SAMRC Microbial Water Quality Monitoring Center, University of Fort Hare, Alice, South Africa.
Applied and Environmental Microbiology Research Group, Department of Biochemistry and Microbiology, University of Fort Hare, Alice, South Africa.
PLoS One. 2022 Jul 6;17(7):e0270993. doi: 10.1371/journal.pone.0270993. eCollection 2022.
The occurrence and the antibiogram signatures of Listeria monocytogenes (Lm) recovered from 65 milk samples and its products within the Eastern Cape province were examined. The EN ISO 11290:2017 procedures Parts 1 and 2 described by the International Organization for Standardization for the enumeration and isolation of Lm was adopted for the study. Lm was detected in 18.46% of all the samples examined, and the strains recovered from the samples belong to serotypes 4b and 1/2b. The virulence determinants including prfA, plcA, plcB, inlA, inlC, hly, mpl, actA, inlJ and inlB were detected in all the isolates. About 95.24% of the studied Lm isolates demonstrated potential capacity for biofilm formation. The antibiogram profile revealed high resistance against sulfamethoxazole (71.43%), trimethoprim (52.86%); erythromycin, cefotetan and oxytetracycline (42.86% respectively). About 85.71% exhibited multiple antibiotic resistance phenotypes against the test antibiotics. The resistance determinants encoding resistance against the β-lactamase antibiotics [such as the blaTEM, blaSHV, blaTEM variants (TEM-1 and TEM-2) and the blaZ], the tetracycline resistance genes (including tetA, tetD, tetG and tetM and tetK) were detected among resistant isolates. In addition, the aminoglycoside resistance gene aph (3)-IIa (aphA2)a was detected only in one isolate. Finally, the sulfonamide resistance genes including the sul2 and the sul1 genes were the most frequently observed among Lm isolates. Generally, 71.43% of all Lm isolates recovered from the samples investigated harboured one or more resistance genes encoding resistance against various antibiotics. The antibiogram signatures of Lm isolates observed in this study is an indication that empirical treatment of listeriosis may be challenging in the future as the pathogen may obliterate the success of antibiotics. We, therefore, advocate for the recognition of the One Health approach to ensuring food safety and curbing the spread of antimicrobial resistance in food.
对东开普省 65 份牛奶样本及其产品中分离出的单核细胞增生李斯特菌(Lm)的发生情况和抗生素谱特征进行了研究。本研究采用了国际标准化组织(ISO)11290:2017 标准中描述的第 1 部分和第 2 部分程序,用于 Lm 的计数和分离。在所有检测的样本中,18.46%检测到了 Lm,从样本中分离出的菌株属于 4b 和 1/2b 血清型。所有分离株均检测到毒力决定因子包括 prfA、plcA、plcB、inlA、inlC、hly、mpl、actA、inlJ 和 inlB。研究中约 95.24%的 Lm 分离株具有形成生物膜的潜在能力。抗生素谱分析显示,对磺胺甲噁唑(71.43%)、甲氧苄啶(52.86%)、红霉素、头孢替坦和土霉素(分别为 42.86%)具有较高的耐药性。约 85.71%的分离株对测试抗生素表现出多药耐药表型。编码对β-内酰胺类抗生素(如 blaTEM、blaSHV、blaTEM 变体(TEM-1 和 TEM-2)和 blaZ)耐药的耐药决定因子、四环素耐药基因(包括 tetA、tetD、tetG 和 tetM 和 tetK)在耐药分离株中均有检出。此外,仅在一个分离株中检测到氨基糖苷类耐药基因 aph(3)-IIa(aphA2)a。最后,在所检测的 Lm 分离株中,磺胺类耐药基因包括 sul2 和 sul1 基因是最常见的。总的来说,从研究中回收的所有 Lm 分离株中,有 71.43%的分离株携带一个或多个编码对各种抗生素耐药的耐药基因。本研究中观察到的 Lm 分离株的抗生素谱特征表明,在未来,李斯特菌病的经验治疗可能会面临挑战,因为病原体可能会破坏抗生素的疗效。因此,我们提倡采用“同一健康”方法来确保食品安全,并遏制食品中抗微生物药物耐药性的传播。