Organization of Joint Laboratory Studies during Sanitary and Epidemiological Interventions in the Republic of the Congo by Rospotrebnadzor Specialists

S. A. Portenko, E. V. Naidenova, D. A. Agafonov, D. A. Kuznetsova, A. V. Evteev, A. A. Tushinsky, L. N. Dmitrieva, A. D. Katyshev, V. E. Kuklev, N. Obissa, V. Mabiala, J. Loubano, M. Mpompolo, J.-C. Mobousse Misse, S. A. Shcherbakova, V. V. Kutyrev
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Abstract

The study presents the data on organization of laboratory testing of clinical and environmental samples within the framework of establishing the etiology of the acute intestinal infections outbreak, performed by the specialists of the joint SAET of the Rospotrebnadzor in Dolisie (Republic of the Congo) in the period of 07–24 July, 2023.Materials and methods. In order to identify the causative agents of cholera and other acute intestinal infections of bacterial and viral nature, 177 clinical and environmental samples were tested, as well as cultures on solid nutrient media and bacterial suspensions. A total of 1023 tests were carried out by polymerase chain reaction (PCR) and 305 – using bacteriological method.Results and discussion. The causative agent of cholera has not been detected in any of the samples tested. Using the PCR method, markers of acute intestinal diseases agents (Salmonella spp., Shigella spp., Campylobacter spp., Rotavirus A) have been identified in 23 clinical samples and 1 sample of bacterial suspension. No DNA/RNA of pathogens has been detected in environmental samples. During culture studies, Salmonella enterica serovar Typhi have been isolated from 8 clinical samples, and their antibiotic sensitivity has been determined. Applying whole-genome nanopore sequencing, using the MinIon platform (Oxford Nanopore Technologies, UK), nucleotide sequences of 4 S. Typhi isolates have been investigated and deposited in the international database NCBI GenBank (No. CP141260, CP141193, CP141194, CP141195). Additionally, the analysis of initially sterile samples (blood, peritoneal fluid, intraoperational samples) from the patients of General and Reference hospitals of Dolisie has resulted in the identification of 5 cultures of non-fermenting bacteria, and their antibiotic sensitivity has been determined.
Rospotrebnadzor 专家在刚果共和国进行卫生和流行病干预期间组织联合实验室研究
本研究介绍了 2023 年 7 月 7 日至 24 日期间多利西(刚果共和国)Rospotrebnadzor 联合 SAET 专家在确定急性肠道传染病爆发病因框架内组织的临床和环境样本实验室检测数据。为了确定霍乱及其他急性肠道细菌和病毒感染的病原体,对 177 份临床和环境样本以及固体营养培养基和细菌悬浮液培养物进行了检测。通过聚合酶链式反应(PCR)共进行了 1023 次检测,通过细菌学方法共进行了 305 次检测。在所有检测样本中均未发现霍乱病原体。利用 PCR 方法,在 23 份临床样本和 1 份细菌悬浮液样本中确定了急性肠道疾病病原体(沙门氏菌属、志贺氏菌属、弯曲杆菌属、轮状病毒 A)的标记。在环境样本中没有检测到病原体的 DNA/RNA。在培养研究中,从 8 份临床样本中分离出了肠炎沙门氏菌(Salmonella enterica serovar Typhi),并确定了它们对抗生素的敏感性。通过使用 MinIon 平台(牛津纳米孔技术公司,英国)进行全基因组纳米孔测序,研究了 4 个伤寒沙门氏菌分离物的核苷酸序列,并将其存入国际数据库 NCBI GenBank(编号:CP141260、CP141193、CP141194、CP141195)。此外,通过对多利西综合医院和参考医院病人的初始无菌样本(血液、腹腔液、术中样本)进行分析,确定了 5 个非发酵菌培养物,并确定了它们对抗生素的敏感性。
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