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Genetic insights into novel lysis suppression by phage CSP1 in Escherichia coli
Moosung Kim, Sangryeol Ryu
J. Microbiol. 2025;63(4):e2501013.   Published online April 29, 2025
DOI: https://doi.org/10.71150/jm.2501013
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AbstractAbstract PDFSupplementary Material

Lysis inhibition (LIN) in bacteriophage is a strategy to maximize progeny production. A clear plaque-forming mutant, CSP1C, was isolated from the turbid plaque-forming CSP1 phage. CSP1C exhibited an adsorption rate and replication dynamics similar to CSP1. Approximately 90% of the phages were adsorbed to the host cell within 12 min, and both phages had a latent period of 25 min. Burst sizes were 171.42 ± 31.75 plaque-forming units (PFU) per infected cell for CSP1 and 168.94 ± 51.67 PFU per infected cell for CSP1C. Both phages caused comparable reductions in viable E. coli cell counts at a low multiplicity of infection (MOI). However, CSP1 infection did not reduce turbidity, suggesting a form of LIN distinct from the well-characterized LIN of T4 phage. Genomic analysis revealed that a 4,672-base pairs (bp) DNA region, encompassing part of the tail fiber gene, CSP1_020, along with three hypothetical genes, CSP1_021, CSP1_022, and part of CSP1_023, was deleted from CSP1 to make CSP1C. Complementation analysis in CSP1C identified CSP1_020, CSP1_021, and CSP1_022 as a minimal gene set required for the lysis suppression in CSP1. Co-expression of these genes in E. coli with holin (CSP1_092) and endolysin (CSP1_091) resulted in lysis suppression. Lysis suppression was abolished by disrupting the proton motive force (PMF), supporting their potential role as antiholin. Additionally, CSP1_021 directly interacts with holin, suggesting that it may function as an antiholin. These findings identify new genetic factors involved in lysis suppression in CSP1, providing broader insights into phage strategies for modulating host cell lysis.

Citations

Citations to this article as recorded by  
  • Characterization and genome analyses of the novel phages targeting extraintestinal Escherichia coli clones ST131 and ST410
    Md Shamsuzzaman, Yoon-Jung Choi, Shukho Kim, Jungmin Kim
    International Microbiology.2025;[Epub]     CrossRef
Research Support, Non-U.S. Gov'ts
Simultaneous Detection of Waterborne Viruses by Multiplex Real-Time PCR
Lae-Hyung Kang , Se-hwan Oh , Jeong-Woong Park , Yu-Jung Won , Sangryeol Ryu , Soon-Young Paik
J. Microbiol. 2013;51(5):671-675.   Published online September 14, 2013
DOI: https://doi.org/10.1007/s12275-013-3199-1
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AbstractAbstract
Norovirus, Rotavirus group A, the Hepatitis A virus, and Coxsackievirus are all common causes of gastroenteritis. Conventional diagnoses of these causative agents are based on antigen detection and electron microscopy. To improve the diagnostic potential for viral gastroenteritis, internally controlled multiplex real-time polymerase chain reaction (PCR) methods have been recently developed. In this study, individual real-time PCRs were developed and optimized for specific detections of Norovirus genogroup I, Norovirus genogroup II, Rotavirus group A, the Hepatitis A virus, and Coxsackievirus group B1. Subsequently, individual PCRs were combined with multiplex PCR reactions. In general, multiplex real-time PCR assays showed comparable sensitivities and specificities with individual assays. A retrospective clinical evaluation showed increased pathogen detection in 29% of samples using conventional PCR methods. Prospective clinical evaluations were detected in 123 of the 227 (54%) total samples used in the multiplex realtime PCR analysis. The Norovirus genogroup II was found most frequently (23%), followed by Rotavirus (20%), the Hepatitis A virus (4.5%), Coxsackievirus (3.5%), and Norovirus genogroup I (2.6%). Internally controlled multiplex real-time PCR assays for the simultaneous detection of Rotavirus, Coxsackievirus group B, the Hepatitis A virus, and Norovirus genogroups I and II showed significant improvement in the diagnosis of viral gastroenteritis.

Citations

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  • Microbiological quality of irrigation water for cultivation of fruits and vegetables: An overview of available guidelines, water testing strategies and some factors that influence compliance.
    Oluwadara Alegbeleye, Anderson S. Sant’Ana
    Environmental Research.2023; 220: 114771.     CrossRef
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    Lisa Paruch
    International Journal of Environmental Research and Public Health.2022; 19(9): 5128.     CrossRef
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    Kyu Bong Cho
    Biomedical Science Letters.2020; 26(4): 302.     CrossRef
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    Mohammad Irshad, Priyanka Gupta, Dhananjay Singh Mankotia, Mohammad Ahmad Ansari
    World Journal of Gastroenterology.2016; 22(20): 4824.     CrossRef
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    Chourouk Ibrahim, Nadia Cherif, Salah Hammami, Pierre Pothier, Abdennaceur Hassen
    CLEAN – Soil, Air, Water.2016; 44(4): 393.     CrossRef
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    Satoshi Ishii, Gaku Kitamura, Takahiro Segawa, Ayano Kobayashi, Takayuki Miura, Daisuke Sano, Satoshi Okabe, C. A. Elkins
    Applied and Environmental Microbiology.2014; 80(24): 7505.     CrossRef
ppGpp-Mediated Stationary Phase Induction of the Genes Encoded by Horizontally Acquired Pathogenicity Islands and cob/pdu Locus in Salmonella enterica serovar Typhimurium
Miryoung Song , Hyun-Ju Kim , Sangryeol Ryu , Hyunjin Yoon , Jiae Yun , Hyon E. Choy
J. Microbiol. 2010;48(1):89-95.   Published online March 11, 2010
DOI: https://doi.org/10.1007/s12275-009-0179-6
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  • 11 Crossref
AbstractAbstract
Salmonella enterica is highly diverse in terms of genome structure, which is at least partly due to the horizontal transfer of genetic elements from various sources. In this study, we examined the expression profiles of such genes in Salmonella Pathogenicity Islands (SPIs) and the cob/pdu locus, horizontally acquired large DNA segments, during growth under standard growth conditions. Transcripts from exponentially growing and early stationary phase Salmonellae were compared using various methods including cDNA microarray analysis. Nearly all genes encoded by SPIs and the cob/pdu locus were induced at the onset of the stationary phase in a stringent molecule ppGpp-dependent but stationary phase σ, σ38-independent manner. Although, it has been suggested that ppGpp acts in concert with DksA, we found the stationary phase induction of those SPI genes was not DksA dependent. It is suggested that ppGpp stimulates the expression of these stress-inducible genes encoded by horizontally acquired DNA, by itself or in concert with DksA.

Citations

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  • Intrinsic antimicrobial resistance: Molecular biomaterials to combat microbial biofilms and bacterial persisters
    Swagatam Barman, Leman Buzoglu Kurnaz, Ryan Leighton, Md Waliullah Hossain, Alan W. Decho, Chuanbing Tang
    Biomaterials.2024; 311: 122690.     CrossRef
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    Khaled S Allemailem
    International Journal of Nanomedicine.2021; Volume 16: 8159.     CrossRef
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