Almeida-Silva Fernando, Rabello Vanessa Brito de Souza, Scramignon-Costa Bruno de Souza, Zancopé-Oliveira Rosely Maria, de Macedo Priscila Marques, Almeida-Paes Rodrigo
Laboratório de Micologia, Instituto Nacional de Infectologia Evandro Chagas, Fundação Oswaldo Cruz, Rio de Janeiro 21040-900, Brazil.
Laboratório de Pesquisa Clínica em Dermatologia Infeciosa, Instituto Nacional de Infectologia Evandro Chagas-Fundação Oswaldo Cruz, Rio de Janeiro 21040-900, Brazil.
J Fungi (Basel). 2022 Jun 4;8(6):604. doi: 10.3390/jof8060604.
In Brazil, sporotrichosis has transitioned from a rural to urban disease, driven by a shift in the initiation of infection from the accidental inoculation of organic matter to the traumatic implantation of the fungus by cats. Since the emergence of zoonotic sporotrichosis caused by , investigations have largely ignored the environmental habitat of the pathogen due to its association with domestic cats. Therefore, we investigated 18 environmental samples collected from rural areas of two cities where zoonotic sporotrichosis is endemic, but where domestic cats are scarce. We utilized traditional culture methods, and samples were also examined with two molecular methods used for the clinical diagnosis of sporotrichosis: a nested-PCR targeting the ITS region and a species-specific PCR targeting the calmodulin gene. No colonies were identified by traditional culture methods. However, the nested-PCR and the species-specific PCR for were positive for 18 and 5 samples, respectively. Sequencing revealed that positive results with the nested-PCR were due to non-specific amplification of other Ophiostomatales DNA, rather than spp. Three of the five amplicons from the species-specific PCR were suitable for sequencing and confirmed the presence of DNA. Hence, we confirmed that , as with other species, has an environmental habitat. Our findings underscore the challenges of nested-PCR for environmental studies and highlight that sequencing must follow PCR protocols to definitively identify spp. in environmental samples.
在巴西,孢子丝菌病已从一种农村疾病转变为城市疾病,这是由感染起始方式的转变所驱动的,即从有机物的意外接种转变为猫造成的真菌创伤性植入。自从由[某种病原体]引起的人畜共患孢子丝菌病出现以来,由于其与家猫的关联,调查在很大程度上忽略了该病原体的环境栖息地。因此,我们调查了从两个人畜共患孢子丝菌病流行但家猫稀少的城市农村地区采集的18份环境样本。我们采用传统培养方法,并且还用两种用于孢子丝菌病临床诊断的分子方法对样本进行了检测:一种靶向ITS区域的巢式PCR和一种靶向钙调蛋白基因的种特异性PCR。通过传统培养方法未鉴定出任何菌落。然而,巢式PCR和针对[某种病原体]的种特异性PCR分别对18份和5份样本呈阳性。测序显示,巢式PCR的阳性结果是由于其他长喙壳目DNA的非特异性扩增,而非[某种病原体]属。种特异性PCR的五个扩增子中有三个适合测序,并证实了[某种病原体]DNA的存在。因此,我们证实,与其他[某种病原体]物种一样,[某种病原体]具有环境栖息地。我们的研究结果强调了巢式PCR用于[某种病原体]环境研究面临的挑战,并突出表明测序必须遵循PCR方案才能明确鉴定环境样本中的[某种病原体]属。