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Biocontrol mechanisms of antagonistic yeasts on postharvest fruits and vegetables and the approaches to enhance the biocontrol potential of antagonistic yeasts 采后水果和蔬菜上拮抗酵母菌的生物防治机制以及提高拮抗酵母菌生物防治潜力的方法。
IF 5 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2024-12-27 DOI: 10.1016/j.ijfoodmicro.2024.111038
Fangfang Wu , Haibo Wang , Yankun Lin , Shun Feng , Xinguo Li
During storage and transportation, fruits and vegetables are susceptible to various pathogens, leading to quality degradation and significant economic losses. Currently, chemical pesticides are primarily used for control; however, their overuse poses serious threats to human health and causes environmental pollution. Biocontrol, known for its environmentally friendly characteristics, has been extensively studied. Among biocontrol agents, yeasts are widely distributed and possesses strong antagonistic abilities, making them crucial agents against numerous pathogenic fungi. Despite their considerable promise, the full potential of antagonistic yeasts for broader application remains untapped. Therefore, this paper reviews the mechanisms of antagonistic yeasts as biocontrol agents for postharvest diseases, including space and nutrients competition, competition for scarce iron resources, parasitism, production of soluble and volatile antifungal compounds, and induction of host systemic resistance. The paper also introduces research on the combined application of antagonistic yeasts with physical, chemical, and other microbial methods. Ultimately, this review provides a potential pathway to enhance the biocontrol effectiveness of antagonistic yeasts and expand their application prospects.
在储存和运输过程中,水果和蔬菜容易受到各种病原体的影响,导致质量下降和重大的经济损失。目前,化学农药主要用于控制;然而,它们的过度使用对人类健康造成严重威胁,并造成环境污染。生物防治因其环境友好性而受到广泛的研究。在生物防治剂中,酵母分布广泛,具有较强的拮抗能力,是防治多种病原真菌的重要药剂。尽管具有相当大的前景,但拮抗酵母的全部潜力仍未得到更广泛的应用。因此,本文综述了拮抗酵母作为采后病害生物防治剂的作用机制,包括空间和养分竞争、对稀缺铁资源的竞争、寄生、可溶性和挥发性抗真菌化合物的产生以及诱导寄主系统抗性等。本文还介绍了拮抗酵母与物理、化学和其他微生物方法联合应用的研究。为提高拮抗酵母的生物防治效果和扩大其应用前景提供了一条可能的途径。
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引用次数: 0
Characterization of non-typhoidal Salmonella reveals the highly prevalent mcr-1-positive S. 1,4,[5],12:i:- within eggs are derived from chickens 对非伤寒沙门氏菌的特征分析表明,鸡蛋中高度流行的mcr-1阳性S. 1,4,[5],12:i:-来源于鸡。
IF 5 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2024-12-26 DOI: 10.1016/j.ijfoodmicro.2024.111048
Ting-Yu Yang , Tiantian Liu , Yan Li , Zeqing Wang , Meijun Chu , Junjie Wang , Ming Zou , Bao-Tao Liu
<div><div><em>Salmonella</em> is one of the most common foodborne pathogens. Antimicrobial-resistant <em>Salmonella</em> isolates, especially those resistant to colistin, pose a significant threat to public health worldwide. However, data about the prevalence of <em>mcr</em>-positive <em>Salmonella</em> in animals was few and the dissemination of <em>mcr</em>-positive <em>Salmonella</em> from animals to food, especially eggs, has not been fully addressed. The role of houseflies in the <em>Salmonella</em> transmission has also not been clarified. Here, we analyzed the prevalence and resistance characteristics of <em>mcr</em>-positive <em>Salmonella</em> in 1707 samples of animals (commercial laying hens, broilers, waterfowls and swine), eggs and flies from 23 farms in four cities of China between July 2021 and October 2022. Pulsed-field gel electrophoresis (PFGE) and whole-genome sequencing (WGS) analyses of <em>Salmonella</em> from different sources were further performed. Among animals, waterfowls had the highest isolation rate of <em>Salmonella</em> (18.1 %, 35/193), followed by swine (6.1 %, 23/377), laying hens (4.2 %, 21/505) and broilers (1.4 %, 7/489). Two of the 53 flies (3.8 %) carried <em>Salmonella</em>. The detection rate of <em>Salmonella</em> in eggs from farms was 26.7 %. All <em>mcr-1</em>-positive <em>Salmonella</em> isolates were <em>S</em>. 1,4,[5],12:i:- and were only found in hens (0.2 %) and eggs (11.1 %). PFGE and WGS analyses showed that the <em>mcr-1</em>-positive <em>S</em>. 1,4,[5],12:i:- from commercial laying hens and eggs in the same farm had no single nucleotide polymorphism (SNP) variation, indicating that the <em>mcr-1</em>-positive <em>S</em>. 1,4,[5],12:i:- in eggs were derived from hens. The phylogenomic analysis also showed that the <em>mcr-1</em>-positive <em>S</em>. 1,4,[5],12:i:- isolates from hens and eggs were closely related to previously reported <em>mcr-1</em>-positive <em>Salmonella</em> from human in China, further confirming that such <em>mcr-1</em>-positive <em>Salmonella</em> in animals could transmit to humans via the food chain. Furthermore, the <em>bla</em><sub>CTX-M-1G</sub>-positive <em>S</em>. Kentucky isolates from broiler and flies in the same farm had a limited number of variations (5–7 SNPs), proving the clonal transmission of <em>Salmonella</em> between broilers and flies. The <em>S</em>. Kentucky isolates carrying <em>bla</em><sub>CTX-M-1G</sub> from broilers were also closely related to the <em>S</em>. Kentucky isolates from chicken meats and humans. Our findings suggest that <em>Salmonella</em> including those carrying <em>mcr-1</em> in animals could transmit to eggs/meats and potentially trigger human infections. The houseflies can play an important role in the <em>Salmonella</em> transmission within farms. <em>Salmonella</em> carrying <em>mcr</em> in animals and animal products should be monitored regularly and control measures are urgently needed to reduce the dissemination of suc
