Yin Hsin-Bai, Boomer Ashley, Chen Chi-Hung, Patel Jitendra
Environmental Microbial and Food Safety Laboratory, U.S. Department of Agriculture, Agricultural Research Service, 10300 Baltimore Avenue, Building 201, BARC-East, Beltsville, Maryland 20705 (ORCID: https://orcid.org/0000-0002-1420-5723 [J.P.]); and.
Department of Animal and Avian Sciences, University of Maryland, College Park, Maryland 20742, USA.
J Food Prot. 2019 Nov;82(11):1837-1843. doi: 10.4315/0362-028X.JFP-19-168.
and Shiga toxigenic (STEC) are important foodborne bacterial pathogens that can form biofilms on equipment surfaces at food processing facilities. Pathogens in biofilms are resistant to conventional antimicrobials and require higher antimicrobial concentrations to be inactivated. In this study, the efficacy of a synthetic innate defense regulator peptide 1018 (peptide 1018) for inactivating and STEC (O26, O111, O145, O157) biofilms on stainless steel and polycarbonate surfaces was investigated. Stainless steel and polycarbonate coupons (12 mm in diameter) were used in a Centers for Disease Control and Prevention biofilm reactor containing 400 mL of 10% tryptic soy broth (TSB) that had been inoculated with an individual strain of or STEC to obtain 6 log CFU/mL populations. The reactor was set with a constant flow rate at 50 mL/h of 10% TSB for 48 h. After 48 h, coupons were treated with peptide 1018 at 0, 10, 20, or 50 μg/mL in phosphate buffer saline (PBS) for 24 h. Surviving bacterial populations were determined by scraping off the coupons and spiral plating on selective media. Significantly higher levels of pathogens in biofilms formed by certain bacterial strains, including F6854, O157:H7 RM4407 and NADC5713, and non-O157 NADC3629, were recovered on polycarbonate surfaces than on stainless steel. Antibiofilm efficacy of peptide 1018 against pathogens was concentration-dependent and varied with the type of pathogen and material surfaces. Peptide 1018 at 50 μg/mL significantly inactivated all tested bacterial biofilms on both surfaces compared with the PBS control ( < 0.05). was the bacterium most sensitive to peptide 1018; on stainless steel surfaces treated with 50 μg/mL peptide 1018, there was a 3.7- to 4.6-log CFU/cm reduction in populations compared with a 1.0- to 3.5-log CFU/cm reduction of STEC. Results suggest that peptide 1018 may be used to inactivate and STEC biofilms on equipment surfaces.
产志贺毒素大肠杆菌(STEC)是重要的食源细菌性病原体,可在食品加工设施的设备表面形成生物膜。生物膜中的病原体对传统抗菌药物具有抗性,需要更高的抗菌浓度才能被灭活。在本研究中,研究了一种合成的天然免疫调节肽1018(肽1018)对不锈钢和聚碳酸酯表面上的产志贺毒素大肠杆菌和STEC(O26、O111、O145、O157)生物膜的灭活效果。直径12毫米的不锈钢和聚碳酸酯试片被用于疾病控制与预防中心的生物膜反应器中,该反应器含有400毫升接种了单个产志贺毒素大肠杆菌菌株或STEC菌株的10%胰蛋白胨大豆肉汤(TSB),以获得6 log CFU/mL的菌量。反应器以50毫升/小时的恒定流速通入10% TSB,持续48小时。48小时后,将试片在磷酸盐缓冲盐水(PBS)中用0、10、20或50微克/毫升的肽1018处理24小时。通过刮下试片并在选择性培养基上进行螺旋平板接种来测定存活的细菌数量。在聚碳酸酯表面上,由某些细菌菌株形成的生物膜中的病原体水平显著高于不锈钢表面,这些菌株包括产志贺毒素大肠杆菌F6854、O157:H7 RM4407和NADC5713,以及非O157的NADC3629。肽1018对病原体的抗生物膜效果呈浓度依赖性,且因病原体类型和材料表面而异。与PBS对照相比,50微克/毫升的肽1018显著灭活了两个表面上所有测试的细菌生物膜(P < 0.05)。产志贺毒素大肠杆菌是对肽1018最敏感的细菌;在50微克/毫升肽1018处理的不锈钢表面上,产志贺毒素大肠杆菌的菌量减少了3.7至4.6 log CFU/cm²,而STEC的菌量减少了1.0至3.5 log CFU/cm²。结果表明,肽1018可用于灭活设备表面上的产志贺毒素大肠杆菌和STEC生物膜。