Walker Travis S, Bais Harsh Pal, Déziel Eric, Schweizer Herbert P, Rahme Laurence G, Fall Ray, Vivanco Jorge M
Department of Horticulture and Landscape Architecture, Colorado State University, Fort Collins, Colorado 80523, USA.
Plant Physiol. 2004 Jan;134(1):320-31. doi: 10.1104/pp.103.027888. Epub 2003 Dec 30.
Pseudomonas aeruginosa is an opportunistic human pathogen capable of forming a biofilm under physiological conditions that contributes to its persistence despite long-term treatment with antibiotics. Here, we report that pathogenic P. aeruginosa strains PAO1 and PA14 are capable of infecting the roots of Arabidopsis and sweet basil (Ocimum basilicum), in vitro and in the soil, and are capable of causing plant mortality 7 d postinoculation. Before plant mortality, PAO1 and PA14 colonize the roots of Arabidopsis and sweet basil and form a biofilm as observed by scanning electron microscopy, phase contrast microscopy, and confocal scanning laser microscopy. Upon P. aeruginosa infection, sweet basil roots secrete rosmarinic acid (RA), a multifunctional caffeic acid ester that exhibits in vitro antibacterial activity against planktonic cells of both P. aeruginosa strains with a minimum inhibitory concentration of 3 microg mL(-1). However, in our studies RA did not attain minimum inhibitory concentration levels in sweet basil's root exudates before P. aeruginosa formed a biofilm that resisted the microbicidal effects of RA and ultimately caused plant mortality. We further demonstrated that P. aeruginosa biofilms were resistant to RA treatment under in vivo and in vitro conditions. In contrast, induction of RA secretion by sweet basil roots and exogenous supplementation of Arabidopsis root exudates with RA before infection conferred resistance to P. aeruginosa. Under the latter conditions, confocal scanning laser microscopy revealed large clusters of dead P. aeruginosa on the root surface of Arabidopsis and sweet basil, and biofilm formation was not observed. Studies with quorum-sensing mutants PAO210 (DeltarhlI), PAO214 (DeltalasI), and PAO216 (DeltalasI DeltarhlI) demonstrated that all of the strains were pathogenic to Arabidopsis, which does not naturally secrete RA as a root exudate. However, PAO214 was the only pathogenic strain toward sweet basil, and PAO214 biofilm appeared comparable with biofilms formed by wild-type strains of P. aeruginosa. Our results collectively suggest that upon root colonization, P. aeruginosa forms a biofilm that confers resistance against root-secreted antibiotics.
铜绿假单胞菌是一种机会性人类病原体,能够在生理条件下形成生物膜,这使得它即使在长期使用抗生素治疗的情况下仍能持续存在。在此,我们报告致病的铜绿假单胞菌菌株PAO1和PA14能够在体外和土壤中感染拟南芥和甜罗勒(Ocimum basilicum)的根部,并在接种后7天导致植物死亡。在植物死亡之前,PAO1和PA14定殖于拟南芥和甜罗勒的根部,并通过扫描电子显微镜、相差显微镜和共聚焦扫描激光显微镜观察到形成了生物膜。在铜绿假单胞菌感染后,甜罗勒根部分泌迷迭香酸(RA),一种多功能咖啡酸酯,其对两种铜绿假单胞菌菌株的浮游细胞均具有体外抗菌活性,最低抑菌浓度为3μg mL(-1)。然而,在我们的研究中,在铜绿假单胞菌形成抵抗RA杀菌作用并最终导致植物死亡的生物膜之前,RA在甜罗勒根分泌物中未达到最低抑菌浓度水平。我们进一步证明,铜绿假单胞菌生物膜在体内和体外条件下均对RA处理具有抗性。相反,甜罗勒根部诱导RA分泌以及在感染前用RA外源补充拟南芥根分泌物可赋予对铜绿假单胞菌的抗性。在后一种条件下,共聚焦扫描激光显微镜显示在拟南芥和甜罗勒的根表面有大量死亡的铜绿假单胞菌簇,并且未观察到生物膜形成。对群体感应突变体PAO210(DeltarhlI)、PAO214(DeltalasI)和PAO216(DeltalasI DeltarhlI)的研究表明,所有这些菌株对拟南芥均具有致病性,拟南芥不会自然分泌RA作为根分泌物。然而,PAO214是唯一对甜罗勒具有致病性的菌株,并且PAO214生物膜与铜绿假单胞菌野生型菌株形成的生物膜相当。我们的结果共同表明,在根部定殖后,铜绿假单胞菌形成生物膜,从而赋予对根部分泌的抗生素的抗性。