Altay Kursat, Coskun Alparslan, Erol Ufuk, Sahin Omer Faruk, Turk Sefer
Department of Parasitology, Faculty of Veterinary Medicine, Sivas Cumhuriyet University, 58140 Sivas, Türkiye.
Department of Internal Medicine, Faculty of Veterinary Medicine, Sivas Cumhuriyet University, 58140 Sivas, Türkiye.
Parasitol Int. 2025 Feb;104:102969. doi: 10.1016/j.parint.2024.102969. Epub 2024 Sep 12.
Three hemoplasma species, Mycoplasma haemofelis, Candidatus Mycoplasma haemominutum, and Candidatus Mycoplasma turicensis, have been identified in domestic and wild felids. M. haemofelis may cause severe clinical manifestations in domestic cats, whereas others can lead to mild infections. Identification of these pathogens is done using molecular diagnostic tools like conventional-PCR or real-time PCR. However, these have disadvantages, such as the failure to differentiate species or high cost. This study aimed to develop a triplex-PCR method for the diagnosis and discrimination of feline hemoplasma species. Furthermore, it is aimed at providing molecular data on the epidemiology of feline hemoplasma species in Türkiye, where there is a paucity of information on these pathogens. Triplex-PCR primers amplifying the 16S rRNA gene regions of M. haemofelis (1022 bp), Ca. Mycoplasma haemominutum (607 bp), and Ca. Mycoplasma turicensis (456 bp) species were designed and optimized. Moreover, the detection limits of the method were also determined and it was found that the primers could detect 0.001 ng/μL amount of DNA for M. haemofelis, 0.0001 ng/μL for Ca. Mycoplasma haemominutum, and 0.0002 ng/μL for Ca. Mycoplasma turicensis in the sample. 286 cat blood samples obtained from Sivas province were researched for feline hemoplasma species. Feline hemoplasma species were detected in samples of 29 out of 286 cats (10.23 %). Five samples (1.74 %) were infected with only M. haemofelis, whereas 22 (7.69 %) were only infected with Ca. Mycoplasma haemominutum. Two samples (0.69 %) were found to be infected with both M. haemofelis and Ca. Mycoplasma haemominutum. Ca. Mycoplasma turicensis was not detected in this study. A triplex-PCR method that can be used for the identification and species differentiation of feline hemoplasma species in hosts was developed. Moreover, hemoplasma species were found to be circulating in cats in the study area, and it is recommended that veterinarians and animal owners take the necessary precautions to protect themselves and their cats from these pathogens.
在 domestic 和 wild felids 中已鉴定出三种血支原体物种,即溶血支原体(Mycoplasma haemofelis)、嗜吞噬细胞无形体(Candidatus Mycoplasma haemominutum)和都柏林无形体(Candidatus Mycoplasma turicensis)。溶血支原体可在家猫中引起严重的临床表现,而其他物种可导致轻度感染。这些病原体的鉴定是使用传统 PCR 或实时 PCR 等分子诊断工具进行的。然而,这些方法存在缺点,如无法区分物种或成本高昂。本研究旨在开发一种用于诊断和区分猫血支原体物种的三重 PCR 方法。此外,旨在提供关于土耳其猫血支原体物种流行病学的分子数据,该国关于这些病原体的信息匮乏。设计并优化了扩增溶血支原体(1022 bp)、嗜吞噬细胞无形体(607 bp)和都柏林无形体(456 bp)物种 16S rRNA 基因区域的三重 PCR 引物。此外,还确定了该方法的检测限,发现引物可检测到样本中溶血支原体的 DNA 量为 0.001 ng/μL,嗜吞噬细胞无形体为 0.0001 ng/μL,都柏林无形体为 0.0002 ng/μL。对从锡瓦斯省采集的 286 份猫血样进行了猫血支原体物种研究。在 286 只猫中的 29 只(10.23%)的样本中检测到猫血支原体物种。5 份样本(1.74%)仅感染了溶血支原体,而 22 份(7.69%)仅感染了嗜吞噬细胞无形体。发现 2 份样本(0.69%)同时感染了溶血支原体和嗜吞噬细胞无形体。本研究未检测到都柏林无形体。开发了一种可用于鉴定宿主中猫血支原体物种并进行物种区分的三重 PCR 方法。此外,在研究区域的猫中发现血支原体物种在传播,建议兽医和动物主人采取必要的预防措施,以保护自己和他们的猫免受这些病原体的侵害。