Waters Paulette F, Snowden Karen F, Holman Patricia J
Department of Veterinary Pathobiology, The Texas Veterinary Medical Center, Texas A&M University, College Station, TX 77843-4467, USA.
Parasitol Res. 2004 Aug;93(5):410-8. doi: 10.1007/s00436-004-1148-y. Epub 2004 Jun 25.
Encephalitozoon cuniculi and E. hellem are often recognized as the agents of human microsporidiosis, but less than optimal therapy is available for treatment. The identification of enzymes critical to the parasitic life cycle is an important step in finding targets for potential drug development. Aminopeptidase gene sequences were obtained from cDNA and gDNA from avian and human E. hellem isolates and from a rabbit E. cuniculi isolate. At the amino acid level, the aminopeptidase sequences from the E. hellem human and bird isolates share >99% identity and are nearly 70% identical with the E. cuniculi sequence. Conserved HEXXH and GAMEN motifs classify the predicted aminopeptidase in the MA clan of the M1 family. The obtained aminopeptidase gene sequences are likely homologous to the previously reported E. cuniculi glutamyl aminopeptidase. The conservation of this aminopeptidase between species and divergence from mammalian aminopeptidases indicate that this enzyme may be a valid target for drug therapy.
兔脑炎微孢子虫和海伦脑炎微孢子虫常被认为是人类微孢子虫病的病原体,但目前可用的治疗方法并不理想。鉴定对寄生虫生命周期至关重要的酶是寻找潜在药物开发靶点的重要一步。从鸟类和人类海伦脑炎微孢子虫分离株以及兔脑炎微孢子虫分离株的cDNA和gDNA中获得了氨肽酶基因序列。在氨基酸水平上,人类和鸟类海伦脑炎微孢子虫分离株的氨肽酶序列具有>99%的同一性,与兔脑炎微孢子虫序列的同一性接近70%。保守的HEXXH和GAMEN基序将预测的氨肽酶归类为M1家族MA族。获得的氨肽酶基因序列可能与先前报道的兔脑炎微孢子虫谷氨酰胺氨肽酶同源。该氨肽酶在物种间的保守性以及与哺乳动物氨肽酶的差异表明,这种酶可能是药物治疗的有效靶点。