首页 > 最新文献

International journal of food microbiology最新文献

英文 中文
Prevalence, antimicrobial resistance and virulence genes of Campylobacter isolated from retail duck meat in Southern China 华南地区零售鸭肉中弯曲杆菌的流行、耐药性和毒力基因分析
IF 5.2 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2025-12-11 DOI: 10.1016/j.ijfoodmicro.2025.111577
Chen Lixuan , He Haishan , Miu Tianshuang , Guan Jin , Xia Ruowei , Zheng Zexin , Zhang Jianmin
Campylobacter is a significant foodborne pathogen. However, most current studies have focused on chicken-derived Campylobacter, while systematic epidemiological investigations on duck-derived Campylobacter remain relatively limited. Given that China is the largest duck meat producer globally, conducting systematic epidemiological surveys on duck-borne Campylobacter is of considerable public health importance. This study analyzed the prevalence, antimicrobial resistance (AMR), and virulence genes of Campylobacter isolates from retail duck meat in Southern China. A total of 350 duck meat samples were collected from retail markets, consisting of 173 fresh, 167 refrigerated, and 10 frozen samples. The ISO 10272 guidelines were used to isolate 61 Campylobacter strains (17.4 %), with Campylobacter jejuni (C. jejuni, 80.3 %) showing a significantly higher prevalence than Campylobacter coli (C. coli, 19.7 %). Antimicrobial susceptibility testing revealed high resistance rates to Erythromycin (96.7 %), Streptomycin (93.4 %), Nalidixic Acid (93.4 %), Ampicillin (78.7 %), and Gentamicin (78.7 %). All isolates exhibited multidrug resistance (MDR). It is noteworthy that mutations were identified in the present study, including the 23S rRNA gene (A2075G and C2113T), ribosomal proteins L4 and L22, as well as the Thr-86-Ile substitution in the gyrA gene. These alterations in key target sites may contribute to the observed resistance phenotypes to erythromycin and fluoroquinolones, though the precise mechanisms warrant further investigation. In addition to antimicrobial resistance, virulence gene analysis revealed a high prevalence of cdtB (59.0 %) and cadF (57.4 %), with C. jejuni carrying a significantly higher number of virulence genes compared to C. coli. The study highlights the significant public health risk posed by MDR Campylobacter in duck meat, emphasizing the need for stricter regulations on antibiotic use in livestock and continuous monitoring to mitigate the spread of resistant strains through the food chain.
弯曲杆菌是一种重要的食源性致病菌。然而,目前的研究大多集中在鸡源弯曲杆菌上,而对鸭源弯曲杆菌的系统流行病学调查仍然相对有限。鉴于中国是全球最大的鸭肉生产国,对鸭源弯曲杆菌进行系统的流行病学调查具有相当大的公共卫生重要性。本研究分析了华南地区零售鸭肉中弯曲杆菌(Campylobacter)的流行、耐药性和毒力基因。在零售市场共采集了350份鸭肉样本,其中新鲜鸭肉173份,冷藏鸭肉167份,冷冻鸭肉10份。采用ISO 10272指南分离出61株弯曲杆菌(17.4%),其中空肠弯曲杆菌(C. jejuni, 80.3%)的流行率明显高于大肠弯曲杆菌(C. coli, 19.7%)。对红霉素(96.7%)、链霉素(93.4%)、萘啶酸(93.4%)、氨苄西林(78.7%)、庆大霉素(78.7%)的耐药率较高。所有分离株均表现出多药耐药(MDR)。值得注意的是,本研究发现的突变包括23S rRNA基因(A2075G和C2113T),核糖体蛋白L4和L22,以及gyrA基因中Thr-86-Ile的替换。这些关键靶点的改变可能有助于观察到的对红霉素和氟喹诺酮类药物的耐药表型,但其确切机制有待进一步研究。除了抗菌素耐药性外,毒力基因分析显示cdtB(59.0%)和cadF(57.4%)的流行率很高,与大肠杆菌相比,空肠梭菌携带的毒力基因数量显著增加。该研究强调了鸭肉中的耐多药弯曲杆菌构成的重大公共卫生风险,强调需要对牲畜使用抗生素制定更严格的法规,并进行持续监测,以减轻耐药菌株在食物链中的传播。
{"title":"Prevalence, antimicrobial resistance and virulence genes of Campylobacter isolated from retail duck meat in Southern China","authors":"Chen Lixuan ,&nbsp;He Haishan ,&nbsp;Miu Tianshuang ,&nbsp;Guan Jin ,&nbsp;Xia Ruowei ,&nbsp;Zheng Zexin ,&nbsp;Zhang Jianmin","doi":"10.1016/j.ijfoodmicro.2025.111577","DOIUrl":"10.1016/j.ijfoodmicro.2025.111577","url":null,"abstract":"<div><div><em>Campylobacter</em> is a significant foodborne pathogen. However, most current studies have focused on chicken-derived <em>Campylobacter</em>, while systematic epidemiological investigations on duck-derived <em>Campylobacter</em> remain relatively limited. Given that China is the largest duck meat producer globally, conducting systematic epidemiological surveys on duck-borne <em>Campylobacter</em> is of considerable public health importance. This study analyzed the prevalence, antimicrobial resistance (AMR), and virulence genes of <em>Campylobacter</em> isolates from retail duck meat in Southern China. A total of 350 duck meat samples were collected from retail markets, consisting of 173 fresh, 167 refrigerated, and 10 frozen samples. The ISO 10272 guidelines were used to isolate 61 <em>Campylobacter</em> strains (17.4 %), with <em>Campylobacter jejuni</em> (<em>C. jejuni</em>, 80.3 %) showing a significantly higher prevalence than <em>Campylobacter coli</em> (<em>C. coli</em>, 19.7 %). Antimicrobial susceptibility testing revealed high resistance rates to Erythromycin (96.7 %), Streptomycin (93.4 %), Nalidixic Acid (93.4 %), Ampicillin (78.7 %), and Gentamicin (78.7 %). All isolates exhibited multidrug resistance (MDR). It is noteworthy that mutations were identified in the present study, including the 23S rRNA gene (A2075G and C2113T), ribosomal proteins L4 and L22, as well as the Thr-86-Ile substitution in the <em>gyrA</em> gene. These alterations in key target sites may contribute to the observed resistance phenotypes to erythromycin and fluoroquinolones, though the precise mechanisms warrant further investigation. In addition to antimicrobial resistance, virulence gene analysis revealed a high prevalence of <em>cdtB</em> (59.0 %) and <em>cadF</em> (57.4 %), with <em>C. jejuni</em> carrying a significantly higher number of virulence genes compared to <em>C. coli</em>. The study highlights the significant public health risk posed by MDR <em>Campylobacter</em> in duck meat, emphasizing the need for stricter regulations on antibiotic use in livestock and continuous monitoring to mitigate the spread of resistant strains through the food chain.</div></div>","PeriodicalId":14095,"journal":{"name":"International journal of food microbiology","volume":"448 ","pages":"Article 111577"},"PeriodicalIF":5.2,"publicationDate":"2025-12-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145788683","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Application of a novel phage vB_Sa_2868B2 and its endolysin LytN with broad antibacterial Spectrum against multidrug-resistant Staphylococcus aureus on food matrices, and metal surfaces 新型噬菌体vB_Sa_2868B2及其内溶素LytN在食品基质和金属表面对耐多药金黄色葡萄球菌的广谱抗菌应用
IF 5.2 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2025-12-11 DOI: 10.1016/j.ijfoodmicro.2025.111575
Feng Zhang , Shi Wu , Jiaxu Gao , Shiyu Ma , Xiaodong Pei , Xu Yang , Zhiping Zhang , Lili Song , Tao Wei
The novel bacteriophage vB_Sa_2868B2 and its endolysin LytN, which were isolated and characterized in this study, demonstrate significant potential as effective biocontrol agents against foodborne multidrug-resistant Staphylococcus aureus, including methicillin-resistant S. aureus (MRSA). Morphological and genomic analyses revealed that vB_Sa_2868B2 is a new species of the genus Rosenblumvirus. Lifecycle and stability assays demonstrated that phage vB_Sa_2868B2 exhibited a short latent period (20 min), a high burst size (126 plaque-forming units [PFU]/cell), and broad tolerance to temperature (4–60 °C) and pH (4.0–11.0) conditions. The phage displayed a wide host range for S. aureus, lysing 49.10 % S. aureus strains with 29 different sequence types (STs). vB_Sa_2868B2 effectively reduced bacterial loads of S. aureus in milk by 5.60–5.80 log10 CFU/mL within 6 h. Furthermore, the purified endolysin LytN of vB_Sa_2868B2 showed robust stability across a wide temperature (0–45 °C) and pH (3.0–12.0) range, coupled with excellent metal ion tolerance. Notably, endolysin LytN demonstrated broad lytic activity, lysing 97.13 % of staphylococcal strains spanning 37 distinct STs, particularly including 99.11 % of the methicillin-resistant S. aureus (MRSA) isolates. Both phage vB_Sa_2868B2 and endolysin LytN exhibited significant bactericidal efficacy against MRSA in pork, with LytN treatment achieving a 3.50 log10 CFU/mL reduction. Additionally, the phage and endolysin effectively disrupted biofilms on stainless steel surfaces, reducing bacterial counts on metal contact surfaces by 4.00 and 4.30 log10 CFU/mL. Collectively, these findings highlight that the novel phage vB_Sa_2868B2 and endolysin LytN are highly effective, promising antibacterial biocontrol candidates for controlling S. aureus in the food industry. This work provides a robust foundation for developing novel, phage-based interventions to enhance food safety and combat antibiotic resistance.
