- σB Affects Biofilm Formation under the Dual Stress Conditions Imposed by Adding Salt and Low Temperatur in Listeria monocytogenes
-
Jin-Ju Lee , Gilho Lee , Ji-Hyun Shin
-
J. Microbiol. 2014;52(10):849-855. Published online October 1, 2014
-
DOI: https://doi.org/10.1007/s12275-014-4369-5
-
-
913
View
-
0
Download
-
11
Crossref
-
Abstract
PDF
-
The food-borne pathogenic bacteria Listeria monocytogenes
can form biofilms on various surfaces including food-processing
equipment. Biofilms offer survival benefits to the organisms
entrapped against environmental insults. Moreover,
the σB transcription factor of L. monocytogenes plays an important
role in its survival under various stress conditions.
In this study, we evaluated whether σB contributes to biofilm
formation when L. monocytogenes is grown under various
temperatures and media. When the wild-type strain was
grown under static biofilm culture below ambient temperature
(15°C) for 72 h, the difference in viable cell number (in
both planktonic and biofilm cells) between the wild-type
and ΔsigB mutant increased by adding NaCl to BHI broth
(9% salt BHI > 6% salt BHI > BHI, w/v), and the specific activity
of β-galactosidase was highly induced in the wild-type
strain grown in 6% salt containing BHI broth. Furthermore,
we measured surface-adhered biofilm forming ability using
the crystal violet staining method. The wild-type strain formed
a four times larger biofilm than that of the ΔsigB mutant in
6% salt-BHI medium at 15°C over a 72 h incubation and also
showed the highest level of β-galactosidase specific activity.
However, both the wild-type and ΔsigB mutant L. monocytogenes
were defective for forming a biofilm in 9% salt-BHI
medium at 15°C. Our results suggest that σB plays an enhanced
role in surface-adhered biofilm formation when L.
monocytogenes encounters dual stress conditions, such as
6% NaCl and low temperature.
-
Citations
Citations to this article as recorded by 
- Estimating the antimicrobial effect of grape seed extract on L. monocytogenes ΔsigB on xanthan gum gels
Melina Kitsiou, Jorge Gutierrez-Merino, Oleksiy V. Klymenko, Kimon Andreas Karatzas, Eirini Velliou Food Control.2025; 176: 111355. CrossRef - Characteristics of Clinical Isolates of Listeria monocytogenes in Sichuan, China, in 2022 Based on Whole Genome Sequencing Analysis
Qian Liang, Weifeng Huang, Tao Xiao, Lin Zhang, Gaopeng Lei, Hong Lv, Xiaorong Yang Foodborne Pathogens and Disease.2024; 21(7): 424. CrossRef - The influence of stress factors on selected phenotypic and genotypic features of Listeria monocytogenes – a pilot study
Natalia Wiktorczyk-Kapischke, Ewa Wałecka-Zacharska, Jakub Korkus, Katarzyna Grudlewska-Buda, Anna Budzyńska, Kacper Wnuk, Eugenia Gospodarek-Komkowska, Krzysztof Skowron BMC Microbiology.2023;[Epub] CrossRef - Marked inter-strain heterogeneity in the differential expression of some key stress response and virulence-related genes between planktonic and biofilm cells in Listeria monocytogenes
Christos Toliopoulos, Efstathios Giaouris International Journal of Food Microbiology.2023; 390: 110136. CrossRef - Proteomic analysis reveals the temperature-dependent presence of extracytoplasmic peptidases in the biofilm exoproteome of Listeria monocytogenes EGD-e
Yue-Jia Lee, Chinling Wang Journal of Microbiology.2020; 58(9): 761. CrossRef - Genomic Differences between Listeria monocytogenes EGDe Isolates Reveal Crucial Roles for SigB and Wall Rhamnosylation in Biofilm Formation
