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Staphylococcus Aureus Dormancy: Waiting for Insurgency Publisher Pubmed



Nasser A1, 2 ; Jahanbakhshi S3 ; Dallal MMS1, 2 ; Banar M1 ; Sattarimaraji A1 ; Azimi T4
Authors
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Authors Affiliations
  1. 1. Department of Pathobiology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran
  2. 2. Department of Pathobiology, Division of Food Microbiology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran
  3. 3. Department of Food Science and Technology, The Ohio State University, Columbus, OH, United States
  4. 4. Department of Bacteriology and Virology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran

Source: Current Pharmaceutical Biotechnology Published:2023


Abstract

Relapse infection usually results from resistance to the antibiotic, acquired genes, or persister cells. Persister cells are formed through mutation, reduced activity or metabolically inac-tive pathways induced by antibiotics, harassing conditions, low ATP, and malnutrition. These factors provide the ground for bacteria to grow slowly. Such a slow growth rate makes traditional antibiotics ineffective against persister cells. Staphylococcus aureus (S. aureus), in addition to this form, can be observed in Small Colony Variants (SCVs), L-forms, and dormant, all of which are characterized by at least one feature, i.e., slow growth. Despite their slow growth, they are meta-bolically active in terms of stringent SOS and cell wall stress responses. The stress response involves resistance against harassing conditions, and it survives until it is reactivated later. The present study aims to discuss the mechanisms of all persister cell formations, circumstances involved, gene mutation, and adoptable strategies against it. © 2023 Bentham Science Publishers.