Bui Thuong Thi Huyen, Thongmeesee Kritsada, Wechtaisong Wittawat, Tiawsirisup Sonthaya
Center of Excellence in Animal Vector-Borne Diseases, Veterinary Parasitology Unit, Department of Veterinary Pathology, Faculty of Veterinary Science, Chulalongkorn University, Bangkok, Thailand.
The International Graduate Program of Veterinary Science and Technology, Faculty of Veterinary Science, Chulalongkorn University, Bangkok, Thailand.
J Feline Med Surg. 2025 May;27(5):1098612X251335211. doi: 10.1177/1098612X251335211. Epub 2025 May 28.
ObjectivesThis study examined feline haemoplasmas (, ' Mycoplasma haemominutum' [Mhm] and ' Mycoplasma turicensis') infecting Thai domestic cats, using the 16S and 23S rRNA genes as genetic markers.MethodsBlood samples from 20 cats were obtained from a diagnostic laboratory and nucleic acids were extracted from each sample using a commercial kit. PCR targeting the 16S rRNA gene was used to screen haemoplasmas in the samples. Positive PCR samples were further sequenced using the 16S and 23S rRNA genes. The sequences from each genetic marker were analysed using Nucleotide BLAST, phylogeny and genetic network analyses.ResultsAmong the 20 samples, five were infected with haemoplasmas. In the 16S rRNA gene sequencing, four sequences were assigned to Mhm and the remaining sequence was likely to be a closely related species of Mhm. In the 23S rRNA gene sequencing, four sequences from the same samples used for 16S rRNA gene sequencing were identified as Mhm and one sequence could be a putative novel haemoplasma species closely related to Mhm.Conclusions and relevanceOnly Mhm and its closely related species were identified in this study. Although Mhm has been recognised as a low-virulence parasite, cases of severe anaemia in cats infected with Mhm have been found. Thus, such cases could be confirmed via the analysis of 16S and 23S rRNA genes. Furthermore, molecular detection and genetic analyses of feline haemoplasmas in additional cat blood samples should be conducted using PCR assay and DNA sequencing based on universal primers of 16S rRNA and 23S rRNA genes to enable more specific identification.
目的
本研究以16S和23S rRNA基因作为遗传标记,检测感染泰国家猫的猫血巴尔通体(“微小支原体”[Mhm]和“图氏支原体”)。
方法
从一家诊断实验室获取20只猫的血样,使用商业试剂盒从每个样本中提取核酸。采用针对16S rRNA基因的聚合酶链反应(PCR)筛选样本中的血巴尔通体。对PCR阳性样本进一步进行16S和23S rRNA基因测序。使用核苷酸基本局部比对搜索工具(Nucleotide BLAST)、系统发育分析和遗传网络分析对每个遗传标记的序列进行分析。
结果
在20个样本中,有5个感染了血巴尔通体。在16S rRNA基因测序中,4个序列被鉴定为Mhm,其余序列可能是与Mhm密切相关的物种。在23S rRNA基因测序中,来自用于16S rRNA基因测序的相同样本的4个序列被鉴定为Mhm,1个序列可能是与Mhm密切相关的一种假定新血巴尔通体物种。
结论与意义
本研究仅鉴定出Mhm及其密切相关的物种。尽管Mhm被认为是一种低毒力寄生虫,但已发现感染Mhm的猫出现严重贫血的病例。因此,此类病例可通过16S和23S rRNA基因分析来确诊。此外,应使用基于16S rRNA和23S rRNA基因通用引物的PCR检测和DNA测序,对更多猫血样本中的猫血巴尔通体进行分子检测和遗传分析,以实现更准确的鉴定。