Enterobacter sp. Strain SM1_HS2B Manifests Transient Elongation and Swimming Motility in Liquid Medium

Bacteria undergo morphological changes in order to cope with external stresses. Among the best-known examples are cell elongation and hyperflagellation in the context of swarming motility. Many species of bacteria change their morphology and behavior under external stresses. In this study, we report...

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Published inMicrobiology spectrum Vol. 10; no. 3; p. e0207821
Main Authors Zhang, Zhiyu, Liu, Haoming, Karani, Hamid, Mallen, Jon, Chen, Weijie, De, Arpan, Mani, Sridhar, Tang, Jay X.
Format Journal Article
LanguageEnglish
Published United States American Society for Microbiology 01.06.2022
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ISSN2165-0497
2165-0497
DOI10.1128/spectrum.02078-21

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Abstract Bacteria undergo morphological changes in order to cope with external stresses. Among the best-known examples are cell elongation and hyperflagellation in the context of swarming motility. Many species of bacteria change their morphology and behavior under external stresses. In this study, we report transient elongation and swimming motility of a novel Enterobacter sp. strain, SM1_HS2B, in liquid broth under a standard growth condition. When growing in the Luria-Bertani medium, HS2B cells delay their cell division and elongate. Although transient over a few hours, the average cell length reaches over 10 times that of the stationary-state cells. The increase is also cumulative following repeated growth cycles stimulated by taking cells out of the exponential phase and adding them into fresh medium every 2 hours. The majority of the cells attain swimming motility during the exponential growth phase, and then they lose swimming motility over the course of several hours. Both daughter cells due to division of a long swimming cell retain the ability to swim. We confirm that the long HS2B cells swim with rigid-body rotation along their body axis. These findings based on microscopic observation following repeated cycles of growth establish HS2B as a prototype strain with sensitive dependence of size and motility on its physical and biochemical environment. IMPORTANCE Bacteria undergo morphological changes in order to cope with external stresses. Among the best-known examples are cell elongation and hyperflagellation in the context of swarming motility. The subject of this report, SM1_HS2B, is a hyperswarming strain of a newly identified species of enterobacteria, noted as Enterobacter sp. SM1. The key finding that SM1_HS2B transiently elongates to extreme length in fresh liquid medium offers new insights on regulation in bacterial growth and division. SM1_HS2B also manifests transient but vigorous swimming motility during the exponential phase of growth in liquid medium. These properties establish HS2B as a prototype strain with sensitive dependence of size and motility on its physical and biochemical environment. Such a dependence may be relevant to swarming behavior with a significant environmental or physiological outcome.
AbstractList Many species of bacteria change their morphology and behavior under external stresses. In this study, we report transient elongation and swimming motility of a novel Enterobacter sp. strain, SM1_HS2B, in liquid broth under a standard growth condition. When growing in the Luria-Bertani medium, HS2B cells delay their cell division and elongate. Although transient over a few hours, the average cell length reaches over 10 times that of the stationary-state cells. The increase is also cumulative following repeated growth cycles stimulated by taking cells out of the exponential phase and adding them into fresh medium every 2 hours. The majority of the cells attain swimming motility during the exponential growth phase, and then they lose swimming motility over the course of several hours. Both daughter cells due to division of a long swimming cell retain the ability to swim. We confirm that the long HS2B cells swim with rigid-body rotation along their body axis. These findings based on microscopic observation following repeated cycles of growth establish HS2B as a prototype strain with sensitive dependence of size and motility on its physical and biochemical environment. Bacteria undergo morphological changes in order to cope with external stresses. Among the best-known examples are cell elongation and hyperflagellation in the context of swarming motility. The subject of this report, SM1_HS2B, is a hyperswarming strain of a newly identified species of enterobacteria, noted as Enterobacter sp. SM1. The key finding that SM1_HS2B transiently elongates to extreme length in fresh liquid medium offers new insights on regulation in bacterial growth and division. SM1_HS2B also manifests transient but vigorous swimming motility during the exponential phase of growth in liquid medium. These properties establish HS2B as a prototype strain with sensitive dependence of size and motility on its physical and biochemical environment. Such a dependence may be relevant to swarming behavior with a significant environmental or physiological outcome.