Chih-Yu Hsu, Lynne Cairns, Laura Hobley, James Abbott, Conor O’Byrne, Nicola R. Stanley-Wall, Tina M. Henkin Journal of Bacteriology.2020;[Epub] CrossRef - Listeria monocytogenes Biofilm Adaptation to Different Temperatures Seen Through Shotgun Proteomics
Tiago Santos, Didier Viala, Christophe Chambon, Julia Esbelin, Michel Hébraud Frontiers in Nutrition.2019;[Epub] CrossRef - Cross Talk between SigB and PrfA in Listeria monocytogenes Facilitates Transitions between Extra- and Intracellular Environments
Ahmed Gaballa, Veronica Guariglia-Oropeza, Martin Wiedmann, Kathryn J. Boor Microbiology and Molecular Biology Reviews.2019;[Epub] CrossRef - Salt stress affects global protein expression profiles of extracellular membrane-derived vesicles of Listeria monocytogenes
Taewon Lee, So Hyun Jun, Chi Won Choi, Seung Il Kim, Je Chul Lee, Ji Hyun Shin Microbial Pathogenesis.2018; 115: 272. CrossRef - Genomic and transcriptomic analyses reveal distinct biological functions for cold shock proteins (VpaCspA and VpaCspD) in Vibrio parahaemolyticus CHN25 during low-temperature survival
Chunhua Zhu, Boyi Sun, Taigang Liu, Huajun Zheng, Wenyi Gu, Wei He, Fengjiao Sun, Yaping Wang, Meicheng Yang, Weicheng Bei, Xu Peng, Qunxin She, Lu Xie, Lanming Chen BMC Genomics.2017;[Epub] CrossRef - Regulation of Escherichia coli RNase III activity
Boram Lim, Minji Sim, Howoon Lee, Seogang Hyun, Younghoon Lee, Yoonsoo Hahn, Eunkyoung Shin, Kangseok Lee Journal of Microbiology.2015; 53(8): 487. CrossRef
- Proteomic Analysis of Acinetobacter baumannii in Biofilm and Planktonic Growth Mode
-
Ji-Hyun Shin , Hee-Woo Lee , Sung-Min Kim , Jungmin Kim
-
J. Microbiol. 2009;47(6):728-735. Published online February 4, 2010
-
DOI: https://doi.org/10.1007/s12275-009-0158-y
-
-
947
View
-
1
Download
-
59
Crossref
-
Abstract
PDF
-
Recently, multidrug-resistant clinical isolates of Acinetobacter baumannii have been found to have a high capacity to form biofilm. It is well known that bacterial cells within biofilms are highly resistant to antibiotics, UV light, acid exposure, dehydration, and phagocytosis in comparison to their planktonic counterparts, which suggests that the cells in a biofilm have altered metabolic activity. To determine which proteins are up-regulated in A. baumannii biofilm cells, we performed a proteomic analysis. A clinical isolate of A. baumannii 1656-2, which was characterized to have a high biofilm forming ability, was cultivated under biofilm and planktonic conditions. Outer membrane enriched A. baumannii 1656-2 proteins were separated by two-dimensional (2-D) gel electrophoresis and the differentially expressed proteins were identified by MALDI-TOF mass spectrometry. The proteins up-regulated or expressed only in biofilm cells of A. baumannii are categorized as follows: (i) proteins processing environmental information such as the outer membrane receptor protein involved in mostly Fe transport, a sensor histidine kinase/response regulator, and diguanylate cyclase (PAS-GGEDF-EAL domain); (ii) proteins involved in metabolism such as NAD- linked malate dehydrogenase, nucleoside-diphosphate sugar epimerase, putative GalE, ProFAR isomerase, and N-acetylmuramoyl-L-alanine amidase; (iii) bacterial antibiotic resistance related proteins; and (iv) proteins related to gene repair such as exodeoxyribonuclease III and GidA. This proteomic analysis provides a fundamental platform for further studies to reveal the role of biofilm in the persistence and tolerance of A. baumannii.