沙门氏菌是最常见的食源性病原体之一。具有抗菌素耐药性的沙门氏菌分离株,特别是对粘菌素具有耐药性的沙门氏菌分离株,对全世界的公共卫生构成重大威胁。然而,关于动物中mcr阳性沙门氏菌流行率的数据很少,并且mcr阳性沙门氏菌从动物传播到食物,特别是鸡蛋的问题尚未得到充分解决。家蝇在沙门氏菌传播中的作用也没有得到澄清。在此,我们分析了2021年7月至2022年10月期间来自中国4个城市23个农场的1707种动物(商品蛋鸡、肉鸡、水禽和猪)、鸡蛋和苍蝇中mcr阳性沙门氏菌的流行情况和耐药性特征。进一步对不同来源的沙门氏菌进行脉冲场凝胶电泳(PFGE)和全基因组测序(WGS)分析。动物中,水禽沙门氏菌分离率最高(18.1%,35/193),其次是猪(6.1%,23/377)、蛋鸡(4.2%,21/505)和肉鸡(1.4%,7/489)。53只苍蝇中有2只(3.8%)携带沙门氏菌。农场产鸡蛋沙门氏菌检出率为26.7%。所有mcr-1阳性沙门氏菌分离株分别为S. 1,4,[5],12:i:-,仅在母鸡(0.2%)和鸡蛋(11.1%)中发现。PFGE和WGS分析显示,同一农场商品蛋鸡和鸡蛋中mcr-1阳性S. 1,4,[5],12:i:-无单核苷酸多态性(SNP)差异,表明鸡蛋中mcr-1阳性S. 1,4,[5],12:i:-来源于母鸡。系统发育分析还表明,鸡和蛋中分离的mcr-1阳性S. 1,4,[5],12:i:-与中国先前报道的人源mcr-1阳性沙门氏菌密切相关,进一步证实了动物中mcr-1阳性沙门氏菌可通过食物链传播给人类。此外,从同一农场的肉鸡和苍蝇中分离出的blactx - m - 1g阳性肯塔基沙门氏菌具有有限数量的变异(5-7个snp),证明了沙门氏菌在肉鸡和苍蝇之间的克隆传播。从肉鸡中分离出的携带blaCTX-M-1G的肯塔基菌株也与从鸡肉和人身上分离出的肯塔基菌株密切相关。我们的研究结果表明,沙门氏菌(包括动物体内携带mcr-1的沙门氏菌)可以传播到鸡蛋/肉类,并可能引发人类感染。家蝇在农场沙门氏菌传播中起着重要作用。应定期监测动物和动物产品中携带mcr的沙门氏菌,并迫切需要采取控制措施以减少此类病原体的传播。
{"title":"Characterization of non-typhoidal Salmonella reveals the highly prevalent mcr-1-positive S. 1,4,[5],12:i:- within eggs are derived from chickens","authors":"Ting-Yu Yang ,&nbsp;Tiantian Liu ,&nbsp;Yan Li ,&nbsp;Zeqing Wang ,&nbsp;Meijun Chu ,&nbsp;Junjie Wang ,&nbsp;Ming Zou ,&nbsp;Bao-Tao Liu","doi":"10.1016/j.ijfoodmicro.2024.111048","DOIUrl":"10.1016/j.ijfoodmicro.2024.111048","url":null,"abstract":"&lt;div&gt;&lt;div&gt;&lt;em&gt;Salmonella&lt;/em&gt; is one of the most common foodborne pathogens. Antimicrobial-resistant &lt;em&gt;Salmonella&lt;/em&gt; isolates, especially those resistant to colistin, pose a significant threat to public health worldwide. However, data about the prevalence of &lt;em&gt;mcr&lt;/em&gt;-positive &lt;em&gt;Salmonella&lt;/em&gt; in animals was few and the dissemination of &lt;em&gt;mcr&lt;/em&gt;-positive &lt;em&gt;Salmonella&lt;/em&gt; from animals to food, especially eggs, has not been fully addressed. The role of houseflies in the &lt;em&gt;Salmonella&lt;/em&gt; transmission has also not been clarified. Here, we analyzed the prevalence and resistance characteristics of &lt;em&gt;mcr&lt;/em&gt;-positive &lt;em&gt;Salmonella&lt;/em&gt; in 1707 samples of animals (commercial laying hens, broilers, waterfowls and swine), eggs and flies from 23 farms in four cities of China between July 2021 and October 2022. Pulsed-field gel electrophoresis (PFGE) and whole-genome sequencing (WGS) analyses of &lt;em&gt;Salmonella&lt;/em&gt; from different sources were further performed. Among animals, waterfowls had the highest isolation rate of &lt;em&gt;Salmonella&lt;/em&gt; (18.1 %, 35/193), followed by swine (6.1 %, 23/377), laying hens (4.2 %, 21/505) and broilers (1.4 %, 7/489). Two of the 53 flies (3.8 %) carried &lt;em&gt;Salmonella&lt;/em&gt;. The detection rate of &lt;em&gt;Salmonella&lt;/em&gt; in eggs from farms was 26.7 %. All &lt;em&gt;mcr-1&lt;/em&gt;-positive &lt;em&gt;Salmonella&lt;/em&gt; isolates were &lt;em&gt;S&lt;/em&gt;. 1,4,[5],12:i:- and were only found in hens (0.2 %) and eggs (11.1 %). PFGE and WGS analyses showed that the &lt;em&gt;mcr-1&lt;/em&gt;-positive &lt;em&gt;S&lt;/em&gt;. 1,4,[5],12:i:- from commercial laying hens and eggs in the same farm had no single nucleotide polymorphism (SNP) variation, indicating that the &lt;em&gt;mcr-1&lt;/em&gt;-positive &lt;em&gt;S&lt;/em&gt;. 1,4,[5],12:i:- in eggs were derived from hens. The phylogenomic analysis also showed that the &lt;em&gt;mcr-1&lt;/em&gt;-positive &lt;em&gt;S&lt;/em&gt;. 1,4,[5],12:i:- isolates from hens and eggs were closely related to previously reported &lt;em&gt;mcr-1&lt;/em&gt;-positive &lt;em&gt;Salmonella&lt;/em&gt; from human in China, further confirming that such &lt;em&gt;mcr-1&lt;/em&gt;-positive &lt;em&gt;Salmonella&lt;/em&gt; in animals could transmit to humans via the food chain. Furthermore, the &lt;em&gt;bla&lt;/em&gt;&lt;sub&gt;CTX-M-1G&lt;/sub&gt;-positive &lt;em&gt;S&lt;/em&gt;. Kentucky isolates from broiler and flies in the same farm had a limited number of variations (5–7 SNPs), proving the clonal transmission of &lt;em&gt;Salmonella&lt;/em&gt; between broilers and flies. The &lt;em&gt;S&lt;/em&gt;. Kentucky isolates carrying &lt;em&gt;bla&lt;/em&gt;&lt;sub&gt;CTX-M-1G&lt;/sub&gt; from broilers were also closely related to the &lt;em&gt;S&lt;/em&gt;. Kentucky isolates from chicken meats and humans. Our findings suggest that &lt;em&gt;Salmonella&lt;/em&gt; including those carrying &lt;em&gt;mcr-1&lt;/em&gt; in animals could transmit to eggs/meats and potentially trigger human infections. The houseflies can play an important role in the &lt;em&gt;Salmonella&lt;/em&gt; transmission within farms. &lt;em&gt;Salmonella&lt;/em&gt; carrying &lt;em&gt;mcr&lt;/em&gt; in animals and animal products should be monitored regularly and control measures are urgently needed to reduce the dissemination of suc","PeriodicalId":14095,"journal":{"name":"International journal of food microbiology","volume":"430 ","pages":"Article 111048"},"PeriodicalIF":5.0,"publicationDate":"2024-12-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142894439","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
