Journal Articles
- Secretions from Serratia marcescens Inhibit the Growth and Biofilm Formation of Candida spp. and Cryptococcus neoformans
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Caiyan Xin , Fen Wang , Jinping Zhang , Quan Zhou , Fangyan Liu , Chunling Zhao , Zhangyong Song
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J. Microbiol. 2023;61(2):221-232. Published online February 21, 2023
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DOI: https://doi.org/10.1007/s12275-022-00007-3
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4
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Abstract
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Candida spp. and Cryptococcus are conditional pathogenic fungi that commonly infect immunocompromised patients.
Over the past few decades, the increase in antifungal resistance has prompted the development of new antifungal agents. In
this study, we explored the potential antifungal effects of secretions from Serratia marcescens on Candida spp. and Cryptococcus
neoformans. We confirmed that the supernatant of S. marcescens inhibited fungal growth, suppressed hyphal and
biofilm formation, and downregulated the expression of hyphae-specific genes and virulence-related genes in Candida spp.
and C. neoformans. Furthermore, the S. marcescens supernatant retained biological stability after heat, pH, and protease
K treatment. The chemical profile of the S. marcescens supernatant was characterized by ultra-high-performance liquid
chromatography–linear ion trap/orbitrap high resolution mass spectrometry analysis and a total of 61 compounds with an
mzCloud best match of greater than 70 were identified. In vivo, treatment with the S. marcescens supernatant reduced the
mortality of fungi-infected Galleria mellonella. Taken together, our results revealed that the stable antifungal substances in
the supernatant of S. marcescens have promising potential applications in the development of new antifungal agents.
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Citations
Citations to this article as recorded by

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Antifungal activities of Equol against
Candida albicans in vitro
and
in vivo
Fen Wang, Jinping Zhang, Qian Zhang, Zhangyong Song, Caiyan Xin
Virulence.2024;[Epub] CrossRef - Antifungal Effect of Vitamin D3 against Cryptococcus neoformans Coincides with Reduced Biofilm Formation, Compromised Cell Wall Integrity, and Increased Generation of Reactive Oxygen Species
Jian Huang, Junwen Lei, Anni Ge, Wei Xiao, Caiyan Xin, Zhangyong Song, Jinping Zhang
Journal of Fungi.2023; 9(7): 772. CrossRef
- RNase G controls tpiA mRNA abundance in response to oxygen availability in Escherichia coli
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Jaejin Lee , Dong-Ho Lee , Che Ok Jeon , Kangseok Lee
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J. Microbiol. 2019;57(10):910-917. Published online September 30, 2019
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DOI: https://doi.org/10.1007/s12275-019-9354-6
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48
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10
Web of Science
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9
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Abstract
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Studies have shown that many enzymes involved in glycolysis
are upregulated in Escherichia coli endoribonuclease G (rng)
null mutants. However, the molecular mechanisms underlying
the RNase G-associated regulation of glycolysis have
not been characterized. Here, we show that RNase G cleaves
the 5untranslated region of triosephosphate isomerase A
(tpiA) mRNA, leading to destabilization of the mRNA in E.
coli. Nucleotide substitutions within the RNase G cleavage
site in the genome resulted in altered tpiA mRNA stability,
indicating that RNase G activity influences tpiA mRNA
abundance. In addition, we observed that tpiA expression was
enhanced, whereas that of RNase G was decreased, in E. coli
cells grown anaerobically. Our findings suggest that RNase
G negatively regulates tpiA mRNA abundance in response
to oxygen availability in E. coli.