-
Citations
Citations to this article as recorded by 
- Development and application of a bacteriophage cocktail for Shigella flexneri biofilm inhibition on the stainless steel surface
Jieun Choi, Siyeon Park, Yoonjee Chang Food Microbiology.2025; 125: 104641. CrossRef - Efficacy of the CHRONOlight biodynamic lighting system for control of nosocomial Gram-negative pathogens
Patricia Pérez-Palacios, Pedro Bustamante, Samuel Domínguez-Amarillo, Maria Jose Caro Ayora, Ignacio Acosta, Jose Manuel Rodríguez-Martínez International Journal of Infectious Diseases.2025; 161: 108120. CrossRef - Multi-omics analysis reveals genes and metabolites involved in Streptococcus suis biofilm formation
Haikun Wang, Qingying Fan, Yuxin Wang, Li Yi, Yang Wang BMC Microbiology.2024;[Epub] CrossRef - Characterization and Biofilm Inhibition of Multidrug‐Resistant Acinetobacter baumannii Isolates
Poonam Yadav, Sreska Shrestha, Deepak Basyal, Ananda Tiwari, Ranjit Sah, Anil Kumar Sah, Bishal Yadav, Mark Willcox, Shyam Kumar Mishra, Kai Zheng International Journal of Microbiology.2024;[Epub] CrossRef - Subunit vaccines for Acinetobacter baumannii
Ning Yang, Xiao Jin, Chenghua Zhu, Fenglin Gao, Zheqi Weng, Xingran Du, Ganzhu Feng Frontiers in Immunology.2023;[Epub] CrossRef - A novel vaccine candidate against A. baumannii based on a new OmpW family protein (OmpW2); structural characterization, antigenicity and epitope investigation, and in-vivo analysis
Sajad Abdollahi, Zeinab Raoufi Microbial Pathogenesis.2023; 183: 106317. CrossRef - Acinetobacter baumannii in the critically ill: complex infections get complicated
Ilaria Cavallo, Alessandra Oliva, Rebecca Pages, Francesca Sivori, Mauro Truglio, Giorgia Fabrizio, Martina Pasqua, Fulvia Pimpinelli, Enea Gino Di Domenico Frontiers in Microbiology.2023;[Epub] CrossRef - Targeting the Holy Triangle of Quorum Sensing, Biofilm Formation, and Antibiotic Resistance in Pathogenic Bacteria
Ronit Vogt Sionov, Doron Steinberg Microorganisms.2022; 10(6): 1239. CrossRef - Development of an Anti-Acinetobacter baumannii Biofilm Phage Cocktail: Genomic Adaptation to the Host
L. Blasco, I. Bleriot, M. González de Aledo, L. Fernández-García, O. Pacios, H. Oliveira, M. López, C. Ortiz-Cartagena, F. Fernández-Cuenca, Á. Pascual, L. Martínez-Martínez, J. Pachón, J. Azeredo, M. Tomás Antimicrobial Agents and Chemotherapy.2022;[Epub] CrossRef - DcaP porin and its epitope-based subunit promise effective vaccines against Acinetobacter baumannii; in-silico and in-vivo approaches
Zeinab Raoufi, Sajad Abdollahi, Raham Armand Microbial Pathogenesis.2022; 162: 105346. CrossRef - Decoding Acinetobacter baumannii biofilm dynamics and associated protein markers: proteomic and bioinformatics approach
Monika Choudhary, Shubham Kaushik, Arti Kapil, Rahul Shrivastava, Jitendraa Vashistt Archives of Microbiology.2022;[Epub] CrossRef - Factors mediating Acinetobacter baumannii biofilm formation: Opportunities for developing therapeutics
Kirti Upmanyu, Qazi Mohd. Rizwanul Haq, Ruchi Singh Current Research in Microbial Sciences.2022; 3: 100131. CrossRef - The prevalence of biofilm encoding genes in multidrug-resistant Acinetobacter baumannii isolates
Mahrokh Saadati, Leila Rahbarnia, Safar Farajnia, Behrooz Naghili, Reza Mohammadzadeh Gene Reports.2021; 23: 101094. CrossRef - Modulation of Quorum Sensing and Biofilms in Less Investigated Gram-Negative ESKAPE Pathogens
Veronica Lazar, Alina Maria Holban, Carmen Curutiu, Mariana Carmen Chifiriuc Frontiers in Microbiology.2021;[Epub] CrossRef - Gram-Negative Bacteria Holding Together in a Biofilm: The Acinetobacter baumannii Way
Arianna Pompilio, Daniela Scribano, Meysam Sarshar, Giovanni Di Bonaventura, Anna Teresa Palamara, Cecilia Ambrosi Microorganisms.2021; 9(7): 1353. CrossRef - Novel Genes Required for Surface-Associated Motility in Acinetobacter baumannii
Ulrike Blaschke, Evelyn Skiebe, Gottfried Wilharm Current Microbiology.2021; 78(4): 1509. CrossRef - Physicochemical and structural characterization, epitope mapping and vaccine potential investigation of a new protein containing Tetratrico Peptide Repeats of Acinetobacter baumannii: An in-silico and in-vivo approach
Sajad Abdollahi, Zeinab Raoufi, Mohammad Hadi Fakoor Molecular Immunology.2021; 140: 22. CrossRef - Proteomic Analyses of Acinetobacter baumannii Clinical Isolates to Identify Drug Resistant Mechanism