ABSTRACT Many species of bacteria change their morphology and behavior under external stresses. In this study, we report transient elongation and swimming motility of a novel Enterobacter sp. strain, SM1_HS2B, in liquid broth under a standard growth condition. When growing in the Luria-Bertani medium, HS2B cells delay their cell division and elongate. Although transient over a few hours, the average cell length reaches over 10 times that of the stationary-state cells. The increase is also cumulative following repeated growth cycles stimulated by taking cells out of the exponential phase and adding them into fresh medium every 2 hours. The majority of the cells attain swimming motility during the exponential growth phase, and then they lose swimming motility over the course of several hours. Both daughter cells due to division of a long swimming cell retain the ability to swim. We confirm that the long HS2B cells swim with rigid-body rotation along their body axis. These findings based on microscopic observation following repeated cycles of growth establish HS2B as a prototype strain with sensitive dependence of size and motility on its physical and biochemical environment. IMPORTANCE Bacteria undergo morphological changes in order to cope with external stresses. Among the best-known examples are cell elongation and hyperflagellation in the context of swarming motility. The subject of this report, SM1_HS2B, is a hyperswarming strain of a newly identified species of enterobacteria, noted as Enterobacter sp. SM1. The key finding that SM1_HS2B transiently elongates to extreme length in fresh liquid medium offers new insights on regulation in bacterial growth and division. SM1_HS2B also manifests transient but vigorous swimming motility during the exponential phase of growth in liquid medium. These properties establish HS2B as a prototype strain with sensitive dependence of size and motility on its physical and biochemical environment. Such a dependence may be relevant to swarming behavior with a significant environmental or physiological outcome.
Many species of bacteria change their morphology and behavior under external stresses. In this study, we report transient elongation and swimming motility of a novel Enterobacter sp. strain, SM1_HS2B, in liquid broth under a standard growth condition. When growing in the Luria-Bertani medium, HS2B cells delay their cell division and elongate. Although transient over a few hours, the average cell length reaches over 10 times that of the stationary-state cells. The increase is also cumulative following repeated growth cycles stimulated by taking cells out of the exponential phase and adding them into fresh medium every 2 hours. The majority of the cells attain swimming motility during the exponential growth phase, and then they lose swimming motility over the course of several hours. Both daughter cells due to division of a long swimming cell retain the ability to swim. We confirm that the long HS2B cells swim with rigid-body rotation along their body axis. These findings based on microscopic observation following repeated cycles of growth establish HS2B as a prototype strain with sensitive dependence of size and motility on its physical and biochemical environment. IMPORTANCE Bacteria undergo morphological changes in order to cope with external stresses. Among the best-known examples are cell elongation and hyperflagellation in the context of swarming motility. The subject of this report, SM1_HS2B, is a hyperswarming strain of a newly identified species of enterobacteria, noted as Enterobacter sp. SM1. The key finding that SM1_HS2B transiently elongates to extreme length in fresh liquid medium offers new insights on regulation in bacterial growth and division. SM1_HS2B also manifests transient but vigorous swimming motility during the exponential phase of growth in liquid medium. These properties establish HS2B as a prototype strain with sensitive dependence of size and motility on its physical and biochemical environment. Such a dependence may be relevant to swarming behavior with a significant environmental or physiological outcome.
