Fowler Elizabeth V, Peters Jennifer M, Gatton Michelle L, Chen Nanhua, Cheng Qin
Malaria Laboratory, Infectious Diseases Unit, The Queensland Institute of Medical Research, P.O. Royal Brisbane Hospital, Queensland 4029, Australia.
Mol Biochem Parasitol. 2002 Mar;120(1):117-26. doi: 10.1016/s0166-6851(01)00443-1.
In Plasmodium falciparum a highly polymorphic multi-copy gene family, var, encodes the variant surface antigen P. falciparum erythrocyte membrane protein 1 (PfEMP1), which has an important role in cytoadherence and immune evasion. Using previously described universal PCR primers for the first Duffy binding-like domain (DBLalpha) of var we analysed the DBLalpha repertoires of Dd2 (originally from Thailand) and eight isolates from the Solomon Islands (n=4), Philippines (n=2), Papua New Guinea (n=1) and Africa (n=1). We found 15-32 unique DBLalpha sequence types among these isolates and estimated detectable DBLalpha repertoire sizes ranging from 33-38 to 52-57 copies per genome. Our data suggest that var gene repertoires generally consist of 40-50 copies per genome. Eighteen DBLalpha sequences appeared in more than one Asia-Pacific isolate with the number of sequences shared between any two isolates ranging from 0 to 6 (mean=2.0 +/-1.6). At the amino acid level DBLalpha sequence similarity within isolates ranged from 45.2 +/- 7.1 to 50.2 +/- 6.9%, and was not significantly different from the DBLalpha amino acid sequence similarity among isolates (P>0.1). Comparisons with published sequences also revealed little overlap among DBLalpha sequences from different regions. High DBLalpha sequence diversity and minimal overlap among these isolates suggest that the global var gene repertoire is immense, and may potentially be selected for by the host's protective immune response to the var gene products, PfEMP1.
在恶性疟原虫中,一个高度多态的多拷贝基因家族——var基因家族,编码变异表面抗原恶性疟原虫红细胞膜蛋白1(PfEMP1),该蛋白在细胞黏附和免疫逃避中起重要作用。我们使用先前描述的针对var基因第一个达菲结合样结构域(DBLα)的通用PCR引物,分析了Dd2(最初来自泰国)以及来自所罗门群岛(n = 4)、菲律宾(n = 2)、巴布亚新几内亚(n = 1)和非洲(n = 1)的8个分离株的DBLα基因库。我们在这些分离株中发现了15 - 32种独特的DBLα序列类型,并估计每个基因组中可检测到的DBLα基因库大小在33 - 38到52 - 57个拷贝之间。我们的数据表明,var基因库通常每个基因组由40 - 50个拷贝组成。18种DBLα序列出现在不止一个亚太地区分离株中,任意两个分离株之间共享的序列数量在0到6之间(平均值 = 2.0 ±1.6)。在氨基酸水平上,分离株内DBLα序列的相似性在45.2 ± 7.1%到50.2 ± 6.9%之间,与分离株之间DBLα氨基酸序列的相似性没有显著差异(P>0.1)。与已发表序列的比较还显示,不同区域的DBLα序列之间几乎没有重叠。这些分离株中高DBLα序列多样性和最小重叠表明,全球var基因库非常庞大,并且可能会被宿主对var基因产物PfEMP1的保护性免疫反应所选择。