Ping Wang, Ren-Qing Li, Lei Wang, Wen-Tao Yang, Qing-Hua Zou, Di Xiao Frontiers in Cellular and Infection Microbiology.2021;[Epub] CrossRef - Galleria mellonella as a Good Model to Study Acinetobacter baumannii Pathogenesis
Ye Tao, Luminita Duma, Yannick Rossez Pathogens.2021; 10(11): 1483. CrossRef - Effect of Glucose Induction on Biofilm Density in Clinical Isolate Acinetobacter baumannii Patients in Intensive Care Unit of Dr. Soetomo Hospital, Surabaya
Wira W Lindarto, Eddy Bagus Wasito, Kartuti Debora Folia Medica Indonesiana.2020; 56(2): 118. CrossRef - Study of biofilms by V. cholerae strains on the surfaces of biotic and abiotic substrates using mass spectrometry
M. V. Poleeva, O. S. Chemisova, E. A. Menshikova, M. M. Sagakyants, E. M. Kurbatova Medical Herald of the South of Russia.2020; 11(2): 94. CrossRef - Insights Into Mechanisms of Biofilm Formation in Acinetobacter baumannii and Implications for Uropathogenesis
Jennifer M. Colquhoun, Philip N. Rather Frontiers in Cellular and Infection Microbiology.2020;[Epub] CrossRef - Proteomic and Systematic Functional Profiling Unveils Citral Targeting Antibiotic Resistance, Antioxidant Defense, and Biofilm-Associated Two-Component Systems of Acinetobacter baumannii To Encumber Biofilm and Virulence Traits
Anthonymuthu Selvaraj, Alaguvel Valliammai, Pandiyan Muthuramalingam, Sivasamy Sethupathy, Ganapathy Ashwinkumar Subramenium, Manikandan Ramesh, Shunmugiah Karutha Pandian, Tricia A. Van Laar mSystems.2020;[Epub] CrossRef - Human Pleural Fluid Elicits Pyruvate and Phenylalanine Metabolism in Acinetobacter baumannii to Enhance Cytotoxicity and Immune Evasion
Nyah Rodman, Jasmine Martinez, Sammie Fung, Jun Nakanouchi, Amber L. Myers, Caitlin M. Harris, Emily Dang, Jennifer S. Fernandez, Christine Liu, Anthony M. Mendoza, Veronica Jimenez, Nikolas Nikolaidis, Catherine A. Brennan, Robert A. Bonomo, Rodrigo Siei Frontiers in Microbiology.2019;[Epub] CrossRef - Comparative proteomics analysis between biofilm and planktonic cells of Mycobacterium tuberculosis
Chao Wang, Qiaoli Zhang, Yang Wang, Xudong Tang, Yanan An, Shulin Li, Hongyue Xu, Yan Li, Wenjing Luan, Xuefei Wang, Mingyuan Liu, Lu Yu ELECTROPHORESIS.2019; 40(20): 2736. CrossRef - An in silico structural and physicochemical characterization of TonB-dependent copper receptor in A. baumannii
Sajad Abdollahi, Iraj Rasooli, Seyed Latif Mousavi Gargari Microbial Pathogenesis.2018; 118: 18. CrossRef - Roles of outer membrane protein W (OmpW) on survival, morphology, and biofilm formation under NaCl stresses in Cronobacter sakazakii
Yingwang Ye, Na Ling, Jina Gao, Xiyan Zhang, Maofeng Zhang, Liaowang Tong, Haiyan Zeng, Jumei Zhang, Qingping Wu Journal of Dairy Science.2018; 101(5): 3844. CrossRef - A transposon mutant library of Bacillus cereus ATCC 10987 reveals novel genes required for biofilm formation and implicates motility as an important factor for pellicle‐biofilm formation
Mira Okshevsky, Matilde Greve Louw, Elena Otero Lamela, Martin Nilsson, Tim Tolker‐Nielsen, Rikke Louise Meyer MicrobiologyOpen.2018;[Epub] CrossRef - The role of TonB-dependent copper receptor in virulence of Acinetobacter baumannii
Sajad Abdollahi, Iraj Rasooli, Seyed Latif Mousavi Gargari Infection, Genetics and Evolution.2018; 60: 181. CrossRef - Human serum albumin alters specific genes that can play a role in survival and persistence in Acinetobacter baumannii
Brettni Quinn, Nyah Rodman, Eugenio Jara, Jennifer S. Fernandez, Jasmine Martinez, German M. Traglia, Sabrina Montaña, Virginia Cantera, Kori Place, Robert A. Bonomo, Andres Iriarte, María Soledad Ramírez Scientific Reports.2018;[Epub] CrossRef - Global Dynamic Proteome Study of a Pellicle-forming Acinetobacter baumannii Strain
Takfarinas Kentache, Ahmed Ben Abdelkrim, Thierry Jouenne, Emmanuelle Dé, Julie Hardouin Molecular & Cellular Proteomics.2017; 16(1): 100. CrossRef - Comparative transcriptomics analyses of the different growth states of multidrug-resistant Acinetobacter baumannii
Shuai Li, Haitao Li, Tianjie Qi, Xixin Yan, Boli Wang, Jitao Guan, Yu Li Biomedicine & Pharmacotherapy.2017; 85: 564. CrossRef - Proteomics dedicated to biofilmology: What have we learned from a decade of research?
