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The protocol describes a step-by-step method to set up an ex vivo ovine wounded skin model infected with Staphylococcus aureus. This high-throughput model better simulates infections in vivo compared with conventional microbiology techniques and presents researchers with a physiologically relevant platform to test the efficacy of emerging antimicrobials.
The development of antimicrobials is an expensive process with increasingly low success rates, which makes further investment in antimicrobial discovery research less attractive. Antimicrobial drug discovery and subsequent commercialization can be made more lucrative if a fail-fast-and-fail-cheap approach can be implemented within the lead optimization stages where researchers have greater control over drug design and formulation. In this article, the setup of an ex vivo ovine wounded skin model infected with Staphylococcus aureus is described, which is simple, cost-effective, high throughput, and reproducible. The bacterial physiology in the model mimics that during infection as bacterial proliferation is dependent on the pathogen's ability to damage the tissue. The establishment of wound infection is verified by an increase in viable bacterial counts compared to the inoculum. This model can be used as a platform to test the efficacy of emerging antimicrobials in the lead optimization stage. It can be contended that the availability of this model will provide researchers developing antimicrobials with a fail-fast-and-fail-cheap model, which will help increase success rates in subsequent animal trials. The model will also facilitate the reduction and refinement of animal use for research and ultimately enable faster and more cost-effective translation of novel antimicrobials for skin and soft tissue infections to the clinic.
Skin infections are an important global issue, with large economic costs to healthcare providers around the world. The development of multidrug resistance and biofilm formation by pathogens plays a key role in the prevalence of non-healing wounds1,2,3,4. As a result of this, skin and soft tissue infections are one of the more common reasons for extended hospitalization and subsequent readmission5. Delays in wound healing are costly for both the patient and healthcare providers, with some estimates suggesting around 6.....
Lambs' heads from the R.B Elliott and Son Abattoir were used as the source of skin samples in this project. All lambs were slaughtered for consumption as food. Instead of discarding the heads, these were repurposed for research. Ethics approval was not required as the tissue was sourced from waste discarded from abattoirs.
1. Sterilization
The identification of a route to sterilize the skin before setting up the wound infection model was challenging. The challenge lay in sterilizing the skin without damaging the different skin layers, which may then go on to have unintended consequences in the outcome of infection. To identify an appropriate sterilization regime, different treatments were tried for varying lengths of time, as outlined in Table 1. Contamination was recorded as the development of turbidity after 48 h in the MK medium used to.......
The development of antimicrobials is an important but expensive venture that is estimated to cost around $1 billion and take around 15 years to complete. Over 90% of antimicrobial drug discovery and preclinical studies of antimicrobial drug efficacy are carried out by academic researchers and small to medium companies with typically less than 50 employees22. These teams are very financially constrained, which makes the failure of lead molecules in later stages of translational research calamitous........
The authors would like to thank EPSRC (EP/R513313/1) for funding. The authors would like to also thank R.B Elliot and Son Abattoir in Calow, Chesterfield, for providing lambs' heads and for being so accommodating in the early stages of the project, Kasia Emery for her support throughout the development of this protocol, and Fiona Wright from the Department of Infection, Immunity and Cardiovascular Disease at the University of Sheffield for processing the histology samples and being so incredibly helpful throughout this project.
....Name | Company | Catalog Number | Comments |
24 Well Companion Plate | SLSÂ | 353504 | |
4 mm Biopsy Punch | Williams Medical | D7484 | |
50 ml centrifuge tubes | Fisher Scientific | 10788561 | |
8 mm Biopsy Punch | Williams Medical | D7488 | |
Amphotericin B solution, sterile | Sigma | A2942 | |
Colour Pro Style Cordless Hair Clipper | Wahl | 9639-2117X | Hair Clippers |
Dual Oven Incubator | SLS | OVe1020 | Sterilising oven |
Epidermal growth factor | SLS | E5036-200UG | |
Ethanol | Honeywell | 458600-2.5L | |
F12 HAM | Sigma | N4888 | |
Foetal bovine serum | Labtech International | CA-115/500 | |
Forceps | Fisher Scientific | 15307805 | |
Hair Removal Cream | Veet | Not applicable | |
Heracell VIOS 160i | Thermo Scientific | 15373212Â | Tissue culture incubator |
Heraeus Megafuge 16R | VWR | 521-2242 | Centrifuge |
Homogenizer 220, Handheld | Fisher Scientific | 15575809 | |
Homogenizer 220, plastic blending cones | Fisher Scientific | 15585819 | |
Insert Individual 24 well 0.4um membrane | VWR International | 353095 | |
Insulin, recombinant Human | SLS | 91077C-1G | |
Medium 199 (MK media) | Sigma | M0393 | |
Microplate, cell culture Costar 96 well | Fisher Scientific | 10687551 | |
Multitron | Infors | Not applicable | Bacterial incubator |
PBS tablets | Sigma | P4417-100TAB | |
Penicillin-Streptomycin | SLSÂ | P0781 | |
Plate seals | Fisher Scientific | ESI-B-100 | |
Safe 2020 | Fisher Scientific | 1284804 | Class II microbiology safety cabinet |
Scalpel blade number 15 | Fisher Scientific | O305 | |
Scalpel Swann Morton | Fisher Scientific | 11849002 | |
Sodium bicarbonate | Sigma | S5761-1KG | |
Toothed Allis Tissue Forceps | Rocialle | RSPU500-322 | |
Tryptic Soy Agar | Merck Life Science UK Limited | 14432-500G-F | |
Tryptic Soy Broth | Merck Life Science UK Limited | 41298-500G-F | |
Vimoba Tablets | Quip Labs | VMTAB75BX |
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