Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2024 Sep 11;17(1):385.
doi: 10.1186/s13071-024-06444-w.

A study on the diversity of phlebotomine sand flies (Diptera, Psychodidae) in karstic limestone areas in Vientiane Province, Laos, with a description of two new species of Sergentomyia França and & Parrot

Affiliations

A study on the diversity of phlebotomine sand flies (Diptera, Psychodidae) in karstic limestone areas in Vientiane Province, Laos, with a description of two new species of Sergentomyia França and & Parrot

Khamsing Vongphayloth et al. Parasit Vectors. .

Abstract

Background: Southeast Asia is well known as a hotspot of biodiversity. However, very little is known about cave-dwelling hematophagous insects that are medically important. Taxonomic knowledge and ecology of phlebotomine sand flies are very poorly studied in Laos, as well as in other countries in the region. Herein, we report species diversity data and some notes on the ecology of the detected species from these karstic limestone areas of Laos.

Methods: Phlebotomine sand flies were collected using Centers for Disease Control and Prevention (CDC) light traps from limestone cave locations in three districts of Vientiane Province, Laos. Both morphological and molecular techniques were used for sand fly identification. Species diversity and abundance were analyzed according to sites, locations, collection seasons, and trapping positions.

Results: A total of 6564 sand flies, of which 5038 were females and 1526 were males, were morphologically identified into 20 species belonging to five genera (Chinius, Idiophlebotomus, Phlebotomus, Sergentomyia, and Grassomyia). The most abundant species were Chinius eunicegalatiae, Phlebotomus stantoni, Sergentomyia hivernus, Se. siamensis, and Idiophlebotomus longiforceps. Cytochrome b analysis results supported the morphological identification and revealed that Se. siamensis was separated from other members of the Se. barraudi group. Two new species, Se. dvoraki n. sp. and Se. marolii n. sp., were described. Sand fly density was generally high except in a cave in Vangvieng, with species richness ranging from 14 to 18 across different caves. Outside caves had higher species richness (R = 20) and diversity (H = 2.50) than cave entrances (R = 18, H = 2.41) and interiors (R = 16, H = 2.13). Seasonal variations showed high sand fly density in Feung and Hinheup during both dry and rainy seasons, while Vangvieng had a notable decrease in density during the dry season (D = 6.29).

Conclusions: This study revealed that the diversity of phlebotomine sand fly fauna in Laos, particularly in karstic limestone areas, is greater than previously known. However, the taxonomic status of many species in Laos, as well as Southeast Asia, still needs more in-depth study using both morphological characters and molecular methods. Many species could be found from inside, at the entrance, and outside of caves, indicating a wide range of host-seeking behavior or possible natural breeding in the karstic cave areas.

Keywords: Chinius; Grassomyia; Idiophlebotomus; Phlebotomus; Sergentomyia; Ecology; Lao PDR.

PubMed Disclaimer

Conflict of interest statement

The authors declare that they have no competing interests.

Figures

Fig. 1
Fig. 1
Study sites and sand fly species composition from karstic limestones in three districts of Vientiane Province. Red dots represent sampling locations
Fig. 2
Fig. 2
Female morphological characteristics of Se. siamensis, Se. brevicaulis-like, and Se. rudnicki found in this study. Sergentomyia siamensis: head with short flagellomere 1 (A), cibarium with about 54 teeth (D), pharyngeal teeth long (G), smooth and ovoid spermathecae (J); Se. brevicaulis-like teeth: head with long flagellomere 1 (B), cibarium with about 50 comb-like teeth (E), pharyngeal teeth long (H), oblong and wrinkled spermathecae (K); and Se. rudnicki: head with long flagellomere 1 (C), cibarium with about 80 comb-like teeth (F), pharyngeal teeth long (I), and oblong and wrinkled spermathecae (L)
Fig. 3
Fig. 3
Female morphological characteristics of Sergentomyia. Sergentomyia khawi: cibarium with three rows of vertical teeth (A), smooth spermathecae and wide individual duct (D); Se. hivenus: cibarium (B) and tubular spermathecae (E); Se. dvoraki n. sp.: cibarium of paratype (C), spermathecae with long and narrow individual ducts (F); Se. gemmea (holotype): red arrow points to the spur of the ascoid (I); Se. phasukae: cibarial teeth, no pigment patch (G), spermathecae (J); and Se. sylvatica: cibarium teeth (H), and spermathecae (K)
Fig. 4
Fig. 4
Sergentomyia perturbans: cibarium (A), pharynx unarmed (D), and mesofurca strongly pigmented (F); and Se. marolii n. sp.: cibarium (B), pharynx armed with teeth (E), and mesofurca strongly pigmented (C)
Fig. 5
Fig. 5
Maximum likelihood tree constructed from cytochrome b gene using the Tamura–Nei model
Fig. 6
Fig. 6
Sergentomyia dvoraki n. sp. female. A Head (paratype LAOS#251-2); B flagellomeres 1, 2, and 3 (= AIII, AIV, and AV) (paratype LAOS#251-2); C pharynx and cibarium (holotype LAOS#251-3); D palp (paratype LAOS#251-2); E third segment of the palp (P3) (paratype LAOS#251-2); F mouth parts (labrum, hypopharynx, mandible, maxilla [paratype LAOS#251-2], and labial furca [paratype LAOS#251-2] from left to right); G wing (holotype LAOS#251-3); H furca and spermathecae (holotype LAOS#251-3)
Fig. 7
Fig. 7
Sergentomyia marolii n. sp. female. A Head (paratype S-1610-2); B pharynx and cibarium (holotype S-2553-4); C mouth parts (labrum, hypopharynx, mandible, maxilla, and labial furca from left to right) (paratype S-1610-2); D flagellomeres 1, 2, and 3 (= AIII, AIV, and AV) (holotype S-2553-4); E third segment of the palp (P3) (holotype S-2553-4); F palp (paratype S-1610-2); G wing (holotype S-2553-4); and H furca and spermathecae (paratype)

References

    1. Jones KE, Patel NG, Levy MA, Storeygard A, Balk D, Gittleman JL, et al. Global trends in emerging infectious diseases. Nature. 2008;451:990–3. - PMC - PubMed
    1. Chan JF, Choi GK, Yip CC, Cheng VC, Yuen KY. Zika fever and congenital Zika syndrome: an unexpected emerging arboviral disease. J Infect. 2016;72:507–24. - PMC - PubMed
    1. Gratz NG. Emerging and resurging vector-borne diseases. Annu Rev Entomol. 1999;44:51–75. - PubMed
    1. Vasconcelos PF, Calisher CH. Emergence of human arboviral diseases in the Americas, 2000–2016. Vector Borne Zoonotic Dis. 2016;16:295–301. - PubMed
    1. Harrus S, Baneth G. Drivers for the emergence and re-emergence of vector-borne protozoal and bacterial diseases. Int J Parasitol. 2005;35:1309–18. - PubMed

Substances

LinkOut - more resources