本研究分离并鉴定的新型噬菌体vB_Sa_2868B2及其内溶素LytN作为食源性耐多药金黄色葡萄球菌(包括耐甲氧西林金黄色葡萄球菌(MRSA))的生物防治剂具有重要潜力。形态学和基因组分析表明,vB_Sa_2868B2是Rosenblumvirus属的一个新种。生命周期和稳定性试验表明,噬菌体vB_Sa_2868B2潜伏期短(20 min),爆发大小高(126个斑块形成单位[PFU]/细胞),对温度(4-60°C)和pH(4.0-11.0)条件具有广泛的耐受性。该噬菌体对金黄色葡萄球菌具有广泛的宿主范围,可裂解29种不同序列类型(st)的49.10%的金黄色葡萄球菌菌株。vB_Sa_2868B2在6 h内可有效降低牛奶中金黄色葡萄球菌的细菌负荷5.60 ~ 5.80 log10 CFU/mL。此外,纯化后的vB_Sa_2868B2在较宽的温度(0 ~ 45℃)和pH(3.0 ~ 12.0)范围内均表现出较强的稳定性,并具有良好的金属离子耐受性。值得注意的是,内溶素LytN显示出广泛的裂解活性,裂解97.13%的葡萄球菌菌株,跨越37个不同的STs,特别是包括99.11%的耐甲氧西林金黄色葡萄球菌(MRSA)分离株。噬菌体vB_Sa_2868B2和内溶素LytN对猪肉MRSA均有显著的杀菌效果,LytN处理后可降低3.50 log10 CFU/mL。此外,噬菌体和内溶素有效地破坏了不锈钢表面的生物膜,使金属接触表面的细菌计数分别减少4.00和4.30 log10 CFU/mL。综上所述,这些研究结果表明,新型噬菌体vB_Sa_2868B2和内溶素LytN是非常有效的、有前景的抗菌生物防治候选物,可用于食品工业中金黄色葡萄球菌的控制。这项工作为开发基于噬菌体的新型干预措施以加强食品安全和对抗抗生素耐药性提供了坚实的基础。
{"title":"Application of a novel phage vB_Sa_2868B2 and its endolysin LytN with broad antibacterial Spectrum against multidrug-resistant Staphylococcus aureus on food matrices, and metal surfaces","authors":"Feng Zhang ,&nbsp;Shi Wu ,&nbsp;Jiaxu Gao ,&nbsp;Shiyu Ma ,&nbsp;Xiaodong Pei ,&nbsp;Xu Yang ,&nbsp;Zhiping Zhang ,&nbsp;Lili Song ,&nbsp;Tao Wei","doi":"10.1016/j.ijfoodmicro.2025.111575","DOIUrl":"10.1016/j.ijfoodmicro.2025.111575","url":null,"abstract":"<div><div>The novel bacteriophage vB_Sa_2868B2 and its endolysin LytN, which were isolated and characterized in this study, demonstrate significant potential as effective biocontrol agents against foodborne multidrug-resistant <em>Staphylococcus aureus</em>, including methicillin-resistant <em>S. aureus</em> (MRSA). Morphological and genomic analyses revealed that vB_Sa_2868B2 is a new species of the genus <em>Rosenblumvirus</em>. Lifecycle and stability assays demonstrated that phage vB_Sa_2868B2 exhibited a short latent period (20 min), a high burst size (126 plaque-forming units [PFU]/cell), and broad tolerance to temperature (4–60 °C) and pH (4.0–11.0) conditions. The phage displayed a wide host range for <em>S. aureus,</em> lysing 49.10 % <em>S. aureus</em> strains with 29 different sequence types (STs). vB_Sa_2868B2 effectively reduced bacterial loads of <em>S. aureus</em> in milk by 5.60–5.80 log<sub>10</sub> CFU/mL within 6 h. Furthermore, the purified endolysin LytN of vB_Sa_2868B2 showed robust stability across a wide temperature (0–45 °C) and pH (3.0–12.0) range, coupled with excellent metal ion tolerance. Notably, endolysin LytN demonstrated broad lytic activity, lysing 97.13 % of staphylococcal strains spanning 37 distinct STs, particularly including 99.11 % of the methicillin-resistant <em>S. aureus</em> (MRSA) isolates. Both phage vB_Sa_2868B2 and endolysin LytN exhibited significant bactericidal efficacy against MRSA in pork, with LytN treatment achieving a 3.50 log<sub>10</sub> CFU/mL reduction. Additionally, the phage and endolysin effectively disrupted biofilms on stainless steel surfaces, reducing bacterial counts on metal contact surfaces by 4.00 and 4.30 log<sub>10</sub> CFU/mL. Collectively, these findings highlight that the novel phage vB_Sa_2868B2 and endolysin LytN are highly effective, promising antibacterial biocontrol candidates for controlling <em>S. aureus</em> in the food industry. This work provides a robust foundation for developing novel, phage-based interventions to enhance food safety and combat antibiotic resistance.</div></div>","PeriodicalId":14095,"journal":{"name":"International journal of food microbiology","volume":"448 ","pages":"Article 111575"},"PeriodicalIF":5.2,"publicationDate":"2025-12-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145774512","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Whole genome sequencing reveals transmission dynamics and persistence of Listeria monocytogenes along the poultry slaughtering and processing chain 全基因组测序揭示了单核细胞增生李斯特菌沿家禽屠宰和加工链的传播动态和持久性。
IF 5.2 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2025-12-11 DOI: 10.1016/j.ijfoodmicro.2025.111568
Ye Wang , Chaohui Huang , Sijie Wu , Jianye Jia , Tianxiang Pan , Ruochen Wang , Jing Li , Zegang Wang , Chuang Meng , Yuelan Yin , Xin'an Jiao
Listeria monocytogenes (Lm) is a gram-positive foodborne pathogen responsible for severe invasive human and livestock listeriosis. The dissemination of Lm throughout the poultry production chain significantly increases the risk of human listeriosis. In this study, we investigated the epidemiology and genetic characteristics of Lm in a poultry slaughterhouse using whole-genome sequencing (WGS). Lm contamination was detected in 8.32 % (77/925) of slaughterhouse carcasses, 9.86 % (102/1035) of environmental samples, and 13.28 % (32/241) of retail chicken, showing a gradual increase along the production chain. Moreover, contamination levels rose progressively throughout processing, reaching their highest at the quick-freezing and refrigeration stages after evisceration. Cross-contamination between poultry carcasses and processing equipment surfaces (8 ≤ single-nucleotide polymorphism distance (SNP) ≤ 21) was major driver of Lm transmission in slaughterhouse. Core-genome multilocus sequence typing (cgMLST) and SNP analyses identified four persistent Lm clusters (clonal complex 8, 9, 19 and 87), indicating long-term contamination on slaughterhouse processing equipment surfaces. Notably, all serotype 1/2b isolates belonged to cluster CC87 and harbored multiple stress resistance genes, demonstrating enhanced adaptability to slaughterhouse environments. In addition, CC87 strains showed reduced susceptibility to ampicillin (100 %) and gentamicin (66.7 %), highlighting significant therapeutic challenges and public health risks. These findings underscore the importance of implementing robust epidemiological surveillance throughout the poultry production chain to prevent Lm contamination and reduce the risk of human listeriosis.
