Krishna Sri, Nema Shrikant, Sangle Ruchika, Ahmad Amreen, Singh Akansha, Kumar Devendra, Verma Anil K, Udhayakumar Venkatachalam, Das Aparup, Anvikar Anup R, Bharti Praveen K
ICMR-National Institute of Research in Tribal Health, Jabalpur, Madhya Pradesh, India.
ICMR-National Institute of Malaria Research, New Delhi, India.
PLoS One. 2024 Dec 18;19(12):e0315662. doi: 10.1371/journal.pone.0315662. eCollection 2024.
Rapid diagnostic tests (RDTs) are crucial for diagnosing malaria in resource-limited settings. These tests, which detect the histidine-rich protein 2 (PfHRP2) and its structural homologue PfHRP3, are specifically designed to identify Plasmodium falciparum. Deletion of the Pfhrp2 gene in parasite has been reported in India and other malaria-endemic countries. Therefore, periodic surveillance of Pfhrp2 and Pfhrp3 genetic deletions is crucial. We conducted a study to examine these gene deletions in P. falciparum isolates from nine malaria-endemic states in India. In this study, we analyzed 1,558 samples that were microscopically confirmed to be P. falciparum positive. We isolated genomic DNA from all the aforementioned samples, followed by PCR amplification of the Pfhrp2/3 gene. The results showed that the deletion rates for Pfhrp2 and Pfhrp3 genes were 0.44% and 1.47%, respectively. These findings indicate that the gene deletions in all nine states are at low level. Despite these low deletion rates, continuous surveillance is crucial to monitor the efficiency of HRP2 based malaria RDTs. It is recommend that conducting large-scale studies which include other endemic states in India to gain a more comprehensive understanding of the prevalence and impact of these gene deletions over time. This ongoing surveillance will ensure that diagnostic strategies remain effective and that any emerging trends in gene deletions are promptly addressed to achieve the malaria control and elimination.
快速诊断检测(RDTs)对于在资源有限的环境中诊断疟疾至关重要。这些检测通过检测富含组氨酸的蛋白2(PfHRP2)及其结构同源物PfHRP3,专门用于鉴定恶性疟原虫。在印度和其他疟疾流行国家已报道寄生虫中Pfhrp2基因的缺失。因此,定期监测Pfhrp2和Pfhrp3基因缺失至关重要。我们开展了一项研究,以检测来自印度九个疟疾流行邦的恶性疟原虫分离株中的这些基因缺失情况。在本研究中,我们分析了1558份经显微镜检查确诊为恶性疟原虫阳性的样本。我们从所有上述样本中分离基因组DNA,随后对Pfhrp2/3基因进行PCR扩增。结果显示,Pfhrp2和Pfhrp3基因的缺失率分别为0.44%和1.47%。这些发现表明,所有九个邦的基因缺失水平较低。尽管缺失率较低,但持续监测对于监测基于HRP2的疟疾RDTs的效率至关重要。建议开展大规模研究,纳入印度其他流行邦,以更全面地了解这些基因缺失的流行情况及其随时间的影响。这种持续监测将确保诊断策略保持有效,并能及时应对基因缺失方面出现的任何新趋势,以实现疟疾控制和消除目标。