Brooks John F, Mandel Mark J
Department of Microbiology-Immunology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Department of Microbiology-Immunology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA
J Bacteriol. 2016 Sep 9;198(19):2596-607. doi: 10.1128/JB.00037-16. Print 2016 Oct 1.
Bacterial colonization of animal epithelial tissue is a dynamic process that relies on precise molecular communication. Colonization of Euprymna scolopes bobtail squid by Vibrio fischeri bacteria requires bacterial aggregation in host mucus as the symbiont transitions from a planktonic lifestyle in seawater to a biofilm-associated state in the host. We have identified a gene, binK (biofilm inhibitor kinase; VF_A0360), which encodes an orphan hybrid histidine kinase that negatively regulates the V. fischeri symbiotic biofilm (Syp) in vivo and in vitro We identified binK mutants as exhibiting a colonization advantage in a global genetic screen, a phenotype that we confirmed in controlled competition experiments. Bacterial biofilm aggregates in the host are larger in strains lacking BinK, whereas overexpression of BinK suppresses biofilm formation and squid colonization. Signaling through BinK is required for temperature modulation of biofilm formation at 28°C. Furthermore, we present evidence that BinK acts upstream of SypG, the σ(54)-dependent transcriptional regulator of the syp biofilm locus. The BinK effects are dependent on intact signaling in the RscS-Syp biofilm pathway. Therefore, we propose that BinK antagonizes the signal from RscS and serves as an integral component in V. fischeri biofilm regulation.
Bacterial lifestyle transitions underlie the colonization of animal hosts from environmental reservoirs. Formation of matrix-enclosed, surface-associated aggregates (biofilms) is common in beneficial and pathogenic associations, but investigating the genetic basis of biofilm development in live animal hosts remains a significant challenge. Using the bobtail squid light organ as a model, we analyzed putative colonization factors and identified a histidine kinase that negatively regulates biofilm formation at the host interface. This work reveals a novel in vivo biofilm regulator that influences the transition of bacteria from their planktonic state in seawater to tight aggregates of cells in the host. The study enriches our understanding of biofilm regulation and beneficial colonization by an animal's microbiome.
细菌在动物上皮组织中的定殖是一个依赖精确分子通讯的动态过程。费氏弧菌在短尾乌贼的定殖需要细菌在宿主黏液中聚集,因为共生菌要从海水中的浮游生活方式转变为宿主中与生物膜相关的状态。我们鉴定出一个基因binK(生物膜抑制激酶;VF_A0360),它编码一种孤儿杂合组氨酸激酶,在体内和体外对费氏弧菌的共生生物膜(Syp)起负调控作用。我们在全基因组筛选中鉴定出binK突变体表现出定殖优势,这一表型在对照竞争实验中得到了证实。在缺乏BinK的菌株中,宿主中的细菌生物膜聚集体更大,而BinK的过表达则抑制生物膜形成和乌贼定殖。通过BinK的信号传导是28°C时生物膜形成温度调节所必需的。此外,我们提供证据表明BinK在SypG上游起作用,SypG是syp生物膜基因座的σ(54)依赖性转录调节因子。BinK的作用依赖于RscS-Syp生物膜途径中完整的信号传导。因此,我们提出BinK拮抗来自RscS的信号,并作为费氏弧菌生物膜调节的一个组成部分。
细菌生活方式的转变是动物宿主从环境储库中定殖的基础。形成被基质包围的、与表面相关的聚集体(生物膜)在有益和致病关联中很常见,但研究活体动物宿主中生物膜发育的遗传基础仍然是一项重大挑战。以短尾乌贼发光器官为模型,我们分析了假定的定殖因子,并鉴定出一种组氨酸激酶,它对宿主界面处的生物膜形成起负调控作用。这项工作揭示了一种新的体内生物膜调节因子,它影响细菌从海水中的浮游状态转变为宿主中紧密的细胞聚集体。该研究丰富了我们对生物膜调节和动物微生物群有益定殖的理解。