Journal Articles
- Comparative Transcriptomic Analysis of Flagellar‑Associated Genes in Salmonella Typhimurium and Its rnc Mutant
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Seungmok Han , Ji-Won Byun , Minho Lee
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J. Microbiol. 2024;62(1):33-48. Published online January 5, 2024
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DOI: https://doi.org/10.1007/s12275-023-00099-5
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Abstract
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Salmonella enterica serovar Typhimurium (S. Typhimurium) is a globally recognized foodborne pathogen that affects both
animals and humans. Endoribonucleases mediate RNA processing and degradation in the adaptation of bacteria to environmental
changes and have been linked to the pathogenicity of S. Typhimurium. Not much is known about the specific regulatory
mechanisms of these enzymes in S. Typhimurium, particularly in the context of environmental adaptation. Thus, this
study carried out a comparative transcriptomic analysis of wild-type S. Typhimurium SL1344 and its mutant (Δrnc), which
lacks the rnc gene encoding RNase III, thereby elucidating the detailed regulatory characteristics that can be attributed to the
rnc gene. Global gene expression analysis revealed that the Δrnc strain exhibited 410 upregulated and 301 downregulated
genes (fold-change > 1.5 and p < 0.05), as compared to the wild-type strain. Subsequent bioinformatics analysis indicated
that these differentially expressed genes are involved in various physiological functions, in both the wild-type and Δrnc
strains. This study provides evidence for the critical role of RNase III as a general positive regulator of flagellar-associated
genes and its involvement in the pathogenicity of S. Typhimurium.
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Citations
Citations to this article as recorded by

- CspA regulates stress resistance, flagellar motility and biofilm formation in Salmonella Enteritidis
Xiang Li, Yan Cui, Xiaohui Sun, Chunlei Shi, Shoukui He, Xianming Shi
Food Bioscience.2025; 66: 106237. CrossRef - Influence of Flagella on Salmonella Enteritidis Sedimentation, Biofilm Formation, Disinfectant Resistance, and Interspecies Interactions
Huixue Hu, Jingguo Xu, Jingyu Chen, Chao Tang, Tianhao Zhou, Jun Wang, Zhuangli Kang
Foodborne Pathogens and Disease.2024;[Epub] CrossRef
- Azohydromonas aeria sp. nov., isolated from air
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Han Xue , Chun-gen Piao , Dan-ran Bian , Min-wei Guo , Yong Li
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J. Microbiol. 2020;58(7):543-549. Published online June 27, 2020
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DOI: https://doi.org/10.1007/s12275-020-9423-x
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Abstract
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A grey pink colored bacterium, strain t3-1-3T, was isolated
from the air at the foot of the Xiangshan Mountain in Beijing,
China. The cells are aerobic, Gram-stain-negative, non-sporeforming,
motile and coccoid-rod shaped (0.9–1.2 × 1.9–2.1
μm). Strain t3-1-3T was catalase-positive and oxidase-negative
and this strain grew at 4–42°C (optimum 28°C), a pH
of 4.0–9.0 (optimum pH 7.0) and under 0–2% (w/v) NaCl
(optimum 0–1% NaCl). A phylogenetic analysis based on 16S
rRNA gene sequences revealed that strain t3-1-3T was closely
related to Azohydromonas riparia UCM-11T (97.4% similarity),
followed by Azohydromonas australica G1-2T (96.8%)
and Azohydromonas ureilytica UCM-80T (96.7%). The genome
of strain t3-1-3T contains 6,895 predicted protein-encoding
genes, 8 rRNA genes, 62 tRNA genes and one sRNA
gene, as well as five potential biosynthetic gene clusters, including
clusters of genes coding for non-ribosomal peptide
synthetase (NRPS), bacteriocin and arylpolyene and two clusters
of genes for terpene. The predominant cellular fatty acids
(> 10.0% of the total) in strain t3-1-3T were summed feature
3 (C16:1ω7c and/or C16:1ω6c, 37.8%), summed feature 8
(C18:1ω7c and/or C18:1ω6c, 29.7%) and C16:0 (17.3%). Strain
t3-1-3T contained ubiquinone-8 (Q-8) as the predominant
respiratory quinone. The polar lipids of strain t3-1-3T comprised
phosphatidyl ethanolamine (PE), phosphatidyl glycerol
(PG), diphosphatidyl glycerol (DPG), an unidentified
glycolipid (GL), an unidentified aminophospholipid (APL),
two unidentified phospholipid (PL1-2) and five unidentified
lipid (L1-5). The DNA G + C content of the type strain
is 70.3%. The broader range of growth temperature, assimilation
of malic acid and trisodium citrate, presence of C18:3ω6c
and an unidentified glycolipid and absence of C12:0 2-OH and
C16:0iso differentiate strain t3-1-3T from related species. Based
on the taxonomic data presented in this study, we suggest
that strain t3-1-3T represents a novel species within the genus
Azohydromonas, for which the name Azohydromonas
aeria sp. nov. is proposed. The type strain of Azohydromonas
aeria is t3-1-3T (= CFCC 13393T = LMG 30135T).