Many species of bacteria change their morphology and behavior under external stresses. In this study, we report transient elongation and swimming motility of a novel Enterobacter sp. strain, SM1_HS2B, in liquid broth under a standard growth condition. When growing in the Luria-Bertani medium, HS2B cells delay their cell division and elongate. Although transient over a few hours, the average cell length reaches over 10 times that of the stationary-state cells. The increase is also cumulative following repeated growth cycles stimulated by taking cells out of the exponential phase and adding them into fresh medium every 2 hours. The majority of the cells attain swimming motility during the exponential growth phase, and then they lose swimming motility over the course of several hours. Both daughter cells due to division of a long swimming cell retain the ability to swim. We confirm that the long HS2B cells swim with rigid-body rotation along their body axis. These findings based on microscopic observation following repeated cycles of growth establish HS2B as a prototype strain with sensitive dependence of size and motility on its physical and biochemical environment. IMPORTANCE Bacteria undergo morphological changes in order to cope with external stresses. Among the best-known examples are cell elongation and hyperflagellation in the context of swarming motility. The subject of this report, SM1_HS2B, is a hyperswarming strain of a newly identified species of enterobacteria, noted as Enterobacter sp. SM1. The key finding that SM1_HS2B transiently elongates to extreme length in fresh liquid medium offers new insights on regulation in bacterial growth and division. SM1_HS2B also manifests transient but vigorous swimming motility during the exponential phase of growth in liquid medium. These properties establish HS2B as a prototype strain with sensitive dependence of size and motility on its physical and biochemical environment. Such a dependence may be relevant to swarming behavior with a significant environmental or physiological outcome.
Many species of bacteria change their morphology and behavior under external stresses. In this study, we report transient elongation and swimming motility of a novel Enterobacter sp. strain, SM1_HS2B, in liquid broth under a standard growth condition. When growing in the Luria-Bertani medium, HS2B cells delay their cell division and elongate. Although transient over a few hours, the average cell length reaches over 10 times that of the stationary-state cells. The increase is also cumulative following repeated growth cycles stimulated by taking cells out of the exponential phase and adding them into fresh medium every 2 hours. The majority of the cells attain swimming motility during the exponential growth phase, and then they lose swimming motility over the course of several hours. Both daughter cells due to division of a long swimming cell retain the ability to swim. We confirm that the long HS2B cells swim with rigid-body rotation along their body axis. These findings based on microscopic observation following repeated cycles of growth establish HS2B as a prototype strain with sensitive dependence of size and motility on its physical and biochemical environment. IMPORTANCE Bacteria undergo morphological changes in order to cope with external stresses. Among the best-known examples are cell elongation and hyperflagellation in the context of swarming motility. The subject of this report, SM1_HS2B, is a hyperswarming strain of a newly identified species of enterobacteria, noted as Enterobacter sp. SM1. The key finding that SM1_HS2B transiently elongates to extreme length in fresh liquid medium offers new insights on regulation in bacterial growth and division. SM1_HS2B also manifests transient but vigorous swimming motility during the exponential phase of growth in liquid medium. These properties establish HS2B as a prototype strain with sensitive dependence of size and motility on its physical and biochemical environment. Such a dependence may be relevant to swarming behavior with a significant environmental or physiological outcome.Many species of bacteria change their morphology and behavior under external stresses. In this study, we report transient elongation and swimming motility of a novel Enterobacter sp. strain, SM1_HS2B, in liquid broth under a standard growth condition. When growing in the Luria-Bertani medium, HS2B cells delay their cell division and elongate. Although transient over a few hours, the average cell length reaches over 10 times that of the stationary-state cells. The increase is also cumulative following repeated growth cycles stimulated by taking cells out of the exponential phase and adding them into fresh medium every 2 hours. The majority of the cells attain swimming motility during the exponential growth phase, and then they lose swimming motility over the course of several hours. Both daughter cells due to division of a long swimming cell retain the ability to swim. We confirm that the long HS2B cells swim with rigid-body rotation along their body axis. These findings based on microscopic observation following repeated cycles of growth establish HS2B as a prototype strain with sensitive dependence of size and motility on its physical and biochemical environment. IMPORTANCE Bacteria undergo morphological changes in order to cope with external stresses. Among the best-known examples are cell elongation and hyperflagellation in the context of swarming motility. The subject of this report, SM1_HS2B, is a hyperswarming strain of a newly identified species of enterobacteria, noted as Enterobacter sp. SM1. The key finding that SM1_HS2B transiently elongates to extreme length in fresh liquid medium offers new insights on regulation in bacterial growth and division. SM1_HS2B also manifests transient but vigorous swimming motility during the exponential phase of growth in liquid medium. These properties establish HS2B as a prototype strain with sensitive dependence of size and motility on its physical and biochemical environment. Such a dependence may be relevant to swarming behavior with a significant environmental or physiological outcome.