Effects of low-salt stress on biological characteristics and transcriptomic profiles of Vibrio parahaemolyticus 低盐胁迫对副溶血性弧菌生物学特性和转录组学的影响。
IF 5 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2024-12-26 DOI: 10.1016/j.ijfoodmicro.2024.111047
Zhiyong Song , Lu Chen , Shiying Tang , Yingjie Pan , Qingchao Xie , Yong Zhao , Haiquan Liu
Studies have proved that halophilic Vibrio parahaemolyticus is widely detected in freshwater environments (salinity <0.5 %). However, the growth and colonization of V. parahaemolyticus in low-salt environments remain unclear. This study was envisaged to assess the effects of low-salt stress on the growth, motility and biofilm formation of V. parahaemolyticus and the transcriptomic changes that the bacterium responds to such stress. The results indicated that low salt concentrations supported the growth (allowing growth to proceed, though at a lower speed) of V. parahaemolyticus, prolonged the lag time (LT), and decreased the maximum specific growth rate (μmax) of V. parahaemolyticus. Additionally, this low salinity inhibited its motility and enhanced its biofilm formation capacity. Notably, the growth of V. parahaemolyticus on both freshwater and marine-cultured Litopenaeus vannamei exhibited a similar trend, suggesting that V. parahaemolyticus might have adapted to thrive in freshwater food. Furthermore, the reasons for the support of V. parahaemolyticus growth in 0.25 % NaCl was analyzed by transcriptome sequencing (RNA-seq). RNA-seq revealed that V. parahaemolyticus can improve resistance to adverse environments by reducing energy consumption and enhancing oxidative stress resistance to adapt to a low-salt environment. This study revealed that the freshwater environment supported the growth of V. parahaemolyticus and its influence on the growth of V. parahaemolyticus, providing valuable theoretical support for risk assessment.
研究证明,嗜盐副溶血性弧菌广泛存在于副溶血性弧菌的淡水环境(盐度最大值)中。此外,这种低盐度抑制了它的运动,增强了它的生物膜形成能力。值得注意的是,副溶血性弧菌在淡水和海洋养殖的凡纳滨对虾上的生长趋势相似,这表明副溶血性弧菌可能已经适应了在淡水食物中繁殖。此外,通过转录组测序(RNA-seq)分析了副溶血性弧菌在0.25% NaCl中生长的原因。RNA-seq结果显示,副溶血性弧菌可以通过降低能量消耗和增强氧化应激抵抗能力来提高对不利环境的抵抗力,以适应低盐环境。本研究揭示了淡水环境对副溶血性弧菌生长的支持作用及其对副溶血性弧菌生长的影响,为风险评估提供了有价值的理论支持。
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引用次数: 0
Use of dielectric-barrier discharge (DBD) cold plasma for control of bread spoilage fungi 介质阻挡放电(DBD)冷等离子体对面包腐坏真菌的控制。
IF 5 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2024-12-25 DOI: 10.1016/j.ijfoodmicro.2024.111034
Jéssica Gonçalves Lemos , Lhwan Philippe Silva , Mailah Ali Abdul Rahman Mahfouz , Leonardo Alvarenga Freire Cazzuni , Liliana Oliveira Rocha , Caroline Joy Steel
Bread is a greatly consumed bakery product worldwide. Unfortunately, it is an optimal substrate for fungal contamination and deterioration (aw > 0.95), commonly caused by the genera Penicillium, Paecilomyces, and Aspergillus, resulting in significant economic losses. Traditional conservation methods, such as the use of calcium propionate, are rejected by some consumers, leading to investment in alternative methods, such as the use of cold plasma. This study aimed to verify the effectiveness of dielectric-barrier discharge (DBD) cold plasma in inhibiting the growth of bread spoilage fungi. The species Penicillium sumatrense (ML1), Penicillium roqueforti (FML125), Penicillium paneum (FML126), Paecilomyces variotii (FML112), Aspergillus niger (ML2) were used. To assess the effect of plasma on fungi, they were inoculated into swabs, stainless steel coupons, and then small plugs were taken directly from the fungal culture and pan bread slices. All strains were inoculated into swabs and pan bread slices, but only the ML1 strain was used for experiments with coupons and plugs. Regarding the swabs of all strains (System I, 50 W/15 min), in addition to the milder treatments on the plug (System II, 50 W/2.5, 5, 10, and 20 min) and all treatments of ML1 strain coupons (System II, 200 W/15 min, 10 W and 8 W/2.5 and 1.5 min), the cold plasma presented fungistatic properties, delaying mycelial growth from 8 to 30 days and reducing the fungal population by 2.24 log when compared to controls. By analyzing the 200 W treatment with the longest exposure (5, 10, and 20 min) on the plug, plasma showed fungicidal action, completely inactivating mycelial growth. Regarding the pan bread slices, plasma System III, when applied for 45 min, reduced strains FML126 and FML112 by 1 log, FML125 and ML2 by 2 logs, and ML1 by 7 logs, demonstrating potential for use as a control method in the baking industry.
