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Dermotropic Leishmania donovani in Sri Lanka: visceralizing potential in clinical and preclinical studies

The visceralizing potential of apparently dermotropic Leishmania donovani in Sri Lanka (L. donovani-SL) was investigated through long-term follow-up of cutaneous leishmaniasis (CL) patients and in vivo and in vitro experimental infection models. CL patients (n = 250) treated effectively with intra-l...

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Autores principales: KARIYAWASAM, K. K. G. D. U. L., SELVAPANDIYAN, A., SIRIWARDANA, H. V. Y. D., DUBE, A., KARUNANAYAKE, P., SENANAYAKE, S. A. S. C., DEY, R., GANNAVARAM, S., NAKHASI, H. L., KARUNAWEERA, N. D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5989320/
https://www.ncbi.nlm.nih.gov/pubmed/29113609
http://dx.doi.org/10.1017/S003118201700169X
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author KARIYAWASAM, K. K. G. D. U. L.
SELVAPANDIYAN, A.
SIRIWARDANA, H. V. Y. D.
DUBE, A.
KARUNANAYAKE, P.
SENANAYAKE, S. A. S. C.
DEY, R.
GANNAVARAM, S.
NAKHASI, H. L.
KARUNAWEERA, N. D.
author_facet KARIYAWASAM, K. K. G. D. U. L.
SELVAPANDIYAN, A.
SIRIWARDANA, H. V. Y. D.
DUBE, A.
KARUNANAYAKE, P.
SENANAYAKE, S. A. S. C.
DEY, R.
GANNAVARAM, S.
NAKHASI, H. L.
KARUNAWEERA, N. D.
author_sort KARIYAWASAM, K. K. G. D. U. L.
collection PubMed
description The visceralizing potential of apparently dermotropic Leishmania donovani in Sri Lanka (L. donovani-SL) was investigated through long-term follow-up of cutaneous leishmaniasis (CL) patients and in vivo and in vitro experimental infection models. CL patients (n = 250) treated effectively with intra-lesional antimony therapy were followed-up six monthly for 4 years. There was no clinical evidence of visceralization of infection (VL) during this period. Infection of BALB/c mice with L. donovani-SL (test) through intra-dermal route led to the development of cutaneous lesions at the site of inoculation with no signs of systemic dissemination, in contrast to the observations made in animals similarly infected with a visceralizing strain of L. donovani-1S (control). Cytokine (IL-10, IFN-γ) release patterns of splenocytes and lymph node cell cultures derived from mice primed with experimental infections (with either test or control parasites) revealed significantly high IFN-γ response associated with test mice with CL, while prominent IL-10 levels were observed in association with control mice with VL. Furthermore, diminished infection efficiency, intracellular growth and survival of L. donovani-SL parasites compared with L. donovani-1S were evident through in vitro macrophage infection experiments. These studies confirm, for the first time, the essential dermotropic nature of L. donovani-SL suggesting natural attenuation of virulence of local parasite strains.
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spelling pubmed-59893202018-06-07 Dermotropic Leishmania donovani in Sri Lanka: visceralizing potential in clinical and preclinical studies KARIYAWASAM, K. K. G. D. U. L. SELVAPANDIYAN, A. SIRIWARDANA, H. V. Y. D. DUBE, A. KARUNANAYAKE, P. SENANAYAKE, S. A. S. C. DEY, R. GANNAVARAM, S. NAKHASI, H. L. KARUNAWEERA, N. D. Parasitology Special Issue Article The visceralizing potential of apparently dermotropic Leishmania donovani in Sri Lanka (L. donovani-SL) was investigated through long-term follow-up of cutaneous leishmaniasis (CL) patients and in vivo and in vitro experimental infection models. CL patients (n = 250) treated effectively with intra-lesional antimony therapy were followed-up six monthly for 4 years. There was no clinical evidence of visceralization of infection (VL) during this period. Infection of BALB/c mice with L. donovani-SL (test) through intra-dermal route led to the development of cutaneous lesions at the site of inoculation with no signs of systemic dissemination, in contrast to the observations made in animals similarly infected with a visceralizing strain of L. donovani-1S (control). Cytokine (IL-10, IFN-γ) release patterns of splenocytes and lymph node cell cultures derived from mice primed with experimental infections (with either test or control parasites) revealed significantly high IFN-γ response associated with test mice with CL, while prominent IL-10 levels were observed in association with control mice with VL. Furthermore, diminished infection efficiency, intracellular growth and survival of L. donovani-SL parasites compared with L. donovani-1S were evident through in vitro macrophage infection experiments. These studies confirm, for the first time, the essential dermotropic nature of L. donovani-SL suggesting natural attenuation of virulence of local parasite strains. Cambridge University Press 2018-04 2017-11-08 /pmc/articles/PMC5989320/ /pubmed/29113609 http://dx.doi.org/10.1017/S003118201700169X Text en © Cambridge University Press 2017 http://creativecommons.org/licenses/by/4.0/ This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Special Issue Article
KARIYAWASAM, K. K. G. D. U. L.
SELVAPANDIYAN, A.
SIRIWARDANA, H. V. Y. D.
DUBE, A.
KARUNANAYAKE, P.
SENANAYAKE, S. A. S. C.
DEY, R.
GANNAVARAM, S.
NAKHASI, H. L.
KARUNAWEERA, N. D.
Dermotropic Leishmania donovani in Sri Lanka: visceralizing potential in clinical and preclinical studies
title Dermotropic Leishmania donovani in Sri Lanka: visceralizing potential in clinical and preclinical studies
title_full Dermotropic Leishmania donovani in Sri Lanka: visceralizing potential in clinical and preclinical studies
title_fullStr Dermotropic Leishmania donovani in Sri Lanka: visceralizing potential in clinical and preclinical studies
title_full_unstemmed Dermotropic Leishmania donovani in Sri Lanka: visceralizing potential in clinical and preclinical studies
title_short Dermotropic Leishmania donovani in Sri Lanka: visceralizing potential in clinical and preclinical studies
title_sort dermotropic leishmania donovani in sri lanka: visceralizing potential in clinical and preclinical studies
topic Special Issue Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5989320/
https://www.ncbi.nlm.nih.gov/pubmed/29113609
http://dx.doi.org/10.1017/S003118201700169X
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