Apoptosis like symptoms associated with abortive infection of Mycobacterium smegmatis by mycobacteriophage D29
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Published on: August 3, 2017
Fatema Calcuttawala1, Rahul Shaw2, Arpita Sarbajna3
1Department of Microbiology, Sister Nivedita University, Kolkata, India.
Abstract:
Mycobacteriophages are phages that infect mycobacteria resulting in their killing. Although lysis is the primary mechanism by which mycobacteriophages cause cell death, others such as abortive infection may also be involved. We took recourse to perform immunofluorescence and electron microscopic studies using mycobacteriophage D29 infected Mycobacterium smegmatis cells to investigate this issue. We could observe the intricate details of the infection process using these techniques such as adsorption, the phage tail penetrating the thick mycolic acid layer, formation of membrane pores, membrane blebbing, and phage release. We observed a significant increase in DNA fragmentation and membrane depolarization using cell-biological techniques symptomatic of programmed cell death (PCD). As Toxin-Antitoxin (TA) systems mediate bacterial PCD, we measured their expression profiles with and without phage infection. Of the three TAs examined, MazEF, VapBC, and phd/doc, we found that in the case of VapBC, a significant decrease in the antitoxin (VapB): toxin (VapC) ratio was observed following phage infection, implying that high VapC may have a role to play in the induction of mycobacterial apoptotic cell death following phage infection. This study indicates that D29 infection causes mycobacteria to undergo morphological and molecular changes that are hallmarks of apoptotic cell death.
Insights
Mycobacteriophage D29 infection triggers programmed cell death in Mycobacterium smegmatis. This involves DNA fragmentation, membrane depolarization, and altered toxin-antitoxin systems, indicating apoptotic cell death.
Area of Science:
- Bacteriology
- Virology
- Molecular Biology
Background:
- Mycobacteriophages kill mycobacteria, primarily through lysis.
- Other cell death mechanisms, like abortive infection, may also occur.
- Understanding these mechanisms is crucial for phage therapy.
Purpose of the Study:
- To investigate the cell death mechanisms induced by mycobacteriophage D29 infection in Mycobacterium smegmatis.
- To examine the role of toxin-antitoxin systems in phage-induced cell death.
Main Methods:
- Immunofluorescence and electron microscopy to visualize infection processes.
- Cell-biological assays to detect DNA fragmentation and membrane depolarization.
- Analysis of toxin-antitoxin (TA) system expression profiles.
Main Results:
- Observed detailed infection events: adsorption, mycolic acid layer penetration, pore formation, blebbing, and phage release.
- Detected significant DNA fragmentation and membrane depolarization, indicative of programmed cell death (PCD).
- Found a decreased VapB:VapC ratio in the VapBC toxin-antitoxin system after phage infection.
Conclusions:
- Mycobacteriophage D29 infection induces morphological and molecular changes in mycobacteria consistent with apoptotic cell death.
- The VapBC toxin-antitoxin system, specifically increased VapC levels, may play a role in this induced cell death.
- This study highlights complex cell death pathways beyond lysis in mycobacteriophage infections.
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