Arbia Khemiri, Thierry Jouenne, Pascal Cosette Medical Microbiology and Immunology.2016; 205(1): 1. CrossRef - Bacterial diguanylate cyclases: Structure, function and mechanism in exopolysaccharide biofilm development
Chris G. Whiteley, Duu-Jong Lee Biotechnology Advances.2015; 33(1): 124. CrossRef - Genetic tools for manipulating Acinetobacter baumannii genome: an overview
Indranil Biswas Journal of Medical Microbiology.2015; 64(7): 657. CrossRef - A Commensal Strain of Staphylococcus epidermidis Overexpresses Membrane Proteins Associated with Pathogenesis When Grown in Biofilms
S. Águila-Arcos, S. Ding, K. Aloria, J. M. Arizmendi, I. M. Fearnley, J. E. Walker, F. M. Goñi, I. Alkorta The Journal of Membrane Biology.2015; 248(3): 431. CrossRef - Effect of iron on expression of efflux pump (adeABC) and quorum sensing (luxI, luxR) genes in clinical isolates of Acinetobacter baumannii
Farzan Modarresi, Omid Azizi, Mohammad Reza Shakibaie, Mohammad Motamedifar, Behnaz Valibeigi, Shahla Mansouri APMIS.2015; 123(11): 959. CrossRef - Microbiota diversity and gene expression dynamics in human oral biofilms
Alfonso Benítez-Páez, Pedro Belda-Ferre, Aurea Simón-Soro, Alex Mira BMC Genomics.2014; 15(1): 311. CrossRef - MALDI-TOF MS Analysis of Anaerobic Bacteria Isolated from Biofilm-Covered Surfaces in Brewery Bottling Halls
Andrea Vávrová, Dagmar Matoulková, Tereza Balážová, Ondrej Šedo Journal of the American Society of Brewing Chemists.2014; 72(2): 95. CrossRef - Effect of Chlorine Exposure on the Survival and Antibiotic Gene Expression of Multidrug Resistant Acinetobacter baumannii in Water
Deepti Karumathil, Hsin-Bai Yin, Anup Kollanoor-Johny, Kumar Venkitanarayanan International Journal of Environmental Research and Public Health.2014; 11(2): 1844. CrossRef - Identification and Characterization of Porphyromonas gingivalis Client Proteins That Bind to Streptococcus oralis Glyceraldehyde-3-Phosphate Dehydrogenase
Kazuhiko Maeda, Hideki Nagata, Masae Kuboniwa, Miki Ojima, Tsukasa Osaki, Naoto Minamino, Atsuo Amano, B. A. McCormick Infection and Immunity.2013; 81(3): 753. CrossRef - H-NS Plays a Role in Expression of Acinetobacter baumannii Virulence Features
Bart A. Eijkelkamp, Uwe H. Stroeher, Karl A. Hassan, Liam D. H. Elbourne, Ian T. Paulsen, Melissa H. Brown, S. M. Payne Infection and Immunity.2013; 81(7): 2574. CrossRef - 1H NMR-Based Metabolite Profiling of Planktonic and Biofilm Cells in Acinetobacter baumannii 1656-2
Jinki Yeom, Ji-Hyun Shin, Ji-Young Yang, Jungmin Kim, Geum-Sook Hwang, Jacob Guy Bundy PLoS ONE.2013; 8(3): e57730. CrossRef - Micropatterning with conical features can control bacterial adhesion on silicone
Stefano Perni, Polina Prokopovich Soft Matter.2013; 9(6): 1844. CrossRef - Electromodulated release of nitric oxide through polymer material from reservoir of inorganic nitrite salt
Lajos Höfler, Dipankar Koley, Jianfeng Wu, Chuanwu Xi, Mark E. Meyerhoff RSC Advances.2012; 2(17): 6765. CrossRef - Unraveling the resistance of microbial biofilms: Has proteomics been helpful?
