Single-Step Multiplex PCR Assay for Characterization of New World Leishmania Complexes

Одностадийный мультиплексный ПЦР-анализ для характеристики комплексов Leishmania Нового Света
Eva Harris, Gerald Kropp, Alejandro Belli, Betzabé Mara Rodríguez, Nina Agabian
1998-07-01

New World Leishmania complexesSingle-step multiplex PCR assaydifferentiation of L. braziliensis L. mexicana L. donovanisensitivity 1 fg–10 pg DNA (0.01–100 parasites)spliced leader RNA (mini-exon) gene repeats
We have developed a PCR assay for one-step differentiation of the three complexes of New World Leishmania (Leishmania braziliensis, Leishmania mexicana, and Leishmania donovani). This multiplex assay is targeted to the spliced leader RNA (mini-exon) gene repeats of these organisms and can detect all three complexes simultaneously, generating differently sized products for each complex. The assay is specific to the Leishmania genus and does not recognize related kinetoplastid protozoa, such as Trypanosoma cruzi, Trypanosoma brucei, and Crithidia fasciculata. It correctly identified Leishmania species with a broad geographic distribution in Central and South America. The sensitivity of the PCR amplification ranged from 1 fg to 10 pg of DNA (0.01 to 100 parasites), depending on the complex detected. Crude extracts of cultured parasites, prepared simply by boiling diluted cultures, served as excellent templates for amplification. Crude preparations of clinical material were also tested. The assay detected L. braziliensis in dermal scrapings from cutaneous leishmanial lesions, Leishmania chagasi in dermal scrapings of atypical cutaneous leishmaniasis, and L. mexicana from lesion aspirates from infected hamsters. We have minimized the material requirements and maximized the simplicity, rapidity, and informative content of this assay to render it suitable for use in laboratories in countries where leishmaniasis is endemic. This assay should be useful for rapid in-country identification of Leishmania parasites, particularly where different Leishmania complexes are found in the same geographical area.
1
Assay design minimizes material requirements and maximizes simplicity and speed, making it suitable for use in leishmaniasis-endemic country laboratories
2
Assay is specific to Leishmania genus and does not amplify related kinetoplastids (Trypanosoma cruzi, Trypanosoma brucei, Crithidia fasciculata)
3
Assay targets spliced leader RNA (mini-exon) gene repeats and produces differently sized products for each complex enabling simultaneous detection
4
Crude boiled extracts of cultured parasites and crude clinical material served as effective PCR templates, enabling simple sample preparation
5
Developed a single-step multiplex PCR that differentiates three New World Leishmania complexes (L. braziliensis, L. mexicana, L. donovani) in one reaction
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Sensitivity ranged from 1 fg to 10 pg of DNA (equivalent to 0.01 to 100 parasites), varying by complex
7
Successfully identified Leishmania species from broad Central and South American distributions, including detection of L. braziliensis, L. chagasi, and L. mexicana from clinical/experimental samples

Single-step multiplex PCR assay for differentiation of New World Leishmania complexes

Ability of the assay to specifically detect and differentiate the three New World Leishmania complexes (L. braziliensis, L. mexicana, L. donovani) via mini-exon (spliced leader RNA) repeats, including sensitivity (1 fg–10 pg DNA), specificity against related kinetoplastids, performance on crude culture and clinical extracts, and field applicability for rapid in-country identification

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1998-07-01
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Authors
Eva Harris
Gerald Kropp
Alejandro Belli
Betzabé Mara Rodríguez
Nina Agabian
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