A Novel Model of Chronic Wounds: Importance of Redox Imbalance and Biofilm-Forming Bacteria for Establishment of Chronicity

Chronic wounds have a large impact on health, affecting ∼6.5 M people and costing ∼$25B/year in the US alone [1]. We previously discovered that a genetically modified mouse model displays impaired healing similar to problematic wounds in humans and that sometimes the wounds become chronic. Here we show how and why these impaired wounds become chronic, describe a way whereby we can drive impaired wounds to chronicity at will and propose that the same processes are involved in chronic wound development in humans. We hypothesize that exacerbated levels of oxidative stress are critical for initiation of chronicity. We show that, very early after injury, wounds with impaired healing contain elevated levels of reactive oxygen and nitrogen species and, much like in humans, these levels increase with age. Moreover, the activity of anti-oxidant enzymes is not elevated, leading to buildup of oxidative stress in the wound environment. To induce chronicity, we exacerbated the redox imbalance by further inhibiting the antioxidant enzymes and by infecting the wounds with biofilm-forming bacteria isolated from the chronic wounds that developed naturally in these mice. These wounds do not re-epithelialize, the granulation tissue lacks vascularization and interstitial collagen fibers, they contain an antibiotic-resistant mixed bioflora with biofilm-forming capacity, and they stay open for several weeks. These findings are highly significant because they show for the first time that chronic wounds can be generated in an animal model effectively and consistently. The availability of such a model will significantly propel the field forward because it can be used to develop strategies to regain redox balance that may result in inhibition of biofilm formation and result in restoration of healthy wound tissue. Furthermore, the model can lead to the understanding of other fundamental mechanisms of chronic wound development that can potentially lead to novel therapies.

[1]  G. Rogers,et al.  G385 RATNO – Reducing Antibiotic Tolerance using Nitric Oxide in Cystic Fibrosis: report of a proof of concept clinical trial , 2014, Archives of Disease in Childhood.

[2]  L. Gould,et al.  Consequences of age on ischemic wound healing in rats: altered antioxidant activity and delayed wound closure , 2014, AGE.

[3]  A. Progulske-Fox,et al.  Development of a novel ex vivo porcine skin explant model for the assessment of mature bacterial biofilms , 2013, Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society.

[4]  Yang Shen,et al.  Purification and Characterization of Biofilm-Associated EPS Exopolysaccharides from ESKAPE Organisms and Other Pathogens , 2013, PloS one.

[5]  G. Huffnagle,et al.  The microbiome in wound repair and tissue fibrosis , 2013, The Journal of pathology.

[6]  Hualiang Jiang,et al.  Oxidation-sensing Regulator AbfR Regulates Oxidative Stress Responses, Bacterial Aggregation, and Biofilm Formation in Staphylococcus epidermidis* , 2012, The Journal of Biological Chemistry.

[7]  T. Agner,et al.  International guidelines for the in vivo assessment of skin properties in non-clinical settings: part 1. pH , 2012, Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging.

[8]  P. Smooker,et al.  Differences between Two Clinical Staphylococcus capitis Subspecies as Revealed by Biofilm, Antibiotic Resistance, and Pulsed-Field Gel Electrophoresis Profiling , 2012, Journal of Clinical Microbiology.

[9]  G. Gurtner,et al.  Tissue engineering for the management of chronic wounds: current concepts and future perspectives , 2012, Experimental dermatology.

[10]  Yves Bayon,et al.  Reactive oxygen species (ROS)--a family of fate deciding molecules pivotal in constructive inflammation and wound healing. , 2012, European cells & materials.

[11]  S. Barnum,et al.  Erythrocyte storage increases rates of NO and nitrite scavenging: implications for transfusion-related toxicity. , 2012, The Biochemical journal.

[12]  R. Takimoto,et al.  Improvement of iron-mediated oxidative DNA damage in patients with transfusion-dependent myelodysplastic syndrome by treatment with deferasirox. , 2012, Free radical biology & medicine.

[13]  S. Britland,et al.  The lactate conundrum in wound healing: Clinical and experimental findings indicate the requirement for a rapid point‐of‐care diagnostic , 2012, Biotechnology progress.

[14]  Julia G. Lyubovitsky,et al.  Deletion of a tumor necrosis superfamily gene in mice leads to impaired healing that mimics chronic wounds in humans , 2012, Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society.