C. Jayampath Seneviratne, Yu Wang, Lijian Jin, Sarah S. W. Wong, Thanuja D. K. Herath, Lakshman P. Samaranayake PROTEOMICS.2012; 12(4-5): 651. CrossRef - LuxS-Dependent AI-2 Regulates Versatile Functions in Enterococcus faecalis V583
Changlin Shao, Wei Shang, Zhan Yang, Zhongke Sun, Yunmei Li, Jing Guo, Xuesong Wang, DaYang Zou, Simiao Wang, Hong Lei, Qian Cui, Zhitao Yin, Xuelian Li, Xiao Wei, Wei Liu, Xiang He, Zheng Jiang, Shuangkui Du, Xiangru Liao, Liuyu Huang, Yufei Wang, Jing Y Journal of Proteome Research.2012; 11(9): 4465. CrossRef - Comparative Proteomic Analysis of Streptococcus suis Biofilms and Planktonic Cells That Identified Biofilm Infection-Related Immunogenic Proteins
Yang Wang, Li Yi, Zongfu Wu, Jing Shao, Guangjin Liu, Hongjie Fan, Wei Zhang, Chengping Lu, Michael Chaussee PLoS ONE.2012; 7(4): e33371. CrossRef - Host-microbe interactions that shape the pathogenesis ofAcinetobacter baumanniiinfection
Brittany L. Mortensen, Eric P. Skaar Cellular Microbiology.2012; 14(9): 1336. CrossRef - Differential Proteomic Analysis of a Polymicrobial Biofilm
Zamirah Zainal-Abidin, Paul D. Veith, Stuart G. Dashper, Ying Zhu, Deanne V. Catmull, Yu-Yen Chen, Deasy C. Heryanto, Dina Chen, James S. Pyke, Kheng Tan, Helen L. Mitchell, Eric C. Reynolds Journal of Proteome Research.2012; 11(9): 4449. CrossRef - A genome-wide study of two-component signal transduction systems in eight newly sequenced mutans streptococci strains
Lifu Song, Padhmanand Sudhakar, Wei Wang, Georg Conrads, Anke Brock, Jibin Sun, Irene Wagner-Döbler, An-Ping Zeng BMC Genomics.2012;[Epub] CrossRef - Proteomic Analysis of Neisseria gonorrhoeae Biofilms Shows Shift to Anaerobic Respiration and Changes in Nutrient Transport and Outermembrane Proteins
Nancy J. Phillips, Christopher T. Steichen, Birgit Schilling, Deborah M. B. Post, Richard K. Niles, Thomas B. Bair, Megan L. Falsetta, Michael A. Apicella, Bradford W. Gibson, Pedro Santos PLoS ONE.2012; 7(6): e38303. CrossRef - Comparative Proteomics of Inner Membrane Fraction from Carbapenem-Resistant Acinetobacter baumannii with a Reference Strain
Vishvanath Tiwari, Jitendraa Vashistt, Arti Kapil, Rajeswari R. Moganty, Pedro Santos PLoS ONE.2012; 7(6): e39451. CrossRef - Nuclear Translocation of Acinetobacter baumannii Transposase Induces DNA Methylation of CpG Regions in the Promoters of E-cadherin Gene
Dong Chan Moon, Chul Hee Choi, Su Man Lee, Jung Hwa Lee, Seung Il Kim, Dong Sun Kim, Je Chul Lee, Riccardo Manganelli PLoS ONE.2012; 7(6): e38974. CrossRef -
Acinetobacter baumannii virulence is enhanced in Galleria mellonella following biofilm adaptation
Matthew E. Wand, Lucy J. Bock, Jane F. Turton, Philip G. Nugent, J. Mark Sutton
Journal of Medical Microbiology
.2012; 61(4): 470. CrossRef - Complete Genome Sequence of Multidrug-Resistant Acinetobacter baumannii Strain 1656-2, Which Forms Sturdy Biofilm
