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Validation of a simple resazurin-based promastigote assay for the routine monitoring of miltefosine susceptibility in clinical isolates of Leishmania donovani
Authors:Arpita Kulshrestha  Vasundhra Bhandari  Rupkatha Mukhopadhyay  V Ramesh  Shyam Sundar  Louis Maes  Jean Claude Dujardin  Syamal Roy  Poonam Salotra
Institution:1. National Institute of Pathology, Indian Council of Medical Research, Safdarjung Hospital Campus, New Delhi, 110029, India
2. Division of Infectious Diseases and Immunology, Indian Institute of Chemical Biology, CSIR, Kolkata, India
3. Department of Dermatology, Safdarjung Hospital, New Delhi, India
4. Institute of Medical Sciences, Banaras Hindu University, Varanasi, India
5. Lab. of Microbiology, Parasitology and Hygiene (LMPH), University of Antwerp, Antwerp, Belgium
6. Unit of Molecular Parasitology, Department of Parasitology, Institute of Tropical Medicine, Antwerp, Belgium
Abstract:Simple, cost-effective approach for routine surveillance of parasite susceptibility to antileishmanial drug miltefosine (MIL) is highly desirable for controlling emergence of drug resistance in visceral leishmaniasis (VL). We validated a simple resazurin-based fluorimetric assay using promastigotes to track natural MIL tolerance in Leishmania donovani parasites from VL cases (n?=?17) against standard amastigote assay, in two different labs in India. The inter-stage MIL susceptibility correlated strongly (r?=?0.70, p?=?0.0018) using J774.A.1 macrophage cell line-based amastigote assay and fluorescence-based resazurin assay for promastigotes. Investigation of inter-stage MIL susceptibility for the same set of clinical isolates in another lab also showed a strong correlation (r?=?0.72, p?=?0.0012) using mouse peritoneal macrophages for amastigote assay and resazurin-based alamar blue assay for promastigotes. Additionally, parasites from post-kala-azar dermal leishmaniasis (PKDL) lesions (n?=?7, r?=?0.78, p?=?0.046) and MIL-induced parasites (r?=?0.92, p?=?0.0001; n?=?3) also exhibited a strongly correlated inter-stage miltefosine susceptibility. Thus, our results support the utility of resazurin assay as a simplified biological tool for MIL susceptibility monitoring in clinical isolates from MIL-treated VL/PKDL patients.
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