Tillack Manuela, Biller Laura, Irmer Henriette, Freitas Michelle, Gomes Maria A, Tannich Egbert, Bruchhaus Iris
Bernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
BMC Genomics. 2007 Jun 14;8:170. doi: 10.1186/1471-2164-8-170.
A number of studies have shown that peptidases and in particular cysteine peptidases constitute major pathogenicity factors in Entamoeba histolytica. Recent studies have suggested that a considerable number of genes coding for proteolytic enzymes are present within the E. histolytica genome and questions remain about the mode of expression of the various molecules.
By homology search within the recently published amoeba genome, we identified a total of 86 E. histolytica genes coding for putative peptidases, including 46 recently described peptidase genes. In total these comprise (i) 50 cysteine peptidases of different families but most of which belong to the C1 papain superfamily, (ii) 22 different metallo peptidases from at least 11 different families, (iii) 10 serine peptidases belonging to 3 different families, and (iv) 4 aspartic peptidases of only one family. Using an oligonucleotide microarray, peptidase gene expression patterns of 7 different E. histolytica isolates as well as of heat stressed cells were analysed. A total of 21 out of 79 amoeba peptidase genes analysed were found to be significantly expressed under standard axenic culture conditions whereas the remaining are not expressed or at very low levels only. In heat-stressed cells the expression of 2 and 3 peptidase genes, respectively, were either decreased or increased. Only minor differences were observed between the various isolates investigated, despite the fact that these isolates were originated from asymptomatic individuals or from patients with various forms of amoebic diseases.
Entamoeba histolytica possesses a large number of genes coding for proteolytic enzymes. Under standard culture conditions or upon heat-stress only a relatively small number of these genes is significantly expressed and only very few variations become apparent between various clinical E. histolytica isolates, calling into question the importance of these enzymes in E. histolytica pathogenicity. Further studies are required to define the precise role of most of the proteolytic enzyme for amoeba cell biology but in particular for E. histolytica virulence.
多项研究表明,肽酶尤其是半胱氨酸肽酶是溶组织内阿米巴的主要致病因素。近期研究表明,溶组织内阿米巴基因组中存在大量编码蛋白水解酶的基因,而各种分子的表达模式仍存在疑问。
通过在最近公布的阿米巴基因组中进行同源性搜索,我们共鉴定出86个溶组织内阿米巴基因,这些基因编码假定的肽酶,其中包括46个最近描述的肽酶基因。这些基因总共包括:(i)50种不同家族的半胱氨酸肽酶,但大多数属于C1木瓜蛋白酶超家族;(ii)来自至少11个不同家族的22种不同的金属肽酶;(iii)属于3个不同家族的10种丝氨酸肽酶;(iv)仅一个家族的4种天冬氨酸肽酶。使用寡核苷酸微阵列,分析了7种不同的溶组织内阿米巴分离株以及热应激细胞的肽酶基因表达模式。在分析的79个阿米巴肽酶基因中,共有21个在标准无菌培养条件下显著表达,而其余基因不表达或仅以极低水平表达。在热应激细胞中,分别有2个和3个肽酶基因的表达降低或增加。尽管这些分离株来自无症状个体或患有各种形式阿米巴病的患者,但在所研究的各种分离株之间仅观察到微小差异。
溶组织内阿米巴拥有大量编码蛋白水解酶的基因。在标准培养条件下或热应激时,这些基因中只有相对较少的一部分显著表达,并且在各种临床溶组织内阿米巴分离株之间仅出现极少数差异,这使人质疑这些酶在溶组织内阿米巴致病性中的重要性。需要进一步研究来确定大多数蛋白水解酶在阿米巴细胞生物学中,特别是在溶组织内阿米巴毒力方面的确切作用。