Mira Milisavljevic
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Mira Milisavljevic has a total of 5 co-authors. Here are the top co-authors by number of shared publications:
- Milorad Kojic
Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Vojvode Stepe 444a, Belgrade, 11042 Belgrade 152, Republic of Serbia.
2 shared publications - Natalija Azanjac
Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Belgrade, Republic of Serbia
2 shared publications - Snezana Kojic
Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Belgrade, Serbia
2 shared publications - Stefan Stanovčić
Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, 11042 Belgrade, Serbia
2 shared publications Milorad Kojic
University of Belgrade
1 shared publication
Latest Publications
- 2 September 2026
- Published by Springer Nature
- p. 227-232
Determination of Spontaneous Mutation Rate by Fluctuation Analysis Using 5-Fluoroorotic Acid (5-FOA)
- 2 September 2026
- Published by Springer Nature
- p. 227-232
Determination of Spontaneous Mutation Rate by Fluctuation Analysis Using 5-Fluoroorotic Acid (5-FOA)
- Open Access
- 5 March 2026
- Published by Springer Nature in Microbial Ecology
- Vol. 89 (1)
Biomolecules Generated During Programmed Cell Death (PCD) Enhance the Capacity of Proliferating Ustilago maydis Cells to Overcome the Negative Impacts of Non-PCD Necromass
This work builds upon our previous “repopulation upon shattering” (RUS) studies in the yeast-like microbe Ustilago maydis, focusing mainly on a deeper understanding of the suicidal type of death caused by self-generated hypoxia (SGH). The key findings are: (1) the massive loss of viability induced by SGH occurs via programmed cell death (PCD), (2) the PCD-released materials are more beneficial for the surviving cells than the nutrients liberated from cells that die through necrotic processes, (3) products of PCD can stimulate growth even in the presence of growth-suppressive necromass, (4) the beneficial effects of substances released through PCD extend to two other species within the family Ustilaginaceae, and (5) U. maydis exhibited a remarkable ability to withstand the negative effects of non-PCD necromass. The third and fifth points are of special note. The third indicates that PCD-derived materials are essential for critical initial regrowth in post-stress environments where there is a high presence of non-PCD necromass. As the revitalized population strengthens, it would correspondingly enhance the communal ability to exploit more challenging nutrients. The robust resilience of U. maydis survivors against non-PCD necromass could represent an important fitness determinant, mediating competitive success in mixed microbial communities where non-PCD necromass imposes selective pressure. Thus, while providing valuable insights, the study also underscores the need for further research, especially in understanding the molecular underpinnings of the RUS phenomenon.
- 5 March 2026
- Published by Springer Nature in Microbial Ecology
- Vol. 89 (1)
Open AccessBiomolecules Generated During Programmed Cell Death (PCD) Enhance the Capacity of Proliferating Ustilago maydis Cells to Overcome the Negative Impacts of Non-PCD Necromass
This work builds upon our previous “repopulation upon shattering” (RUS) studies in the yeast-like microbe Ustilago maydis, focusing mainly on a deeper understanding of the suicidal type of death caused by self-generated hypoxia (SGH). The key findings are: (1) the massive loss of viability induced by SGH occurs via programmed cell death (PCD), (2) the PCD-released materials are more beneficial for the surviving cells than the nutrients liberated from cells that die through necrotic processes, (3) products of PCD can stimulate growth even in the presence of growth-suppressive necromass, (4) the beneficial effects of substances released through PCD extend to two other species within the family Ustilaginaceae, and (5) U. maydis exhibited a remarkable ability to withstand the negative effects of non-PCD necromass. The third and fifth points are of special note. The third indicates that PCD-derived materials are essential for critical initial regrowth in post-stress environments where there is a high presence of non-PCD necromass. As the revitalized population strengthens, it would correspondingly enhance the communal ability to exploit more challenging nutrients. The robust resilience of U. maydis survivors against non-PCD necromass could represent an important fitness determinant, mediating competitive success in mixed microbial communities where non-PCD necromass imposes selective pressure. Thus, while providing valuable insights, the study also underscores the need for further research, especially in understanding the molecular underpinnings of the RUS phenomenon.
- Open Access
- 14 August 2025
- Published by MDPI AG in Preprints.org
Biomolecules Generated During Programmed Cell Death (PCD) Improve the Capacity of Proliferating Ustilago maydis Cells to Overcome the Negative Impacts of Non-PCD Necromass
This work builds upon our previous “repopulation upon shattering” (RUS) studies in the yeast-like microbe Ustilago maydis, focusing mainly on a deeper understanding of the suicidal type of death caused by self-generated hypoxia (SGH). The key findings are: 1) the massive loss of viability induced by SGH occurs via programmed cell death (PCD), 2) the PCD-released materials are more beneficial for the surviving cells than the nutrients liberated from cells that die through necrotic processes, 3) products of PCD can stimulate growth even in the presence of growth-suppressive necromass, and 4) the beneficial effects of substances released through PCD extend to two other species within the family Ustilaginaceae. Additionally, U. maydis exhibited a remarkable ability to withstand the negative effects of non-PCD necromass. These results suggest PCD-released materials are essential for critical initial regrowth in post-stress environments where there is a high presence of non-PCD necromass. As the revitalized population strengthens, it would correspondingly enhance the communal ability to exploit more challenging nutrients. Alongside with the robust resilience of U. maydis survivors against non-PCD necromass, the PCD mode of dying may improve the fitness of this microorganism in harsh and fluctuating environments, warranting further investigation.
- 14 August 2025
- Published by MDPI AG in Preprints.org
Open AccessBiomolecules Generated During Programmed Cell Death (PCD) Improve the Capacity of Proliferating Ustilago maydis Cells to Overcome the Negative Impacts of Non-PCD Necromass
This work builds upon our previous “repopulation upon shattering” (RUS) studies in the yeast-like microbe Ustilago maydis, focusing mainly on a deeper understanding of the suicidal type of death caused by self-generated hypoxia (SGH). The key findings are: 1) the massive loss of viability induced by SGH occurs via programmed cell death (PCD), 2) the PCD-released materials are more beneficial for the surviving cells than the nutrients liberated from cells that die through necrotic processes, 3) products of PCD can stimulate growth even in the presence of growth-suppressive necromass, and 4) the beneficial effects of substances released through PCD extend to two other species within the family Ustilaginaceae. Additionally, U. maydis exhibited a remarkable ability to withstand the negative effects of non-PCD necromass. These results suggest PCD-released materials are essential for critical initial regrowth in post-stress environments where there is a high presence of non-PCD necromass. As the revitalized population strengthens, it would correspondingly enhance the communal ability to exploit more challenging nutrients. Alongside with the robust resilience of U. maydis survivors against non-PCD necromass, the PCD mode of dying may improve the fitness of this microorganism in harsh and fluctuating environments, warranting further investigation.