Sanguinetti Maurizio, Posteraro Brunella, La Sorda Marilena, Torelli Riccardo, Fiori Barbara, Santangelo Rosaria, Delogu Giovanni, Fadda Giovanni
Istituto di Microbiologia, Università Cattolica del Sacro Cuore, Largo F. Vito 1, Rome 00168, Italy.
Infect Immun. 2006 Feb;74(2):1352-9. doi: 10.1128/IAI.74.2.1352-1359.2006.
We have recently demonstrated that upregulation of the ATP binding cassette (ABC) transporter-encoding gene AFR1 in Cryptococcus neoformans is involved in the in vitro resistance to fluconazole of this yeast. In the present study, we investigated the role of AFR1 in the in vivo response to fluconazole in a mouse model of systemic cryptococcosis. Mice were infected with a wild-type fluconazole-susceptible strain of C. neoformans, strain BPY22; an afr1 mutant, BPY444, which displayed hypersusceptibility to fluconazole in vitro; or an AFR1-overexpressing strain, BPY445, which exhibited in vitro resistance to the drug. In each of the three groups, infected animals were randomly assigned to fluconazole treatment or untreated-control subgroups. As expected, fluconazole prolonged survival and reduced fungal tissue burdens (compared with no treatment) in BPY22- and BPY444-infected mice, whereas it had no significant effects in mice infected with BPY445. When the pathogenicities of these strains in mice were investigated, strain BPY445 was significantly more virulent than BPY22 following inhalational or intravenous inoculation, but mice infected with BPY444 survived significantly longer than BPY22-infected animals only when infection was acquired via the respiratory tract. In in vitro macrophage infection studies, strain BPY445 also displayed enhanced intracellular survival compared with strains BPY22 and BPY444, suggesting that its increased virulence may be due to its reduced vulnerability to the antimicrobial factors produced by phagocytic cells. These findings indicate that the upregulation of the AFR1 gene is an important factor in either determining the in vivo resistance to fluconazole or influencing the virulence of C. neoformans.
我们最近证明,新型隐球菌中ATP结合盒(ABC)转运蛋白编码基因AFR1的上调与该酵母对氟康唑的体外耐药性有关。在本研究中,我们在系统性隐球菌病小鼠模型中研究了AFR1在体内对氟康唑反应中的作用。用野生型对氟康唑敏感的新型隐球菌菌株BPY22、体外对氟康唑高度敏感的afr1突变体BPY444或对该药物表现出体外耐药性的AFR1过表达菌株BPY445感染小鼠。在这三组中的每组中,将感染动物随机分配至氟康唑治疗组或未治疗对照组亚组。正如预期的那样,氟康唑延长了BPY22和BPY444感染小鼠的存活时间并降低了真菌组织负荷(与未治疗相比),而对BPY445感染的小鼠没有显著影响。当研究这些菌株在小鼠中的致病性时,吸入或静脉接种后,BPY445菌株的毒性明显高于BPY22,但仅在通过呼吸道感染时,感染BPY444的小鼠比感染BPY22的动物存活时间明显更长。在体外巨噬细胞感染研究中,与BPY22和BPY444菌株相比,BPY445菌株在细胞内存活能力也增强,这表明其毒力增加可能是由于其对吞噬细胞产生的抗菌因子的敏感性降低。这些发现表明,AFR1基因的上调是决定体内对氟康唑耐药性或影响新型隐球菌毒力的重要因素。