Bacteria undergo morphological changes in order to cope with external stresses. Among the best-known examples are cell elongation and hyperflagellation in the context of swarming motility. Many species of bacteria change their morphology and behavior under external stresses. In this study, we report transient elongation and swimming motility of a novel Enterobacter sp. strain, SM1_HS2B, in liquid broth under a standard growth condition. When growing in the Luria-Bertani medium, HS2B cells delay their cell division and elongate. Although transient over a few hours, the average cell length reaches over 10 times that of the stationary-state cells. The increase is also cumulative following repeated growth cycles stimulated by taking cells out of the exponential phase and adding them into fresh medium every 2 hours. The majority of the cells attain swimming motility during the exponential growth phase, and then they lose swimming motility over the course of several hours. Both daughter cells due to division of a long swimming cell retain the ability to swim. We confirm that the long HS2B cells swim with rigid-body rotation along their body axis. These findings based on microscopic observation following repeated cycles of growth establish HS2B as a prototype strain with sensitive dependence of size and motility on its physical and biochemical environment. IMPORTANCE Bacteria undergo morphological changes in order to cope with external stresses. Among the best-known examples are cell elongation and hyperflagellation in the context of swarming motility. The subject of this report, SM1_HS2B, is a hyperswarming strain of a newly identified species of enterobacteria, noted as Enterobacter sp. SM1. The key finding that SM1_HS2B transiently elongates to extreme length in fresh liquid medium offers new insights on regulation in bacterial growth and division. SM1_HS2B also manifests transient but vigorous swimming motility during the exponential phase of growth in liquid medium. These properties establish HS2B as a prototype strain with sensitive dependence of size and motility on its physical and biochemical environment. Such a dependence may be relevant to swarming behavior with a significant environmental or physiological outcome.
Author Zhang, Zhiyu
Chen, Weijie
Mani, Sridhar
Liu, Haoming
Tang, Jay X.
Karani, Hamid
Mallen, Jon
De, Arpan
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Cites_doi 10.1103/PhysRevLett.114.018105
10.1016/j.ijantimicag.2009.12.011
10.1007/BF02013529
10.1053/j.gastro.2021.03.017
10.1046/j.1365-2672.1999.00602.x
10.1038/s41598-018-34192-2
10.1016/j.tim.2008.07.004
10.1128/AEM.02191-18
10.1128/JB.181.6.1703-1712.1999
10.1073/pnas.1420702111
10.1128/jb.175.19.6238-6244.1993
10.1039/c3sm53127a
10.1007/s00253-020-10590-3
10.1101/gad.1373905
10.1111/j.1365-2958.2008.06469.x
10.3184/003685003783238725
10.1111/mmi.13218
10.1016/j.celrep.2013.07.026
10.1128/AEM.66.4.1274-1279.2000
10.1111/j.1472-765X.2007.02187.x
10.3389/fmicb.2015.00657
10.1128/MMBR.00001-06
10.1038/nrmicro2405
10.1016/j.bpj.2017.02.019
10.1046/j.1365-2958.2003.03584.x
10.1016/j.cub.2007.04.050
10.1016/0021-9290(94)00116-l
10.1128/aem.50.2.364-372.1985
10.1016/s1369-5274(99)00033-8
10.1016/j.ijfoodmicro.2006.04.026
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Issue 3
Keywords swarming
cell division
hyperswarming
bacterial growth
bacterial swarming
hyperswarmer
flagellar
septa
bacterial motility
flagella
swimming
Enterobacter
bacterial swimming
bacterial elongation
Language English
License This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license. https://creativecommons.org/licenses/by/4.0
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The authors declare no conflict of interest.
Zhiyu Zhang and Haoming Liu contributed equally to this article. Author order was determined by based on chronology in participation.
