Joel Gil, Michael Solis, Ryan Strong, Roger Cassagnol, Ivan Jozic, Stephen C. Davis
{"title":"多模式伤口基质在猪体外和体内伤口模型中对耐甲氧西林金黄色葡萄球菌和铜绿假单胞菌的抗菌效果。","authors":"Joel Gil, Michael Solis, Ryan Strong, Roger Cassagnol, Ivan Jozic, Stephen C. Davis","doi":"10.1111/iwj.70059","DOIUrl":null,"url":null,"abstract":"<p>Chronic non-healing wounds pose significant challenges due to an elevated inflammatory response caused in part by bacterial contamination (<i>Physiol Rev.</i> 2019;99:665). These wounds lead to billions being spent in the health care system worldwide (<i>N Engl J Med</i>. 2017;376:2367, <i>Int J Pharm</i>. 2014;463:119). We studied the <i>in-vitro</i> and <i>in-vivo</i> antimicrobial effects of a multimodal wound matrix (MWM) against two common wound pathogens, Methicillin-Resistant <i>Staphylococcus aureus</i> (MRSA USA300) and <i>Pseudomonas aeruginosa</i> ATCC 27312 (PA27312) (<i>Int Wound J</i>. 2019;16:634). The <i>in-vitro</i> study conducted was a zone of inhibition test with the two microbes at 104 Log CFU/mL inoculated on Tryptic soy agar with 5% sheep blood (TSAII) plates. Treatments used were MWM, Mupirocin (Positive control for MRSA), Silver Sulfadiazine (Positive Control for PA), Petrolatum and Sterile Saline (both serving as Negative Controls). Treatments were allowed to diffuse into the agar for 3 h and then were incubated for 24 h at 37°C. The <i>in-vivo</i> study utilized a deep dermal porcine wound model (22 × 22 × 3 mm) created on six animals. Three animals were inoculated with MRSA USA300 and the other three with PA27312 with each allowing a 72-h biofilm formation. After 72 h, baseline wounds were assessed for bacterial concentration and all remaining wounds were treated with either MWM alone, Silver Treatment or Untreated Control. Wounds were assessed on days 4, 8 and 12 after treatment application for microbiological analysis. <i>In-vitro</i>, MWM exhibited significant inhibition of MRSA USA300 and PA27312 growth when compared to negative controls (<i>p</i> ≤ 0.05). Likewise, <i>in-vivo</i>, the MWM-treated wounds exhibited a significant (<i>p</i> ≤ 0.05) bacterial reduction compared to all other treatment groups, especially on days 8 and 12 for both pathogens. MWM demonstrated promise in addressing colonized wounds with biofilms. Additional studies on MWM's benefits and comparisons with existing treatments are warranted to optimize wound care strategies (<i>Adv Wound Care</i>. 2021;10:281).</p>","PeriodicalId":14451,"journal":{"name":"International Wound Journal","volume":"21 10","pages":""},"PeriodicalIF":2.6000,"publicationDate":"2024-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11447198/pdf/","citationCount":"0","resultStr":"{\"title\":\"Antimicrobial effects of a multimodal wound matrix against methicillin-resistant Staphylococcus aureus and Pseudomonas aeruginosa in an in vitro and an in vivo porcine wound model\",\"authors\":\"Joel Gil, Michael Solis, Ryan Strong, Roger Cassagnol, Ivan Jozic, Stephen C. Davis\",\"doi\":\"10.1111/iwj.70059\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Chronic non-healing wounds pose significant challenges due to an elevated inflammatory response caused in part by bacterial contamination (<i>Physiol Rev.</i> 2019;99:665). These wounds lead to billions being spent in the health care system worldwide (<i>N Engl J Med</i>. 2017;376:2367, <i>Int J Pharm</i>. 2014;463:119). We studied the <i>in-vitro</i> and <i>in-vivo</i> antimicrobial effects of a multimodal wound matrix (MWM) against two common wound pathogens, Methicillin-Resistant <i>Staphylococcus aureus</i> (MRSA USA300) and <i>Pseudomonas aeruginosa</i> ATCC 27312 (PA27312) (<i>Int Wound J</i>. 