Department of Microbiology, School of Science & Technology, Babcock University, PMB 4005, Ilisan-Remo, Ogun State, Nigeria.
Department of Nature Conservation, Faculty of Natural Sciences, Mangosuthu University of Technology, P.O. Box 12363, Jacobs, 4026, Durban, Kwa-Zulu Natal, South Africa.
Afr Health Sci. 2020 Sep;20(3):1109-1117. doi: 10.4314/ahs.v20i3.12.
The potential of transmitting multidrug resistant from asymptomatic individuals to healthy individuals could constitute a great challenge to antimicrobial therapy.
The antibiograms of the from asymptomatic individuals were determined by disk diffusion and agar dilution assay techniques with different antibiotics and vancomycin.
Of the 152 isolated, (59)38.8% isolates were multi-drug resistant strains. Streptomycin was the most effective and inhibited (135)88.82% of the isolates while ceftazidime inhibited (24)15.8% of the isolates. While (82)54.0% of the isolates inhibited by cefuroxime had resistant colonies within their inhibition zones (Rc) and ofloxacin inhibited (100)65.8% of the isolates without having resistant colonies within the inhibition zones, ceftazidime inhibited (7)4.6% of the isolates with resistant colonies within the inhibition zones. Subjecting the isolates to vancomycin showed that (27)17.8% were resistant to 2 µg/ml, (43)28.3% were resistant to 4 µg/ml and (27)17.8% of the isolates were simultaneously resistant to both concentrations of vancomycin. Although (100)65.8% of the isolates had MAR ≥0.2, (52)34.2% of the isolates had MAR ≤ 0.2 and (65)428% of the isolates were considered multidrug resistant strains.
The isolation of multi-drug and vancomycin intermediate resistant strains of in high percentage, in this study, presents a great threat to clinicians and general populace. The vancomycin intermediate resistant (VISA) in asymptomatic individuals could be a critical concern to the therapeutic dilemma to be added to the presence of multi-drug resistance. A more sustainable therapy must be in place to prevent its dissemination or the outbreak of its infection.
无症状个体传播耐多药 的可能性对抗菌治疗构成了巨大挑战。
采用纸片扩散法和琼脂稀释法测定无症状个体 的药敏谱,使用不同的抗生素和万古霉素。
在分离的 152 株 中,有 59 株(38.8%)为多药耐药株。链霉素最有效,抑制了 135 株(88.82%)的 ,而头孢他啶抑制了 24 株(15.8%)的 。在头孢呋肟抑制的 82 株(54.0%)中,抑制区内有耐药菌落(Rc),氧氟沙星抑制了 100 株(65.8%)的 ,而抑制区内没有耐药菌落,但头孢他啶抑制了 7 株(4.6%)的 ,抑制区内有耐药菌落。万古霉素药敏试验结果显示,有 27 株(17.8%)对 2μg/ml 万古霉素耐药,43 株(28.3%)对 4μg/ml 万古霉素耐药,27 株(17.8%)对两种浓度的万古霉素均耐药。虽然有 100 株(65.8%)的 MAR 值≥0.2,但仍有 52 株(34.2%)的 MAR 值≤0.2,有 65 株(42.8%)的 被认为是多药耐药株。
本研究中,从无症状个体中分离出高比例的耐多药和万古霉素中介耐药 ,对临床医生和普通人群构成了巨大威胁。无症状个体中的万古霉素中介耐药 (VISA)可能会加剧治疗困境,增加多药耐药的发生。必须采取更可持续的治疗方法来防止其传播或感染的爆发。