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References e_1_3_3_17_2
e_1_3_3_16_2
e_1_3_3_19_2
e_1_3_3_18_2
e_1_3_3_13_2
e_1_3_3_12_2
e_1_3_3_15_2
e_1_3_3_14_2
e_1_3_3_32_2
e_1_3_3_33_2
e_1_3_3_11_2
e_1_3_3_30_2
e_1_3_3_10_2
e_1_3_3_31_2
Kusumaningrum HD (e_1_3_3_23_2) 2003
e_1_3_3_6_2
e_1_3_3_5_2
e_1_3_3_8_2
e_1_3_3_7_2
e_1_3_3_28_2
e_1_3_3_9_2
e_1_3_3_27_2
e_1_3_3_29_2
e_1_3_3_24_2
e_1_3_3_25_2
e_1_3_3_2_2
e_1_3_3_20_2
Li M (e_1_3_3_26_2) 2010
e_1_3_3_4_2
e_1_3_3_22_2
e_1_3_3_3_2
e_1_3_3_21_2
Benisty, S, Ben-Jacob, E, Ariel, G, Be’er, A (B14) 2015; 114
Eberl, L, Molin, S, Givskov, M (B20) 1999; 181
Ghaffar, NM, Connerton, PL, Connerton, IF (B27) 2015; 6
De, A, Chen, W, Li, H, Wright, JR, Lamendella, R, Lukin, DJ, Szymczak, WA, Sun, K, Kelly, L, Ghosh, S, Kearns, DB, He, Z, Jobin, C, Luo, X, Byju, A, Chatterjee, S, San Yeoh, B, Vijay-Kumar, M, Tang, JX, Prajapati, M, Bartnikas, TB, Mani, S (B16) 2021; 161
Verstraeten, N, Braeken, K, Debkumari, B, Fauvart, M, Fransaer, J, Vermant, J, Michiels, J (B11) 2008; 16
Fraser, GM, Hughes, C (B19) 1999; 2
Hazeleger, WC, Dalvoorde, M, Beumer, RR (B7) 2006; 112
Mattick, KL, Jørgensen, F, Legan, JD, Cole, MB, Porter, J, Lappin-Scott, HM, Humphrey, TJ (B21) 2000; 66
Jensen, RH, Woolfolk, CA (B4) 1985; 50
Patrick, JE, Kearns, DB (B29) 2008; 70
Mattick, KL, Rowbury, RJ, Humphrey, TJ (B5) 2003; 86
Dev Kumar, G, Macarisin, D, Micallef, SA (B28) 2019; 85
Martínez, LE, Hardcastle, JM, Wang, J, Pincus, Z, Tsang, J, Hoover, TR, Bansil, R, Salama, NR (B17) 2016; 99
Deforet, M, van Ditmarsch, D, Carmona-Fontaine, C, Xavier, JB (B31) 2014; 10
van Ditmarsch, D, Boyle, KE, Sakhtah, H, Oyler, JE, Nadell, CD, Déziel, É, Dietrich, LEP, Xavier, JB (B30) 2013; 4
Güde, H (B2) 1979; 5
McMahon, MAS, McDowell, DA, Blair, IS (B23) 2007; 45
Høiby, N, Bjarnsholt, T, Givskov, M, Molin, S, Ciofu, O (B15) 2010; 35
Kearns, DB, Losick, R (B26) 2005; 19
Rizzo, MG, De Plano, LM, Franco, D (B8) 2020; 104
Kearns, DB, Losick, R (B18) 2003; 49
Kusumaningrum, HD (B22) 2003
Yang, A, Tang, WS, Si, T, Tang, JX (B10) 2017; 112
Young, KD (B1) 2006; 70
Li, M (B25) 2010
Kearns, DB (B9) 2010; 8
Challis, JH (B24) 1995; 28
Amsler, CD, Cho, M, Matsumura, P (B32) 1993; 175
Wainwright, M, Canham, LT, Al-Wajeeh, K, Reeves, CL (B3) 1999; 29
Partridge, JD, Ariel, G, Schvartz, O, Harshey, RM, Be’er, A (B13) 2018; 8
Bos, J, Zhang, Q, Vyawahare, S, Rogers, E, Rosenberg, SM, Austin, RH (B6) 2015; 112
Kaiser, D (B12) 2007; 17
References_xml – ident: e_1_3_3_15_2
  doi: 10.1103/PhysRevLett.114.018105
– ident: e_1_3_3_16_2
  doi: 10.1016/j.ijantimicag.2009.12.011
– ident: e_1_3_3_3_2
  doi: 10.1007/BF02013529
– ident: e_1_3_3_17_2
  doi: 10.1053/j.gastro.2021.03.017
– ident: e_1_3_3_4_2
  doi: 10.1046/j.1365-2672.1999.00602.x
– ident: e_1_3_3_14_2
  doi: 10.1038/s41598-018-34192-2
– ident: e_1_3_3_12_2
  doi: 10.1016/j.tim.2008.07.004
– ident: e_1_3_3_29_2
  doi: 10.1128/AEM.02191-18
– ident: e_1_3_3_21_2
  doi: 10.1128/JB.181.6.1703-1712.1999
– ident: e_1_3_3_7_2
  doi: 10.1073/pnas.1420702111
– ident: e_1_3_3_33_2
  doi: 10.1128/jb.175.19.6238-6244.1993
– ident: e_1_3_3_32_2
  doi: 10.1039/c3sm53127a
– ident: e_1_3_3_9_2
  doi: 10.1007/s00253-020-10590-3
– ident: e_1_3_3_27_2
  doi: 10.1101/gad.1373905
– ident: e_1_3_3_30_2
  doi: 10.1111/j.1365-2958.2008.06469.x
