» Articles » PMID: 27581188

Bacterial Diversity of the American Sand Fly Lutzomyia Intermedia Using High-throughput Metagenomic Sequencing

Abstract

Background: Parasites of the genus Leishmania cause a broad spectrum of diseases, collectively known as leishmaniasis, in humans worldwide. American cutaneous leishmaniasis is a neglected disease transmitted by sand fly vectors including Lutzomyia intermedia, a proven vector. The female sand fly can acquire or deliver Leishmania spp. parasites while feeding on a blood meal, which is required for nutrition, egg development and survival. The microbiota composition and abundance varies by food source, life stages and physiological conditions. The sand fly microbiota can affect parasite life-cycle in the vector.

Methods: We performed a metagenomic analysis for microbiota composition and abundance in Lu. intermedia, from an endemic area in Brazil. The adult insects were collected using CDC light traps, morphologically identified, carefully sterilized, dissected under a microscope and the females separated into groups according to their physiological condition: (i) absence of blood meal (unfed = UN); (ii) presence of blood meal (blood-fed = BF); and (iii) presence of developed ovaries (gravid = GR). Then, they were processed for metagenomics with Illumina Hiseq Sequencing in order to be sequence analyzed and to obtain the taxonomic profiles of the microbiota.

Results: Bacterial metagenomic analysis revealed differences in microbiota composition based upon the distinct physiological stages of the adult insect. Sequence identification revealed two phyla (Proteobacteria and Actinobacteria), 11 families and 15 genera; 87 % of the bacteria were Gram-negative, while only one family and two genera were identified as Gram-positive. The genera Ochrobactrum, Bradyrhizobium and Pseudomonas were found across all of the groups.

Conclusions: The metagenomic analysis revealed that the microbiota of the Lu. intermedia female sand flies are distinct under specific physiological conditions and consist of 15 bacterial genera. The Ochrobactrum, Bradyrhizobium and Pseudomonas were the common genera. Our results detailing the constituents of Lu. intermedia native microbiota contribute to the knowledge regarding the bacterial community in an important sand fly vector and allow for further studies to better understand how the microbiota interacts with vectors of human parasites and to develop tools for biological control.

Citing Articles

Comparative analysis of the microbiota of sand fly vectors of Leishmania major and L. tropica in a mixed focus of cutaneous leishmaniasis in southeast Tunisia; ecotype shapes the bacterial community structure.

Tabbabi A, Mizushima D, Yamamoto D, Zhioua E, Kato H PLoS Negl Trop Dis. 2024; 18(9):e0012458.

PMID: 39236074 PMC: 11407667. DOI: 10.1371/journal.pntd.0012458.


Effects of Leishmania major infection on the gut microbiome of resistant and susceptible mice.

Mrazek J, Mrazkova L, Mekadim C, Jarosikova T, Krayem I, Sohrabi Y Appl Microbiol Biotechnol. 2024; 108(1):145.

PMID: 38240984 PMC: 10799115. DOI: 10.1007/s00253-024-13002-y.


Beyond canonical models: why a broader understanding of Diptera-microbiota interactions is essential for vector-borne disease control.

Arellano A, Sommer A, Coon K Evol Ecol. 2023; 37(1):165-188.

PMID: 37153630 PMC: 10162596. DOI: 10.1007/s10682-022-10197-2.


Molecular detection of Wolbachia and Bartonella as part of the microbiome of phlebotomine sand flies from Chiapas, Mexico.

Lozano-Sardaneta Y, Marina C, Torres-Monzon J, Sanchez-Cordero V, Becker I Parasitol Res. 2023; 122(6):1293-1301.

PMID: 37055642 PMC: 10172221. DOI: 10.1007/s00436-023-07829-z.


Bacteriota and Antibiotic Resistance in Spiders.

Kacaniova M, Terentjeva M, Kowalczewski P, Babosova M, Porhajasova J, Hikal W Insects. 2022; 13(8).

PMID: 36005303 PMC: 9409187. DOI: 10.3390/insects13080680.


References
1.
Peterkova-Koci K, Robles-Murguia M, Ramalho-Ortigao M, Zurek L . Significance of bacteria in oviposition and larval development of the sand fly Lutzomyia longipalpis. Parasit Vectors. 2012; 5:145. PMC: 3414784. DOI: 10.1186/1756-3305-5-145. View

2.
Maleki-Ravasan N, Oshaghi M, Hajikhani S, Saeidi Z, Akhavan A, Gerami-Shoar M . Aerobic Microbial Community of Insectary Population of Phlebotomus papatasi. J Arthropod Borne Dis. 2015; 8(1):69-81. PMC: 4289513. View

3.
Moraes C, Seabra S, Castro D, Brazil R, De Souza W, Garcia E . Leishmania (Leishmania) chagasi interactions with Serratia marcescens: ultrastructural studies, lysis and carbohydrate effects. Exp Parasitol. 2008; 118(4):561-8. DOI: 10.1016/j.exppara.2007.11.015. View

4.
SUDIA W, CHAMBERLAIN R . Battery-operated light trap, an improved model. By W. D. Sudia and R. W. Chamberlain, 1962. J Am Mosq Control Assoc. 1988; 4(4):536-8. View

5.
Dillon R, El Kordy E, Shehata M, Lane R . The prevalence of a microbiota in the digestive tract of Phlebotomus papatasi. Ann Trop Med Parasitol. 1996; 90(6):669-73. DOI: 10.1080/00034983.1996.11813102. View