Nautlyal C Shekhar, Johri J K, Singh H B
National Botanical Research Institute, Lucknow, India.
Can J Microbiol. 2002 Jul;48(7):588-601. doi: 10.1139/w02-054.
Pseudomonas fluorescens NBRI2650 was isolated after screening 360 bacterial strains from the rhizosphere of chickpea (Cicer arietinum L.) grown in fungal-disease-suppressive field soil. The strain was selected because of its high rhizosphere competence and ability to inhibit the growth of Fusarium oxysporum f.sp. ciceri, Rhizoctonia bataticola, and Pythium sp. under in vitro conditions. Survival and colonization of NBRI2650 in the phytosphere of chickpea, cotton (Gossypium hirsutum L.), cucumber (Cucumis sativus L.), and tomato (Lycopersicon seculentum Mill.) were monitored using a chromosomally located rifampicin-marked mutant P. fluorescens NBRI2650R. The strain showed variable ability to invade and survive in the phytosphere of different plants. Chickpea was used as a tester plant for further work, as it was not invaded by NBRI2650R. The interaction between NBRI2650R and F oxysporum fsp. ciceri was studied by both light microscopy and scanning electron microscopy. The lysis of the fungal cell wall by NBRI2650R was clearly demonstrated. Treatment of the chickpea seeds with NBRI2650R in prerelease experiments in the greenhouse using disease-conducive field soils from Jhansi and Kanpur resulted in increased plant growth and did not result in any perturbation of the indigenous microbial community that inhabited the rhizosphere of chickpea compared with nonbacterized seeds. Direct fermentation of diluted NBRI2650R on vermiculite without the need of expensive fermentors offers a reliable process for manufacturing bacterial inoculants in developing countries. Under field conditions, the horizontal and vertical movement of NBRI2650R was restricted to 30 and 60 cm, respectively, and the strain could not survive in the field during the 7 months before the chickpea could be planted for next cropping season. Field trials conducted at Jhansi, Kanpur, and Pantnagar resulted in higher grain yield increase in the bacteria-treated seed compared with the nonbacterized control. Seed and furrow treatment of the two chickpeas ('Radhey' and 'H-208') at Pantnagar resulted in significantly (P = 0.05) greater seedling mortality in nonbacterized seedlings compared with bacterized ones. The seed dry weight and yield for each variety were also significantly higher in bacterized seedlings than in nonbacterized ones. The population of NBRI2650R persisted throughout the growing season of chickpea in the range of 5.4-6.4 log10 CFU/g root.
荧光假单胞菌NBRI2650是从鹰嘴豆(Cicer arietinum L.)根际筛选的360株细菌菌株中分离得到的,这些鹰嘴豆生长在具有真菌病害抑制作用的田间土壤中。该菌株因其较高的根际定殖能力以及在体外条件下抑制尖孢镰刀菌鹰嘴豆专化型、茄丝核菌和腐霉菌生长的能力而被选中。使用染色体定位的利福平标记突变体荧光假单胞菌NBRI2650R监测了NBRI2650在鹰嘴豆、棉花(Gossypium hirsutum L.)、黄瓜(Cucumis sativus L.)和番茄(Lycopersicon seculentum Mill.)根际的存活和定殖情况。该菌株在不同植物根际的侵入和存活能力各不相同。由于NBRI2650R不会侵入鹰嘴豆,因此将鹰嘴豆用作进一步研究的受试植物。通过光学显微镜和扫描电子显微镜研究了NBRI2650R与尖孢镰刀菌鹰嘴豆专化型之间的相互作用。结果清楚地表明NBRI2650R能够裂解真菌细胞壁。在温室预释放实验中,使用来自占西和坎普尔的致病田间土壤,用NBRI2650R处理鹰嘴豆种子,与未接种细菌的种子相比,植物生长得到促进,且未对鹰嘴豆根际的本土微生物群落造成任何干扰。在蛭石上直接稀释发酵NBRI2650R,无需昂贵的发酵罐,为发展中国家生产细菌接种剂提供了一种可靠的方法。在田间条件下,NBRI2650R的水平和垂直移动分别限制在30厘米和60厘米,并且在鹰嘴豆下一季种植前的7个月里,该菌株无法在田间存活。在占西、坎普尔和潘特纳加尔进行的田间试验表明,与未接种细菌的对照相比,用该细菌处理种子后鹰嘴豆的谷物产量有更高的增加。在潘特纳加尔,对两个鹰嘴豆品种(“Radhey”和“H - 208”)进行种子和沟施处理,结果表明,与接种细菌的幼苗相比,未接种细菌的幼苗死亡率显著更高(P = 0.05)。接种细菌的幼苗的种子干重和产量也显著高于未接种细菌的幼苗。在鹰嘴豆的整个生长季节,NBRI2650R的数量在5.4 - 6.4 log10 CFU/g根的范围内持续存在。