Mohammad Rahimi Hanieh, Karamati Seyed Ahmad, Nemati Sara, Mirjalali Hamed, Zali Mohammad Reza
Foodborne and Waterborne Diseases Research Center, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Department of Medical Parasitology and Mycology, Faculty of Medicine, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran.
Iran J Parasitol. 2022 Apr-Jun;17(2):184-193. doi: 10.18502/ijpa.v17i2.9534.
sp., is a prevalent protist isolated from humans and animals, which its opportunistic role in immunocompromised patients is still controversial. The current study aimed to evaluate the subtype and alleles distribution of sp., among immunocompromised patients.
Totally, 33 microscopically -positive stool samples, isolated from Guilan province during April 2018 to May 2019 were investigated. Total DNA extraction was performed and the barcoding region of the small subunit ribosomal RNA (SSU rRNA) gene was amplified. Targeted fragments were sequenced to characterize subtypes and relevant alleles. Phylogenetic tree was constructed using Maximum-likelihood and Tamura 3-parameter to illustrate the correlation between subtypes and certain immunodeficiency.
Subtype analysis revealed the presence of ST1, ST2, ST3, and ST7 among 13/33 (39.4%), 5 (15.2%), 14/33 (42.4%), and 1/33 (3%), of samples, respectively. ST1 was the major subtype among cancer patients 5/7 (71.42%), while ST3 was the predominant subtype among rheumatoid arthritis (RA) patients 3/6 (50%), internal ward patients 5/10 (50%), and asthma and allergy patients 2/3 (66.66%). ST7 was isolated from a patient hospitalized in internal ward. No significant correlation was seen between the type of immunodeficiency and subtypes (-value = 0.771). The phylogenetic tree showed no separation regarding the type of immunodeficiency.
Among studied immunocompromised patients, ST3 was the most prevalent subtype followed by ST1. There was no specific correlation between subtypes and alleles with type of immunodeficiency. Putative zoonotic alleles were highlighted the probability of zoonotic transmission for sp.
[具体物种名]是一种从人类和动物中分离出的常见原生生物,其在免疫功能低下患者中的机会性作用仍存在争议。本研究旨在评估免疫功能低下患者中[具体物种名]的亚型和等位基因分布情况。
共调查了2018年4月至2019年5月期间从吉兰省分离出的33份显微镜检查呈阳性的粪便样本。进行了总DNA提取,并扩增了小亚基核糖体RNA(SSU rRNA)基因的条形码区域。对靶向片段进行测序以鉴定亚型和相关等位基因。使用最大似然法和 Tamura 3 参数构建系统发育树,以阐明亚型与某些免疫缺陷之间的相关性。
亚型分析显示,在13/33(39.4%)、5(15.2%)、14/33(42.4%)和1/(33.0%)的样本中分别存在ST1、ST2、ST3和ST7。ST1是癌症患者中的主要亚型,占5/7(71.42%),而ST3是类风湿性关节炎(RA)患者中的主要亚型,占3/6(50%),内科病房患者中占5/10(50%),哮喘和过敏患者中占2/3(66.66%)。ST7是从一名内科病房住院患者中分离出来的。免疫缺陷类型与亚型之间未发现显著相关性(P值 = 0.771)。系统发育树显示在免疫缺陷类型方面没有分离。
在所研究的免疫功能低下患者中,ST3是最常见的亚型,其次是ST1。亚型和等位基因与免疫缺陷类型之间没有特定的相关性。推测的人畜共患等位基因突出了[具体物种名]人畜共患传播的可能性。