– ident: e_1_3_3_6_2
  doi: 10.3184/003685003783238725
– ident: e_1_3_3_18_2
  doi: 10.1111/mmi.13218
– ident: e_1_3_3_31_2
  doi: 10.1016/j.celrep.2013.07.026
– volume-title: Behaviour and cross-contamination of pathogenic bacteria in household kitchens-relevance to exposure assessment.
  year: 2003
  ident: e_1_3_3_23_2
– ident: e_1_3_3_22_2
  doi: 10.1128/AEM.66.4.1274-1279.2000
– ident: e_1_3_3_24_2
  doi: 10.1111/j.1472-765X.2007.02187.x
– ident: e_1_3_3_28_2
  doi: 10.3389/fmicb.2015.00657
– ident: e_1_3_3_2_2
  doi: 10.1128/MMBR.00001-06
– ident: e_1_3_3_10_2
  doi: 10.1038/nrmicro2405
– volume-title: Experimental study of swimming flagellated bacteria and their collective behaviour in concentrated suspensions.
  year: 2010
  ident: e_1_3_3_26_2
– ident: e_1_3_3_11_2
  doi: 10.1016/j.bpj.2017.02.019
– ident: e_1_3_3_19_2
  doi: 10.1046/j.1365-2958.2003.03584.x
– ident: e_1_3_3_13_2
  doi: 10.1016/j.cub.2007.04.050
– ident: e_1_3_3_25_2
  doi: 10.1016/0021-9290(94)00116-l
– ident: e_1_3_3_5_2
  doi: 10.1128/aem.50.2.364-372.1985
– ident: e_1_3_3_20_2
  doi: 10.1016/s1369-5274(99)00033-8
– ident: e_1_3_3_8_2
  doi: 10.1016/j.ijfoodmicro.2006.04.026
– volume: 86
  start-page: 103
  year: 2003
  end-page: 113
  ident: B5
  article-title: Morphological changes to Escherichia coli O157:H7, commensal E. coli and Salmonella spp in response to marginal growth conditions, with special reference to mildly stressing temperatures
  publication-title: Sci Prog
  doi: 10.3184/003685003783238725
– volume: 112
  start-page: 1462
  year: 2017
  end-page: 1471
  ident: B10
  article-title: Influence of physical effects on the swarming motility of Pseudomonas aeruginosa
  publication-title: Biophys J
  doi: 10.1016/j.bpj.2017.02.019
– volume: 70
  start-page: 1166
  year: 2008
  end-page: 1179
  ident: B29
  article-title: MinJ (YvjD) is a topological determinant of cell division in Bacillus subtilis
  publication-title: Mol Microbiol
  doi: 10.1111/j.1365-2958.2008.06469.x
– volume: 28
  start-page: 733
  year: 1995
  end-page: 737
  ident: B24
  article-title: A procedure for determining rigid body transformation parameters
  publication-title: J Biomech
  doi: 10.1016/0021-9290(94)00116-l
– volume: 70
  start-page: 660
  year: 2006
  end-page: 703
  ident: B1
  article-title: The selective value of bacterial shape
  publication-title: Microbiol Mol Biol Rev
  doi: 10.1128/MMBR.00001-06
– volume: 8
  start-page: 15823
  year: 2018
  ident: B13
  article-title: The 3D architecture of a bacterial swarm has implications for antibiotic tolerance
  publication-title: Sci Rep
  doi: 10.1038/s41598-018-34192-2
– volume: 175
  start-page: 6238
  year: 1993
  end-page: 6244
  ident: B32
  article-title: Multiple factors underlying the maximum motility of Escherichia coli as cultures enter post-exponential growth
  publication-title: J Bacteriol
  doi: 10.1128/jb.175.19.6238-6244.1993
– volume: 112
  start-page: 288
  year: 2006
  end-page: 290
  ident: B7
  article-title: Fluorescence microscopy of NaCl-stressed, elongated Salmonella and Listeria cells reveals the presence of septa in filaments
  publication-title: Int J Food Microbiol
  doi: 10.1016/j.ijfoodmicro.2006.04.026
– volume: 50
  start-page: 364
  year: 1985
  end-page: 372
  ident: B4