面包是世界范围内消费最多的烘焙产品。不幸的是,它是真菌污染和变质的最佳底物(aw >.95),通常由青霉属、拟青霉属和曲霉属引起,造成重大的经济损失。传统的保存方法,如使用丙酸钙,被一些消费者拒绝,导致投资于替代方法,如使用冷等离子体。本研究旨在验证介质阻挡放电(DBD)冷等离子体对面包腐败真菌生长的抑制作用。选用苏门答腊青霉(ML1)、罗氏青霉(FML125)、paneum青霉(FML126)、拟青霉(FML112)、黑曲霉(ML2)。为了评估血浆对真菌的影响,将它们接种到棉签、不锈钢片中,然后直接从真菌培养物中取出小塞,并平底锅烤面包片。所有菌株均接种于棉签和面包片上,但只有ML1菌株接种于面包片和面包片上。对于所有菌株(系统I, 50 W/15 min)的拭子,除了塞上较温和的处理(系统II, 50 W/2.5, 5, 10和20 min)以及ML1菌株片的所有处理(系统II, 200 W/15 min, 10 W和8 W/2.5和1.5 min)外,冷浆具有抑菌特性,将菌丝生长延迟8至30天,真菌数量比对照减少2.24 log。通过分析200w处理下最长暴露时间(5、10和20分钟),血浆显示出杀真菌作用,完全灭活菌丝生长。对于烤面包片,等离子体系统III在应用45分钟后,菌株FML126和FML112减少了1个对数,FML125和ML2减少了2个对数,ML1减少了7个对数,显示了在烘焙行业作为控制方法使用的潜力。
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引用次数: 0
Fungi associated with orange juice production and assessment of adhesion ability and resistance to sanitizers 与橙汁生产有关的真菌以及对消毒剂的粘附能力和抗性的评估。
IF 5 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2024-12-22 DOI: 10.1016/j.ijfoodmicro.2024.111035
Larissa Pereira Margalho , Camila Siedlarczyk Martins , Naara Aparecida Almeida , Juliana Carusi , Mailah Ali Abdul Rahman Mahfouz , Anderson S. Sant'Ana , Maristela Silva Nascimento , Liliana de Oliveira Rocha
Orange juice is widely consumed worldwide due to its sensory and nutritional characteristics. This beverage is susceptible to contamination by acidic-tolerant microorganisms due to its low pH, especially filamentous fungi and yeasts. To minimize fungal spoilage, companies usually submit juice to thermal treatments; sanitizers are also applied on surfaces to maintain the microbiological quality. This study aimed to identify potential contamination sources in a juice processing line and to verify the susceptibility of isolated yeasts and filamentous fungi to food-grade sanitizers. Also, their ability to form single and binary adherent cells was assessed. The results revealed the presence of fungi in all samplings performed, with the most prominent microorganisms identified as Paecilomyces variotii, P. paravariotii, Pichia kudriavzevii and Wickerhamomyces anomalus. After obtaining results for sanitizer resistance and adhesion ability of the isolates, these were submitted to multivariate analysis using hierarchical cluster analysis (HCA), and two groups were found: one composed mostly of filamentous fungi (16/18) with low adhesion potential and one group formed by yeasts with high adhesion ability and resistance to sanitizers. Microscopy images corroborate those data, demonstrating the importance of yeast cell agglomerates along germinated spores of filamentous fungi and the importance of adhered biomass to protect cells against the sanitizers tested. This study is the first to combine fungi isolated from a beverage processing line and aims to contribute to the current knowledge of fungal adhesion and sanitizer resistance.
橙汁因其感官和营养特性在世界范围内被广泛消费。由于其pH值低,这种饮料容易受到耐酸微生物的污染,特别是丝状真菌和酵母。为了尽量减少真菌的破坏,公司通常会将果汁进行热处理;消毒剂也应用于表面,以保持微生物的质量。本研究旨在确定果汁加工生产线中潜在的污染源,并验证分离的酵母和丝状真菌对食品级消毒剂的敏感性。此外,还评估了它们形成单贴壁细胞和双贴壁细胞的能力。结果显示,所有样品中都存在真菌,其中鉴定出最突出的微生物是拟青霉(Paecilomyces variotii)、副拟青霉(P. paravariotii)、毕赤酵母(Pichia kudriavzevii)和异常维克霉(Wickerhamomyces anomalus)。获得菌株对消毒剂的抗性和粘附能力结果后,采用层次聚类分析(HCA)进行多变量分析,发现菌株主要由丝状真菌(16/18)组成,粘附潜力低;菌株主要由酵母组成,粘附能力高,对消毒剂有抗性。显微镜图像证实了这些数据,证明了沿着丝状真菌萌发孢子的酵母细胞聚集的重要性,以及粘附的生物量对保护细胞免受消毒剂测试的重要性。这项研究首次将从饮料加工生产线分离的真菌结合起来,旨在为真菌粘附和消毒剂抗性的当前知识做出贡献。
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引用次数: 0
Untargeted metabolomics to relate changes produced by biocontrol agents against Aspergillus westerdijkiae and Penicillium nordicum in vitro on dry-cured ham 非靶向代谢组学研究:生物防治剂对西曲霉和北方青霉对干腌火腿的影响。
IF 5 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2024-12-22 DOI: 10.1016/j.ijfoodmicro.2024.111036
Eva Cebrián , Elia Roncero , João Luz , Marta Sousa Silva , Carlos Cordeiro , Ana Belén Peromingo , Mar Rodríguez , Félix Núñez
Dry-cured ham is a highly appreciated meat product. During the ripening, moulds grow on its surface such as Penicillium nordicum and Aspergillus westerdijkiae producers of ochratoxin A (OTA). This mycotoxin poses a risk to consumers that must be controlled. The aim of this work is to evaluate the effectiveness of Debaryomyces hansenii and Staphylococcus xylosus isolated from dry-cured ham as a combined biocontrol culture (BCA) to reduce the OTA produced by one strain of A. westerdijkiae and two strain of P. nordicum, and to assess the metabolomic changes they cause. Each mould was inoculated alone and in combination with BCA on dry-cured ham for 14 days at 20 °C. OTA and total metabolites were analysed in a mass spectrometer Orbitrap Q- Exactive Plus. The Compound Discoverer software, in-house Python-based software and the Metaboanalyst software were used for metabolite analysis. BCA reduced the OTA of A. westerdijkiae, P. nordicum 15 and P. nordicum 856 by 78 %, 99 % and 65 % respectively. BCA caused changes in their metabolome, mainly in the phenylalanine metabolism pathway altering compounds such as Phenylacetaldehyde, Phenylpyruvate or trans-2-hydroxycinnamate, the synthesis of phenylalanine, tyrosine, and tryptophan altering compounds such as 4-hydroxyphenylpyruvate or L-tryptophan, and in the synthesis of oxylipins derived from the linoleic acid metabolism such as 13-OxoODE, 9(S)-HODE or 9(10)-EpOME.
