Can Hüseyin, Döşkaya Mert, Özdemir H Gökhan, Şahar Esra Atalay, Karakavuk Muhammet, Pektaş Bayram, Karakuş Mehmet, Töz Seray, Caner Ayşe, Döşkaya Aysu Değirmenci, İz Sultan Gülce, Özbel Yusuf, Gürüz Yüksel
Ege University Faculty of Science, Department of Biology, Molecular Biology Section, Bornova, İzmir, Turkey.
Ege University Faculty of Medicine, Department of Parasitology, Bornova, İzmir, Turkey.
Exp Parasitol. 2016 Aug;167:109-14. doi: 10.1016/j.exppara.2016.05.011. Epub 2016 May 31.
Leishmaniasis caused by more than 20 species of genus Leishmania is transmitted by the bite of infected phlebotomine sand flies. The studies on Leishmania infection in cats is very few in Turkey and therefore we aimed to screen stray cats living in city of İzmir located in western Turkey using nested PCR targeting kinetoplast DNA and serological techniques (ELISA and IFA). Leishmania DNA positive samples were also studied by ITS1 real time PCR. Whole blood and serum samples were obtained from stray cats (n: 1101) living in different counties of İzmir. In serological assays, a serum sample was considered positive in 1:40 dilution in IFA and for ELISA a serum sample was accepted positive when the absorbance value (AV) exceeded the mean AV + Standard Deviation (SD) of the negative control serum samples. According to the results, the seropositivity rates were 10.8% (119/1101) and 15.2% (167/1101) by in house ELISA and IFA, respectively. Among serology coherent samples, the seropositivity rate was 11.1% (116/1047) as detected by both assays after discordant samples (n: 54) were discarded. Of the 1101 stray cats, six (0.54%) were positive by nested PCR while only one of these six samples was positive by ITS1 real time PCR. During PCR, three controls designated as Leishmania infantum, Leishmania tropica, and Leishmania major were used for species identification. According to nested PCR results, L. tropica was identified in two cats (no.76 and 95). In another cat (no. 269), there were two bands in which one of them was well-matched with L. infantum and the other band had ∼850 bp size which does not match with any controls. Remaining three cats (no. 86, 514, and 622) also had the ∼850 bp atypical band size. ITS1 real time PCR detected L. tropica in only one cat (no. 622) which showed an atypical band size in nested PCR. These results indicated that three cats with only one atypical band (no. 86, 514, and 622) and the cat with mixed infection (no. 269) were infected with L. tropica. Altogether, L. tropica was detected in all six DNA positive cats and L. infantum was detected in one cat with mixed infection. In conclusion, although the reservoir role of cats in nature is still unclear the high seroprevalence rate against Leishmania parasites and detecting parasite DNA in stray cats in İzmir indicates that the stray cats are frequently bitten by infected sand flies. Further research activities are required to reveal the frequency of leishmaniasis in cats in different regions of Turkey where Leishmania species are endemic.
由20多种利什曼原虫属物种引起的利什曼病通过受感染的白蛉叮咬传播。在土耳其,关于猫感染利什曼原虫的研究非常少,因此我们旨在使用针对动基体DNA的巢式PCR和血清学技术(ELISA和IFA),对生活在土耳其西部伊兹密尔市的流浪猫进行筛查。对利什曼原虫DNA阳性样本也采用ITS1实时PCR进行研究。从生活在伊兹密尔不同县的流浪猫(n = 1101)中采集全血和血清样本。在血清学检测中,IFA检测时血清样本在1:40稀释度下被视为阳性,ELISA检测时当吸光度值(AV)超过阴性对照血清样本的平均AV + 标准差(SD)时,血清样本被判定为阳性。根据结果,内部ELISA和IFA检测的血清阳性率分别为10.8%(119/1101)和15.2%(167/1101)。在血清学结果一致的样本中,排除不一致样本(n = 54)后,两种检测方法检测到的血清阳性率为11.1%(116/1047)。在1101只流浪猫中,6只(0.54%)通过巢式PCR检测为阳性,而这6个样本中只有1个通过ITS1实时PCR检测为阳性。在PCR过程中,使用了三个分别指定为婴儿利什曼原虫、热带利什曼原虫和硕大利什曼原虫的对照品进行物种鉴定。根据巢式PCR结果,在两只猫(编号76和95)中鉴定出热带利什曼原虫。在另一只猫(编号269)中,有两条条带,其中一条与婴儿利什曼原虫匹配良好,另一条条带大小约为850 bp,与任何对照品都不匹配。其余三只猫(编号86、514和622)也有大小约为850 bp的非典型条带。ITS1实时PCR仅在一只猫(编号622)中检测到热带利什曼原虫,这只猫在巢式PCR中显示出非典型条带大小。这些结果表明,三只只有一条非典型条带的猫(编号86、514和622)以及一只混合感染的猫(编号269)感染了热带利什曼原虫。总共,在所有六只DNA阳性猫中检测到热带利什曼原虫,在一只混合感染的猫中检测到婴儿利什曼原虫。总之,虽然猫在自然界中的储存宿主作用仍不清楚,但伊兹密尔流浪猫中针对利什曼原虫的高血清阳性率以及检测到寄生虫DNA表明,流浪猫经常被受感染的白蛉叮咬。需要进一步开展研究活动,以揭示在利什曼原虫物种流行的土耳其不同地区猫利什曼病的发病频率。