2019;16:634). The <i>in-vitro</i> study conducted was a zone of inhibition test with the two microbes at 104 Log CFU/mL inoculated on Tryptic soy agar with 5% sheep blood (TSAII) plates. Treatments used were MWM, Mupirocin (Positive control for MRSA), Silver Sulfadiazine (Positive Control for PA), Petrolatum and Sterile Saline (both serving as Negative Controls). Treatments were allowed to diffuse into the agar for 3 h and then were incubated for 24 h at 37°C. The <i>in-vivo</i> study utilized a deep dermal porcine wound model (22 × 22 × 3 mm) created on six animals. Three animals were inoculated with MRSA USA300 and the other three with PA27312 with each allowing a 72-h biofilm formation. After 72 h, baseline wounds were assessed for bacterial concentration and all remaining wounds were treated with either MWM alone, Silver Treatment or Untreated Control. Wounds were assessed on days 4, 8 and 12 after treatment application for microbiological analysis. <i>In-vitro</i>, MWM exhibited significant inhibition of MRSA USA300 and PA27312 growth when compared to negative controls (<i>p</i> ≤ 0.05). Likewise, <i>in-vivo</i>, the MWM-treated wounds exhibited a significant (<i>p</i> ≤ 0.05) bacterial reduction compared to all other treatment groups, especially on days 8 and 12 for both pathogens. MWM demonstrated promise in addressing colonized wounds with biofilms. Additional studies on MWM's benefits and comparisons with existing treatments are warranted to optimize wound care strategies (<i>Adv Wound Care</i>. 2021;10:281).</p>\",\"PeriodicalId\":14451,\"journal\":{\"name\":\"International Wound Journal\",\"volume\":\"21 10\",\"pages\":\"\"},\"PeriodicalIF\":2.6000,\"publicationDate\":\"2024-10-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11447198/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Wound Journal\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/iwj.70059\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"DERMATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Wound Journal","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/iwj.70059","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"DERMATOLOGY","Score":null,"Total":0}
Antimicrobial effects of a multimodal wound matrix against methicillin-resistant Staphylococcus aureus and Pseudomonas aeruginosa in an in vitro and an in vivo porcine wound model
Chronic non-healing wounds pose significant challenges due to an elevated inflammatory response caused in part by bacterial contamination (Physiol Rev. 2019;99:665). These wounds lead to billions being spent in the health care system worldwide (N Engl J Med. 2017;376:2367, Int J Pharm. 2014;463:119). We studied the in-vitro and in-vivo antimicrobial effects of a multimodal wound matrix (MWM) against two common wound pathogens, Methicillin-Resistant Staphylococcus aureus (MRSA USA300) and Pseudomonas aeruginosa ATCC 27312 (PA27312) (Int Wound J. 2019;16:634). The in-vitro study conducted was a zone of inhibition test with the two microbes at 104 Log CFU/mL inoculated on Tryptic soy agar with 5% sheep blood (TSAII) plates. Treatments used were MWM, Mupirocin (Positive control for MRSA), Silver Sulfadiazine (Positive Control for PA), Petrolatum and Sterile Saline (both serving as Negative Controls). Treatments were allowed to diffuse into the agar for 3 h and then were incubated for 24 h at 37°C. The in-vivo study utilized a deep dermal porcine wound model (22 × 22 × 3 mm) created on six animals. Three animals were inoculated with MRSA USA300 and the other three with PA27312 with each allowing a 72-h biofilm formation. After 72 h, baseline wounds were assessed for bacterial concentration and all remaining wounds were treated with either MWM alone, Silver Treatment or Untreated Control. Wounds were assessed on days 4, 8 and 12 after treatment application for microbiological analysis. In-vitro, MWM exhibited significant inhibition of MRSA USA300 and PA27312 growth when compared to negative controls (p ≤ 0.05). Likewise, in-vivo, the MWM-treated wounds exhibited a significant (p ≤ 0.05) bacterial reduction compared to all other treatment groups, especially on days 8 and 12 for both pathogens. MWM demonstrated promise in addressing colonized wounds with biofilms. Additional studies on MWM's benefits and comparisons with existing treatments are warranted to optimize wound care strategies (Adv Wound Care. 2021;10:281).
期刊介绍:
The Editors welcome papers on all aspects of prevention and treatment of wounds and associated conditions in the fields of surgery, dermatology, oncology, nursing, radiotherapy, physical therapy, occupational therapy and podiatry. The Journal accepts papers in the following categories:
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The Editors are supported by a board of international experts and a panel of reviewers across a range of disciplines and specialties which ensures only the most current and relevant research is published.