干腌火腿是一种非常受欢迎的肉制品。在成熟过程中,霉菌在其表面生长,如产赭曲霉A (OTA)的北方青霉和西曲霉。这种霉菌毒素对消费者构成风险,必须加以控制。本研究的目的是评估从干腌火腿中分离的汉斯德巴氏菌和木糖葡萄球菌作为联合生物防治培养物(BCA)减少一株西部拟南弧菌和两株北方拟南弧菌产生的OTA的有效性,并评估它们引起的代谢组学变化。每种霉菌单独接种和与BCA联合接种于20℃干腌火腿上14天。用Orbitrap Q- Exactive Plus质谱仪分析OTA和总代谢物。使用Compound Discoverer软件、内部python软件和Metaboanalyst软件进行代谢物分析。BCA可使西部野鸡、北方野鸡15和北方野鸡856的OTA分别降低78%、99%和65%。BCA引起了它们代谢组的变化,主要是改变苯丙氨酸代谢途径的化合物,如苯乙醛、苯丙酮酸酯或反式2-羟基肉桂酸酯,改变苯丙氨酸、酪氨酸和色氨酸的化合物,如4-羟基苯丙酮酸酯或l -色氨酸,以及由亚油酸代谢衍生的氧脂类的合成,如13-OxoODE、9(S)-HODE或9(10)-EpOME。
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引用次数: 0
Effective control of snake fruit (Salacca zalacca) rot using Trichoderma asperelloides SKRU-01: A safe approach to preserving fruit quality 利用曲霉SKRU-01有效防治蛇果腐病:保品质的安全途径
IF 5 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2024-12-21 DOI: 10.1016/j.ijfoodmicro.2024.111037
Sawai Boukaew , Julalak Chuprom , Jirayu Buatong , Sujirat Sornprasit , Sureeporn Wijitsopa , Karistsapol Nooprom , Rachasak Boonhok
Rot disease, caused by the fungal pathogen Peniophora salaccae SKRU002, affects the quality of snake fruit production. In the pursuit of sustainable disease management, biocontrol using Trichoderma asperelloides SKRU-01 offers a promising solution. This study evaluated the antagonistic potential of T. asperelloides SKRU-01 against P. salaccae SKRU002 in both in vitro assays and snake fruit trials, while also assessing its impact on fruit quality. In vitro dual culture assays revealed that T. asperelloides SKRU-01 inhibited P. salaccae SKRU002 growth by 62.5 % over 10 days through efficient nutrient colonization. Microscopic analysis confirmed that T. asperelloides SKRU-01 hyphae penetrated and wrapped around P. salaccae SKRU002, causing cytoplasmic lysis. Additionally, T. asperelloides SKRU-01 culture filtrates (20 % v/v) completely inhibited P. salaccae SKRU002 growth in both solid and liquid media. LC-QTOF/MS analysis identified 31 secondary metabolites, including toyocamycin and antimycin A1. In snake fruit trials, T. asperelloides SKRU-01 culture filtrates provided 100 % protection against disease incidence (DI) and severity (DS), comparable to Mancozeb®. The application of T. asperelloides SKRU-01 spores (107 spores/mL) reduced DI and DS to 0 % within 1–3 days post-pathogen inoculation, demonstrating both protective and curative effects. Furthermore, while P. salaccae SKRU002 significantly affected fruit quality—causing weight loss, color changes, and reductions in total soluble solids, phenolic content, titratable acidity, and antioxidant activity—the simultaneous application of T. asperelloides SKRU-01 mitigated these effects without compromising fruit quality. These findings indicate the antagonistic activity of T. asperelloides SKRU-01 and its metabolites against P. salaccae SKRU002, suggesting their potential as biofungicidal agents for managing rot disease in snake fruit.
蛇果腐烂病是由蛇果真菌病原菌SKRU002引起的,影响蛇果生产质量。在追求可持续疾病管理的过程中,利用曲霉SKRU-01进行生物防治提供了一个很有前途的解决方案。本研究通过体外试验和蛇果试验,评价了曲霉SKRU-01对salaccae SKRU002的拮抗潜力,并评估了其对果实品质的影响。体外双培养实验表明,曲霉SKRU-01通过有效的营养定殖,在10天内抑制salaccae SKRU002生长62.5%。显微镜分析证实,曲霉SKRU-01菌丝穿透并包裹P. salaccae SKRU002,引起细胞质溶解。此外,曲霉skru01培养滤液(20% v/v)在固体和液体培养基中均能完全抑制salaccae SKRU002的生长。LC-QTOF/MS分析鉴定出31种次生代谢物,包括toyocamycin和antiycin A1。在蛇果试验中,曲霉SKRU-01培养滤液对疾病发病率(DI)和严重程度(DS)提供了100%的保护,与Mancozeb®相当。病原菌接种后1 ~ 3 d内施用107孢子/mL的曲霉SKRU-01孢子可使DI和DS降至0%,具有保护和治疗双重作用。此外,尽管salaccae SKRU002显著影响果实质量——导致重量下降、颜色变化、可溶性固体总量、酚类含量、可滴定酸度和抗氧化活性降低——但同时施用曲霉SKRU-01可以在不影响果实质量的情况下减轻这些影响。这些结果表明,曲霉SKRU-01及其代谢物对salaccae P. SKRU002具有拮抗作用,提示其有可能作为防治蛇果腐病的生物杀菌剂。
{"title":"Effective control of snake fruit (Salacca zalacca) rot using Trichoderma asperelloides SKRU-01: A safe approach to preserving fruit quality","authors":"Sawai Boukaew ,&nbsp;Julalak Chuprom ,&nbsp;Jirayu Buatong ,&nbsp;Sujirat Sornprasit ,&nbsp;Sureeporn Wijitsopa ,&nbsp;Karistsapol Nooprom ,&nbsp;Rachasak Boonhok","doi":"10.1016/j.ijfoodmicro.2024.111037","DOIUrl":"10.1016/j.ijfoodmicro.2024.111037","url":null,"abstract":"<div><div>Rot disease, caused by the fungal pathogen <em>Peniophora salaccae</em> SKRU002, affects the quality of snake fruit production. In the pursuit of sustainable disease management, biocontrol using <em>Trichoderma asperelloides</em> SKRU-01 offers a promising solution. This study evaluated the antagonistic potential of <em>T. asperelloides</em> SKRU-01 against <em>P. salaccae</em> SKRU002 in both <em>in vitro</em> assays and snake fruit trials, while also assessing its impact on fruit quality. <em>In vitro</em> dual culture assays revealed that <em>T. asperelloides</em> SKRU-01 inhibited <em>P. salaccae</em> SKRU002 growth by 62.5 % over 10 days through efficient nutrient colonization. Microscopic analysis confirmed that <em>T. asperelloides</em> SKRU-01 hyphae penetrated and wrapped around <em>P. salaccae</em> SKRU002, causing cytoplasmic lysis. Additionally, <em>T. asperelloides</em> SKRU-01 culture filtrates (20 % <em>v/v</em>) completely inhibited <em>P. salaccae</em> SKRU002 growth in both solid and liquid media. LC-QTOF/MS analysis identified 31 secondary metabolites, including toyocamycin and antimycin A1. In snake fruit trials, <em>T. asperelloides</em> SKRU-01 culture filtrates provided 100 % protection against disease incidence (DI) and severity (DS), comparable to Mancozeb®. The application of <em>T. asperelloides</em> SKRU-01 spores (10<sup>7</sup> spores/mL) reduced DI and DS to 0 % within 1–3 days post-pathogen inoculation, demonstrating both protective and curative effects. Furthermore, while <em>P. salaccae</em> SKRU002 significantly affected fruit quality—causing weight loss, color changes, and reductions in total soluble solids, phenolic content, titratable acidity, and antioxidant activity—the simultaneous application of <em>T. asperelloides</em> SKRU-01 mitigated these effects without compromising fruit quality. These findings indicate the antagonistic activity of <em>T. asperelloides</em> SKRU-01 and its metabolites against <em>P. salaccae</em> SKRU002, suggesting their potential as biofungicidal agents for managing rot disease in snake fruit.