2005
DOI: 10.1111/j.1462-2920.2005.00806.x
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Swarmer cell differentiation in Proteus mirabilis

Abstract: SummaryUnder the appropriate environmental conditions, the Gram-negative bacterium Proteus mirabilis undergoes a remarkable differentiation to form a distinct cell type called a swarmer cell. The swarmer cell is characterized by a 20-to 40-fold increase in both cell length and the number of flagella per cell. Environmental conditions required for swarmer cell differentiation include: surface contact, inhibition of flagellar rotation, a sufficient cell density and cell-to-cell signalling. The differentiated swa… Show more

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Cited by 169 publications
(152 citation statements)
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References 72 publications
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“…Most probably putrescine can form a complex with galacturonic acid which is component of CPS. This suggests a possibility that putrescine complexed with cell surface polysaccharide acts as a signal factor or putrescine regulates expression of CPS (RATHER 2005, MORGENSTEIN et al 2010.…”
Section: Swarming Phenomenonmentioning
confidence: 99%
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“…Most probably putrescine can form a complex with galacturonic acid which is component of CPS. This suggests a possibility that putrescine complexed with cell surface polysaccharide acts as a signal factor or putrescine regulates expression of CPS (RATHER 2005, MORGENSTEIN et al 2010.…”
Section: Swarming Phenomenonmentioning
confidence: 99%
“…It was found that extracellular signal AI-2 (autoinducer-2) does not play a role in swarming. Cyclic dipeptides were also shown as P. mirabilis signaling molecules out of importance in swarming (RATHER 2005). Other signal molecules N-acyl homoserine lactones crucial in quorum sensing are not produced by P. mirabilis (MORGENSTEIN et al 2010).…”
Section: Swarming Phenomenonmentioning
confidence: 99%
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“…This form of motility allows P. mirabilis to migrate across the infected ulcer, spreading the infection (Rather, 2005; Jacobsen et al, 2008). Moreover, P. mirabilis biofilms contain protruding swarm cells which enhance the microbial resistance (Jones et al, 2007).…”
Section: Discussionmentioning
confidence: 99%
“…8.55 mM NaCl, 9.35 mM NH4Cl) 액체배지 또는 1.5% (w/v) agar를 첨가한 고체배지를 사용하여 37℃에서 배 양하였다 [3]. 최소배지는 M9 CK214 균주의 효소액을 분리하 기 위해서 0.2% (w/v) agar가 첨가된 LB 액체배지에서 24 시 간 동안 배양하였다.…”
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