Gil-Lamaignere Cristina, Roilides Emmanuel, Lyman Caron A, Simitsopoulou Maria, Stergiopoulou Theodouli, Maloukou Avgi, Walsh Thomas J
Third Pediatric Department, Aristotle University, Thessaloniki, Greece 54642.
Infect Immun. 2003 Nov;71(11):6472-8. doi: 10.1128/IAI.71.11.6472-6478.2003.
Scedosporium apiospermum (Pseudallescheria boydii) is an emerging opportunistic filamentous fungus that causes serious infections in both immunocompetent and immunocompromised patients. To gain insight into the immunopathogenesis of infections due to S. apiospermum, the antifungal activities of human polymorphonuclear leukocytes (PMNs), mononuclear leukocytes (MNCs), and monocyte-derived macrophages (MDMs) against two clinical isolates of S. apiospermum were evaluated. Isolate SA54A was amphotericin B resistant and was the cause of a fatal disseminated infection. Isolate SA1216 (cultured from a successfully treated localized subcutaneous infection) was susceptible to amphotericin B. MDMs exhibited similar phagocytic activities against conidia of both isolates. However, PMNs and MNCs responded differently to the hyphae of these two isolates. Serum opsonization of hyphae resulted in a higher level of superoxide anion (O(2)(-)) release by PMNs in response to SA54A (amphotericin B resistant) than that seen in response to SA1216 (amphotericin B susceptible; P < 0.001). Despite this increased O(2)(-) production, PMNs and MNCs induced less hyphal damage to SA54A than to SA1216 (P < 0.001). To investigate the potential mechanisms responsible for these differences, hyphal damage was evaluated in the presence of antifungal oxidative metabolites as well as in the presence of a series of inhibitors and scavengers of antifungal PMN function. Mannose, catalase, superoxide dismutase, dimethyl sulfoxide, and heparin had no effect on PMN-induced hyphal damage to either of the two isolates. However, azide, which inhibits PMN myeloperoxidase activity, significantly reduced hyphal damage to SA1216 (P < 0.01) but not to SA54A. Hyphae of SA1216 were slightly more susceptible to oxidative pathway products, particularly HOCl, than those of SA54A. Thus, S. apiospermum is susceptible to antifungal phagocytic function to various degrees. The selective inhibitory pattern of azide with respect to hyphal damage and the parallel susceptibility to HOCl suggests an important difference in susceptibilities to myeloperoxidase products that may be related to the various levels of pathogenicity and amphotericin B resistance of S. apiospermum.
阿氏丝孢霉(波氏假阿利什霉)是一种新出现的机会致病性丝状真菌,可在免疫功能正常和免疫功能低下的患者中引起严重感染。为深入了解阿氏丝孢霉感染的免疫发病机制,评估了人类多形核白细胞(PMN)、单核白细胞(MNC)和单核细胞衍生巨噬细胞(MDM)对两株阿氏丝孢霉临床分离株的抗真菌活性。分离株SA54A对两性霉素B耐药,是一例致命播散性感染的病因。分离株SA1216(从成功治疗的局限性皮下感染中培养获得)对两性霉素B敏感。MDM对两株分离株的分生孢子表现出相似的吞噬活性。然而,PMN和MNC对这两株分离株的菌丝反应不同。菌丝的血清调理作用导致PMN对SA54A(两性霉素B耐药)释放的超氧阴离子(O₂⁻)水平高于对SA1216(两性霉素B敏感;P < 0.001)的反应。尽管O₂⁻产生增加,但PMN和MNC对SA54A的菌丝损伤比对SA1216的损伤小(P < 0.001)。为研究造成这些差异的潜在机制,在存在抗真菌氧化代谢产物以及一系列抗真菌PMN功能抑制剂和清除剂的情况下评估了菌丝损伤。甘露糖、过氧化氢酶、超氧化物歧化酶、二甲基亚砜和肝素对PMN诱导的两株分离株中任何一株的菌丝损伤均无影响。然而,抑制PMN髓过氧化物酶活性的叠氮化物显著降低了对SA1216的菌丝损伤(P < 0.01),但对SA54A没有影响。SA1216的菌丝比SA54A的菌丝对氧化途径产物,特别是次氯酸(HOCl)稍更敏感。因此,阿氏丝孢霉对抗真菌吞噬功能有不同程度的敏感性。叠氮化物对菌丝损伤的选择性抑制模式以及对HOCl的平行敏感性表明,对髓过氧化物酶产物的敏感性存在重要差异,这可能与阿氏丝孢霉的不同致病水平和两性霉素B耐药性有关。