单核细胞增生李斯特菌(Lm)是一种革兰氏阳性食源性病原体,负责严重侵袭性人类和牲畜李斯特菌病。Lm在整个家禽生产链中的传播显著增加了人类李斯特菌病的风险。本研究采用全基因组测序(WGS)技术对某家禽屠宰场Lm的流行病学和遗传特征进行了研究。在8.32%(77/925)的屠宰胴体、9.86%(102/1035)的环境样本和13.28%(32/241)的零售鸡中检测到Lm污染,呈沿生产链逐渐增加的趋势。此外,污染水平在整个加工过程中逐渐上升,在去除内脏后的速冻和冷藏阶段达到最高水平。家禽胴体与加工设备表面交叉污染(8≤单核苷酸多态性距离(SNP)≤21)是Lm在屠宰场传播的主要驱动因素。核心基因组多位点序列分型(cgMLST)和SNP分析鉴定出4个持久性Lm簇(克隆复合体8、9、19和87),表明屠宰场加工设备表面存在长期污染。值得注意的是,所有血清型1/2b分离株均属于CC87集群,并携带多种抗逆性基因,表明对屠宰场环境的适应性增强。此外,CC87菌株对氨苄西林(100%)和庆大霉素(66.7%)的敏感性降低,突出了显著的治疗挑战和公共卫生风险。这些发现强调了在整个家禽生产链中实施强有力的流行病学监测以防止Lm污染和降低人类李斯特菌病风险的重要性。
{"title":"Whole genome sequencing reveals transmission dynamics and persistence of Listeria monocytogenes along the poultry slaughtering and processing chain","authors":"Ye Wang ,&nbsp;Chaohui Huang ,&nbsp;Sijie Wu ,&nbsp;Jianye Jia ,&nbsp;Tianxiang Pan ,&nbsp;Ruochen Wang ,&nbsp;Jing Li ,&nbsp;Zegang Wang ,&nbsp;Chuang Meng ,&nbsp;Yuelan Yin ,&nbsp;Xin'an Jiao","doi":"10.1016/j.ijfoodmicro.2025.111568","DOIUrl":"10.1016/j.ijfoodmicro.2025.111568","url":null,"abstract":"<div><div><em>Listeria monocytogenes</em> (Lm) is a gram-positive foodborne pathogen responsible for severe invasive human and livestock listeriosis. The dissemination of Lm throughout the poultry production chain significantly increases the risk of human listeriosis. In this study, we investigated the epidemiology and genetic characteristics of Lm in a poultry slaughterhouse using whole-genome sequencing (WGS). Lm contamination was detected in 8.32 % (77/925) of slaughterhouse carcasses, 9.86 % (102/1035) of environmental samples, and 13.28 % (32/241) of retail chicken, showing a gradual increase along the production chain. Moreover, contamination levels rose progressively throughout processing, reaching their highest at the quick-freezing and refrigeration stages after evisceration. Cross-contamination between poultry carcasses and processing equipment surfaces (8 ≤ single-nucleotide polymorphism distance (SNP) ≤ 21) was major driver of Lm transmission in slaughterhouse. Core-genome multilocus sequence typing (cgMLST) and SNP analyses identified four persistent Lm clusters (clonal complex 8, 9, 19 and 87), indicating long-term contamination on slaughterhouse processing equipment surfaces. Notably, all serotype 1/2b isolates belonged to cluster CC87 and harbored multiple stress resistance genes, demonstrating enhanced adaptability to slaughterhouse environments. In addition, CC87 strains showed reduced susceptibility to ampicillin (100 %) and gentamicin (66.7 %), highlighting significant therapeutic challenges and public health risks. These findings underscore the importance of implementing robust epidemiological surveillance throughout the poultry production chain to prevent Lm contamination and reduce the risk of human listeriosis.</div></div>","PeriodicalId":14095,"journal":{"name":"International journal of food microbiology","volume":"448 ","pages":"Article 111568"},"PeriodicalIF":5.2,"publicationDate":"2025-12-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145819349","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Comparative evaluation of LAB proteolytic activities in soy-based dairy alternatives and bovine milk for selecting plant-based food starter strains 选择植物性食品发酵剂时大豆基乳制品替代品和牛乳中乳酸菌蛋白水解活性的比较评价。
IF 5.2 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2025-12-09 DOI: 10.1016/j.ijfoodmicro.2025.111566
Joanna Ivy Irorita Fugaban , Steffen Yde Bak , Pascal Fourcassie , Claus Heiner Bang-Berthelsen , Egon Bech Hansen
The green transition in food production has intensified the search for novel starter cultures to produce plant-based dairy alternatives (PBDAs) that match dairy products in quality, taste, and texture. Traditional dairy starters have shown clear limitations in these matrices, particularly in nitrogen metabolism and proteolysis. This study aimed to screen and characterize lactic acid bacteria (LAB) with proteolytic traits better suited for plant-based food fermentations. Diverse LAB strains from different genera were screened in a soy-based drink (SBD), identifying 14 different clades of cell envelope proteinases (CEPs). Representative strains were then comparatively profiled in bovine milk and SBD, revealing that Clade I proteases have three distinct phenotypes, with proteases that are active predominantly in milk, predominantly in SBD, or in both matrices. Sequence and three-dimensional structure analyses identified amino acid differences in the Fn2 domain that may modulate substrate specificity. Soy-specific proteases were observed to have a tandem deletion in the pro-peptide and mutation at H763 in the active enzyme. Additionally, proteomics analysis revealed that these proteases target the disordered regions of soy proteins as the primary sources of peptides. The soy proteins dehydrin (K7LEQ5) and a late embryogenesis abundant protein (I1L957), which have highly disordered structures similar to caseins, were found to be susceptible to these proteases. Comparative peptide profiling showed that Lactococcus proteinases generated highly varied peptide sequences with consistent peptide lengths, whereas prtS gene-coded proteinases produced more uniform peptide sets, which highlights key functional difference between these two groups of traditional dairy starters. Overall, our findings indicate that Clade I proteases can be beneficial for hybrid dairy fermentation and plant-based fermentation, while Clade IV are highly conserved and ubiquitous in plant-adapted Leuconostoc spp. Although further investigation of these proteases is needed, these findings help fill a gap in comprehensive studies of the proteolytic capacity across different food matrices and provide detailed criteria for selecting suitable starter strains for plant-based foods.