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Citations to this article as recorded by

- Relaxed Cleavage Specificity of Hyperactive Variants of Escherichia coli RNase E on RNA I
Dayeong Bae, Hana Hyeon, Eunkyoung Shin, Ji-Hyun Yeom, Kangseok Lee
Journal of Microbiology.2023; 61(2): 211. CrossRef - Transcript-specific selective translation by specialized ribosomes bearing genome-encoded heterogeneous rRNAs in V. vulnificus CMCP6
Younkyung Choi, Minju Joo, Wooseok Song, Minho Lee, Hana Hyeon, Hyun-Lee Kim, Ji-Hyun Yeom, Kangseok Lee, Eunkyoung Shin
Journal of Microbiology.2022; 60(12): 1162. CrossRef - Regulator of RNase E activity modulates the pathogenicity of Salmonella Typhimurium
Jaejin Lee, Eunkyoung Shin, Ji-Hyun Yeom, Jaeyoung Park, Sunwoo Kim, Minho Lee, Kangseok Lee
Microbial Pathogenesis.2022; 165: 105460. CrossRef - Endoribonuclease-mediated control of hns mRNA stability constitutes a key regulatory pathway for Salmonella Typhimurium pathogenicity island 1 expression
Minho Lee, Minkyung Ryu, Minju Joo, Young-Jin Seo, Jaejin Lee, Hong-Man Kim, Eunkyoung Shin, Ji-Hyun Yeom, Yong-Hak Kim, Jeehyeon Bae, Kangseok Lee, William Navarre
PLOS Pathogens.2021; 17(2): e1009263. CrossRef - Trans-acting regulators of ribonuclease activity
Jaejin Lee, Minho Lee, Kangseok Lee
Journal of Microbiology.2021; 59(4): 341. CrossRef - The effect of two ribonucleases on the production of Shiga toxin and stx-bearing bacteriophages in Enterohaemorrhagic Escherichia coli
Patricia B. Lodato
Scientific Reports.2021;[Epub] CrossRef - Regulator of ribonuclease activity modulates the pathogenicity of Vibrio vulnificus
Jaejin Lee, Eunkyoung Shin, Jaeyeong Park, Minho Lee, Kangseok Lee
Journal of Microbiology.2021; 59(12): 1133. CrossRef - An alternative miRISC targets a cancer‐associated coding sequence mutation in FOXL2
Eunkyoung Shin, Hanyong Jin, Dae‐Shik Suh, Yongyang Luo, Hye‐Jeong Ha, Tae Heon Kim, Yoonsoo Hahn, Seogang Hyun, Kangseok Lee, Jeehyeon Bae
The EMBO Journal.2020;[Epub] CrossRef - The coordinated action of RNase III and RNase G controls enolase expression in response to oxygen availability in Escherichia coli
Minho Lee, Minju Joo, Minji Sim, Se-Hoon Sim, Hyun-Lee Kim, Jaejin Lee, Minkyung Ryu, Ji-Hyun Yeom, Yoonsoo Hahn, Nam-Chul Ha, Jang-Cheon Cho, Kangseok Lee
Scientific Reports.2019;[Epub] CrossRef
Research Support, Non-U.S. Gov't
- RNase G Participates in Processing of the 5′-end of 23S Ribosomal RNA
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Woo-Seok Song , Minho Lee , Kangseok Lee
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J. Microbiol. 2011;49(3):508-511. Published online June 30, 2011
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DOI: https://doi.org/10.1007/s12275-011-1198-7
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Abstract
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In Escherichia coli, primary rRNA transcripts must be processed by a complex process in which several ribonucleases are involved in order to generate mature 16S, 23S, and 5S rRNA molecules. While it is known that RNase G, a single-stranded RNA-specific endoribonuclease encoded by the rng gene, plays an active role in the maturation of the 5′-end of 16S rRNA, its involvement in the maturation of the 5′-end of 23S rRNA remains unclear. Here we show that E. coli cells deleted for the rng gene accumulate the 23S rRNA precursor containing an extra 77 nucleotides at its mature 5′-end. In vitro cleavage assays show that RNase G cleaves synthetic RNA containing a sequence encompassing the 5′-end to 77 nucleotides upstream of mature 23S rRNA at two sites present in single-stranded regions. Our results suggest the involvement of RNase G in the processing of the 5′-region of 23S rRNA precursors.