» Articles » PMID: 29958283

Molecular Detection of Leishmania Infantum DNA and Host Blood Meal Identification in Phlebotomus in a Hypoendemic Focus of Human Leishmaniasis in Northern Algeria

Overview
Date 2018 Jun 30
PMID 29958283
Citations 14
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Leishmania parasites are transmitted by female phlebotomine sand flies that maintain the enzootic cycle by circulating between sylvatic and domestic mammals. Humans are part of this cycle as accidental hosts due to the vector's search for a source of blood. In Algeria, Human Leishmaniases (HL) are endemic and represent a serious public health problem because of their high annual incidence and their spread across the country. The aim of this study is to identify sand fly species fauna (vectors of Leishmania), determine their infection rate and identify their feeding preferences using molecular tools in a hypoendemic focus of HL located in the province of Tipaza, northern Algeria.

Methodology/principal Findings: An entomological survey using CDC light traps was conducted between July and October of 2015 in four HL affected peri-urban locations in the province of Tipaza, northern Algeria. Sand flies were identified using the morphological criteria of the genitalia for the males and spermathecae for the females. Leishmania DNA was detected in pooled female sand flies (N = 81 pools with 8-10 specimens per pool) using quantitative real-time polymerase chain reaction (qPCR) targeting two different genes: kDNA-PCR and 18S rRNA. To identify their blood meal sources, blood-fed female sand flies were analyzed by PCR-sequencing targeting the vertebrate cytochrome c oxidase I (COI) gene. A total of 4,045 sand flies were caught, of which 3,727 specimens were morphologically identified. Seven species were recorded: P. (L.) perniciosus (50.28%), P. (L.) perfiliewi (26.13%), P. (L.) longicuspis (21.92%), Sergentomyia (S.) minuta (0.85%), P. (P.) papatasi (0.42%), P. (L.) langeroni (0.32%) and P. (L.) ariasi (0.05%). Afterwards, 740 female specimens were randomly selected and divided into 81 pools and were then screened to investigate the presence of Leishmania spp. L. infantum DNA was detected in three pools, corresponding to three sand fly specimens (one each). The infection rate was 0.33% (2/600) for P. (L.) perniciosus and 2.56% (1/39) for P. (L.) perfiliewi. Analysis of the blood feeding sources (N = 88 specimens) revealed that sand flies belonging to Larroussius subgenera, mainly (71.5%) feed on small ruminants. Human blood is the second feeding source (17%), eight specimens (9%) were found to feed on equines and no domestic reservoir (dog) blood was found.

Conclusions/significance: The presence of human leishmaniasis cases, the high abundance of Phlebotomus (Larroussius) species which are proven or suspected vectors of L. infantum, and the detection of L. infantum DNA from its natural vectors (P. (L.) perniciosus, P. (L.) perfiliewi), in addition to the blood-feeding of positive females for L. infantum on humans blood, prove that the major elements of the epidemiological transmission cycle of L. infantum are present and indicate risk factors for an outbreak of the disease in the province of Tipaza.

Citing Articles

First Comprehensive List of Phlebotomine Sand Fly Species (Diptera: Psychodidae) in a Leishmaniasis Focus (Djelfa, Algeria), Including the First Record of Females in Algeria.

Messaoudene F, Boukraa S, Chaouki-Boubidi S, Guerzou A J Arthropod Borne Dis. 2025; 18(2):94-112.

PMID: 39850255 PMC: 11752668. DOI: 10.18502/jad.v18i2.17532.


First Detection and Molecular Analysis of DNA in Sand Flies of Kosovo.

Xhekaj B, Hoxha I, Platzgummer K, Kniha E, Walochnik J, Sherifi K Pathogens. 2023; 12(10).

PMID: 37887706 PMC: 10610191. DOI: 10.3390/pathogens12101190.


Experimental feeding of Sergentomyia minuta on reptiles and mammals: comparison with Phlebotomus papatasi.

Ticha L, Volfova V, Mendoza-Roldan J, Bezerra-Santos M, Maia C, Sadlova J Parasit Vectors. 2023; 16(1):126.

PMID: 37055860 PMC: 10103492. DOI: 10.1186/s13071-023-05758-5.


Investigation of the Sandfly Fauna of Central Arid Areas and Northern Humid Regions of Tunisia, with Morphological and Molecular Identification of the Recently Established Population of () .

Chelbi I, Abdi A, Depaquit J, Fares W, Abdo Saghir Abbas M, Dachraoui K Insects. 2022; 13(11).

PMID: 36421960 PMC: 9696294. DOI: 10.3390/insects13111057.


Diversity, Abundance and Infection Rate of Phlebotomine Sandflies in an Area with Low Incidence of Visceral Leishmaniasis in Northern Tunisia.

Weslati M, Ghrab J, Benabid M, Souissi O, Aoun K, Bouratbine A Microorganisms. 2022; 10(5).

PMID: 35630455 PMC: 9144524. DOI: 10.3390/microorganisms10051012.


References
1.
. Control of the leishmaniases. World Health Organ Tech Rep Ser. 2011; (949):xii-xiii, 1-186, back cover. View

2.
Feliciangeli M . Natural breeding places of phlebotomine sandflies. Med Vet Entomol. 2004; 18(1):71-80. DOI: 10.1111/j.0269-283x.2004.0487.x. View

3.
Izri M, Belazzoug S, Boudjebla Y, Dereure J, Pratlong S, Rioux J . [Leishmania infantum MON-1 isolated from Phlebotomus perniciosus, in Kabylia (Algeria)]. Ann Parasitol Hum Comp. 1990; 65(3):151-2. View

4.
Hamad I, Forestier C, Peeters M, Delaporte E, Raoult D, Bittar F . Wild gorillas as a potential reservoir of Leishmania major. J Infect Dis. 2014; 211(2):267-73. PMC: 4342692. DOI: 10.1093/infdis/jiu380. View

5.
Zait H, Ferhani Y, Achir I, Hamrioui B . [Study of 71 cases of visceral leishmaniasis diagnosed at the Mustapha University Hospital (Algiers) from 1998 to 2009]. Med Mal Infect. 2012; 42(3):119-25. DOI: 10.1016/j.medmal.2012.01.001. View