食品生产的绿色转型已经加强了对新型发酵剂的研究,以生产在质量、味道和质地上与乳制品相匹配的植物性乳制品替代品(pbda)。传统的乳制品发酵剂在这些基质中表现出明显的局限性,特别是在氮代谢和蛋白质水解方面。本研究旨在筛选和表征具有更适合植物性食品发酵的蛋白水解特性的乳酸菌(LAB)。在大豆基饮料(SBD)中筛选了来自不同属的多种LAB菌株,鉴定出14种不同的细胞膜蛋白酶(cep)分支。然后在牛奶和SBD中比较代表性菌株,揭示了进化枝I蛋白酶具有三种不同的表型,蛋白酶主要在牛奶中活性,主要在SBD中活性,或在两种基质中活性。序列和三维结构分析发现,Fn2结构域的氨基酸差异可能会调节底物特异性。大豆特异性蛋白酶在前肽上有串联缺失,在活性酶上有H763突变。此外,蛋白质组学分析表明,这些蛋白酶靶向大豆蛋白的紊乱区域作为肽的主要来源。大豆脱氢蛋白(K7LEQ5)和胚胎发育晚期丰富蛋白(I1L957)具有与酪蛋白相似的高度无序结构,易受这些蛋白酶的影响。比较肽谱分析显示,乳球菌蛋白酶产生的肽序列变化很大,但肽长度一致,而prtS基因编码的蛋白酶产生的肽集更均匀,这凸显了两组传统乳制品启动物之间的关键功能差异。总的来说,我们的研究结果表明,Clade I蛋白酶可能有利于混合乳制品发酵和植物发酵,而Clade IV蛋白酶高度保守且普遍存在于植物适应的Leuconostoc spp中。尽管需要对这些蛋白酶进行进一步的研究,但这些发现有助于填补在不同食物基质中蛋白质水解能力综合研究的空白,并为选择合适的植物性食品发酵剂提供详细的标准。
{"title":"Comparative evaluation of LAB proteolytic activities in soy-based dairy alternatives and bovine milk for selecting plant-based food starter strains","authors":"Joanna Ivy Irorita Fugaban ,&nbsp;Steffen Yde Bak ,&nbsp;Pascal Fourcassie ,&nbsp;Claus Heiner Bang-Berthelsen ,&nbsp;Egon Bech Hansen","doi":"10.1016/j.ijfoodmicro.2025.111566","DOIUrl":"10.1016/j.ijfoodmicro.2025.111566","url":null,"abstract":"<div><div>The green transition in food production has intensified the search for novel starter cultures to produce plant-based dairy alternatives (PBDAs) that match dairy products in quality, taste, and texture. Traditional dairy starters have shown clear limitations in these matrices, particularly in nitrogen metabolism and proteolysis. This study aimed to screen and characterize lactic acid bacteria (LAB) with proteolytic traits better suited for plant-based food fermentations. Diverse LAB strains from different genera were screened in a soy-based drink (SBD), identifying 14 different clades of cell envelope proteinases (CEPs). Representative strains were then comparatively profiled in bovine milk and SBD, revealing that Clade I proteases have three distinct phenotypes, with proteases that are active predominantly in milk, predominantly in SBD, or in both matrices. Sequence and three-dimensional structure analyses identified amino acid differences in the Fn2 domain that may modulate substrate specificity. Soy-specific proteases were observed to have a tandem deletion in the pro-peptide and mutation at H763 in the active enzyme. Additionally, proteomics analysis revealed that these proteases target the disordered regions of soy proteins as the primary sources of peptides. The soy proteins dehydrin (K7LEQ5) and a late embryogenesis abundant protein (I1L957), which have highly disordered structures similar to caseins, were found to be susceptible to these proteases. Comparative peptide profiling showed that <em>Lactococcus</em> proteinases generated highly varied peptide sequences with consistent peptide lengths, whereas <em>prtS</em> gene-coded proteinases produced more uniform peptide sets, which highlights key functional difference between these two groups of traditional dairy starters. Overall, our findings indicate that Clade I proteases can be beneficial for hybrid dairy fermentation and plant-based fermentation, while Clade IV are highly conserved and ubiquitous in plant-adapted <em>Leuconostoc</em> spp. Although further investigation of these proteases is needed, these findings help fill a gap in comprehensive studies of the proteolytic capacity across different food matrices and provide detailed criteria for selecting suitable starter strains for plant-based foods.</div></div>","PeriodicalId":14095,"journal":{"name":"International journal of food microbiology","volume":"448 ","pages":"Article 111566"},"PeriodicalIF":5.2,"publicationDate":"2025-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145774547","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Genomic characterization of five novel Salmonella phages and the assessment of their biocontrol potential for the preservation of chicken meat 五种新型沙门氏菌噬菌体的基因组鉴定及其对鸡肉保鲜的生物防治潜力评价
IF 5.2 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2025-12-08 DOI: 10.1016/j.ijfoodmicro.2025.111574
Gizem Cufaoglu , Gorkem Cengiz , Bahar Onaran Acar , Ozlem Kardogan , Nurhan Ertas Onmaz , Gultekin Unal , Erva Eser , Bilge Alpaslan Kocamemi , Muammer Goncuoglu , Irfan Erol , TÜBİTAK-121Z447 project scholars and consultants , Naim Deniz Ayaz
The rise of multidrug-resistant Salmonella poses a significant threat to food safety and public health, necessitating novel antimicrobial strategies. The primary objective of this study was to characterize novel bacteriophages and assess their biocontrol potential against predominant Salmonella serotypes. A total of 84 lytic bacteriophages specific to various Salmonella enterica serotypes were isolated from wastewater sources across Türkiye. Five phages (S.Hadar 4–5-1, S.Inf 5–2, S.Typ Adana, S.Ent 1–35-3, and S.Kent 1–2-1) demonstrating broad lytic activity to tested major serotypes (S. Enteritidis, S. Typhimurium, S. Infantis, S. Kentucky, S. Newport, S. Hadar, S. Gallinarum and S. Pullorum) and genetic diversity were selected for detailed phenotypic and genomic analysis. These phages, four from Siphoviridae and one from Podoviridae, exhibited tolerance to thermal (up to 60 °C) and mildly acidic conditions (pH 4), as well as 12-month stability when stored in Tris-Buffered Saline (TBS) with 20 % (v/v) glycerol at −20 °C and − 80 °C. Whole-genome sequencing confirmed their novelty and the absence of antimicrobial resistance and virulence genes. A cocktail formulated from these phages was applied against Salmonella Enteritidis both in-vitro (at 37 °C) and on artificially contaminated chicken wings (at 4 °C). The phage cocktail effectively reduced Salmonella counts in both environments, keeping levels below the detection limit (< 1 log CFU/g) over 24 h. For chicken wings food model, bacterial reductions reached 3.30 log CFU/g and 4.86 log CFU/g. These results underscore the potential of the newly characterized Salmonella phages as effective tools for controlling bacterial contamination on chicken meat, supporting their use as a natural, and antibiotic-free strategy in modern food safety management.
