Bricker J, Mulks M, Moxon E R, Plaut A G, Wright A
Infect Immun. 1985 Feb;47(2):370-4. doi: 10.1128/iai.47.2.370-374.1985.
The structural gene for immunoglobulin A protease (iga) from Haemophilus influenzae serotype d was cloned in pBR322. The gene was used as a probe for Southern hybridization analysis of chromosomal DNA from the five other H. influenzae serotypes (a, b, c, e, and f). In most cases strains from a single serotype exhibited a distinct pattern of restriction fragment(s) homologous to the iga gene probe which was unique for that serotype. Serotype f strains were unique in that they gave two distinct patterns of homologous restriction fragments which correlated well with the production of two different protease types by members of this group. An iga mutant of H. influenzae serotype d was isolated by introducing a 4-base-pair insertion into the cloned iga gene and using the altered DNA for transformation of an H. influenzae recipient. The resulting iga- mutant produced no immunoglobulin A protease but was otherwise indistinguishable from its iga+ parent in growth characteristics. Transformation of mutant cells with chromosomal DNA isolated from either a serotype d or a serotype c strain gave rise to iga+ transformants. Those obtained with serotype d DNA produced a type 1 protease, whereas those obtained with serotype c DNA produced either a type 1 protease (characteristic of serotype d) or a type 2 protease (characteristic of serotype c). Southern analysis of the latter transformants, using the iga gene probe, indicated that the type 1 transformants had a serotype d pattern of restriction fragments whereas the type 2 transformants had either a serotype c or a novel pattern of restriction fragments. These results indicate that there is considerable homology between the iga genes of the various serotypes and that the homologous sequences identified with the serotype d probe are the immunoglobulin A protease-coding sequences in each case.
将来自d型流感嗜血杆菌的免疫球蛋白A蛋白酶(iga)的结构基因克隆到pBR322中。该基因用作探针,对其他五种流感嗜血杆菌血清型(a、b、c、e和f)的染色体DNA进行Southern杂交分析。在大多数情况下,来自单一血清型的菌株表现出与iga基因探针同源的独特限制性片段模式,该模式对该血清型而言是独一无二的。f血清型菌株的独特之处在于,它们产生两种不同的同源限制性片段模式,这与该组菌株产生两种不同类型的蛋白酶密切相关。通过在克隆的iga基因中引入一个4碱基对的插入片段,并使用改变后的DNA转化流感嗜血杆菌受体,分离出了d型流感嗜血杆菌的iga突变体。产生的iga-突变体不产生免疫球蛋白A蛋白酶,但在生长特性方面与它的iga+亲本没有区别。用从d血清型或c血清型菌株中分离的染色体DNA转化突变细胞,产生了iga+转化体。用d血清型DNA获得的转化体产生1型蛋白酶,而用c血清型DNA获得的转化体产生1型蛋白酶(d血清型的特征)或2型蛋白酶(c血清型的特征)。使用iga基因探针对后一种转化体进行Southern分析表明,1型转化体具有d血清型的限制性片段模式,而2型转化体具有c血清型或一种新的限制性片段模式。这些结果表明,各种血清型的iga基因之间存在相当大的同源性,并且用d血清型探针鉴定的同源序列在每种情况下都是免疫球蛋白A蛋白酶编码序列。