de Goes Tayná C, de Morais Rayana C S, de Melo Maria G N, E Silva Rômulo P, Rezende Antônio M, de Paiva-Cavalcanti Milena
Aggeu Magalhães Institute, Av. Moraes Rego, Cidade Universitária, 50670-420 Recife, PE, Brazil.
J Parasitol Res. 2020 Oct 6;2020:8885070. doi: 10.1155/2020/8885070. eCollection 2020.
The causative species is an important factor influencing the evolution of American cutaneous leishmaniasis (ACL). Due to its wide distribution in endemic areas, (.) is considered one of the most important species in circulation in Brazil. Molecular targets derived from ribosomal RNA (rRNA) were used in studies to identify spp.; however, the Intergenic Spacer (IGS) region has not yet been explored in parasite species differentiation. Besides, there is a shortage of sequences deposited in public repositories for this region. Thus, it was proposed to analyze and provide sequences of the IGS rRNA region from different spp. and to evaluate their potential as biomarkers to characterize . A set of primers was designed for complete amplification of the IGS rRNA region of spp. PCR products were submitted to Sanger sequencing. The sequences obtained were aligned and analyzed for size and similarity, as well as deposited in GenBank. Characteristics of the repetitive elements (IGSRE) present in the IGS rRNA were also verified. In addition, a set of primers for identification for qPCR was developed and optimized. Sensitivity (), specificity (), and efficiency () tests were applied. It was found that the mean size for the IGS rRNA region is 3 kb, and the similarity analysis of the sequences obtained demonstrated high conservation among the species. It was observed that the size for the IGSRE repetitive region varies between 61 and 71 bp, and there is a high identity between some species. Fifteen sequences generated for the IGS rRNA partial region of nine different species were deposited in GenBank so far. The specific primer system for showed = 10 fg, = 98.08%, and log = 10 for ; log = 10 for ; and log = 10 for . This protocol system can be used for diagnosis, identification, and quantification of a patient's parasite load, aiding in the direction of a more appropriate therapeutic management to the cases of infection by this etiological agent. Besides that, the unpublished sequences deposited in databases can be used for multiple analyses in different contexts.
致病物种是影响美洲皮肤利什曼病(ACL)演变的一个重要因素。由于其在流行地区分布广泛,(.)被认为是巴西传播最广的重要物种之一。核糖体RNA(rRNA)衍生的分子靶点被用于研究以鉴定 spp.;然而,基因间隔区(IGS)区域尚未在寄生虫物种分化研究中得到探索。此外,该区域在公共数据库中 deposited 的序列短缺。因此,有人提议分析并提供不同 spp. 的IGS rRNA区域序列,并评估其作为生物标志物来表征 的潜力。设计了一组引物用于完全扩增 spp. 的IGS rRNA区域。PCR产物进行桑格测序。对获得的序列进行比对,分析其大小和相似性,并存入GenBank。还验证了IGS rRNA中存在的重复元件(IGSRE)的特征。此外,开发并优化了一组用于qPCR鉴定 的引物。进行了灵敏度()、特异性()和效率()测试。发现IGS rRNA区域的平均大小为3 kb,对获得的序列进行的相似性分析表明各物种间具有高度保守性。观察到IGSRE重复区域的大小在61至71 bp之间变化,一些物种之间具有高度同一性。到目前为止,九个不同物种的IGS rRNA部分区域产生的15个序列已存入GenBank。针对 的特异性引物系统显示 = 10 fg, = 98.08%, 时log = 10; 时log = 10; 时log = 10。该方案系统可用于诊断、鉴定和定量患者的寄生虫载量,有助于针对该病原体感染病例进行更适当的治疗管理。除此之外,数据库中未发表的序列可用于不同背景下的多种分析。