耐多药沙门氏菌的增加对食品安全和公众健康构成重大威胁,需要新的抗微生物策略。本研究的主要目的是表征新型噬菌体,并评估其对主要沙门氏菌血清型的生物防治潜力。从全国各地的废水源中分离出84种不同肠道沙门氏菌血清型的裂解噬菌体。5个噬菌体(S.Hadar 4-5-1、s.f inf 5-2、S.Typ Adana、s.t ent 1-35-3和s.t kent 1-2-1)对主要血清型(肠炎沙门氏菌、鼠伤寒沙门氏菌、婴儿沙门氏菌、肯塔基沙门氏菌、新港沙门氏菌、S.Hadar、s.g allinarum和s.p ullorum)具有广泛的裂解活性,并具有遗传多样性,对其进行了详细的表型和基因组分析。这些噬菌体,4个来自Siphoviridae, 1个来自Podoviridae,表现出对高温(高达60°C)和轻度酸性条件(pH 4)的耐受性,并且在- 20°C和- 80°C下储存在含有20% (v/v)甘油的tris缓冲盐水(TBS)中12个月的稳定性。全基因组测序证实了它们的新颖性和抗菌素耐药性和毒力基因的缺失。由这些噬菌体配制的鸡尾酒在体外(37°C)和人工污染的鸡翅(4°C)上用于对抗肠炎沙门氏菌。噬菌体鸡尾酒有效降低了两种环境中的沙门氏菌计数,在24小时内保持在检测限(1 log CFU/g)以下。对于鸡翅食物模型,细菌减少量分别达到3.30 log CFU/g和4.86 log CFU/g。这些结果强调了新鉴定的沙门氏菌噬菌体作为控制鸡肉细菌污染的有效工具的潜力,支持它们作为一种天然的、无抗生素的策略在现代食品安全管理中使用。
{"title":"Genomic characterization of five novel Salmonella phages and the assessment of their biocontrol potential for the preservation of chicken meat","authors":"Gizem Cufaoglu ,&nbsp;Gorkem Cengiz ,&nbsp;Bahar Onaran Acar ,&nbsp;Ozlem Kardogan ,&nbsp;Nurhan Ertas Onmaz ,&nbsp;Gultekin Unal ,&nbsp;Erva Eser ,&nbsp;Bilge Alpaslan Kocamemi ,&nbsp;Muammer Goncuoglu ,&nbsp;Irfan Erol ,&nbsp;TÜBİTAK-121Z447 project scholars and consultants ,&nbsp;Naim Deniz Ayaz","doi":"10.1016/j.ijfoodmicro.2025.111574","DOIUrl":"10.1016/j.ijfoodmicro.2025.111574","url":null,"abstract":"<div><div>The rise of multidrug-resistant <em>Salmonella</em> poses a significant threat to food safety and public health, necessitating novel antimicrobial strategies. The primary objective of this study was to characterize novel bacteriophages and assess their biocontrol potential against predominant <em>Salmonella</em> serotypes. A total of 84 lytic bacteriophages specific to various <em>Salmonella enterica</em> serotypes were isolated from wastewater sources across Türkiye. Five phages (S.Hadar 4–5-1, S.Inf 5–2, S.Typ Adana, S.Ent 1–35-3, and S.Kent 1–2-1) demonstrating broad lytic activity to tested major serotypes (<em>S.</em> Enteritidis, <em>S.</em> Typhimurium, <em>S.</em> Infantis, <em>S</em>. Kentucky, <em>S</em>. Newport, <em>S</em>. Hadar, <em>S.</em> Gallinarum and <em>S</em>. Pullorum) and genetic diversity were selected for detailed phenotypic and genomic analysis. These phages, four from <em>Siphoviridae</em> and one from <em>Podoviridae</em>, exhibited tolerance to thermal (up to 60 °C) and mildly acidic conditions (pH 4), as well as 12-month stability when stored in Tris-Buffered Saline (TBS) with 20 % (<em>v</em>/v) glycerol at −20 °C and − 80 °C. Whole-genome sequencing confirmed their novelty and the absence of antimicrobial resistance and virulence genes. A cocktail formulated from these phages was applied against <em>Salmonella</em> Enteritidis both in-vitro (at 37 °C) and on artificially contaminated chicken wings (at 4 °C). The phage cocktail effectively reduced <em>Salmonella</em> counts in both environments, keeping levels below the detection limit (&lt; 1 log CFU/g) over 24 h. For chicken wings food model, bacterial reductions reached 3.30 log CFU/g and 4.86 log CFU/g. These results underscore the potential of the newly characterized <em>Salmonella</em> phages as effective tools for controlling bacterial contamination on chicken meat, supporting their use as a natural, and antibiotic-free strategy in modern food safety management.</div></div>","PeriodicalId":14095,"journal":{"name":"International journal of food microbiology","volume":"448 ","pages":"Article 111574"},"PeriodicalIF":5.2,"publicationDate":"2025-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145736180","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Peracetic acid efficacy and decay kinetics in poultry processing under chiller conditions 过氧乙酸在低温条件下家禽加工中的功效和腐烂动力学
IF 5.2 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2025-12-08 DOI: 10.1016/j.ijfoodmicro.2025.111572
Vyshnavi Ciluveru , Jason Simon , Jeffery M. Farber , Shawn D. Ryan , Chandrasekhar R. Kothapalli , Daniel S. Munther
Pathogens on poultry products continue to pose critical public health risks. While chilling is a critical control point, the mechanisms of sanitizer efficacy in terms of pathogen and organic load, sanitizer levels, and exposure duration have not been clearly quantified. Moving beyond descriptive sanitizer-pathogen reduction experiments, we utilized experimentally-informed-mathematical-modeling to determine pathogen dynamics during chilling. Under realistic conditions in 10-L chiller tanks, whole chicken carcasses were exposed to peracetic acid (PAA; 70 and 200 mg⋅L−1) with process water parameters and PAA levels monitored up to 60 min. Additionally, the shedding and survival of a five-strain cocktail of poultry plant derived Salmonella enterica serovars, at high and low loads, with exposure to PAA (0–75 mg⋅L−1) for up to 10 min, in the presence/absence of inoculated chicken thighs, were measured. A mathematical model for PAA decay and pathogen shedding/inactivation was developed. Results indicate total dissolved solids (TDS) predict PAA decay more consistently than chemical oxygen demand (COD), with accurate forecasting of PAA level changes in the pre/main chiller of a high-speed poultry processing plant in North America. Without organic load, residual PAA (1 mg⋅L−1) inactivated bacteria given sufficient exposure time, although PAA levels >5 mg⋅L−1 were essential for rapid inactivation. With organic load, initial PAA concentration (> 40 mg⋅L−1) and exposure time (> 2 min) were critical for bacterial reduction, with model results contrasting when shed or sanitizer inactivation dominate. The data and insights from this study provide novel tools for processors to improve pathogen control during chilling.
家禽产品上的病原体继续构成严重的公共卫生风险。虽然冷却是一个关键的控制点,但从病原体和有机负荷、消毒剂水平和暴露时间等方面来看,消毒剂功效的机制尚未得到明确的量化。除了描述性消毒剂-病原体减少实验之外,我们利用实验信息数学模型来确定冷却期间的病原体动态。在实际条件下,在10-L冷水箱中,将全鸡尸体暴露于过氧乙酸(PAA; 70和200 mg⋅L−1)中,监测工艺水参数和PAA水平长达60分钟。此外,在接种鸡腿和不接种鸡腿的情况下,在高负荷和低负荷条件下,暴露于PAA (0-75 mg·L−1)达10分钟,测定了五株家禽植物源性肠炎沙门氏菌鸡尾酒的脱落和存活情况。建立了PAA腐烂和病原体脱落/失活的数学模型。结果表明,总溶解固体(TDS)对PAA衰变的预测比化学需氧量(COD)更一致,可以准确预测北美一家高速家禽加工厂前置/主制冷机中PAA水平的变化。在没有有机负荷的情况下,在足够的暴露时间内,残留的PAA (1 mg⋅L−1)灭活了细菌,尽管PAA水平为5 mg⋅L−1是快速灭活所必需的。在有机负荷下,初始PAA浓度(> 40 mg·L−1)和暴露时间(> 2 min)是细菌减少的关键,模型结果与棚子或消毒剂失活的结果相反。本研究的数据和见解为加工商在冷藏过程中提高病原体控制提供了新的工具。
{"title":"Peracetic acid efficacy and decay kinetics in poultry processing under chiller conditions","authors":"Vyshnavi Ciluveru ,&nbsp;Jason Simon ,&nbsp;Jeffery M. Farber ,&nbsp;Shawn D. Ryan ,&nbsp;Chandrasekhar R. Kothapalli ,&nbsp;Daniel S. Munther","doi":"10.1016/j.ijfoodmicro.2025.111572","DOIUrl":"10.1016/j.ijfoodmicro.2025.111572","url":null,"abstract":"<div><div>Pathogens on poultry products continue to pose critical public health risks. While chilling is a critical control point, the mechanisms of sanitizer efficacy in terms of pathogen and organic load, sanitizer levels, and exposure duration have not been clearly quantified. Moving beyond descriptive sanitizer-pathogen reduction experiments, we utilized experimentally-informed-mathematical-modeling to determine pathogen dynamics during chilling. Under realistic conditions in 10-L chiller tanks, whole chicken carcasses were exposed to peracetic acid (PAA; 70 and 200 mg⋅L<sup>−1</sup>) with process water parameters and PAA levels monitored up to 60 min. Additionally, the shedding and survival of a five-strain cocktail of poultry plant derived <em>Salmonella enterica</em> serovars, at high and low loads, with exposure to PAA (0–75 mg⋅L<sup>−1</sup>) for up to 10 min, in the presence/absence of inoculated chicken thighs, were measured. A mathematical model for PAA decay and pathogen shedding/inactivation was developed. Results indicate total dissolved solids (TDS) predict PAA decay more consistently than chemical oxygen demand (COD), with accurate forecasting of PAA level changes in the pre/main chiller of a high-speed poultry processing plant in North America. Without organic load, residual PAA (1 mg⋅L<sup>−1</sup>) inactivated bacteria given sufficient exposure time, although PAA levels &gt;5 mg⋅L<sup>−1</sup> were essential for rapid inactivation. With organic load, initial PAA concentration (&gt; 40 mg⋅L<sup>−1</sup>) and exposure time (&gt; 2 min) were critical for bacterial reduction, with model results contrasting when shed or sanitizer inactivation dominate. The data and insights from this study provide novel tools for processors to improve pathogen control during chilling.</div></div>","PeriodicalId":14095,"journal":{"name":"International journal of food microbiology","volume":"448 ","pages":"Article 111572"},"PeriodicalIF":5.2,"publicationDate":"2025-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145719040","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
From phyllosphere to fermentation: Impact of fermentation scale and temperature on sauerkraut fermentation 从层球到发酵:发酵规模和温度对酸菜发酵的影响。
IF 5.2 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2025-12-07 DOI: 10.1016/j.ijfoodmicro.2025.111571
Nanzhen Qiao, Michael G. Gänzle
The spontaneous fermentation of vegetables such as kimchi, pao cai and sauerkraut, relies on lactic acid bacteria (LAB) from the plant phyllosphere. Plant-associated LAB occur only at low abundance. This study investigated the impact of fermentation scale, temperature and cabbage source on the LAB diversity. Fermentations were conducted at a scale of 0.8 g to 30 g by immersion of chopped interior leaves of white cabbage obtained from two supermarkets, SF and SW, in 2.5 % (w/w) NaCl solution at 10 °C and 20 °C. Fermentations were monitored by pH determination, metabolite analysis and microbial cell counts, and by 16S rRNA gene amplicon sequencing. Fermentation of 0.8 g cabbage SF with 20 replicates per group supported growth of Enterobacterales but not of LAB. Cabbage SW was fermented by Leuconostoc spp., with an average relative abundance of 98.8 % after 28 d. In fermentations with 8 g cabbage, Lactiplantibacillus established as dominating fermentation microorganism. At the 30 g scale, Lactiplantibacillus dominated at 20 °C regardless of cabbage source, whereas Leuconostoc or Rahnella remained dominant at 10 °C. The organic acid concentrations and the metabolism of phenolic compounds differed depending on whether Lactiplantibacillus, Leuconostoc or Rahnella were the predominant fermentation microorganisms. Collectively, our data highlight that the establishment of LAB communities in sauerkraut fermentation is influenced by both the fermentation scale and temperature, underscoring the critical roles of Lactiplantibacillus at higher temperatures and Leuconostoc at lower temperatures.