[15]  J. Olerud,et al.  Time course study of delayed wound healing in a biofilm‐challenged diabetic mouse model , 2012, Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society.

[16]  R. Losick,et al.  RETRACTED: A Self-Produced Trigger for Biofilm Disassembly that Targets Exopolysaccharide , 2012, Cell.

[17]  J. Zweier,et al.  Aldehyde oxidase functions as a superoxide generating NADH oxidase: an important redox regulated pathway of cellular oxygen radical formation. , 2012, Biochemistry.

[18]  M. Blaser,et al.  The human microbiome: at the interface of health and disease , 2012, Nature Reviews Genetics.

[19]  P. Clegg,et al.  The role of endogenous and exogenous enzymes in chronic wounds: A focus on the implications of aberrant levels of both host and bacterial proteases in wound healing , 2012, Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society.

[20]  D. Spitz,et al.  Manipulation of cellular redox parameters for improving therapeutic responses in B‐cell lymphoma and multiple myeloma , 2012, Journal of cellular biochemistry.

[21]  Marshall Summar,et al.  Requirement of argininosuccinate lyase for systemic nitric oxide production , 2011, Nature Medicine.

[22]  C. Colton,et al.  Nitric oxide and redox mechanisms in the immune response , 2011, Journal of leukocyte biology.

[23]  F. Schreiber,et al.  The role of nitric-oxide-synthase-derived nitric oxide in multicellular traits of Bacillus subtilis 3610: biofilm formation, swarming, and dispersal , 2011, BMC Microbiology.

[24]  T. Tolker-Nielsen,et al.  Quantitative analysis of the cellular inflammatory response against biofilm bacteria in chronic wounds , 2011, Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society.

[25]  K. Scharffetter-Kochanek,et al.  An unrestrained proinflammatory M1 macrophage population induced by iron impairs wound healing in humans and mice. , 2011, The Journal of clinical investigation.

[26]  Abdul R Siddiqui,et al.  Chronic wound infection: facts and controversies. , 2010, Clinics in dermatology.

[27]  A. Vetrano,et al.  Mechanisms of oxidant generation by catalase , 2010, Annals of the New York Academy of Sciences.

[28]  M. Landthaler,et al.  Oxygen in acute and chronic wound healing , 2010, The British journal of dermatology.

[29]  A. Daley,et al.  Antibiotic susceptibility of coagulase-negative staphylococci isolated from very low birth weight babies: comprehensive comparisons of bacteria at different stages of biofilm formation , 2010, Annals of Clinical Microbiology and Antimicrobials.

[30]  J. Kaplan,et al.  Biofilm Dispersal: Mechanisms, Clinical Implications, and Potential Therapeutic Uses , 2010, Journal of dental research.

[31]  L. DiPietro,et al.  Factors Affecting Wound Healing , 2010, Journal of dental research.

[32]  J. Parvizi,et al.  Reactive oxygen and nitrogen species induce protein and DNA modifications driving arthrofibrosis following total knee arthroplasty , 2009, Fibrogenesis & tissue repair.

[33]  T. K. Hunt,et al.  Human skin wounds: A major and snowballing threat to public health and the economy , 2009, Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society.

[34]  Xianzhong Xiao,et al.  Role of Foxa1 in regulation of bcl2 expression during oxidative-stress-induced apoptosis in A549 type II pneumocytes , 2009, Cell Stress and Chaperones.

[35]  C. Sen,et al.  Redox signals in wound healing. , 2008, Biochimica et biophysica acta.

[36]  J. Zweier,et al.  Phosphorylation of Endothelial Nitric-oxide Synthase Regulates Superoxide Generation from the Enzyme* , 2008, Journal of Biological Chemistry.

[37]  R. Clark Oxidative stress and "senescent" fibroblasts in non-healing wounds as potential therapeutic targets. , 2008, The Journal of investigative dermatology.

[38]  C. Ware,et al.  Vascular endothelial growth factor promotes macrophage apoptosis through stimulation of tumor necrosis factor superfamily member 14 (TNFSF14/LIGHT). , 2008, Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society.

[39]  F. Rossi,et al.  Investigation of an outbreak of Enterobacter cloacae in a neonatal unit and review of the literature. , 2008, The Journal of hospital infection.

[40]  Blaise R. Boles,et al.  Endogenous oxidative stress produces diversity and adaptability in biofilm communities , 2008, Proceedings of the National Academy of Sciences.

