Norris Michael H, Kang Yun, Lu Diana, Wilcox Bruce A, Hoang Tung T
Department of Microbiology, University of Hawaii at Manoa, Honolulu, Hawaii 96822, USA.
Appl Environ Microbiol. 2009 Oct;75(19):6062-75. doi: 10.1128/AEM.00820-09. Epub 2009 Jul 31.
Genetic manipulation of the category B select agents Burkholderia pseudomallei and Burkholderia mallei has been stifled due to the lack of compliant selectable markers. Hence, there is a need for additional select-agent-compliant selectable markers. We engineered a selectable marker based on the gat gene (encoding glyphosate acetyltransferase), which confers resistance to the common herbicide glyphosate (GS). To show the ability of GS to inhibit bacterial growth, we determined the effective concentrations of GS against Escherichia coli and several Burkholderia species. Plasmids based on gat, flanked by unique flip recombination target (FRT) sequences, were constructed for allelic-replacement. Both allelic-replacement approaches, one using the counterselectable marker pheS and the gat-FRT cassette and one using the DNA incubation method with the gat-FRT cassette, were successfully utilized to create deletions in the asd and dapB genes of wild-type B. pseudomallei strains. The asd and dapB genes encode an aspartate-semialdehyde dehydrogenase (BPSS1704, chromosome 2) and dihydrodipicolinate reductase (BPSL2941, chromosome 1), respectively. Mutants unable to grow on media without diaminopimelate (DAP) and other amino acids of this pathway were PCR verified. These mutants displayed cellular morphologies consistent with the inability to cross-link peptidoglycan in the absence of DAP. The B. pseudomallei 1026b Deltaasd::gat-FRT mutant was complemented with the B. pseudomallei asd gene on a site-specific transposon, mini-Tn7-bar, by selecting for the bar gene (encoding bialaphos/PPT resistance) with PPT. We conclude that the gat gene is one of very few appropriate, effective, and beneficial compliant markers available for Burkholderia select-agent species. Together with the bar gene, the gat cassette will facilitate various genetic manipulations of Burkholderia select-agent species.
由于缺乏符合要求的选择标记,对B类选择病原体类鼻疽伯克霍尔德菌和鼻疽伯克霍尔德菌的基因操作受到了阻碍。因此,需要更多符合选择病原体要求的选择标记。我们基于gat基因(编码草甘膦乙酰转移酶)设计了一个选择标记,该标记赋予对常用除草剂草甘膦(GS)的抗性。为了证明GS抑制细菌生长的能力,我们测定了GS对大肠杆菌和几种伯克霍尔德菌属细菌的有效浓度。构建了基于gat基因且两侧带有独特的翻转重组靶点(FRT)序列的质粒用于等位基因替换。两种等位基因替换方法,一种使用反选择标记pheS和gat-FRT盒,另一种使用带有gat-FRT盒的DNA孵育方法,均成功用于在野生型类鼻疽伯克霍尔德菌菌株的asd和dapB基因中产生缺失。asd和dapB基因分别编码天冬氨酸-半醛脱氢酶(BPSS1704,位于2号染色体)和二氢吡啶二羧酸还原酶(BPSL2941,位于1号染色体)。通过PCR验证了在不含二氨基庚二酸(DAP)和该途径其他氨基酸的培养基上无法生长的突变体。这些突变体显示出的细胞形态与在缺乏DAP时无法交联肽聚糖一致。通过用草丁膦选择bar基因(编码bialaphos/PPT抗性),用位点特异性转座子mini-Tn7-bar上的类鼻疽伯克霍尔德菌asd基因对类鼻疽伯克霍尔德菌1026b Deltaasd::gat-FRT突变体进行了互补。我们得出结论,gat基因是可用于伯克霍尔德菌属选择病原体物种的极少数合适、有效且有益的符合要求的标记之一。与bar基因一起,gat盒将促进伯克霍尔德菌属选择病原体物种的各种基因操作。