Identification and Genotyping of Anaplasma phagocytophylum Strains with Zoonotic Potential in Dogs from Mashhad Shelters, Khorasan-Razavi Province, Iran

Q4 Medicine
Naghmeh Mehrabifar, H. Staji, Morteza Keywanlou, M. S. Salimi Bejestani, Ehsan Gallehdar Kakhki
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Abstract

Background and Aim: Anaplasmosis caused by Anaplasma spp. is an important arthropod-borne disease of various vertebrates with health concerns to humans. The present study aimed to investigate the detection and genotype of Anaplasma phagocytophilum using microscopic examination, real-time PCR technique, and phylogenetic analysis in dogs from Mashhad shelters, Khorasan-Razavi province. Materials and Methods: For this purpose, 250 blood specimens were collected during routine health checkups from dogs in different shelters in Mashhad, Iran, in 2020. First, smears were prepared from the blood specimens, stained with Giemsa, and examined under the light microscope for Anaplasma inclusions. Then, the genomic DNAs were extracted from buffy coats of blood specimens and screened by real-time PCR for the presence of Anaplasma infection by amplifying a 1400 bp sequence of 16S rRNA belonging to the Anaplasma genus. Finally, sequencing and BLAST analyses were carried out on the amplified fragments for the phylogenetic assessments in positive specimens. Results: A total of 9 dogs (3.60%), including 5 females (3.40%) and 4 males (3.88%) were found to be positive for Anaplasma infection in real-time PCR. Moreover, in blood smear observation, A. phagocytophilum morulae were detected in the neutrophils of 3 PCR positive animals. Conclusion: This study provides important data regarding A. phagocytophilum in dogs and the degree of genetic homology/heterogeneities among these pathogen strains from dogs and humans in Iran and other countries. To our knowledge, this is the first molecular evidence on the infection of A. phagocytophilum in sheltered dogs of the region.
伊朗呼罗珊-拉扎维省马什哈德收容所犬具人畜共患性吞噬细胞无原体菌株的鉴定和基因分型
背景与目的:由无形体虫引起的无形体病是一种重要的节肢动物传播的脊椎动物疾病,对人类健康有重要影响。本研究旨在利用显微检查、实时PCR技术和系统发育分析方法对来自呼罗珊-拉扎维省马什哈德收容所的狗进行嗜吞噬细胞无原体的检测和基因分型研究。材料和方法:为此目的,在2020年对伊朗马什哈德不同收容所的狗进行常规健康检查时收集了250份血液样本。首先,从血液标本中制备涂片,用吉姆萨染色,并在光镜下检查无原体包涵体。然后,从血液标本的黄皮毛中提取基因组dna,通过扩增属于无原体属的16S rRNA的1400 bp序列,通过实时PCR筛选无原体感染的存在。最后,对扩增片段进行测序和BLAST分析,用于阳性标本的系统发育评估。结果:共9只犬(3.60%),其中母犬5只(3.40%),公犬4只(3.88%),实时PCR检测无原体感染阳性。此外,在血涂片观察中,3只PCR阳性动物的中性粒细胞中检出了嗜吞噬细胞芽胞杆菌。结论:本研究为了解伊朗等国犬类嗜吞噬细胞芽胞杆菌及其与人犬类病原菌的遗传同源/异质性程度提供了重要资料。据我们所知,这是该地区收容犬感染嗜吞噬单胞杆菌的第一个分子证据。
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来源期刊
Iranian Journal of Medical Microbiology
Iranian Journal of Medical Microbiology Medicine-Infectious Diseases
CiteScore
1.60
自引率
0.00%
发文量
70
审稿时长
8 weeks
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