Zeaki Nikoleta, Susilo Yusak Budi, Pregiel Anna, Rådström Peter, Schelin Jenny
Applied Microbiology, Department of Chemistry, Lund University, Lund 22100, Sweden.
Toxins (Basel). 2015 Dec 9;7(12):5359-76. doi: 10.3390/toxins7124889.
The present study investigates the nature of the link between the staphylococcal enterotoxin A (SEA) gene and the lifecycle of Siphoviridae bacteriophages, including the origin of strain variation regarding SEA production after prophage induction. Five strains representing three different genetic lines of the sea region were studied under optimal and prophage-induced growth conditions and the Siphoviridae lifecycle was followed through the phage replicative form copies and transcripts of the lysogenic repressor, cro. The role of SOS response on prophage induction was addressed through recA transcription in a recA-disruption mutant. Prophage induction was found to increase the abundance of the phage replicative form, the sea gene copies and transcripts and enhance SEA production. Sequence analysis of the sea regions revealed that observed strain variances were related to strain capacity for prophage induction, rather than sequence differences in the sea region. The impact of SOS response activation on the phage lifecycle was demonstrated by the absence of phage replicative form copies in the recA-disruption mutant after prophage induction. From this study it emerges that all aspects of SEA-producing strain, the Siphoviridae phage and the food environment must be considered when evaluating SEA-related hazards.
本研究调查了葡萄球菌肠毒素A(SEA)基因与长尾噬菌体科噬菌体生命周期之间联系的本质,包括原噬菌体诱导后SEA产生的菌株变异起源。在最佳生长条件和原噬菌体诱导生长条件下,研究了代表SEA区域三种不同遗传谱系的五株菌株,并通过噬菌体复制形式拷贝和溶原性阻遏物cro的转录本来追踪长尾噬菌体科的生命周期。通过recA破坏突变体中recA的转录来探讨SOS反应对原噬菌体诱导的作用。发现原噬菌体诱导可增加噬菌体复制形式、SEA基因拷贝和转录本的丰度,并提高SEA的产生。SEA区域的序列分析表明,观察到的菌株差异与原噬菌体诱导能力有关,而非SEA区域的序列差异。原噬菌体诱导后,recA破坏突变体中缺乏噬菌体复制形式拷贝,证明了SOS反应激活对噬菌体生命周期的影响。从这项研究可以看出,在评估与SEA相关的危害时,必须考虑产生SEA的菌株、长尾噬菌体科噬菌体和食品环境的各个方面。