</div></div>","PeriodicalId":14095,"journal":{"name":"International journal of food microbiology","volume":"430 ","pages":"Article 111037"},"PeriodicalIF":5.0,"publicationDate":"2024-12-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142894440","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
Survey of foodborne pathogenic Vibrio species in commercial Tasmanian bivalve shellfish and predictors of risk at harvest
IF 5 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2024-12-20 DOI: 10.1016/j.ijfoodmicro.2024.111033
Valeria Anna Torok , Khandaker Rayhan Mahbub , Paul A. Grey , Graham Clive Fletcher , Alison R. Turnbull
<div><div>There has been an increase in foodborne vibriosis outbreaks globally, with <em>Vibrio parahaemolyticus</em> emerging as a foodborne issue in temperate commercial shellfish growing regions, including southern Australia. The food safety concerns associated with these microorganisms have led to the need for specific guidance on potential risk management strategies for their control. This is the first Australian multi-seasonal survey of <em>V. parahaemolyticus</em> and <em>Vibrio vulnificus</em> in commercial shellfish growing areas aimed at understanding their occurrence and regional environmental drivers of risk at harvest. Eleven commercial Tasmanian shellfish (oyster and mussel) growing areas were surveyed for the prevalence and levels of <em>V. parahaemolyticus</em>, including presence of pathogenicity associated <em>tdh</em> and <em>trh</em> genes, and <em>V. vulnificus</em> at harvest between 2020 and 2022. <em>Vibrio parahaemolyticus</em> was detected in all surveyed growing areas during the three summer/autumn sampling periods, with a prevalence of 8–100 %. Prevalence was generally higher in the north (north-west, Moulting Bay and upper east coast) as compared with the mid-east coast and south-east and Bruny regions. <em>Vibrio parahaemolyticus</em> was only detected in five of the eleven growing areas during the two surveyed winter/spring seasons: Duck Bay, Moulting Bay, Great Swanport, Little Swanport and Boomer Bay East. Where it was detected, the prevalence was much lower in the winter/spring seasons (17–33 %). Levels of <em>V. parahaemolyticus</em> detected during the survey were generally low (<10 MPN/g) for most growing areas. Some higher levels (100–1100 MPN/g) were observed in Duck Bay, Moulting Bay, Great Swanport and Little Swanport. Only one sample from Great Swanport had a level of over 1000 MPN/g (1,100 MPN/g). The higher levels were only observed in the summer/autumn sampling periods. <em>Vibrio parahaemolyticus tdh</em>, <em>trh</em> or <em>tdh</em>/<em>trh</em> gene detections only occurred in the summer/autumn months with a prevalence of 0–21 %, 0–18 % or 0–7 %, respectively, depending on the growing area surveyed. Despite low levels <em>of V. parahaemolyticus</em> being detected in southern commercial growing areas, five sporadic cases of vibriosis associated with oysters from southern Tasmania were reported during the survey period, predominantly from oysters harvested recreationally. Levels of <em>V. vulnificus</em> detected were generally very low in most Tasmanian growing areas (<1 MPN/g). However, levels of 35–460 MPN/g were detected in shellfish at harvest in one area (Great Swanport). Predictive models for <em>V. parahaemolyticus</em> at harvest were developed from survey data which were area specific. Water temperature was the sole or primary driver in most areas. Predictive models for <em>V. vulnificus</em> at harvest were developed for Great Swanport and were driven by river flow and rainfall.</di
{"title":"Survey of foodborne pathogenic Vibrio species in commercial Tasmanian bivalve shellfish and predictors of risk at harvest","authors":"Valeria Anna Torok ,&nbsp;Khandaker Rayhan Mahbub ,&nbsp;Paul A. Grey ,&nbsp;Graham Clive Fletcher ,&nbsp;Alison R. Turnbull","doi":"10.1016/j.ijfoodmicro.2024.111033","DOIUrl":"10.1016/j.ijfoodmicro.2024.111033","url":null,"abstract":"&lt;div&gt;&lt;div&gt;There has been an increase in foodborne vibriosis outbreaks globally, with &lt;em&gt;Vibrio parahaemolyticus&lt;/em&gt; emerging as a foodborne issue in temperate commercial shellfish growing regions, including southern Australia. The food safety concerns associated with these microorganisms have led to the need for specific guidance on potential risk management strategies for their control. This is the first Australian multi-seasonal survey of &lt;em&gt;V. parahaemolyticus&lt;/em&gt; and &lt;em&gt;Vibrio vulnificus&lt;/em&gt; in commercial