Dafalla Ommer, Abdulhaq Ahmed A, Almutairi Hatim, Noureldin Elsiddig, Ghzwani Jaber, Mashi Omar, Shrwani Khalid J, Hobani Yahya, Sufyani Ohood, Ayed Reem, Alamri Abdullah, Al-Mekhlafi Hesham M, Eisa Zaki M
Saudi Public Health Authority, Jazan, Kingdom of Saudi Arabia.
Jazan University, Jazan, Kingdom of Saudi Arabia.
Trop Dis Travel Med Vaccines. 2023 Mar 15;9(1):5. doi: 10.1186/s40794-023-00188-8.
Dengue virus (DENV) infection is a global economic and public health concern, particularly in tropical and subtropical countries where it is endemic. Saudi Arabia has seen an increase in DENV infections, especially in the western and southwestern regions. This study aims to investigate the genetic variants of DENV-2 that were circulating during a serious outbreak in Jazan region in 2019.
A total of 482 serum samples collected during 2019 from Jazan region were tested with reverse transcription-polymerase chain reaction (RT-PCR) to detect and classify DENV; positive samples underwent sequencing and bioinformatics analyses.
Out of 294 positive samples, type-specific RT-PCR identified 58.8% as DENV-2 but could not identify 41.2%. Based on sequencing and bioinformatics analyses, the samples tested PCR positive in the first round but PCR negative in the second round were found to be imported genetic variant of DENV-2. The identified DENV-2 imported variant showed similarities to DENV-2 sequences reported in Malaysia, Singapore, Korea and China. The results revealed the imported genetic variant of DENV-2 was circulating in Jazan region that was highly prevalent and it was likely a major factor in this outbreak.
The emergence of imported DENV variants is a serious challenge for the dengue fever surveillance and control programmes in endemic areas. Therefore, further investigations and continuous surveillance of existing and new viral strains in the region are warranted.
登革病毒(DENV)感染是一个全球性的经济和公共卫生问题,在其流行的热带和亚热带国家尤为如此。沙特阿拉伯的登革病毒感染有所增加,特别是在西部地区和西南部地区。本研究旨在调查2019年贾赞地区严重疫情期间流行的DENV-2基因变异情况。
对2019年从贾赞地区采集的482份血清样本进行逆转录-聚合酶链反应(RT-PCR)检测,以检测和分类登革病毒;对阳性样本进行测序和生物信息学分析。
在294份阳性样本中,型特异性RT-PCR鉴定出58.8%为DENV-2,但有41.2%无法鉴定。基于测序和生物信息学分析,发现第一轮PCR检测呈阳性但第二轮PCR检测呈阴性的样本为DENV-2的输入性基因变异。鉴定出的DENV-2输入性变异与马来西亚、新加坡、韩国和中国报告的DENV-2序列相似。结果显示,DENV-2的输入性基因变异在贾赞地区流行,且高度普遍,这可能是此次疫情的一个主要因素。
输入性DENV变异的出现对流行地区的登革热监测和控制计划构成了严峻挑战。因此,有必要对该地区现有和新出现的病毒株进行进一步调查和持续监测。