- Whole genome and RNA sequencing of oral commensal bacterium Streptococcus anginosus subsp. anginosus with vancomycin tolerance
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Kyu Hwan Kwack , Jae-Hyung Lee , Ji-Hoi Moon
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J. Microbiol. 2022;60(2):167-176. Published online January 7, 2022
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DOI: https://doi.org/10.1007/s12275-022-1425-4
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“Antibiotic tolerance” promotes the rapid subsequent evolution
of “antibiotic resistance,” however, it is often overlooked
because it is difficult to distinguish between tolerant
and susceptible organisms. A commensal bacterium S. anginosus
subsp. anginosus strain KHUD_S1, isolated from dental
biofilm was found to exhibit a high MBC/MIC ratio of 32
against vancomycin. We observed KHUD_S1 cells exposed
to vancomycin did not grow but maintained viability. Transmission
electron microscope showed KHUD_S1 cells possessed
a dense, thick capsule and maintained the cell wall integrity
upon vancomycin exposure. To infer the underlying
mechanisms of the vancomycin tolerance in KHUD_S1, we
performed whole genome sequencing and RNA sequencing.
The KHUD_S1 genome carried three genes encoding branching
enzymes that can affect peptidoglycan structure through
interpeptide bridge formation. Global gene expression profiling
revealed that the vancomycin-induced downregulation
of carbohydrate and inorganic ion transport/metabolism as
well as translation is less prominent in KHUD_S1 than in the
vancomycin susceptible strain KHUD_S3. Based on the transcriptional
levels of genes related to peptidoglycan synthesis,
KHUD_S1 was determined to have a 3D peptidoglycan architecture
distinct from KHUD_S3. It was found that, under
vancomycin exposure, the peptidoglycan was remodeled
through changes in the interpeptide bridge and transpeptidation
reactions. Collectively, these features of S. anginosus
KHUD_S1, including a dense capsule and differential gene
expression in peptidoglycan synthesis, may contribute to vancomycin
tolerance. Our results showing the occurrence of
vancomycin tolerance amongst oral commensal bacteria highlight
the need for considering future strategies for screening
of antibiotic tolerance as an effort to reduce antibiotic resistance.
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Citations
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- From commensal to pathogen: recent advances in the pathogenicity and clinical implications of Streptococcus anginosus
Ying Chen, Hongjie Zheng, Wenhua Huang, Shaolong Chen, Yongqiang Jiang, Shengwei Zhang, Peng Liu Frontiers in Microbiology.2026;[Epub] CrossRef - Development of a Novel Multi‐Epitope Vaccine Against Streptococcus anginosus Infection via Reverse Vaccinology Approach
Linglan Xu, Nan Xie, Yiqing Liu, Hongmei Tang, Tian Li, Jiaofeng Peng, Ranhui Li Immunology.2025; 175(3): 339. CrossRef - Gut resistome profiling reveals high diversity and fluctuations in pancreatic cancer cohorts
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- Antibacterial effects of N-acetylcysteine against endodontic pathogens
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Ji-Hoi Moon , Young-Suk Choi , Hyeon-Woo Lee , Jung Sun Heo , Seok Woo Chang , Jin-Yong Lee
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J. Microbiol. 2016;54(4):322-329. Published online April 1, 2016
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DOI: https://doi.org/10.1007/s12275-016-5534-9
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2,026
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The success of endodontic treatment depends on the eradication
of microorganisms from the root canal system and
the prevention of reinfection. The purpose of this investigation
was to evaluate the antibacterial and antibiofilm efficacy
of N-acetylcysteine (NAC), an antioxidant mucolytic
agent, as an intracanal medicament against selected endodontic
pathogens. Minimum inhibitory concentrations (MICs)
of NAC for Actinomyces naeslundii, Lactobacillus salivarius,
Streptococcus mutans, and Enterococcus faecalis were determined
using the broth microdilution method. NAC showed
antibacterial activity, with MIC values of 0.78–1.56 mg/ml.
The effect of NAC on biofilm formation of each bacterium
and a multispecies culture consisting of the four bacterial species
was assessed by crystal violet staining. NAC significantly
inhibited biofilm formation by all the monospecies and multispecies
bacteria at minimum concentrations of 0.78–3.13
mg/ml. The efficacy of NAC for biofilm disruption was evaluated
by scanning electron microscopy and ATP-bioluminescence
quantification using mature multispecies biofilms.
Preformed mature multispecies biofilms on saliva-coated hydroxyapatite
disks were disrupted within 10 min by treatment
with NAC at concentrations of 25 mg/ml or higher.