shellfish growing areas aimed at understanding their occurrence and regional environmental drivers of risk at harvest. Eleven commercial Tasmanian shellfish (oyster and mussel) growing areas were surveyed for the prevalence and levels of &lt;em&gt;V. parahaemolyticus&lt;/em&gt;, including presence of pathogenicity associated &lt;em&gt;tdh&lt;/em&gt; and &lt;em&gt;trh&lt;/em&gt; genes, and &lt;em&gt;V. vulnificus&lt;/em&gt; at harvest between 2020 and 2022. &lt;em&gt;Vibrio parahaemolyticus&lt;/em&gt; was detected in all surveyed growing areas during the three summer/autumn sampling periods, with a prevalence of 8–100 %. Prevalence was generally higher in the north (north-west, Moulting Bay and upper east coast) as compared with the mid-east coast and south-east and Bruny regions. &lt;em&gt;Vibrio parahaemolyticus&lt;/em&gt; was only detected in five of the eleven growing areas during the two surveyed winter/spring seasons: Duck Bay, Moulting Bay, Great Swanport, Little Swanport and Boomer Bay East. Where it was detected, the prevalence was much lower in the winter/spring seasons (17–33 %). Levels of &lt;em&gt;V. parahaemolyticus&lt;/em&gt; detected during the survey were generally low (&lt;10 MPN/g) for most growing areas. Some higher levels (100–1100 MPN/g) were observed in Duck Bay, Moulting Bay, Great Swanport and Little Swanport. Only one sample from Great Swanport had a level of over 1000 MPN/g (1,100 MPN/g). The higher levels were only observed in the summer/autumn sampling periods. &lt;em&gt;Vibrio parahaemolyticus tdh&lt;/em&gt;, &lt;em&gt;trh&lt;/em&gt; or &lt;em&gt;tdh&lt;/em&gt;/&lt;em&gt;trh&lt;/em&gt; gene detections only occurred in the summer/autumn months with a prevalence of 0–21 %, 0–18 % or 0–7 %, respectively, depending on the growing area surveyed. Despite low levels &lt;em&gt;of V. parahaemolyticus&lt;/em&gt; being detected in southern commercial growing areas, five sporadic cases of vibriosis associated with oysters from southern Tasmania were reported during the survey period, predominantly from oysters harvested recreationally. Levels of &lt;em&gt;V. vulnificus&lt;/em&gt; detected were generally very low in most Tasmanian growing areas (&lt;1 MPN/g). However, levels of 35–460 MPN/g were detected in shellfish at harvest in one area (Great Swanport). Predictive models for &lt;em&gt;V. parahaemolyticus&lt;/em&gt; at harvest were developed from survey data which were area specific. Water temperature was the sole or primary driver in most areas. Predictive models for &lt;em&gt;V. vulnificus&lt;/em&gt; at harvest were developed for Great Swanport and were driven by river flow and rainfall.&lt;/di","PeriodicalId":14095,"journal":{"name":"International journal of food microbiology","volume":"430 ","pages":"Article 111033"},"PeriodicalIF":5.0,"publicationDate":"2024-12-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143065477","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
Characterization of novel mutations involved in the development of resistance to colistin in Salmonella isolates from retail pork in Shanghai, China
IF 5 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2024-12-19 DOI: 10.1016/j.ijfoodmicro.2024.111027
Zeqiang Zhan, Shoukui He, Jiang Chang, Mengjun Hu, Zengfeng Zhang, Yan Cui, Xianming Shi
Salmonella is an important foodborne pathogen that poses a significant threat to food safety. This study aims to assess the prevalence, genomic features, and colistin-resistant mechanisms of Salmonella isolates collected from 118 retail pork samples from January 2021 to January 2022 in Shanghai, China. Overall, 46 (39.0 %, 46/118) Salmonella isolates were collected, which were identified as 12 serotypes by genomic analysis, including Salmonella Typhimurium (n = 17) and Salmonella London (n = 6). Antimicrobial resistance profiling revealed that the resistance rate of these isolates to colistin was 13.0 % (6/46), while 60.9 % (28/46) exhibited multidrug-resistant. It was found that there were 51 distinct antimicrobial resistance genes in these 46 isolates, which were predominantly associated with resistance to aminoglycosides, fluoroquinolones, and β-lactams. More importantly, among six colistin-resistant isolates, two isolates (Salmonella Schwarzengrund and Salmonella Indiana) were found to carry the mcr-1 gene. The mechanism of resistance in the remaining four colistin-resistant isolates was further studied, and it was found that there were nine amino acid substitutions in PmrAB. It was demonstrated by site-directed mutagenesis that novel substitutions G53W in PmrA and I83V in PmrB led to colistin resistance in Salmonella (MIC = 2 or 4 μg/mL). Analysis results by real-time quantitative PCR and mass spectrometry indicated that the mutants PmrAG53W and PmrBI83V displayed higher expression levels of the gene pmrE than in the parental strain. This upregulation resulted in an increase in the production of 4-amino-4-deoxy-l-arabinose (L-Ara4N) that modified lipid A, thereby conferring resistance to colistin. These findings demonstrated that there was a high prevalence of MDR Salmonella isolates in retail pork in Shanghai, and the substitution G53W in PmrA and I83V in PmrB were independent factors contributing to the development of resistance to colistin in Salmonella via modification of lipid A with L-Ara4N.
