity in July confirming the results obtained in Marrakech province [23].

Ph. perniciosus, one of the most competent L. infantum vectors in the Mediterranean foci [24], was present during all the period of our study. This species showed a biphasic activity and dominating in September (5.29%). This is in line with the results obtained by Guernaoui et al. [25] in the province of Chichaoua, southwest of Morocco.

Ph. papatasi was also present in our study even if it is considered to be adapted to arid climate [26]; Ph. papatasi populations were present from May to October with two peaks. These results are in accordance with the data obtained in Marrakech area in southwestern Morocco [27].

Ph. longicuspis was collected in Aichoun locality. The highest density of this species was observed in August. This result is in accordance with Guernaoui et al. [28] in Chichaoua province where this species showed a monophasic cycle, with one density peak in August-September.

In the region of Fez Boulmane one similar study of the species inventory sand flies in a focus of cutaneous leishmaniasis nominated Ouled aid and belonging to a neighboring province than that Sefrou was realized in 2011 during a year between April 2011 and March 2012 [29, 30]. If we compare our results with those found in this study, we can infer that the same species were encountered but not in the same abundance. Indeed, the most abundant species found were, respectively, Phlebotomus papatasi (50.52%), Phlebotomus sergenti (24.7%), Phlebotomus perniciosus (9.69%), and Phlebotomus longicuspis (5.54%) [29].

According Lahouiti et al. [30], the destruction of vectors’ habitats, the improvement of human habitats, the treatment of scraps, animal drop-pings, dung, and the separation between animal and human dwellings could be an efficient way to get rid of sand flies and consequently diminish the risks of contamination.

In addition to means mentioned above, we must remember that the companions of information-education-communication and the process of integrated management of vector control piloted together by the health services are very efficient tools to prevent cases of leishmaniasis.

Also, these means will be very efficient not only to fight the mosquito sand fly vector of such diseases but also to combat the parasite tanks such as rats and stray dogs who are increasingly responsible for many emerging zoonoses [31, 32].

5. Conclusion

This study, conducted in Aichoun locality during the months of April to October 2012, was aimed at studying the spatial and temporal trends of the main vectors of Leishmania in sand flies in this focus. 1171 sand flies, belonging to the four species, were collected by sticky traps. Phlebotomus sergenti was the predominant species (78.4%) followed by Ph. perniciosus (10.5%), Ph. papatasi (7.94%), and Ph. longicuspis (3.16%). Sand flies were active during 6 months (May–October).

The large distribution and the long activity period of Ph. sergenti and species of the subgenus Larroussius in Aichoun locality indicate the high potential risk of L. tropica and L. infantum transmission in this area.

Conflict of Interests

The authors declare that they have no conflict of interests.

Acknowledgments

The authors thank Mr. El Kohli Mohamed, M. Adlaoui El Bachir, Lakraa Lhoussine, El Rhazi Mohamed, and Ouahabi Souad Laboratory Medical Entomology, for the constant support made during this study. Likewise, the authors thank the regional direction of the Fes-Boulemane Health, provincial delegate of Ministry of Health, Sefrou province, and staff of Aichoun locality for their cooperation, assistance, information, and help.

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