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Citations
Citations to this article as recorded by

- The phylogeny of the genus Azohydromonas supports its transfer to the family Comamonadaceae
Ezequiel Gerardo Mogro, Juan Hilario Cafiero, Mauricio Javier Lozano, Walter Omar Draghi
International Journal of Systematic and Evolutionary Microbiology.2022;[Epub] CrossRef - In situ injectable nano-complexed hydrogel based on chitosan/dextran for combining tumor therapy via hypoxia alleviation and TAMs polarity regulation
Wenxue Zhang, Yan Shi, Hu Li, Miao Yu, Jiaxuan Zhao, Hao Chen, Ming Kong
Carbohydrate Polymers.2022; 288: 119418. CrossRef - Transformation of N and S pollutants and characterization of microbial communities in constructed wetlands with Vallisneria natans
Feichao Fu, Shaobin Huang, Heping Hu, Yao Lu, Yanlin Wang, Jianqi Yuan, Zerui Gong, Jinhua Wu, Yongqing Zhang
Journal of Water Process Engineering.2021; 42: 102186. CrossRef - Azohydromonas caseinilytica sp. nov., a Nitrogen-Fixing Bacterium Isolated From Forest Soil by Using Optimized Culture Method
Ram Hari Dahal, Dhiraj Kumar Chaudhary, Dong-Uk Kim, Jaisoo Kim
Frontiers in Microbiology.2021;[Epub] CrossRef
Research Support, Non-U.S. Gov't
- Immunological Responses Induced by asd and wzy/asd Mutant Strains of Salmonella enterica serovar Typhimurium in BALB/c Mice
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Hong Hua Piao , Vo Thi Minh Tam , Hee Sam Na , Hyun Ju Kim , Phil Youl Ryu , Soo Young Kim , Joon Haeng Rhee , Hyon E. Choy , Suhng Wook Kim , Yeongjin Hong
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J. Microbiol. 2010;48(4):486-495. Published online August 20, 2010
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DOI: https://doi.org/10.1007/s12275-010-0023-z
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Abstract
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Attenuated bacteria have long been developed as vaccine candidates but can have some disadvantages, such as the potential for damage to immune organs due to insufficient clearance. To minimize these disadvantages, we generated Salmonella enterica serovar Typhimurium mutants SHJ2104 (asd::cm) and HTSaYA (wzy::km, asd::cm). The wzy gene codes for the O-antigen polymerase, which is involved in lipopolysaccharide (LPS) biosynthesis, and asd codes for aspartate ß- semialdehyde dehydrogenase, which participates in cell wall formation. The strains synthesized LPS with a short-chain length, and showed lower cytotoxicity and reduced intracellular proliferation in animal cells compared to wild-type bacteria. After oral infection, the mutants were cleared in immune tissues, including the Peyer’s patch, mesenteric lymph node, and spleen, within 5 days. The LD50 of the mutants in Balb/c mice was estimated to be 106 higher than wild-type bacteria when administered either via an oral or i.p. route, indicating that the two strains are highly attenuated. To compare the immune response to and protective effects of the mutants against wild-type bacterial infection, we inoculated the mutants into mice via an oral (1×1010 CFU) or i.p. (1×107 CFU) route once or twice at a two week interval. All immune responses, such as serum IgG and secretory IgA levels, cytokine production, and delayed hypersensitivity, were highly induced by two rounds of immunization. HTSaYA and SHJ2104 induced similar immune responses, and mice immunized with HTSaYA or SHJ2104 via an i.p. route were protected against wild-type Salmonella infection even at 100-fold of the LD50 (5×106 CFU). Taken together, these data indicate that HTSaYA and SHJ2104 could be developed as live attenuated Salmonella vaccine candidates.