After 24 h of treatment, the viability of mature biofilms was
reduced by > 99% compared with the control. Moreover, the
biofilm disrupting activity of NAC was significantly higher
than that of saturated calcium hydroxide or 2% chlorhexidine
solution. Within the limitations of this in vitro study, we
conclude that NAC has excellent antibacterial and antibiofilm
efficacy against endodontic pathogens and may be used as an
alternative intracanal medicament in root canal therapies.
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- In vitro effects of N-acetyl cysteine alone and in combination with antibiotics on Prevotella intermedia
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Ji-Hoi Moon , Eun-Young Jang , Kyu Sang Shim , Jin-Yong Lee
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J. Microbiol. 2015;53(5):321-329. Published online May 3, 2015
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DOI: https://doi.org/10.1007/s12275-015-4500-2
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1,640
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Abstract
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N-acetyl cysteine (NAC) is an antioxidant that possesses
anti-inflammatory activities in tissues. In the field of dentistry,
NAC was demonstrated to prevent the expression of
LPS-induced inflammatory mediators in phagocytic cells
and gingival fibroblasts during the inflammatory process,
but the effect of NAC on oral pathogens has been rarely
studied. Here, we examined the effect of NAC against planktonic
and biofilm cells of Prevotella intermedia, a major oral
pathogen. NAC showed antibacterial activity against the
planktonic P. intermedia with MIC value of 3 mg/ml and
significantly decreased biofilm formation by the bacterium
even at sub MIC. NAC did not affect the antibiotic susceptibility
of planktonic P. intermedia, showing indifference (fractional
inhibitory concentration index of 0.5?) results against
the bacterium in combination with ampicillin, ciprofloxacin,
tetracycline or metronidazole. On the other hand, viability
of the pre-established bacterial biofilm exposed to the antibiotics
except metronidazole was increased in the presence
of NAC. Collectively, NAC may be used for prevention of
the biofilm formation by P. intermedia rather than eradication
of the pre-established bacterial biofilm. Further studies
are required to explore antibacterial and anti-biofilm activity
of NAC against mixed population of oral bacteria and its
modulatory effect on antibiotics used for oral infectious
diseases.
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Young-Suk Choi, Cheul Kim, Ji-Hoi Moon, Jin-Yong Lee Brazilian Journal of Microbiology.2018; 49(1): 184. CrossRef - Biological Activities and Potential Oral Applications of N‐Acetylcysteine: Progress and Prospects
Yanping Pei, Huan Liu, Yi Yang, Yanwei Yang, Yang Jiao, Franklin R. Tay, Jihua Chen, Jolanta Czuczejko Oxidative Medicine and Cellular Longevity.2018;[Epub] CrossRef - Poly(silsesquioxanes) and poly(siloxanes) grafted with N-acetylcysteine for eradicating mature bacterial biofilms in water environment
Maria Nowacka, Anna Rygała, Dorota Kręgiel, Anna Kowalewska Colloids and Surfaces B: Biointerfaces.2018; 172: 627. CrossRef -
N
-Acetyl-
l
-Cysteine and Cysteamine as New Strategies against Mixed Biofilms of Nonencapsulated Streptococcus pneumoniae and Nontypeable Haemophilus influenzae
Mirian Domenech, Ernesto García Antimicrobial Agents and Chemotherapy.2017;[Epub] CrossRef - N‐acetylcysteine eradicates Pseudomonas aeruginosa biofilms in bone cement
Mehmet Emin Onger, Hasan Gocer, Dilek Emir, Suleyman Kaplan Scanning.2016; 38(6): 766. CrossRef - Antibacterial effect of N‐acetylcysteine on common canine otitis externa isolates
Elizabeth R. May, Katherine A. Conklin, David A. Bemis Veterinary Dermatology.2016; 27(3): 188. CrossRef - Antibacterial effects of N-acetylcysteine against endodontic pathogens
Ji-Hoi Moon, Young-Suk Choi, Hyeon-Woo Lee, Jung Sun Heo, Seok Woo Chang, Jin-Yong Lee Journal of Microbiology.2016; 54(4): 322. CrossRef -
In Vitro
Effects of Polyphosphate against Prevotella intermedia in Planktonic Phase and Biofilm
Eun-Young Jang, Minjung Kim, Mi Hee Noh, Ji-Hoi Moon, Jin-Yong Lee Antimicrobial Agents and Chemotherapy.2016; 60(2): 818. CrossRef
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