[41]  Matthias Schäfer,et al.  Oxidative stress in normal and impaired wound repair. , 2008, Pharmacological research.

[42]  S. Dowd,et al.  Survey of bacterial diversity in chronic wounds using Pyrosequencing, DGGE, and full ribosome shotgun sequencing , 2008, BMC Microbiology.

[43]  J. Frick,et al.  Hypoxia Inducible Factor (HIF)-1 Coordinates Induction of Toll-Like Receptors TLR2 and TLR6 during Hypoxia , 2007, PloS one.

[44]  M. Toledano,et al.  ROS as signalling molecules: mechanisms that generate specificity in ROS homeostasis , 2007, Nature Reviews Molecular Cell Biology.

[45]  M. Rollins,et al.  Wounds: an overview of the role of oxygen. , 2007, Antioxidants & redox signaling.

[46]  C. Denis,et al.  Importance of pH regulation and lactate/H+ transport capacity for work production during supramaximal exercise in humans. , 2007, Journal of applied physiology.

[47]  Joachim Dissemond,et al.  Influence of pH on wound-healing: a new perspective for wound-therapy? , 2007, Archives of Dermatological Research.

[48]  D. Hassett,et al.  Involvement of Nitric Oxide in Biofilm Dispersal of Pseudomonas aeruginosa , 2006, Journal of bacteriology.

[49]  K. Krogfelt,et al.  Multiple bacterial species reside in chronic wounds: a longitudinal study , 2006, International wound journal.

[50]  J. Pollock,et al.  Coupled and uncoupled NOS: separate but equal? Uncoupled NOS in endothelial cells is a critical pathway for intracellular signaling. , 2006, Circulation research.

[51]  K. Scharffetter-Kochanek,et al.  Oxidative stress in chronic venous leg ulcers , 2005, Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society.

[52]  Alex F. Chen,et al.  Nitric oxide: a newly discovered function on wound healing , 2005, Acta Pharmacologica Sinica.

[53]  K. E. Hill,et al.  A review of the microbiology, antibiotic usage and resistance in chronic skin wounds. , 2005, The Journal of antimicrobial chemotherapy.

[54]  F. Gonzalez,et al.  Role of cytochromes P450 in chemical toxicity and oxidative stress: studies with CYP2E1. , 2005, Mutation research.

[55]  K. Harding,et al.  Comparison of oxidative stress biomarker profiles between acute and chronic wound environments , 2004, Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society.

[56]  L. DiPietro,et al.  Neutrophil function in the healing wound: adding insult to injury? , 2004, Thrombosis and Haemostasis.

[57]  A. Barbul,et al.  Nitric Oxide and Wound Healing , 2004, World Journal of Surgery.

[58]  M. Parsek,et al.  Bacterial biofilms: an emerging link to disease pathogenesis. , 2003, Annual review of microbiology.

[59]  M. Stacey,et al.  Iron and 8-isoprostane levels in acute and chronic wounds. , 2003, The Journal of investigative dermatology.

[60]  P. Bowler Wound pathophysiology, infection and therapeutic options , 2002, Annals of medicine.

[61]  C. McCollum,et al.  Expression of nitric oxide synthase isoforms and arginase in normal human skin and chronic venous leg ulcers , 2000, The Journal of pathology.

[62]  S. Kun,et al.  Determination of a relationship between bacteria levels and tissue pH in wounds: animal studies , 2000, Proceedings of the IEEE 26th Annual Northeast Bioengineering Conference (Cat. No.00CH37114).

[63]  S. Stepanović,et al.  A modified microtiter-plate test for quantification of staphylococcal biofilm formation. , 2000, Journal of microbiological methods.

[64]  N. Schiller,et al.  Competition of Various β-Lactam Antibiotics for the Major Penicillin-Binding Proteins of Helicobacter pylori: Antibacterial Activity and Effects on Bacterial Morphology , 1999, Antimicrobial Agents and Chemotherapy.

[65]  J. Costerton,et al.  Bacterial biofilms: a common cause of persistent infections. , 1999, Science.

[66]  J. Cooke,et al.  Endogenous nitric oxide synthase inhibitor: a novel marker of atherosclerosis. , 1999, Circulation.

