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A mouse model of Leishmania braziliensis braziliensis infection produced by coinjection with sand fly saliva
To development a reliable murine model of Leishmania braziliensis braziliensis infection, parasites were injected into BALB/c mice in the presence of phlebotomine sand fly salivary gland lysates, which have previously been shown to greatly increase the infectivity of L. major in mice. When injected...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1991
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2118755/ https://www.ncbi.nlm.nih.gov/pubmed/1985126 |
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collection | PubMed |
description | To development a reliable murine model of Leishmania braziliensis braziliensis infection, parasites were injected into BALB/c mice in the presence of phlebotomine sand fly salivary gland lysates, which have previously been shown to greatly increase the infectivity of L. major in mice. When injected with salivary gland lysates, L. braziliensis braziliensis produced progressively enlarging cutaneous nodules, containing many macrophages filled with Leishmania amastigotes. In contrast, L. braziliensis injected without gland extracts produced small and rapidly regressing lesions. Isoenzyme analysis, monoclonal antibodies, and the polymerase chain reaction with L. braziliensis- specific oligonucleotide primers and probes confirmed that parasites causing the lesions were L. braziliensis. |
format | Text |
id | pubmed-2118755 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1991 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21187552008-04-17 A mouse model of Leishmania braziliensis braziliensis infection produced by coinjection with sand fly saliva J Exp Med Articles To development a reliable murine model of Leishmania braziliensis braziliensis infection, parasites were injected into BALB/c mice in the presence of phlebotomine sand fly salivary gland lysates, which have previously been shown to greatly increase the infectivity of L. major in mice. When injected with salivary gland lysates, L. braziliensis braziliensis produced progressively enlarging cutaneous nodules, containing many macrophages filled with Leishmania amastigotes. In contrast, L. braziliensis injected without gland extracts produced small and rapidly regressing lesions. Isoenzyme analysis, monoclonal antibodies, and the polymerase chain reaction with L. braziliensis- specific oligonucleotide primers and probes confirmed that parasites causing the lesions were L. braziliensis. The Rockefeller University Press 1991-01-01 /pmc/articles/PMC2118755/ /pubmed/1985126 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Articles A mouse model of Leishmania braziliensis braziliensis infection produced by coinjection with sand fly saliva |
title | A mouse model of Leishmania braziliensis braziliensis infection produced by coinjection with sand fly saliva |
title_full | A mouse model of Leishmania braziliensis braziliensis infection produced by coinjection with sand fly saliva |
title_fullStr | A mouse model of Leishmania braziliensis braziliensis infection produced by coinjection with sand fly saliva |
title_full_unstemmed | A mouse model of Leishmania braziliensis braziliensis infection produced by coinjection with sand fly saliva |
title_short | A mouse model of Leishmania braziliensis braziliensis infection produced by coinjection with sand fly saliva |
title_sort | mouse model of leishmania braziliensis braziliensis infection produced by coinjection with sand fly saliva |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2118755/ https://www.ncbi.nlm.nih.gov/pubmed/1985126 |