88 BIOTECHNOLOGY
Table 1. Cumulative counts from 14 floor, 36 wall and 14 active air samples Growth Direct System Count
Location
Pre Cleaning Post Cleaning
Floor 205 9
profile required will depend on the flora found in the facility under test. In this site example a 96-hour incubation scheme can be used. Tis amounts to a three-day reduction in incubation time. An evaluation of the growth characteristics is recommended as part of the validation process.
Microorganism identification Because this method is non- destructive, the colonies could be picked following the test run for 16S identification. Table 2 shows some of the organisms detected pre- and post-disinfection of the facility.
Tis RMM can be used to generate equivalent data to
Wall 148 76
Air 50 2
Floor 158 6
the traditional test with no requirement for changing action or alert levels. Te automated, rapid technology allows for the faster enumeration of micro- colonies, reducing the time to results. Te faster time to results allows a clean room facility to be commissioned more quickly than can be performed with traditional methods. Using RMMs can achieve substantial cost and time savings when compared to the traditional environmental monitoring method.
For more information ✔ at
www.scientistlive.com/eurolab
David Jones is director technical services and Nathan Storie is validation specialist
at Rapid Micro Biosystems in Boston, USA.
www.rapidmicrobio.com
Visual Count
Wall 141 64
Air 48 2
Floor 145% 150%
System Recovery
Wall 105% 119%
Table 2. Recovered organisms both pre and post disinfection Pre disinfection Aspergillus niger
Aspergillus phoenicis/tubingenisis Bacillus amyloliquefaciens
Bacillus cereus Bacillus thuringiensis Brevundimonas sp.
Kocuria rosea Kytococcus schroeteri Microbacterium paraoxydans Pseudomonas stutzeri
Discovery paves the way for new drugs to fight bacterial infections
Scientists from the UK and France have gained the first structural insights into the warfare that takes place when bacteria are starved of nutrients. Bacteria produce antimicrobial lasso peptides, which have a unique knotted structure; when they come face-to-face with receptors at the outer membranes of cells of other bacteria that cause human infections, such as E coli or Salmonella, these peptides can hijack the receptor and kill the target bacteria. To uncover the bacterial war tactics,
scientists used structural data collected on the crystallography beamlines at Diamond Light Source, the UK’s national synchrotron science facility, combined with modelling and biochemical experiments. The team brought together scientists
from Imperial College London, the Muséum National d’Histoire Naturelle in
www.scientistlive.com
Paris and the University of Oxford, and their results have just been published in Nature Chemical Biology. Battle lines are drawn when the E.
coli bacteria are starved of iron and seek it out via iron receptors on their outer membrane. These receptors are important and
help bacteria to track down iron, but covert operations come into force as the lasso peptides hijack these receptors for their own purposes and kill the bacteria in the process. Ironically, such clashes between
bacteria could actually prove very useful to humans in our fight against bacterial infections. Konstantinos Beis, from the
Department of Life Sciences at Imperial College London, said: “Successfully treating infectious diseases is currently a huge challenge as bacteria are so good
at shrugging off existing antibiotics by developing resistance to them. “The structural studies we carried
out at Diamond are very exciting as we have identified a key residue in this particular peptide that is important for the recognition of the E. coli receptor and this detailed knowledge, coupled with the fact it has a very stable lasso structure, leads us to believe the peptide could act as a platform for new drugs against bacterial infection.” There is growing interest in new
approaches to tackling bacterial infections as traditional antibiotics made from purely synthetic compounds prove themselves to be not up to the job in the long term. The European Centre for Disease Prevention and Control estimates that 25,000 patients die each year from infections caused by anti microbial resistant bacteria.
Sylvie Rebuffat, from the Muséum
National d’Histoire Naturelle-CNRS in Paris, commented: “My team has been working on this particular peptide for over a decade now and, while these are early stage results, they provide the structural information that we have been waiting for to enable us to establish it as a front runner to aid in the design of new medicine to fight bacterial infections.” The research was funded by the Medical Research Council, the Wellcome Trust and the Biotechnology and Biological Sciences Research Council. Diamond Light Source is funded by
the UK Government through the Science and Technology Facilities Council (STFC), and by the Wellcome Trusyt
For more information, visit
www.diamond.ac.uk or
www.imperial.ac.uk
Post disinfection Aspergillus niger
Aspergillus phoenicis/tubingenisis Bacillus amyloliquefaciens
Bacillus circulans Bacillus pumilis Bacillus subtilis
Kocuria marina Lysinibacillus fusiform Micrococcus luteus Staphylococcus epidermidis
Air
104% 100%
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