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Mansfield, R.

Publications and source records attributed to Mansfield, R..

2 recordsLinked to original sources

Creation of Novel Methylating Conjugal Donor Strains for Genetically Recalcitrant Bacteria

A methodology is presented to integrate DNA methyltransferase genes of interest into the single copy, IncP{beta} R Factor conjugal plasmid, R702. This is to enable DNA transfer, or improved frequency thereof, by mirroring the recipient native DNA methylation signature prior to transfer of plasmid DNA by conjugation, evading native restriction modification systems in the organism of study, without target strain modification. As proof of concept, the bacteriophage derived methyltransferase [FE]3TI, known to facilitate DNA transfer into the industrially important model solventogenic organism, Clostridium acetobutylicum ATCC 824, was inserted into the single copy R702 to create an in vivo methylating strain. Plasmids extracted from this strain were transferred by electroporation at a comparable frequency to the established method which uses the multi-copy accessory plasmids pAN1 or pAN2, harbouring [FE]3TI. The methodology was further exemplified and employed to enable high frequency of DNA transfer into the clinically relevant Clostridioides difficile ribotype 027 outbreak strain, R20291. The modification (hsdM) and specificity (hsdS) components of the native Type I restriction modification system of R20291 were inserted into R702 to create a functional methylating conjugal donor Escherichia coli strain. This approach of coupling methylation and the native transfer functions of R702 creates a system which can easily be mobilised into a genotypically appropriate E. coli strain; creating an in vivo methylating donor strain which may be utilized to protect and transfer DNA to the organism of study by conjugation.

microbiology↗

Functional and diffusion MRI reveal the functional and structural basis of infants' noxious-evoked brain activity

Understanding the neurophysiology underlying pain perception in infants is central to improving early life pain management. In this multimodal MRI study, we use resting-state functional and white matter diffusion MRI to investigate individual variability in infants noxious-evoked brain activity. In an 18-infant nociception-paradigm dataset, we show it is possible to predict infants cerebral haemodynamic responses to experimental noxious stimulation using their resting-state activity across nine networks from a separate stimulus-free scan. In an independent 215-infant Developing Human Connectome Project dataset, we use this resting-state-based prediction model to generate noxious responses. We identify a significant correlation between these predicted noxious responses and infants white matter mean diffusivity, and this relationship is subsequently confirmed within our nociception-paradigm dataset. These findings reveal that a newborn infants pain-related brain activity is tightly coupled to both their spontaneous resting-state activity and underlying white matter microstructure. This work provides proof-of-concept that knowledge of an infants functional and structural brain architecture could be used to predict pain responses, informing infant pain management strategies and facilitating evidence-based personalisation of care.

neuroscience↗