泡菜、白菜和酸菜等蔬菜的自发发酵依赖于植物层圈中的乳酸菌(LAB)。植物相关的LAB仅在低丰度时发生。本试验研究了发酵规模、温度和白菜源对乳酸菌多样性的影响。在10°C和20°C条件下,将从SF和SW两家超市买来的白卷心菜切碎的内叶浸泡在2.5% (w/w)的NaCl溶液中,发酵量为0.8 g ~ 30 g。通过pH测定、代谢物分析、微生物细胞计数和16S rRNA基因扩增子测序来监测发酵过程。发酵0.8 g白菜SF,每组20个重复,有利于肠杆菌的生长,但不利于乳酸菌的生长。白菜SW由Leuconostoc spp.发酵,28 d后平均相对丰度为98.8%。在8 g白菜发酵中,乳酸杆菌确立为主导发酵微生物。在30 g尺度下,无论白菜来源如何,乳酸杆菌在20°C下占优势,而Leuconostoc或Rahnella在10°C下仍占优势。有机酸浓度和酚类化合物的代谢取决于乳酸杆菌、白菌和Rahnella是否是主要发酵微生物。综上所述,我们的数据强调了酸菜发酵过程中LAB群落的建立受发酵规模和温度的影响,强调了高温下Lactiplantibacillus和低温下Leuconostoc的关键作用。
{"title":"From phyllosphere to fermentation: Impact of fermentation scale and temperature on sauerkraut fermentation","authors":"Nanzhen Qiao,&nbsp;Michael G. Gänzle","doi":"10.1016/j.ijfoodmicro.2025.111571","DOIUrl":"10.1016/j.ijfoodmicro.2025.111571","url":null,"abstract":"<div><div>The spontaneous fermentation of vegetables such as kimchi, pao cai and sauerkraut, relies on lactic acid bacteria (LAB) from the plant phyllosphere. Plant-associated LAB occur only at low abundance. This study investigated the impact of fermentation scale, temperature and cabbage source on the LAB diversity. Fermentations were conducted at a scale of 0.8 g to 30 g by immersion of chopped interior leaves of white cabbage obtained from two supermarkets, SF and SW, in 2.5 % (<em>w</em>/w) NaCl solution at 10 °C and 20 °C. Fermentations were monitored by pH determination, metabolite analysis and microbial cell counts, and by 16S rRNA gene amplicon sequencing. Fermentation of 0.8 g cabbage SF with 20 replicates per group supported growth of <em>Enterobacterales</em> but not of LAB. Cabbage SW was fermented by <em>Leuconostoc</em> spp., with an average relative abundance of 98.8 % after 28 d. In fermentations with 8 g cabbage, <em>Lactiplantibacillus</em> established as dominating fermentation microorganism. At the 30 g scale, <em>Lactiplantibacillus</em> dominated at 20 °C regardless of cabbage source, whereas <em>Leuconostoc</em> or <em>Rahnella</em> remained dominant at 10 °C. The organic acid concentrations and the metabolism of phenolic compounds differed depending on whether <em>Lactiplantibacillus</em>, <em>Leuconostoc</em> or <em>Rahnella</em> were the predominant fermentation microorganisms. Collectively, our data highlight that the establishment of LAB communities in sauerkraut fermentation is influenced by both the fermentation scale and temperature, underscoring the critical roles of <em>Lactiplantibacillus</em> at higher temperatures and <em>Leuconostoc</em> at lower temperatures.</div></div>","PeriodicalId":14095,"journal":{"name":"International journal of food microbiology","volume":"447 ","pages":"Article 111571"},"PeriodicalIF":5.2,"publicationDate":"2025-12-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145714069","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Supercritical carbon dioxide inactivation technology for food product preservation 食品保鲜用超临界二氧化碳失活技术
IF 5.2 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2025-12-06 DOI: 10.1016/j.ijfoodmicro.2025.111573
Pietro Andrigo , Sara Spilimbergo , Alessandro Zambon
Supercritical carbon dioxide (scCO2) is increasingly recognized as a non-thermal food preservation technology capable of ensuring microbial safety while preserving nutritional and sensory quality. Operating at moderate temperatures (<50 °C), scCO2 offers an environmentally friendly alternative to thermal pasteurization, leveraging its unique physicochemical properties to penetrate cells, induce acidification, and disrupt microbial structures. This review provides a comprehensive overview of the antimicrobial mechanisms of scCO2, including effects on membranes, enzymes, and intracellular pH, as well as its limitations in low-moisture systems and against spores, which require higher temperature, water, or synergistic co-treatments. The inactivation of viruses and fungal spores is also discussed, highlighting the potential of scCO2 in combination with additives such as hydrogen peroxide or natural antimicrobials. Attention is given to sublethal injury and viable-but-non-culturable (VBNC) states, which pose risks for microbial recovery and underscore the need for robust detection and storage strategies. The review explores hurdle technology approaches, integrating scCO2 with pulsed electric fields, high-power ultrasound, high-pressure processing, and food-grade additives to enhance lethality while maintaining product integrity. Current applications remain limited to pilot- or small-scale operations, with promising results in juices, dairy, and ready-to-eat foods. However, industrial adoption faces persistent challenges such as high equipment costs, regulatory uncertainties, and limited scalability. Future efforts should prioritize standardization of process parameters, validation of continuous systems, and regulatory harmonization. Overall, scCO2 emerges as a versatile, sustainable, and gentle alternative for microbial inactivation, well-suited to meet consumer demand for safe, minimally processed foods.
