scholarly journals Programmed hierarchical patterning of bacterial populations

2017 ◽  
Author(s):  
Christian R. Boehm ◽  
Paul K. Grant ◽  
Jim Haseloff

AbstractModern genetic tools allow the dissection and emulation of fundamental mechanisms shaping morphogenesis in multicellular organisms. Several synthetic genetic circuits for control of multicellular patterning have been reported to date. However, hierarchical induction of gene expression domains has received little attention from synthetic biologists, despite its importance in biological self-organization. We report the first synthetic genetic system implementing population-based AND logic for programmed autonomous induction of bacterial gene expression domains. We develop a ratiometric assay for bacteriophage T7 RNA polymerase activity and use it to systematically characterize different intact and split enzyme variants. We then utilize the best-performing variant to build a three-color patterning system responsive to two different homoserine lactones. We validate the AND gate-like behavior of this system both in cell suspension and in surface culture. Finally, we use the synthetic circuit in a membrane-based spatial assay to demonstrate programmed hierarchical patterning of gene expression across bacterial populations.Abbreviations3OC6HSLN-(3-oxohexanoyl)-L-homoserine lactone3OC12HSLN-(3-oxododecanoyl)-L-homoserine lactoneCFPcyan fluorescent proteinIPTGisopropyl-β-D-thiogalactopyranosideParts RegistryMIT Registry of Standard Biological PartsPIpositional informationRDreaction-diffusionRFPred fluorescent proteinRFUrelative fluorescence unitss.d.standard deviationT7RNAPbacteriophage T7 RNA polymeraseYFPyellow fluorescent protein

Gene ◽  
1989 ◽  
Vol 83 (2) ◽  
pp. 371-375 ◽  
Author(s):  
John Davison ◽  
Nathalie Chevalier ◽  
Françoise Brunel

1996 ◽  
Vol 77 (5) ◽  
pp. 963-967 ◽  
Author(s):  
P. Britton ◽  
P. Green ◽  
S. Kottier ◽  
K. L. Mawditt ◽  
Z. Penzes ◽  
...  

2003 ◽  
Vol 71 (6) ◽  
pp. 3454-3462 ◽  
Author(s):  
Kevin M. Mason ◽  
Robert S. Munson ◽  
Lauren O. Bakaletz

ABSTRACT The gram-negative bacterium nontypeable Haemophilus influenzae (NTHI) is the predominant pathogen in chronic otitis media with effusion and, with Streptococcus pneumoniae and Moraxella catarrhalis, is a causative agent of acute otitis media. To identify potential virulence determinants, bacterial gene expression was monitored by differential fluorescence induction during early disease progression in one specific anatomical niche of a chinchilla model of NTHI-induced otitis media. Genomic DNA fragments from NTHI strain 86-028NP were cloned upstream of the promoterless gfpmut3 gene. NTHI strain 86-028NP served as the host for the promoter trap library. Pools of 2,000 transformants were inoculated into the left and right middle ear cavities of chinchillas. Middle ear effusions were recovered by epitympanic tap at 24 and 48 h, and clones containing promoter elements that were induced in vivo and producing green fluorescent protein were isolated by two-color fluorescence-activated cell sorting. Insert DNA was sequenced and compared to the complete genome sequence of H. influenzae strain Rd. In a screen of 16,000 clones, we have isolated 44 clones that contain unique gene fragments encoding biosynthetic enzymes, metabolic and regulatory proteins, and hypothetical proteins of unknown function. An additional eight clones contain gene fragments unique to our NTHI isolate. Using quantitative reverse transcription-PCR, we have confirmed that 26 clones demonstrated increased gene expression in vivo relative to expression in vitro. These data provide insight into the response of NTHI bacteria as they sense and respond to the middle ear microenvironment during early events of otitis media.


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