Nanoparticle-mediated magnetic hyperthermia is an effective method for killing the human-infective protozoan parasite Leishmania mexicana in vitro

被引:25
作者
Berry, Sarah L. [1 ]
Walker, Karen [2 ]
Hoskins, Clare [3 ]
Telling, Neil D. [4 ]
Price, Helen P. [1 ]
机构
[1] Keele Univ, Sch Life Sci, Ctr Appl Entomol & Parasitol, Newcastle Under Lyme ST5 5BG, Staffs, England
[2] Keele Univ, Sch Life Sci, Cent Electron Microscope Unit, Newcastle Under Lyme ST5 5BG, Staffs, England
[3] Keele Univ, Sch Pharm, Newcastle Under Lyme ST5 5BG, Staffs, England
[4] Keele Univ, Guy Hilton Res Ctr, Inst Sci & Technol Med, Newcastle Under Lyme ST4 7QB, Staffs, England
基金
英国惠康基金;
关键词
CUTANEOUS LEISHMANIASIS; THERMOTHERAPY;
D O I
10.1038/s41598-018-37670-9
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cutaneous leishmaniasis is a neglected tropical disease characterized by disfiguring skin lesions. Current chemotherapeutic options depend on toxic, expensive drugs that are both difficult to administer and becoming less effective due to increasing levels of resistance. In comparison, thermotherapy displays greater patient compliance and less adverse systemic effects, but there are still significant issues associated with this. The procedure is painful, requiring local anaesthetic, and is less effective against large lesions. Using nanoparticles to controllably generate heat in a localized manner may provide an alternative solution. Here we evaluate magnetic hyperthermia, using iron oxide magnetic nanoparticles, as a localized, heat-based method to kill the human-infective parasite in vitro. We assessed the effectiveness of this method against the differentiated, amastigote form of the parasite using three distinct viability assays: PrestoBlue, Live/Dead stain and a novel luciferase-based assay. Changes in amastigote morphology and ultrastructure were assessed by immunofluorescence, scanning and transmission electron microscopy. Our findings show that magnetic hyperthermia is an effective method to kill host-infective amastigotes, with morphological changes consistent with heat treatment. This method has the potential to be a step-change for research into new therapeutic options that moves away from the expensive chemotherapeutics currently dominating the research climate.
引用
收藏
页数:9
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共 34 条
[1]   Cutaneous Leishmaniasis and Conflict in Syria [J].
Ai-Salem, Waleed S. ;
Pigott, David M. ;
Subramaniam, Krishanthi ;
Haines, Lee Rafuse ;
Kelly-Hope, Louise ;
Molyneux, David H. ;
Hay, Simon I. ;
Acosta-Serrano, Alvaro .
EMERGING INFECTIOUS DISEASES, 2016, 22 (05) :931-933
[2]   Leishmaniasis Worldwide and Global Estimates of Its Incidence [J].
Alvar, Jorge ;
Velez, Ivan D. ;
Bern, Caryn ;
Herrero, Merce ;
Desjeux, Philippe ;
Cano, Jorge ;
Jannin, Jean ;
den Boer, Margriet .
PLOS ONE, 2012, 7 (05)
[3]   Serum Proteins Enhance Dispersion Stability and Influence the Cytotoxicity and Dosimetry of ZnO Nanoparticles in Suspension and Adherent Cancer Cell Models [J].
Anders, Catherine B. ;
Chess, Jordan J. ;
Wingett, Denise G. ;
Punnoose, Alex .
NANOSCALE RESEARCH LETTERS, 2015, 10 :1-22
[4]   Efficacy of Thermotherapy to Treat Cutaneous Leishmaniasis: A Meta-Analysis of Controlled Clinical Trials [J].
Antonio Cardona-Arias, Jaiberth ;
Dario Velez, Ivan ;
Lopez-Carvajal, Liliana .
PLOS ONE, 2015, 10 (05)
[5]   AXENIC CULTIVATION AND CHARACTERIZATION OF LEISHMANIA-MEXICANA AMASTIGOTE-LIKE FORMS [J].
BATES, PA ;
ROBERTSON, CD ;
TETLEY, L ;
COOMBS, GH .
PARASITOLOGY, 1992, 105 :193-202
[6]   Development of NanoLuc-PEST expressing Leishmania mexicana as a new drug discovery tool for axenic-and intramacrophage-based assays [J].
Berry, Sarah L. ;
Hameed, Hamza ;
Thomason, Anna ;
Maciej-Hulme, Marissa L. ;
Abou-Akkada, Somaia Saif ;
Horrocks, Paul ;
Price, Helen P. .
PLOS NEGLECTED TROPICAL DISEASES, 2018, 12 (07)
[7]   Advances in Development of New Treatment for Leishmaniasis [J].
Bezerra de Menezes, Juliana Perrone ;
Sampaio Guedes, Carlos Eduardo ;
de Oliveira Almeida Petersen, Antonio Luis ;
Mothe Fraga, Deborah Bittencourt ;
Tavares Veras, Patricia Sampaio .
BIOMED RESEARCH INTERNATIONAL, 2015, 2015
[8]   Nanoparticle-Based Medicines: A Review of FDA-Approved Materials and Clinical Trials to Date [J].
Bobo, Daniel ;
Robinson, Kye J. ;
Islam, Jiaul ;
Thurecht, Kristofer J. ;
Corrie, Simon R. .
PHARMACEUTICAL RESEARCH, 2016, 33 (10) :2373-2387
[9]   Reevaluation of colorimetric iron determination methods commonly used in geomicrobiology [J].
Braunschweig, Juliane ;
Bosch, Julian ;
Heister, Katja ;
Kuebeck, Christine ;
Meckenstock, Rainer U. .
JOURNAL OF MICROBIOLOGICAL METHODS, 2012, 89 (01) :41-48
[10]   Nanoparticle-mediated hyperthermia in cancer therapy [J].
Chatterjee, Dev Kumar ;
Diagaradjane, Parmeswaran ;
Krishnan, Sunil .
THERAPEUTIC DELIVERY, 2011, 2 (08) :1001-1014