Development of a natural model of cutaneous leishmaniasis:: Powerful effects of vector saliva and saliva preexposure on the long-term outcome of Leishmania major infection in the mouse ear dermis
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作者:
Belkaid, Y
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机构:NIAID, Parasit Dis Lab, NIH, Bethesda, MD 20892 USA
Belkaid, Y
Kamhawi, S
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机构:NIAID, Parasit Dis Lab, NIH, Bethesda, MD 20892 USA
Kamhawi, S
Modi, G
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机构:NIAID, Parasit Dis Lab, NIH, Bethesda, MD 20892 USA
Modi, G
Valenzuela, J
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机构:NIAID, Parasit Dis Lab, NIH, Bethesda, MD 20892 USA
Valenzuela, J
Noben-Trauth, N
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机构:NIAID, Parasit Dis Lab, NIH, Bethesda, MD 20892 USA
Noben-Trauth, N
Rowton, E
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机构:NIAID, Parasit Dis Lab, NIH, Bethesda, MD 20892 USA
Rowton, E
Ribeiro, J
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机构:NIAID, Parasit Dis Lab, NIH, Bethesda, MD 20892 USA
Ribeiro, J
Sacks, DL
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机构:NIAID, Parasit Dis Lab, NIH, Bethesda, MD 20892 USA
Sacks, DL
机构:
[1] NIAID, Parasit Dis Lab, NIH, Bethesda, MD 20892 USA
[2] NIAID, Immunol Lab, NIH, Bethesda, MD 20892 USA
[3] Walter Reed Army Med Ctr, Walter Reed Army Inst Res, Dept Entomol, Washington, DC 20307 USA
We have developed a model of cutaneous leishmaniasis due to Leishmania major that seeks to mimic the natural conditions of infection. 1,000 metacyclic promastigotes were coinoculated with a salivary gland sonicate (SGS) obtained from a natural vector, Phlebotomus payatasii, into the ear dermis of naive mice or of mice preexposed to SGS. The studies reveal a dramatic exacerbating effect of SGS on lesion development in the dermal site, and a complete abrogation of this effect in mice preexposed to salivary components. In both BALB/c and C57B1/6 (B/6) mice, the dermal lesions appeared earlier, were more destructive, and contained greater numbers of parasites after infection ill the presence of SGS. Furthermore, coinoculation of SGS converted B/6 mice into a nonhealing phenotype. No effect of SGS was seen in either IL-4-deficient or in SCID mice. Disease exacerbation in both BALB/c and B/6 mice was associated with an early (6 h) increase in the frequency of epidermal cells producing type 2 cytokines. SGS did not elicit type 2 cytokines in the epidermis of mice previously injected with SGS. These mice made antisaliva antibodies that were able to neutralize the ability of SGS to enhance infection and to elicit IL-4 and IL-5 responses in the epidermis. These results are the first to suggest that for individuals at risk of vector-borne infections, history of exposure to vector saliva, might influence the outcome of exposure to transmitted parasites.