Garbaj Aboubaker M, Gawella Tahani B Ben, Sherif Jihan A, Naas Hesham T, Eshamah Hanan L, Azwai Salah M, Gammoudi Fatim T, Abolghait Said K, Moawad Ashraf A, Barbieri Ilaria, Eldaghayes Ibrahim M
Department of Food Hygiene and Control, Faculty of Veterinary Medicine, University of Tripoli, Tripoli, Libya.
Department of Microbiology and Parasitology, Faculty of Veterinary Medicine, University of Tripoli, Tripoli, Libya.
Vet World. 2022 May;15(5):1185-1190. doi: 10.14202/vetworld.2022.1185-1190. Epub 2022 May 17.
Foodborne illnesses are a serious challenge to human health and the economic sector. For example, salmonellosis remains a burden in developed and developing nations. Rapid and reliable molecular methods to identify strains are essential for minimizing human infection. This study aimed to identify spp. in raw milk and dairy products using conventional and molecular techniques and to test the antibiotic susceptibility of the isolated strains.
One hundred and thirty-one milk and dairy product samples were randomly collected from different localities in Libya. Samples were examined for the presence of by conventional culture techniques, including cultivation in Rappaport-Vassiliadis broth and streaking on xylose lysine deoxycholate agar. Identification also used polymerase chain reaction and partial sequencing of 16S rDNA. Twenty-four antibiotics were used for the examination of antimicrobial resistance of spp. isolates with the agar disk diffusion method (Kirby-Bauer technique). Multi-antibiotic resistance index and antibiotic resistance index (ARI)for isolates were calculated.
Twenty-one of 131 samples (16%) were positive for spp. recovered from 9 (16%), 2 (11%), 4 (22.2%), and 6 (46%) samples of raw cow milk, fermented raw milk, and fresh locally made soft cheeses, Maasora and Ricotta), respectively. Samples of ice cream, milk powder, and infant formula showed no spp. contamination. Only 9 of 21 (42.8%) isolates were confirmed as . by partial sequence 16S rDNA analysis. All isolates were resistant to amoxycillin, bacitracin, penicillin G, lincomycin, vancomycin, clindamycin, and cloxacillin with an ARI of 0.042. In contrast, all tested strains were sensitive to levofloxacin, doxycycline, and ciprofloxacin. In addition, all of the tested isolates (100%) were resistant to more than one antibiotic.
This study demonstrated the applicability of molecular techniques, compared with conventional methods, as preferable for the identification of in milk and dairy products and thus reduction of milk-borne transmission to the consumers. From the view of public health, isolation and identification of multidrug-resistant strains from raw cow`s milk and locally prepared dairy products sold in the Libyan markets indicate the need to improve the handling and processing of milk and dairy products to minimize the prevalence of , one of the most important foodborne microorganisms that cause food poisoning.
食源性疾病对人类健康和经济部门构成严峻挑战。例如,沙门氏菌病在发达国家和发展中国家仍是一项负担。快速可靠的分子方法来鉴定菌株对于将人类感染降至最低至关重要。本研究旨在使用传统和分子技术鉴定生乳和乳制品中的沙门氏菌属,并检测分离菌株的抗生素敏感性。
从利比亚不同地区随机采集了131份牛奶和乳制品样本。通过传统培养技术检测样本中沙门氏菌的存在,包括在Rappaport-Vassiliadis肉汤中培养以及在木糖赖氨酸脱氧胆酸盐琼脂上划线接种。鉴定还采用了聚合酶链反应和16S rDNA的部分测序。使用24种抗生素通过琼脂纸片扩散法(Kirby-Bauer技术)检测沙门氏菌属分离株的抗菌耐药性。计算了沙门氏菌分离株的多重耐药指数和抗生素耐药指数(ARI)。
131份样本中有21份(16%)沙门氏菌属呈阳性,分别从9份(16%)生牛乳、2份(11%)发酵生乳以及4份(22.2%)和6份(46%)当地新鲜制作的软奶酪(Maasora和Ricotta)样本中分离得到。冰淇淋、奶粉和婴儿配方奶粉样本未检测到沙门氏菌属污染。通过16S rDNA部分序列分析,21份分离株中仅有9份(42.8%)被确认为沙门氏菌。所有分离株对阿莫西林、杆菌肽、青霉素G、林可霉素、万古霉素、克林霉素和氯唑西林耐药,ARI为0.042。相比之下,所有测试菌株对左氧氟沙星、多西环素和环丙沙星敏感。此外,所有测试分离株(100%)对一种以上抗生素耐药。
本研究表明,与传统方法相比,分子技术适用于鉴定牛奶和乳制品中的沙门氏菌,从而减少通过牛奶传播给消费者的风险。从公共卫生角度来看,从利比亚市场销售的生牛乳和当地制作的乳制品中分离和鉴定出多重耐药的沙门氏菌菌株表明,需要改进牛奶和乳制品的处理和加工,以尽量减少沙门氏菌(导致食物中毒的最重要食源微生物之一)的流行。