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. 2008 Jul 22;105(29):10125-30.
doi: 10.1073/pnas.0802331105. Epub 2008 Jul 14.

Quantification of the infectious dose of Leishmania major transmitted to the skin by single sand flies

Affiliations

Quantification of the infectious dose of Leishmania major transmitted to the skin by single sand flies

Nicola Kimblin et al. Proc Natl Acad Sci U S A. .

Abstract

Leishmaniasis is transmitted between mammalian hosts by the bites of bloodsucking vector sand flies. The dose of parasites transmitted to the mammalian host has never been directly determined. We developed a real-time PCR-based method to determine the number of Leishmania major parasites inoculated into the ears of living mice during feeding by individual infected flies (Phlebotomus duboscqi). The number of parasites transmitted varied over a wide range in the 58 ears in which Leishmania were detected and demonstrated a clear bimodal distribution. Most of the infected mice were inoculated with a low dose of <600 parasites. One in four received a higher dose of >1,000 and up to 100,000 cells. High-dose transmission was associated with a heavy midgut infection of >30,000 parasites, incomplete blood feeding, and transmission of a high percentage of the parasite load in the fly. To test the impact of inoculum size on infection outcome, we compared representative high- (5,000) and low- (100) dose intradermal needle infections in the ears of C57BL/6 mice. To mimic natural transmission, we used sand fly-derived metacyclic forms of L. major and preexposed the injection site to the bites of uninfected flies. Large lesions developed rapidly in the ears of mice receiving the high-dose inoculum. The low dose resulted in only minor pathology but a higher parasite titer in the chronic phase, and it established the host as an efficient long-term reservoir of infection back to vector sand flies.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Fig. 1.
Fig. 1.
Summary of transmitted dose and midgut infection intensity of transmitting flies. (A) Pooled data showing the number of L. major parasites, determined by real-time PCR, that were transmitted to BALB/c mice by individual infected P. duboscqi sand flies allowed access to a section of mouse ear for up to 3 h. (B) Pooled data showing the relationship between the number of L. major parasites in the gut of P. duboscqi sand flies and the infectious dose transmitted by those flies. Two-dimensional Gaussian mixture cluster analysis detects two clusters, identified by different symbols, and plotted together with mean and associated ellipse, representing a two-dimensional analog of the standard deviation. There was a strong correlation between prefeeding parasite load and the dose of transmitted parasites among the 14 flies in the high prefeed, high-dose cluster (Spearman's correlation, 0.754; P = 0.0027; 95% C.I., 0.435–1).
Fig. 2.
Fig. 2.
Transmitted dose as a function of midgut infection intensity. Pooled data showing the relationship between the prefeeding parasite load in the gut and the percentage of the load delivered. Squares, low-dose transmitters; triangles, high-dose transmitters.
Fig. 3.
Fig. 3.
Relationship among parasite load, blood meal engorgement, and the infectious dose transmitted to the mammalian host. (A) Pooled data showing the parasite load in sand flies that took different sizes of blood meals. Flies with greater parasite loads took smaller, partial meals: Jonckheere–Terpstra test, P = 0.0002. (B) Pooled data showing the infectious dose transmitted by sand flies that took different sizes of blood meals. Flies that took smaller blood meals tended to transmit a larger infectious dose: Jonckheere–Terpstra test, P = 0.019.
Fig. 4.
Fig. 4.
Cutaneous leishmaniasis in C57BL/6 mice after infection with high- and low-dose inocula and the transmissibility of parasites in chronic lesions back to vector sand flies. (A) Ear lesion diameters after intradermal injection by needle of sand fly-derived metacyclics into mouse ears preexposed to the bites of uninfected sand flies. Shown are means ± 1 SD, 8–22 ears, 4–11 mice per group; *, P < 0.01 comparing high- and low-dose groups at the same time point. (B) Parasite load in individual ears from mice shown in A during acute and chronic stages of infection, as estimated by limiting-dilution analysis of ear tissue. Bars represent geometric means; *, P < 0.0001 comparing high- (triangles) and low- (squares) dose groups at the same time point. (C) Independent experiment, showing the percentage of blood-fed flies positive for L. major after feeding on ear lesions in C57BL/6 mice at day 151 after challenge with 5,000 or 100 sand fly-derived metacyclics plus uninfected sand fly bites. Percentage positive flies was calculated from 9 or 10 blood-fed flies per ear. No significant difference was observed in the probability of flies becoming infected after exposure to the two groups of mice (P = 0.579).

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