首页> 外文期刊>Photodermatology, photoimmunology and photomedicine >Ultraviolet radiation enhances both the nodular and ulcerative forms of Mycobacterium ulcerans infection in a Crl:IAF(HA)-hrBR hairless guinea pig model of Buruli ulcer disease.
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Ultraviolet radiation enhances both the nodular and ulcerative forms of Mycobacterium ulcerans infection in a Crl:IAF(HA)-hrBR hairless guinea pig model of Buruli ulcer disease.

机译:紫外线辐射可在布鲁氏溃疡病的Crl:IAF(HA)-hrBR无毛豚鼠模型中增强溃疡分支杆菌感染的结节和溃疡形式。

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BACKGROUND: Ultraviolet radiation (UV) pre-exposure enhances intracellular mycobacterial infections, however, its effect upon the pathogenesis of the extracellular Mycobacterium ulcerans parasite had not been previously examined. The hypothesis tested was that UV pre-exposure enhances both the nodular and ulcerative forms of M. ulcerans infection in the Crl:IAF(HA)-hrBR hairless guinea pig. METHODS: Groups of five animals were exposed to total cumulative UV doses of 0 (control), 3 or 30 kJ/m2 followed 3 days later by subcutaneous infection with 3 x 10(4) CFU of M. ulcerans in order to induce the nodular form of the disease. The resultant nodules were then measured for the next 22 days. The experiment was then repeated using intradermal infection with 2 x 10(6) CFU in order to induce the ulcerative form of the disease. The resultant ulcers were measured for the next 30 days. In both experiments, the animals were tested for delayed-type hypersensitivity (DTH) reactivity to Burulin-S as a marker of the onset of the reactive phase of the disease. RESULTS: Following low inoculum subcutaneous infection, distinct, well-demarcated, subcutaneously situated skin nodules were present at infected skin sites between 7 and 22 days post-infection. Between days 14 and 21, the mean nodule diameters of the UV irradiated groups were significantly (P < 0.03) greater than that of the control group. UV pre-exposure resulted in significant (P < 0.035) suppression of DTH responses to Burulin-S challenge. High inoculum intradermal infection resulted in the development of ulcerative lesions. Between 10 and 30 days post-infection, the mean lesion diameters and mean ulcer development times of UV irradiated groups were significantly (P < 0.05) greater than those of the controls. However, UV irradiation did not affect DTH responses to Burulins in the high inoculum experiment. In both experiments, the lesions were histologically consistent with human Buruli ulcer disease. These results demonstrate that UV pre-exposure results in enhanced M. ulcerans infection in the hairless guinea pig model of Buruli ulcer disease and suggest that UV exposure may be a relevant factor in the pathogenesis of human forms of the disease.
机译:背景:紫外线(UV)预暴露可增强细胞内分枝杆菌感染,但是,其对细胞外分枝杆菌溃疡性寄生虫发病机理的影响以前尚未进行过检查。测试的假设是紫外线预暴露可增强Crl:IAF(HA)-hrBR无毛豚鼠的溃疡分枝杆菌感染的结节性和溃疡性形式。方法:将五只动物的组暴露于总累积紫外线剂量为0(对照),3或30 kJ / m2,然后三天后皮下感染3 x 10(4)CFU溃疡分支杆菌,以诱导结节状疾病的形式。然后在接下来的22天中测量所得结节。然后使用2 x 10(6)CFU的皮内感染重复该实验,以诱导该疾病的溃疡性形式。在接下来的30天中测量由此产生的溃疡。在两个实验中,测试动物对Burulin-S的迟发型超敏反应(DTH)反应性,以此作为疾病反应期发作的标志。结果:在低接种量皮下感染后,感染后7到22天之间,受感染的皮肤部位出现了明显的,划定的,皮下定位的皮肤结节。在第14天和第21天之间,紫外线照射组的平均结节直径显着(P <0.03)比对照组大。紫外线预暴露导致DTH对Burulin-S攻击的反应显着(P <0.035)抑制。高接种量的皮内感染导致溃疡性病变的发展。感染后10到30天之间,紫外线照射组的平均病变直径和平均溃疡形成时间显着(P <0.05)大于对照组。但是,在高接种量实验中,紫外线照射不会影响DTH对Burulins的反应。在两个实验中,病变在组织学上与人布鲁里溃疡病一致。这些结果表明,紫外线预暴露在布鲁里溃疡病的无毛豚鼠模型中导致溃疡分枝杆菌感染的增强,并且表明紫外线暴露可能是该疾病人型发病机理的相关因素。

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