  article-title: Formation of filaments by Pseudomonas putida
  publication-title: Appl Environ Microbiol
  doi: 10.1128/aem.50.2.364-372.1985
– volume: 17
  start-page: R561
  year: 2007
  end-page: R570
  ident: B12
  article-title: Bacterial swarming: a re-examination of cell-movement patterns
  publication-title: Curr Biol
  doi: 10.1016/j.cub.2007.04.050
– volume: 99
  start-page: 88
  year: 2016
  end-page: 110
  ident: B17
  article-title: Helicobacter pylori strains vary cell shape and flagellum number to maintain robust motility in viscous environments
  publication-title: Mol Microbiol
  doi: 10.1111/mmi.13218
– volume: 6
  start-page: 657
  year: 2015
  ident: B27
  article-title: Filamentation of Campylobacter in broth cultures
  publication-title: Front Microbiol
  doi: 10.3389/fmicb.2015.00657
– year: 2003
  ident: B22
  publication-title: Behaviour and cross-contamination of pathogenic bacteria in household kitchens-relevance to exposure assessment. ;University of Edinburgh ;Edinburgh, United Kingdom
– volume: 85
  year: 2019
  ident: B28
  article-title: Salmonella enterica filamentation induced by pelargonic acid is a transient morphotype
  publication-title: Appl Environ Microbiol
  doi: 10.1128/AEM.02191-18
– volume: 4
  start-page: 697
  year: 2013
  end-page: 708
  ident: B30
  article-title: Convergent evolution of hyperswarming leads to impaired biofilm formation in pathogenic bacteria
  publication-title: Cell Rep
  doi: 10.1016/j.celrep.2013.07.026
– volume: 181
  start-page: 1703
  year: 1999
  end-page: 1712
  ident: B20
  article-title: Surface motility of Serratia liquefaciens MG1
  publication-title: J Bacteriol
  doi: 10.1128/JB.181.6.1703-1712.1999
– volume: 16
  start-page: 496
  year: 2008
  end-page: 506
  ident: B11
  article-title: Living on a surface: swarming and biofilm formation
  publication-title: Trends Microbiol
  doi: 10.1016/j.tim.2008.07.004
– volume: 161
  start-page: 211
  year: 2021
  end-page: 224
  ident: B16
  article-title: Bacterial swarmers enriched during intestinal stress ameliorate damage
  publication-title: Gastroenterology
  doi: 10.1053/j.gastro.2021.03.017
– volume: 49
  start-page: 581
  year: 2003
  end-page: 590
  ident: B18
  article-title: Swarming motility in undomesticated Bacillus subtilis
  publication-title: Mol Microbiol
  doi: 10.1046/j.1365-2958.2003.03584.x
– volume: 112
  start-page: 178
  year: 2015
  end-page: 183
  ident: B6
  article-title: Emergence of antibiotic resistance from multinucleated bacterial filaments
  publication-title: Proc Natl Acad Sci USA
  doi: 10.1073/pnas.1420702111
– volume: 104
  start-page: 4631
  year: 2020
  end-page: 4642
  ident: B8
  article-title: Regulation of filamentation by bacteria and its impact on the productivity of compounds in biotechnological processes
  publication-title: Appl Microbiol Biotechnol
  doi: 10.1007/s00253-020-10590-3
– volume: 35
  start-page: 322
  year: 2010
  end-page: 332
  ident: B15
  article-title: Antibiotic resistance of bacterial biofilms
  publication-title: Int J Antimicrob Agents
  doi: 10.1016/j.ijantimicag.2009.12.011
– year: 2010
  ident: B25
  publication-title: Experimental study of swimming flagellated bacteria and their collective behaviour in concentrated suspensions. ;University of Edinburgh ;Edinburgh, United Kingdom