Jin Yeol Park, Shukho Kim, Sung-Min Kim, Sun Ho Cha, Si-Kyu Lim, Jungmin Kim Journal of Bacteriology.2011; 193(22): 6393. CrossRef - Biofilm formation byAcinetobacter baumanniistrains isolated from urinary tract infection and urinary catheters
Nadia Kazemi Pour, Devendra H. Dusane, Prashant K. Dhakephalkar, Farokh Rokhbakhsh Zamin, Smita S. Zinjarde, Balu A. Chopade FEMS Immunology & Medical Microbiology.2011; 62(3): 328. CrossRef - Proteomic and Functional Analyses Reveal a Unique Lifestyle for Acinetobacter baumannii Biofilms and a Key Role for Histidine Metabolism
Maria P. Cabral, Nelson C. Soares, Jesús Aranda, José R. Parreira, Carlos Rumbo, Margarita Poza, Jaione Valle, Valentina Calamia, Íñigo Lasa, Germán Bou Journal of Proteome Research.2011; 10(8): 3399. CrossRef - YibK is the 2′-O-methyltransferase TrmL that modifies the wobble nucleotide in Escherichia coli tRNALeu isoacceptors
Alfonso Benítez-Páez, Magda Villarroya, Stephen Douthwaite, Toni Gabaldón, M.-Eugenia Armengod RNA.2010; 16(11): 2131. CrossRef
- Targeting the rpoB Gene Using Nested PCR-Restriction Fragment Length Polymorphism for Identification of Nontuberculous Mycobacteria in Hospital Tap Water
-
Ji-Hyun Shin , Hae-Kyung Lee , Eun-Jin Cho , Jae-Yon Yu , Yeon-Ho Kang
-
J. Microbiol. 2008;46(6):608-614. Published online December 24, 2008
-
DOI: https://doi.org/10.1007/s12275-008-0102-6
-
-
787
View
-
0
Download
-
15
Crossref
-
Abstract
PDF
-
Nontuberculous mycobacteria (NTM) are ubiquitous in the environment and can cause nosocomial infections in immunocompromised patients. Recently the presence of NTM in public drinking water and hospital water distribution systems has been reported. Their ability to form biofilms and their resistance to chlorine both contribute to their survival and colonization in water distribution systems. Here we analyzed thirty-two hospital tap water samples that were collected from different locations in three hospitals so as to evaluate the prevalence of NTM species. The water samples were concentrated by membrane filtration and then eluted with sterilized water following sonication. Two-step direct PCR targeting the rpoB gene, restriction fragment length polymorphism (RFLP) using the MspI restriction enzyme, and sequence analysis were performed for identification of NTM to the species level. The sequences of each PCR product were analyzed using BLASTN. Seven samples (7/32, 21.9%) were positive for NTM as determined by nested-PCR. The PCR-RFLP results indicated five different patterns among the seven positive PCR samples. The waterborn NTM were identified, including M. peregrinum, M. chelonae (2 cases), M. abscessus, M. gordonae (2 cases), and Mycobacterium sp. JLS. The direct two-step PCR-RFLP method targeting the rpoB gene was effective for the detection and the differentiation of NTM species from hospital tap water.
