Mehmood Nasir, Akram Muhammad Waseem, Majeed Muhammad Irfan, Nawaz Haq, Aslam Muhammad Aamir, Naman Abdul, Wasim Muhammad, Ghaffar Usman, Kamran Ali, Nadeem Sana, Kanwal Naeema, Imran Muhammad
Department of Chemistry, University of Agriculture Faisalabad Faisalabad (38000) Pakistan
Institute of Microbiology, Faculty of Veterinary, University of Agriculture Faisalabad Faisalabad (38000) Pakistan.
RSC Adv. 2024 Feb 12;14(8):5425-5434. doi: 10.1039/d3ra07575c. eCollection 2024 Feb 7.
Drug-resistant pathogenic bacteria are a major cause of infectious diseases in the world and they have become a major threat through the reduced efficacy of developed antibiotics. This issue can be addressed by using bacteriophages, which can kill lethal bacteria and prevent them from causing infections. Surface-enhanced Raman spectroscopy (SERS) is a promising technique for studying the degradation of infectious bacteria by the interaction of bacteriophages to break the vicious cycle of drug-resistant bacteria and help to develop chemotherapy-independent remedial strategies. The phage (viruses)-sensitive () bacteria are exposed to bacteriophages (Siphoviridae family) in the time frame from 0 min (control) to 50 minutes with intervals of 5 minutes and characterized by SERS using silver nanoparticles as SERS substrate. This allows us to explore the effects of the bacteriophages against lethal bacteria () at different time intervals. The differentiating SERS bands are observed at 575 (C-C skeletal mode), 620 (phenylalanine), 649 (tyrosine, guanine (ring breathing)), 657 (guanine (COO deformation)), 728-735 (adenine, glycosidic ring mode), 796 (tyrosine (C-N stretching)), 957 (C-N stretching (amide lipopolysaccharides)), 1096 (PO (nucleic acid)), 1113 (phenylalanine), 1249 (CH of amide III, N-H bending and C-O stretching (amide III)), 1273 (CH, N-H, C-N, amide III), 1331 (C-N stretching mode of adenine), 1373 (in nucleic acids (ring breathing modes of the DNA/RNA bases)) and 1454 cm (CH deformation of saturated lipids), indicating the degradation of bacteria and replication of bacteriophages. Multivariate data analysis was performed by employing principal component analysis (PCA) and partial least squares-discriminant analysis (PLS-DA) to study the biochemical differences in the bacteria infected by the bacteriophage. The SERS spectral data sets were successfully differentiated by PLS-DA with 94.47% sensitivity, 98.61% specificity, 94.44% precision, 98.88% accuracy and 81.06% area under the curve (AUC), which shows that at 50 min interval bacteria is degraded by the replicating bacteriophages.
耐药病原菌是全球传染病的主要病因,随着已开发抗生素疗效的降低,它们已成为重大威胁。可以通过使用噬菌体来解决这个问题,噬菌体能够杀死致命细菌并防止其引发感染。表面增强拉曼光谱(SERS)是一种很有前景的技术,可用于研究噬菌体相互作用对感染性细菌的降解作用,以打破耐药细菌的恶性循环,并有助于制定不依赖化疗的治疗策略。将对噬菌体(病毒)敏感的()细菌在0分钟(对照)至50分钟的时间范围内,每隔5分钟暴露于噬菌体(长尾噬菌体科),并使用银纳米颗粒作为SERS底物通过SERS进行表征。这使我们能够探究噬菌体在不同时间间隔对致命细菌()的影响。在575(C-C骨架模式)、620(苯丙氨酸)、649(酪氨酸、鸟嘌呤(环呼吸))、657(鸟嘌呤(COO变形))、728 - 735(腺嘌呤、糖苷环模式)、796(酪氨酸(C-N伸缩))、957(C-N伸缩(酰胺脂多糖))、1096(PO(核酸))、1113(苯丙氨酸)、1249(酰胺III的CH、N-H弯曲和C-O伸缩(酰胺III))、1273(CH、N-H、C-N、酰胺III)、1331(腺嘌呤的C-N伸缩模式)、1373(核酸中(DNA/RNA碱基的环呼吸模式))和1454 cm(饱和脂质的CH变形)处观察到有差异的SERS谱带,表明细菌的降解和噬菌体的复制。通过主成分分析(PCA)和偏最小二乘判别分析(PLS-DA)进行多变量数据分析,以研究受噬菌体感染的细菌中的生化差异。PLS-DA成功区分了SERS光谱数据集,灵敏度为94.47%,特异性为98.61%,精确度为94.44%,准确度为98.88%,曲线下面积(AUC)为81.06%,这表明在50分钟的时间间隔内,细菌被复制的噬菌体降解。