Cheng Peini, Dong Kui, Kang Zhiming, Li Jing, Wang Wenjuan, Zhang Xiaodan, Zhou Guohong
Department of School of the 1st Clinical Medical Sciences, Shanxi Medical University, TaiYuan, Shanxi 030000, China.
Department of Ophthalmology, Shanxi Eye Hospital, TaiYuan, Shanxi 030000, China.
J Ophthalmol. 2022 Aug 27;2022:4024260. doi: 10.1155/2022/4024260. eCollection 2022.
Infectious endophthalmitis is an important cause of vision loss worldwide. It is an inflammatory reaction caused by bacteria, fungi, and other micro-organisms and often occurs as a complication of intraocular surgery, especially following cataract surgery or intravitreal injection. The focus of the prevention and treatment of infectious endophthalmitis is the early detection of microbial flora, such as fungi or bacteria. Current identification methods for bacteria include Gram staining-based, culture-based, and polymerase chain reaction (PCR)-based methods. The matrix-assisted laser desorption/ionization time-of-flight mass spectrometry technology is now the standard identification method of bacteria and fungi after their isolation in culture. The remarkable sensitivity of PCR technology for the direct detection of micro-organisms in clinical samples makes it particularly useful in culture-positive and culture-negative endophthalmitis. Furthermore, PCR increases the rate of microorganism detection in intraocular samples by 20% and can provide a microbiology diagnosis in approximately 44.7-100% of the culture-negative cases. This review aims to introduce the development of different methods for the detection and identification of micro-organisms causing endophthalmitis through a literature review; introduce the research status of the first, second, and third-generation sequencing technologies in infectious endophthalmitis; and understand the research status of endophthalmitis microbial flora. For slow-growing and rare micro-organisms, high-throughput sequencing (HTS) offers advantages over conventional methods and provides a basis for the identification of pathogens in endophthalmitis cases with negative culture. It is a reliable platform for the identification of pathogenic bacteria of infectious endophthalmitis in the future and provides a reference for the clinical diagnosis and treatment of infectious endophthalmitis. The application of HTS technology may also be transformative for clinical microbiology and represents an exciting future direction for the epidemiology of ocular infections.
感染性眼内炎是全球视力丧失的一个重要原因。它是由细菌、真菌和其他微生物引起的炎症反应,常作为眼内手术的并发症出现,尤其是在白内障手术或玻璃体内注射后。感染性眼内炎的防治重点是早期检测微生物菌群,如真菌或细菌。目前细菌的鉴定方法包括基于革兰氏染色、培养和聚合酶链反应(PCR)的方法。基质辅助激光解吸/电离飞行时间质谱技术现在是细菌和真菌在培养物中分离后的标准鉴定方法。PCR技术对临床样本中微生物的直接检测具有显著的敏感性,这使得它在培养阳性和培养阴性的眼内炎中特别有用。此外,PCR可使眼内样本中的微生物检测率提高20%,并能在约44.7%-100%的培养阴性病例中提供微生物学诊断。本综述旨在通过文献回顾介绍检测和鉴定引起眼内炎的微生物的不同方法的发展;介绍第一代、第二代和第三代测序技术在感染性眼内炎中的研究现状;并了解眼内炎微生物菌群的研究现状。对于生长缓慢和罕见的微生物,高通量测序(HTS)比传统方法具有优势,并为培养阴性的眼内炎病例中的病原体鉴定提供了依据。它是未来鉴定感染性眼内炎病原菌的可靠平台,为感染性眼内炎的临床诊断和治疗提供参考。HTS技术的应用也可能对临床微生物学产生变革,并代表了眼部感染流行病学一个令人兴奋的未来方向。