超临界二氧化碳(scCO2)越来越被认为是一种非热食品保鲜技术,能够确保微生物安全,同时保持营养和感官质量。scCO2在中等温度(50°C)下工作,利用其独特的物理化学性质穿透细胞,诱导酸化,破坏微生物结构,为热巴氏灭菌提供了一种环保的替代方案。本文综述了scCO2的抗菌机制,包括对膜、酶和细胞内pH值的影响,以及它在低湿度系统和对孢子的限制,这些系统需要更高的温度、水或协同共处理。还讨论了病毒和真菌孢子的失活,强调了scCO2与添加剂(如过氧化氢或天然抗菌剂)结合的潜力。关注亚致死损伤和存活但不可培养(VBNC)状态,这对微生物恢复构成风险,并强调需要强大的检测和储存策略。该综述探讨了障碍技术方法,将scCO2与脉冲电场、高功率超声、高压加工和食品级添加剂相结合,以提高致死率,同时保持产品完整性。目前的应用仍局限于试点或小规模操作,在果汁、乳制品和即食食品方面取得了可喜的成果。然而,工业应用面临着持续的挑战,如高设备成本、监管不确定性和有限的可扩展性。未来的工作应优先考虑工艺参数的标准化、连续系统的验证和监管协调。总的来说,scCO2作为一种多功能、可持续和温和的微生物灭活替代品,非常适合满足消费者对安全、最低加工食品的需求。
{"title":"Supercritical carbon dioxide inactivation technology for food product preservation","authors":"Pietro Andrigo ,&nbsp;Sara Spilimbergo ,&nbsp;Alessandro Zambon","doi":"10.1016/j.ijfoodmicro.2025.111573","DOIUrl":"10.1016/j.ijfoodmicro.2025.111573","url":null,"abstract":"<div><div>Supercritical carbon dioxide (scCO<sub>2</sub>) is increasingly recognized as a non-thermal food preservation technology capable of ensuring microbial safety while preserving nutritional and sensory quality. Operating at moderate temperatures (&lt;50 °C), scCO<sub>2</sub> offers an environmentally friendly alternative to thermal pasteurization, leveraging its unique physicochemical properties to penetrate cells, induce acidification, and disrupt microbial structures. This review provides a comprehensive overview of the antimicrobial mechanisms of scCO<sub>2</sub>, including effects on membranes, enzymes, and intracellular pH, as well as its limitations in low-moisture systems and against spores, which require higher temperature, water, or synergistic co-treatments. The inactivation of viruses and fungal spores is also discussed, highlighting the potential of scCO<sub>2</sub> in combination with additives such as hydrogen peroxide or natural antimicrobials. Attention is given to sublethal injury and viable-but-non-culturable (VBNC) states, which pose risks for microbial recovery and underscore the need for robust detection and storage strategies. The review explores hurdle technology approaches, integrating scCO<sub>2</sub> with pulsed electric fields, high-power ultrasound, high-pressure processing, and food-grade additives to enhance lethality while maintaining product integrity. Current applications remain limited to pilot- or small-scale operations, with promising results in juices, dairy, and ready-to-eat foods. However, industrial adoption faces persistent challenges such as high equipment costs, regulatory uncertainties, and limited scalability. Future efforts should prioritize standardization of process parameters, validation of continuous systems, and regulatory harmonization. Overall, scCO<sub>2</sub> emerges as a versatile, sustainable, and gentle alternative for microbial inactivation, well-suited to meet consumer demand for safe, minimally processed foods.</div></div>","PeriodicalId":14095,"journal":{"name":"International journal of food microbiology","volume":"448 ","pages":"Article 111573"},"PeriodicalIF":5.2,"publicationDate":"2025-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145719039","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Comparative genomics and functional traits of Weissella cibaria and Weissella confusa isolated from kimchi 泡菜中两种魏塞拉的比较基因组学和功能性状分析。
IF 5.2 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2025-12-06 DOI: 10.1016/j.ijfoodmicro.2025.111565
Md. Ashikur Rahman , Hyunhee Hong , Md. Ashrafudoulla , Shirin Akter , Sang-Do Ha , Si Hong Park
Weissella is a fascinating genus that has garnered increasing attention for its probiotic potential and industrial versatility. In this study, we present a detailed genomic and phenotypic investigation of six Weissella strains isolated from kimchi, identified as W. cibaria (254, 256, 258, 260) and W. confusa (255, 257). Genomic analysis revealed species-specific differences, with W. cibaria linked to cell cycle regulation and replication, while W. confusa displayed adaptations for motility and metabolic diversity. Antibiotic resistance gene analysis revealed the presence of daunorubicin resistance (drrA), multidrug resistance determinants (bmr3, lmrA, ykkCD), and species-specific resistance to bicyclomycin (bcr1, bcr2) and quaternary ammonium compounds (qacC). Phenotypic antibiotic susceptibility testing demonstrated intrinsic resistance to vancomycin alongside high sensitivity to ampicillin, erythromycin, chloramphenicol, and gentamicin. Probiotic assessments highlighted significant tolerance to acid, bile salts, and enzymatic stress, with W. cibaria 256 and W. confusa 255 showing superior survivability under simulated gastrointestinal conditions. High surface hydrophobicity observed in W. confusa 255 and 257 further underscores their adhesion capabilities, which are crucial for gut colonization. Exopolysaccharide (EPS) production was further characterized by FTIR analysis, revealing diverse functional groups associated with structural protection and probiotic functionality. Morphological characteristics as determined by field emission scanning electron microscopy (FE-SEM) revealed rod-shaped cells of 1.39–1.87 μm in length and 0.50–0.70 μm in width for W. cibaria strains versus 1.02–1.45 μm in length and 0.54–0.62 μm in width for W. confusa strains. These findings provide novel insights into the genomic and phenotypic underpinnings of Weissella species' probiotic properties, resistance mechanisms, and adaptability to fermented food environments, highlighting their promising applications in functional food development and human health enhancement.
Weissella是一种迷人的属,因其益生菌潜力和工业用途而受到越来越多的关注。在这项研究中,我们对从泡菜中分离的6株魏塞尔菌进行了详细的基因组和表型研究,鉴定为W. cibaria(254, 256, 258, 260)和W. confusa(255, 257)。基因组分析揭示了物种特异性差异,与细胞周期调节和复制有关的水蛭,而对运动和代谢多样性的适应性的水蛭。抗生素耐药基因分析显示存在柔红霉素耐药(drrA),多药耐药决定因素(bmr3, lmrA, ykkCD),以及对双环霉素(bcr1, bcr2)和季铵化合物(qacC)的物种特异性耐药。表型抗生素敏感性测试显示对万古霉素具有内在耐药性,同时对氨苄西林、红霉素、氯霉素和庆大霉素具有高度敏感性。益生菌评估强调了对酸、胆盐和酶胁迫的显著耐受性,W. cibaria 256和W. confusa 255在模拟胃肠道条件下表现出更强的生存能力。在W. confusa 255和257中观察到的高表面疏水性进一步强调了它们的粘附能力,这对肠道定植至关重要。通过FTIR分析进一步表征了外多糖(EPS)的产生,揭示了与结构保护和益生菌功能相关的多种官能团。通过场发射扫描电镜(FE-SEM)观察,菌株的棒状细胞长度为1.39 ~ 1.87 μm,宽度为0.50 ~ 0.70 μm,而菌株的棒状细胞长度为1.02 ~ 1.45 μm,宽度为0.54 ~ 0.62 μm。这些发现为Weissella物种的益生菌特性、抗性机制和对发酵食品环境的适应性的基因组和表型基础提供了新的见解,突出了它们在功能食品开发和人类健康促进方面的应用前景。
{"title":"Comparative genomics and functional traits of Weissella cibaria and Weissella confusa isolated from kimchi","authors":"Md. Ashikur Rahman ,&nbsp;Hyunhee Hong ,&nbsp;Md. Ashrafudoulla ,&nbsp;Shirin Akter ,&nbsp;Sang-Do Ha ,&nbsp;Si Hong Park","doi":"10.1016/j.ijfoodmicro.2025.111565","DOIUrl":"10.1016/j.ijfoodmicro.2025.111565","url":null,"abstract":"<div><div><em>Weissella</em> is a fascinating genus that has garnered increasing attention for its probiotic potential and industrial versatility. In this study, we present a detailed genomic and phenotypic investigation of six <em>Weissella</em> strains isolated from kimchi, identified as <em>W. cibaria</em> (254, 256, 258, 260) and <em>W. confusa</em> (255, 257). Genomic analysis revealed species-specific differences, with <em>W. cibaria</em> linked to cell cycle regulation and replication, while <em>W. confusa</em> displayed adaptations for motility and metabolic diversity. Antibiotic resistance gene analysis revealed the presence of daunorubicin resistance (<em>drrA</em>), multidrug resistance determinants (<em>bmr3</em>, <em>lmrA</em>, <em>ykkCD</em>), and species-specific resistance to bicyclomycin (<em>bcr1</em>, <em>bcr2</em>) and quaternary ammonium compounds (<em>qacC</em>). Phenotypic antibiotic susceptibility testing demonstrated intrinsic resistance to vancomycin alongside high sensitivity to