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Int J Infect Dis. 2017 Apr;57:132-137. doi: 10.1016/j.ijid.2017.01.036. Epub 2017 Feb 3.

Is Leishmania (Viannia) braziliensis parasite load associated with disease pathogenesis?

Author information

1
Laboratório de Pesquisa em Leishmaniose, IOC, FIOCRUZ, Rio de Janeiro, RJ, Brazil. Electronic address: luizaper@ioc.fiocruz.br.
2
Laboratório Interdisciplinar de Pesquisas Médicas, IOC, FIOCRUZ, Rio de Janeiro, RJ, Brazil.
3
Instituto Nacional de Infectologia Evandro Chagas, FIOCRUZ, Rio de Janeiro, RJ, Brazil.

Abstract

BACKGROUND:

Leishmania (Viannia) braziliensis is the main etiological agent of tegumentary leishmaniasis in the Americas. Parasite molecular diversity and host immune status contribute to extensive variations in its clinical presentation within endemic areas of Brazil. Pentavalent antimonials have been used for more than 60 years as the first-line drug for all cases, despite the potential for severe side effects and refractoriness. In Rio de Janeiro, Brazil, most L. (V.) braziliensis infections are benign with a scarcity of parasites, although metastasis and refractory infections can arise. In this scenario, the use of novel molecular tools can be useful for diagnosis and to assess tissue parasitism, and is of benefit to clinical and therapeutic management.

METHODS:

In this study, parasite load was assessed by real-time PCR based on the leishmanial small subunit ribosomal RNA gene.

RESULTS AND CONCLUSION:

The data revealed a tendency to higher tissue parasitism in the skin compared to mucous lesion sites and a reduction with disease progression. Parasite load was lower in poor compared to good responders to antimonials, and was also reduced in recurrent lesions compared to primary ones. However, parasite load became higher with sequential relapses, pointing to an immune system inability to control the infection. Therefore the parasite burden does not seem to be a good predictor of disease progression.

KEYWORDS:

Leishmania (Viannia) braziliensis; Parasitic load; Small subunit ribosomal RNA gene; Therapeutic failure

PMID:
28167253
DOI:
10.1016/j.ijid.2017.01.036
[Indexed for MEDLINE]
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