-
Citations
Citations to this article as recorded by 
- Occurrence of opportunistic pathogens in private wells after major flooding events: A four state molecular survey
Kris Mapili, William J. Rhoads, Mary Coughter, Kelsey J. Pieper, Marc A. Edwards, Amy Pruden Science of The Total Environment.2022; 826: 153901. CrossRef - Omadacycline for management of Mycobacterium abscessus infections: a review of its effectiveness, place in therapy, and considerations for use
Ashley R. Rizzo, Nader H. Moniri BMC Infectious Diseases.2022;[Epub] CrossRef - Threat in Water for Drinking and Domestic Use
Dursun Atik, Sukrü Oksuz, Elif Ozturk, Emel Çaliskan, Nida Akar, Mehmet Ali Sungur The International Journal of Mycobacteriology.2021; 10(2): 188. CrossRef - Prevalence of Non-Tuberculous Mycobacteria in Hospital Waters of Major Cities of Khuzestan Province, Iran
Azar Dokht Khosravi, Abdolrazagh Hashemi Shahraki, Mohammad Hashemzadeh, Rasa Sheini Mehrabzadeh, Ali Teimoori Frontiers in Cellular and Infection Microbiology.2016;[Epub] CrossRef - Nosocomial pseudo-outbreak of Mycobacterium gordonae associated with a hospital's water supply contamination: a case series of 135 patients
Marija Zlojtro, Mateja Jankovic, Miroslav Samarzija, Ljiljana Zmak, Vera Katalinic Jankovic, Mihaela Obrovac, Igor Zlojtro, Marko Jakopovic Journal of Water and Health.2015; 13(1): 125. CrossRef - Endosymbiotic Mycobacterium chelonae in a Vermamoeba vermiformis strain isolated from the nasal mucosa of an HIV patient in Lima, Peru
Alfonso Martín Cabello-Vílchez, Rosmery Mena, Johanna Zuñiga, Pablo Cermeño, Carmen Ma Martín-Navarro, Ana C. González, Atteneri López-Arencibia, María Reyes-Batlle, José E. Piñero, Basilio Valladares, Jacob Lorenzo-Morales Experimental Parasitology.2014; 145: S127. CrossRef - Sacroiliitis secondary to catheter-related bacteremia due to Mycobacterium abscessus (sensu stricto)
Chrislène Laurens, Geneviève Héry-Arnaud, Raphael Chiron, Eric Oziol, Hélène Jean-Pierre, Nicolas Bouzinbi, Philippe Vande Perre, Anne-Laure Bañuls, Sylvain Godreuil Annals of Clinical Microbiology and Antimicrobials.2014;[Epub] CrossRef - Mycobacterium abscessus Induces a Limited Pattern of Neutrophil Activation That Promotes Pathogen Survival
Kenneth C. Malcolm, E. Michelle Nichols, Silvia M. Caceres, Jennifer E. Kret, Stacey L. Martiniano, Scott D. Sagel, Edward D. Chan, Lindsay Caverly, George M. Solomon, Paul Reynolds, Donna L. Bratton, Jennifer L. Taylor-Cousar, David P. Nichols, Milene T. PLoS ONE.2013; 8(2): e57402. CrossRef - Standardization of multilocus sequence typing scheme for Mycobacterium abscessus and Mycobacterium massiliense
Song Yee Kim, Young Ae Kang, Il Kwon Bae, Jae-Joon Yim, Moo Suk Park, Young Sam Kim, Se Kyu Kim, Joon Chang, Seok Hoon Jeong Diagnostic Microbiology and Infectious Disease.2013; 77(2): 143. CrossRef - Mycobacterium abscessus multispacer sequence typing
Mohamed Sassi, Imen Ben Kahla, Michel Drancourt BMC Microbiology.2013;[Epub] CrossRef - Diversity, Community Composition, and Dynamics of Nonpigmented and Late-Pigmenting Rapidly Growing Mycobacteria in an Urban Tap Water Production and Distribution System
S. Dubrou, J. Konjek, E. Macheras, B. Welté, L. Guidicelli, E. Chignon, M. Joyeux, J. L. Gaillard, B. Heym, T. Tully, G. Sapriel Applied and Environmental Microbiology.2013; 79(18): 5498. CrossRef - Isolation of nontuberculous mycobacteria from hospital waters in Turkey
Gonca Erkose Genc, Elvira Richter, Zayre Erturan APMIS.2013; 121(12): 1192. CrossRef - Mycobacteria in water, soil, plants and air: a review
K. Hruska, M. Kaevska Veterinární medicína.2012; 57(12): 623. CrossRef - Molecular Survey of the Occurrence of Legionella spp., Mycobacterium spp., Pseudomonas aeruginosa, and Amoeba Hosts in Two Chloraminated Drinking Water Distribution Systems
Hong Wang, Marc Edwards, Joseph O. Falkinham, Amy Pruden Applied and Environmental Microbiology.2012; 78(17): 6285. CrossRef -
Multilocus Sequence Analysis and
rpoB
Sequencing of Mycobacterium abscessus (Sensu Lato) Strains
Edouard Macheras, Anne-Laure Roux, Sylvaine Bastian, Sylvia Cardoso Leão, Moises Palaci, Valérie Sivadon-Tardy, Cristina Gutierrez, Elvira Richter, Sabine Rüsch-Gerdes, Gaby Pfyffer, Thomas Bodmer, Emmanuelle Cambau, Jean-Louis Gaillard, Beate Heym Journal of Clinical Microbiology.2011; 49(2): 491. CrossRef
|