– volume: 66
  start-page: 1274
  year: 2000
  end-page: 1279
  ident: B21
  article-title: Survival and filamentation of Salmonella enterica serovar Enteritidis PT4 and Salmonella enterica serovar Typhimurium DT104 at low water activity
  publication-title: Appl Environ Microbiol
  doi: 10.1128/AEM.66.4.1274-1279.2000
– volume: 10
  start-page: 2405
  year: 2014
  end-page: 2413
  ident: B31
  article-title: Hyperswarming adaptations in a bacterium improve collective motility without enhancing single cell motility
  publication-title: Soft Matter
  doi: 10.1039/c3sm53127a
– volume: 5
  start-page: 225
  year: 1979
  end-page: 237
  ident: B2
  article-title: Grazing by protozoa as selection factor for activated sludge bacteria
  publication-title: Microb Ecol
  doi: 10.1007/BF02013529
– volume: 2
  start-page: 630
  year: 1999
  end-page: 635
  ident: B19
  article-title: Swarming motility
  publication-title: Curr Opin Microbiol
  doi: 10.1016/s1369-5274(99)00033-8
– volume: 45
  start-page: 276
  year: 2007
  end-page: 281
  ident: B23
  article-title: The pattern of pleiomorphism in stressed Salmonella Virchow populations is nutrient and growth phase dependent
  publication-title: Lett Appl Microbiol
  doi: 10.1111/j.1472-765X.2007.02187.x
– volume: 19
  start-page: 3083
  year: 2005
  end-page: 3094
  ident: B26
  article-title: Cell population heterogeneity during growth of Bacillus subtilis
  publication-title: Genes Dev
  doi: 10.1101/gad.1373905
– volume: 114
  year: 2015
  ident: B14
  article-title: Antibiotic-induced anomalous statistics of collective bacterial swarming
  publication-title: Phys Rev Lett
  doi: 10.1103/PhysRevLett.114.018105
– volume: 29
  start-page: 224
  year: 1999
  end-page: 227
  ident: B3
  article-title: Morphological changes (including filamentation) in Escherichia coli grown under starvation conditions on silicon wafers and other surfaces
  publication-title: Lett Appl Microbiol
  doi: 10.1046/j.1365-2672.1999.00602.x
– volume: 8
  start-page: 634
  year: 2010
  end-page: 644
  ident: B9
  article-title: A field guide to bacterial swarming motility
  publication-title: Nat Rev Microbiol
  doi: 10.1038/nrmicro2405
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Snippet Bacteria undergo morphological changes in order to cope with external stresses. Among the best-known examples are cell elongation and hyperflagellation in the...
Many species of bacteria change their morphology and behavior under external stresses. In this study, we report transient elongation and swimming motility of a...
ABSTRACT Many species of bacteria change their morphology and behavior under external stresses. In this study, we report transient elongation and swimming...
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SubjectTerms bacterial elongation
Bacterial Proteins - genetics
Bacteriology
Cell Division
Enterobacter - genetics
Enterobacter - metabolism
flagella
Flagella - metabolism
hyperswarmer
Research Article
septa
swarming
swimming
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Title Enterobacter sp. Strain SM1_HS2B Manifests Transient Elongation and Swimming Motility in Liquid Medium
URI https://www.ncbi.nlm.nih.gov/pubmed/35647691
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