Amphotericin B induces apoptosis-like programmed cell death in Naegleria fowleri and Naegleria gruberi

• Published in: Microbiology (Society for General Microbiology) Vol. 163; no. 7; pp. 940 - 949
• Main Authors: Cárdenas-Zúñiga, Roberto, Silva-Olivares, Angélica, Villalba-Magdaleno, José D' Artagnan, Sánchez-Monroy, Virginia, Serrano-Luna, Jesús, Shibayama, Mineko
• Format: Journal Article
• Language: English
• Published: England 01.07.2017
• Subjects: Amphotericin B - pharmacology; Antiprotozoal Agents - pharmacology; Apoptosis - drug effects; Central Nervous System Protozoal Infections - parasitology; Naegleria - cytology; Naegleria - drug effects; Naegleria - genetics; Naegleria - growth & development; Naegleria fowleri - cytology; Naegleria fowleri - drug effects; Naegleria fowleri - genetics; Naegleria fowleri - growth & development; Protozoan Proteins - genetics; Protozoan Proteins - metabolism; Reactive Oxygen Species - metabolism; Trophozoites - drug effects; Trophozoites - growth & development
• ISSN: 1350-0872; 1465-2080
• DOI: 10.1099/mic.0.000500

Naegleria fowleri and Naegleria gruberi belong to the free-living amoebae group. It is widely known that the non-pathogenic species N. gruberi is usually employed as a model to describe molecular pathways in this genus, mainly because its genome has been recently described. However, N. fowleri is an aetiological agent of primary amoebic meningoencephalitis, an acute and fatal disease. Currently, the most widely used drug for its treatment is amphotericin B (AmB). It was previously reported that AmB has an amoebicidal effect in both N. fowleri and N. gruberi trophozoites by inducing morphological changes that resemble programmed cell death (PCD). PCD is a mechanism that activates morphological, biochemical and genetic changes. However, PCD has not yet been characterized in the genus Naegleria. The aim of the present work was to evaluate the typical markers to describe PCD in both amoebae. These results showed that treated trophozoites displayed several parameters of apoptosis-like PCD in both species. We observed ultrastructural changes, an increase in reactive oxygen species, phosphatidylserine externalization and a decrease in intracellular potassium, while DNA degradation was evaluated using the TUNEL assay and agarose gels, and all of these parameters are related to PCD. Finally, we analysed the expression of apoptosis-related genes, such as sir2 and atg8, in N. gruberi. Taken together, our results showed that AmB induces the morphological, biochemical and genetic changes of apoptosis-like PCD in the genus Naegleria.