[67]  E. H. Frazier,et al.  Aerobic and anaerobic microbiology of chronic venous ulcers , 1998, International journal of dermatology.

[68]  Roberto Kolter,et al.  Initiation of biofilm formation in Pseudomonas fluorescens WCS365 proceeds via multiple, convergent signalling pathways: a genetic analysis , 1998, Molecular microbiology.

[69]  J S Beckman,et al.  Nitric oxide, superoxide, and peroxynitrite: the good, the bad, and ugly. , 1996, The American journal of physiology.

[70]  H. Westh,et al.  Bacterial colonization and healing of venous leg ulcers , 1996, APMIS : acta pathologica, microbiologica, et immunologica Scandinavica.

[71]  B. Friguet,et al.  Peroxynitrite-mediated nitration of tyrosine residues in Escherichia coli glutamine synthetase mimics adenylylation: relevance to signal transduction. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[72]  D. Gerding Foot infections in diabetic patients: the role of anaerobes. , 1995, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

[73]  C. Hansson,et al.  The microbial flora in venous leg ulcers without clinical signs of infection. Repeated culture using a validated standardised microbiological technique. , 1995, Acta dermato-venereologica.

[74]  D. M. Cooper,et al.  Definitions and guidelines for assessment of wounds and evaluation of healing , 1994, Archives of dermatology.

[75]  B. Ames,et al.  Oxidative damage to DNA during aging: 8-hydroxy-2'-deoxyguanosine in rat organ DNA and urine. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[76]  A. Benabid,et al.  Correlation between intracellular pH and lactate levels in the rat brain during potassium cyanide induced metabolism blockade: A combined 31P-1H in vivo nuclear magnetic spectroscopy study , 1989, Neuroscience Letters.

[77]  C Torrance,et al.  The physiology of wound healing. , 1986, Nursing.

[78]  L. Baddour,et al.  Adherence of coagulase-negative staphylococci to plastic tissue culture plates: a quantitative model for the adherence of staphylococci to medical devices , 1985, Journal of clinical microbiology.

[79]  T. McNitt,et al.  Demonstration of uronic acid capsular material in the cerebrospinal fluid of a patient with meningitis caused by mucoid Pseudomonas aeruginosa , 1984, Journal of clinical microbiology.

[80]  J. Montgomerie,et al.  The infected foot of the diabetic patient: quantitative microbiology and analysis of clinical features. , 1984, Reviews of infectious diseases.

[81]  A. Tappel,et al.  Mechanism of selenium-glutathione peroxidase and its inhibition by mercaptocarboxylic acids and other mercaptans. , 1984, The Journal of biological chemistry.

[82]  C. Sharp,et al.  Microbiology of Deep Tissue in Diabetic Gangrene , 1978, Diabetes Care.

[83]  J. Smilack The Biologic and Clinical Basis of Infectious Diseases , 1976 .

[84]  O. Warburg [Origin of cancer cells]. , 1956, Oncologia.

[85]  R. Losick,et al.  A self-produced trigger for biofilm disassembly that targets exopolysaccharide. , 2012, Cell.

[86]  David W Williams,et al.  Antimicrobial tolerance and the significance of persister cells in recalcitrant chronic wound biofilms , 2011, Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society.

[87]  J. Zenilman,et al.  Molecular microbiology: new dimensions for cutaneous biology and wound healing. , 2010, The Journal of investigative dermatology.

[88]  P. Stewart,et al.  Biofilms in chronic wounds , 2008, Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society.

[89]  K. Krause,et al.  The NOX family of ROS-generating NADPH oxidases: physiology and pathophysiology. , 2007, Physiological reviews.

[90]  G. Gethin,et al.  The significance of surface pH in chronic wounds , 2007 .

[91]  Savita Khanna,et al.  Dermal wound healing is subject to redox control. , 2006, Molecular therapy : the journal of the American Society of Gene Therapy.

[92]  W. Dröge Free radicals in the physiological control of cell function. , 2002, Physiological reviews.

[93]  S. Shaw,et al.  The role of cellular oxidases and catalytic iron in the pathogenesis of ethanol-induced liver injury. , 1992, Life sciences.

[94]  K. Schleifer,et al.  Isolation and Characterization of Staphylococci from Human Skin II. Descriptions of Four New Species: Staphylococcus warneri, Staphylococcus capitis, Staphylococcus hominis, and Staphylococcus simulans1 , 1975 .