Phenotypic and molecular detection of multi-drug resistant Salmonella Enteritidis, Salmonella Typhimurium and Salmonella species in retail raw beef and chicken

R. E. Uzeh, Venatius Chinenye Ihekire, S. Smith, M. Fowora
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引用次数: 1

Abstract

Globally, Salmonella is a major cause of foodborne diseases[1,2]. The incidence of non-typhoidal Salmonella is estimated at 1.3 billion cases with annual death rate of 3 million[3]. It results in morbidity, mortality and great economic loss[4,5]. Human salmonellosis is most frequently caused by Salmonella Typhimurium (S. Typhimurium) and Salmonella Enteritidis (S. Enteritidis)[6]. Among the over 2 500 serovars identified within Salmonella enterica subspecies enterica, S. Typhimurium continues to be one of the most frequently recovered from food animals worldwide[7]. Due to its broad host range, S. Typhimurium is also one of the most common serotype isolated from human clinical cases of food-borne salmonellosis. Poor sanitary conditions have been identified to be responsible for the transmission of Salmonella spp., S. Typhimurium (group D) and S. Enteritidis (group B) in developing countries. In sub-Saharan Africa, they have been reported to be the cause of 79%–95% of all bacteriaemic non-typhoidal Salmonella infections or foodborne outbreaks[8,9], and are associated with case fatality rate of 20%– 25%[10]. Salmonella can be transmitted to humans from animals and by consuming foods from animal sources such as milk, egg, poultry meat and beef which serve as reservoirs[11,12]. During the production of meat, the major source of Salmonella contamination of carcasses is the evisceration stage in slaughter house[13]. In order to ensure food safety and for the purpose of food borne disease surveillance, foods should be examined routinely for the presence of Salmonella. Conventional typing methods such as, biotyping, serotyping and phage typing which are based on phenotypic characteristics have been used extensively for this purpose[14]. However, they are less discriminative. Molecular typing methods offer higher discrimination[14] and have been employed for identification of Salmonella spp.[9]. Studies on the molecular typing of microbial isolates have ARTICLE INFO ABSTRACT
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零售生牛肉和鸡肉中多重耐药肠炎沙门氏菌、鼠伤寒沙门氏菌和沙门氏菌的表型和分子检测
在全球范围内,沙门氏菌是食源性疾病的主要原因[1,2]。非伤寒沙门氏菌的发病率估计为13亿例,年死亡率为300万[3]。它会导致发病率、死亡率和巨大的经济损失[4,5]。人类沙门氏菌病最常见由鼠伤寒沙门氏菌(S.Typhimurium)和肠炎沙门氏菌引起[6]。在肠炎沙门氏菌亚种肠炎中发现的2500多种血清型中,鼠伤寒沙门氏菌仍然是世界上最常见的食用动物之一[7]。由于其宿主范围广泛,鼠伤寒沙门氏菌也是从人类食源性沙门氏菌病临床病例中分离出的最常见的血清型之一。卫生条件差已被确定是沙门氏菌属、鼠伤寒沙门氏菌(D组)和肠炎沙门氏杆菌(B组)在发展中国家传播的原因。据报道,在撒哈拉以南非洲,它们是所有细菌性非伤寒沙门氏菌感染或食源性疫情的79%-95%[8,9]的病因,病死率为20%-25%[10]。沙门氏菌可以通过动物和食用动物来源的食物传播给人类,如牛奶、鸡蛋、禽肉和牛肉,这些食物是宿主[11,12]。在肉类生产过程中,胴体沙门氏菌污染的主要来源是屠宰场的内脏摘除阶段[13]。为了确保食品安全和监测食源性疾病,应定期检查食品中是否存在沙门氏菌。基于表型特征的传统分型方法,如生物分型、血清分型和噬菌体分型,已被广泛用于此目的[14]。然而,他们的歧视性较小。分子分型方法提供了更高的辨别力[14],并已用于鉴定沙门氏菌。[9]。对微生物分离株分子分型的研究有文章信息摘要
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