ampicillin, erythromycin, chloramphenicol, and gentamicin. Probiotic assessments highlighted significant tolerance to acid, bile salts, and enzymatic stress, with <em>W. cibaria</em> 256 and <em>W. confusa</em> 255 showing superior survivability under simulated gastrointestinal conditions. High surface hydrophobicity observed in <em>W. confusa</em> 255 and 257 further underscores their adhesion capabilities, which are crucial for gut colonization. Exopolysaccharide (EPS) production was further characterized by FTIR analysis, revealing diverse functional groups associated with structural protection and probiotic functionality. Morphological characteristics as determined by field emission scanning electron microscopy (FE-SEM) revealed rod-shaped cells of 1.39–1.87 μm in length and 0.50–0.70 μm in width for <em>W. cibaria</em> strains versus 1.02–1.45 μm in length and 0.54–0.62 μm in width for <em>W. confusa</em> strains. These findings provide novel insights into the genomic and phenotypic underpinnings of <em>Weissella</em> species' probiotic properties, resistance mechanisms, and adaptability to fermented food environments, highlighting their promising applications in functional food development and human health enhancement.</div></div>","PeriodicalId":14095,"journal":{"name":"International journal of food microbiology","volume":"448 ","pages":"Article 111565"},"PeriodicalIF":5.2,"publicationDate":"2025-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145827415","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Environmental microorganisms as heterogeneous sources and shapers of the fermentation microbiome in Zhejiang rosy vinegar 环境微生物是浙江玫瑰红醋发酵微生物群的异质来源和塑造者。
IF 5.2 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2025-12-05 DOI: 10.1016/j.ijfoodmicro.2025.111554
Guoli Chang , Jun Zhang , Xiaoyue Fang , Shenchenyu Zhang , Haixia Lu , Yipeng Jiang , Junli Zhu
Zhejiang rosy vinegar (ZRV) fermentation is a complex, spontaneous open-system process, where microbial communities are key to its unique characteristics. However, the precise influence of the brewing workshop environment on these dynamic microbial communities remains underexplored, hindering consistent product quality. Here, we characterized the environmental and fermentation microbial communities across three factories using high-throughput sequencing (16S rRNA and ITS), qPCR, and advanced ecological network analyses. Our results establish that the brewing environment acts as a critical, heterogeneous, and factory-specific microbial reservoir, and provides the primary inoculum for fermentation initiation. Our findings revealed significant inter-factory differences in environmental microbial loads and community structures. For instance, the SX environment was characterized by a unique composition, including the notable presence of Monascus on jar lids. Source tracking confirmed this environmental “seeding” significantly shapes initial fermentation communities, with contributions from floor and jar surfaces. During fermentation, bacterial communities consistently shifted (LAB decrease, Acetobacter increase), but fungal successions varied notably by factory. Specifically, the natural fermentation at the SX factory fostered a distinct fungal community trajectory, characterized by a unique decrease in Saccharomyces and the emergence of Monascus as the dominant genus in later stages. This trajectory was directly linked to its distinct environmental fungal populations and their pronounced influence from the initial solid-state phase. While internal selective pressures eventually govern community structure, environmental conditions profoundly dictate overall microbial diversity and succession. A core microbiome (Bacillus, Sphingomonas, Cryptococcus, Monascus), consistently present in both environmental and fermentation niches, served as key microbial bridges. Our results provide a vital basis for optimizing ZRV production by strategically managing the environmental microbiome to enhance quality and consistency.
浙江玫瑰红醋发酵是一个复杂的、自发的开放系统过程,其中微生物群落是其独特特性的关键。然而,酿造车间环境对这些动态微生物群落的确切影响仍未得到充分研究,这阻碍了产品质量的一致性。在这里,我们利用高通量测序(16S rRNA和ITS)、qPCR和先进的生态网络分析对三家工厂的环境和发酵微生物群落进行了表征。我们的研究结果表明,酿造环境是一个关键的、异构的、工厂特有的微生物库,并为发酵起始提供了主要的接种物。我们的研究结果揭示了工厂间环境微生物负荷和群落结构的显著差异。例如,SX环境的特点是独特的组成,包括在罐盖上显著存在红曲霉。来源跟踪证实,这种环境“播种”显著地塑造了最初的发酵群落,来自地板和罐子表面的贡献。在发酵过程中,细菌群落不断变化(乳酸杆菌减少,醋酸杆菌增加),但不同工厂的真菌演替差异显著。具体来说,SX工厂的自然发酵培养了一个独特的真菌群落轨迹,其特征是Saccharomyces的独特减少和红曲霉(Monascus)在后期作为优势属的出现。这一轨迹与其独特的环境真菌种群及其从初始固态阶段开始的显著影响直接相关。虽然内部选择压力最终决定了群落结构,但环境条件深刻地决定了整体微生物多样性和演替。核心微生物组(芽孢杆菌、鞘单胞菌、隐球菌、红曲霉)始终存在于环境和发酵生态位中,是关键的微生物桥梁。我们的研究结果为通过战略性地管理环境微生物群来优化ZRV生产以提高质量和一致性提供了重要的基础。
{"title":"Environmental microorganisms as heterogeneous sources and shapers of the fermentation microbiome in Zhejiang rosy vinegar","authors":"Guoli Chang ,&nbsp;Jun Zhang ,&nbsp;Xiaoyue Fang ,&nbsp;Shenchenyu Zhang ,&nbsp;Haixia Lu ,&nbsp;Yipeng Jiang ,&nbsp;Junli Zhu","doi":"10.1016/j.ijfoodmicro.2025.111554","DOIUrl":"10.1016/j.ijfoodmicro.2025.111554","url":null,"abstract":"<div><div>Zhejiang rosy vinegar (ZRV) fermentation is a complex, spontaneous open-system process, where microbial communities are key to its unique characteristics. However, the precise influence of the brewing workshop environment on these dynamic microbial communities remains underexplored, hindering consistent product quality. Here, we characterized the environmental and fermentation microbial communities across three factories using high-throughput sequencing (16S rRNA and ITS), qPCR, and advanced ecological network analyses. Our results establish that the brewing environment acts as a critical, heterogeneous, and factory-specific microbial reservoir, and provides the primary inoculum for fermentation initiation. Our findings revealed significant inter-factory differences in environmental microbial loads and community structures. For instance, the SX environment was characterized by a unique composition, including the notable presence of <em>Monascus</em> on jar lids. Source tracking confirmed this environmental “seeding” significantly shapes initial fermentation communities, with contributions from floor and jar surfaces. During fermentation, bacterial communities consistently shifted (LAB decrease, <em>Acetobacter</em> increase), but fungal successions varied notably by factory. Specifically, the natural fermentation at the SX factory fostered a distinct fungal community trajectory, characterized by a unique decrease in <em>Saccharomyces</em> and the emergence of <em>Monascus</em> as the dominant genus in later stages. This trajectory was directly linked to its distinct environmental fungal populations and their pronounced influence from the initial solid-state phase. While internal selective pressures eventually govern community structure, environmental conditions profoundly dictate overall microbial diversity and succession. A core microbiome (<em>Bacillus</em>, <em>Sphingomonas</em>, <em>Cryptococcus</em>, <em>Monascus</em>), consistently present in both environmental and fermentation niches, served as key microbial bridges. Our results provide a vital basis for optimizing ZRV production by strategically managing the environmental microbiome to enhance quality and consistency.</div></div>","PeriodicalId":14095,"journal":{"name":"International journal of food microbiology","volume":"447 ","pages":"Article 111554"},"PeriodicalIF":5.2,"publicationDate":"2025-12-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145713993","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
International journal of food microbiology
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1