{"title":"Characterization of novel mutations involved in the development of resistance to colistin in Salmonella isolates from retail pork in Shanghai, China","authors":"Zeqiang Zhan,&nbsp;Shoukui He,&nbsp;Jiang Chang,&nbsp;Mengjun Hu,&nbsp;Zengfeng Zhang,&nbsp;Yan Cui,&nbsp;Xianming Shi","doi":"10.1016/j.ijfoodmicro.2024.111027","DOIUrl":"10.1016/j.ijfoodmicro.2024.111027","url":null,"abstract":"<div><div><em>Salmonella</em> is an important foodborne pathogen that poses a significant threat to food safety. This study aims to assess the prevalence, genomic features, and colistin-resistant mechanisms of <em>Salmonella</em> isolates collected from 118 retail pork samples from January 2021 to January 2022 in Shanghai, China. Overall, 46 (39.0 %, 46/118) <em>Salmonella</em> isolates were collected, which were identified as 12 serotypes by genomic analysis, including <em>Salmonella Typhimurium</em> (<em>n</em> = 17) and <em>Salmonella</em> London (<em>n</em> = 6). Antimicrobial resistance profiling revealed that the resistance rate of these isolates to colistin was 13.0 % (6/46), while 60.9 % (28/46) exhibited multidrug-resistant. It was found that there were 51 distinct antimicrobial resistance genes in these 46 isolates, which were predominantly associated with resistance to aminoglycosides, fluoroquinolones, and β-lactams. More importantly, among six colistin-resistant isolates, two isolates (<em>Salmonella</em> Schwarzengrund and <em>Salmonella</em> Indiana) were found to carry the <em>mcr-1</em> gene. The mechanism of resistance in the remaining four colistin-resistant isolates was further studied, and it was found that there were nine amino acid substitutions in PmrAB. It was demonstrated by site-directed mutagenesis that novel substitutions G53W in PmrA and I83V in PmrB led to colistin resistance in <em>Salmonella</em> (MIC = 2 or 4 μg/mL). Analysis results by real-time quantitative PCR and mass spectrometry indicated that the mutants PmrA<sup>G53W</sup> and PmrB<sup>I83V</sup> displayed higher expression levels of the gene <em>pmrE</em> than in the parental strain. This upregulation resulted in an increase in the production of 4-amino-4-deoxy-l-arabinose (L-Ara4N) that modified lipid A, thereby conferring resistance to colistin. These findings demonstrated that there was a high prevalence of MDR <em>Salmonella</em> isolates in retail pork in Shanghai, and the substitution G53W in PmrA and I83V in PmrB were independent factors contributing to the development of resistance to colistin in <em>Salmonella</em> via modification of lipid A with L-Ara4N.</div></div>","PeriodicalId":14095,"journal":{"name":"International journal of food microbiology","volume":"430 ","pages":"Article 111027"},"PeriodicalIF":5.0,"publicationDate":"2024-12-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143065475","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
Characterization of fusidic acid-resistant Staphylococcus aureus isolated from food animals during 2010–2021 in South Korea 2010-2021年韩国食用动物中分离的耐夫西地酸金黄色葡萄球菌的特征
IF 5 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2024-12-19 DOI: 10.1016/j.ijfoodmicro.2024.111026
Su-Jeong Kim , Md. Sekendar Ali , Hee-Seung Kang , Bo-Youn Moon , Yu-Jeong Hwang , Soon-Seek Yoon , Seung-Chun Park , Suk-Kyung Lim
Livestock-associated fusidic acid-resistant Staphylococcus aureus (FRSA) is frequently linked to global public health hazards. This study aimed to ascertain the prevalence and molecular characteristics of FRSA isolated from food animal products in South Korea from 2010 to 2021. We obtained a total of 3980 S. aureus isolates from cattle carcasses (n = 482), pig carcasses (n = 1531), and chicken carcasses (n = 1967). The isolates were evaluated for antimicrobial susceptibility using the broth microdilution method. Antimicrobial resistance genes, spa types, sequence types (STs), and Staphylococcus cassette chromosome mec (SCCmec) types were determined by polymerase chain reaction (PCR) and sequencing analysis. In total, 187 isolates (4.7 %) demonstrated resistance to fusidic acid, with the maximum recovered from cattle (16.2 %), followed by pigs (6.5 %) and chickens (0.5 %). In addition, the majority of the isolates showed resistance to penicillin (86.6 %), while comparatively low resistance rates (7–13.9 %) were observed for erythromycin, gentamicin, kanamycin, and tetracycline. Moreover, multidrug resistance (MDR) comprised 8.6 % (16/187) of the isolates. Among the fusidic acid resistance determinants, the fusA mutation was the highest, containing 54 % (101/187), followed by fusC (29.4 %, 55/187) and fusB (15.5 %, 29/187). A high level of resistance regarding the substitution of L461K in the fusA gene was identified in 97 % of isolates. In addition, the most commonly detected resistance patterns include penicillin (87.1 %, 88/101) among the FRSA. The nucleotide sequencing analysis showed that all 29 fusB-carrying isolates possess the structural gene blaZ of the bla operon and the insertion sequences orf152, orf170, IS257, and orf152. In total, 21 spa types were found, where t126 was detected the most (81.2 %, 82/101) in fusA, followed by t127 (81.8 %, 45/55) in fusC, and t189 (27.6 %, 8/29) in fusB. Furthermore, all t002 harboring fusC were detected as ST5-MRSA-SCCmecII clones. This is the first report of fusA and fusB carrying S. aureus and linkage fusB and blaZ genes in FRSA isolated from food animal products. Taken together, the FRSA in food animals with different resistance determinants and spa types could pose a threat to public health.
家畜相关的耐富西地酸金黄色葡萄球菌(FRSA)经常与全球公共卫生危害有关。本研究旨在确定2010年至2021年韩国食用动物产品中分离的FRSA的流行率和分子特征。从牛尸体(n = 482)、猪尸体(n = 1531)和鸡尸体(n = 1967)中共分离出3980株金黄色葡萄球菌。采用微量肉汤稀释法对分离菌株进行药敏试验。采用聚合酶链式反应(PCR)和测序方法检测耐药基因、spa型、序列型(STs)和葡萄球菌盒染色体mec型(SCCmec)。共有187株菌株(4.7%)对夫西地酸表现出耐药性,其中从牛中分离出的菌株最多(16.2%),其次是猪(6.5%)和鸡(0.5%)。此外,大多数菌株对青霉素(86.6%)有耐药率,而对红霉素、庆大霉素、卡那霉素和四环素的耐药率较低(7- 13.9%)。多药耐药(MDR)占8.6%(16/187)。其中,fusA突变最多,占54%(101/187),其次是fusC(29.4%, 55/187)和fusB(15.5%, 29/187)。97%的菌株对fusA基因中L461K的替代具有高水平的抗性。此外,在FRSA中最常见的耐药模式包括青霉素(87.1%,88/101)。核苷酸测序结果表明,29株携带fusb的分离株均含有bla操纵子的结构基因blaZ和插入序列orf152、orf170、IS257和orf152。共检测到21种spa类型,其中fusA中t126的检出率最高(81.2%,82/101),其次是fusC中t127 (81.8%, 45/55), fusB中t189(27.6%, 8/29)。此外,所有携带fusC的t002均被检测为ST5-MRSA-SCCmecII克隆。这是首次报道从食用动物产品中分离到携带金黄色葡萄球菌的fusA和fusB以及fusB和blaZ基因连锁的FRSA。综上所述,具有不同抗性决定因素和spa类型的食用动物中的FRSA可能对公众健康构成威胁。
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International journal of food microbiology
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