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Strain-specific quantification of root colonization by plant growth promoting rhizobacteria Bacillus firmus I-1582 and Bacillus amyloliquefaciens QST713 in non-sterile soil and field conditions
被引:88
作者:
Mendis, Hajeewaka C.
[1
]
Thomas, Varghese P.
[2
]
Schwientek, Patrick
[2
]
Salamzade, Rauf
[2
,4
]
Chien, Jung-Ting
[2
]
Waidyarathne, Pramuditha
[3
,5
]
Kloepper, Joseph
[1
]
De La Fuente, Leonardo
[1
]
机构:
[1] Auburn Univ, Dept Entomol & Plant Pathol, Auburn, AL 36849 USA
[2] Bayer, Crop Sci Div, Biol, West Sacramento, CA USA
[3] Lincoln Univ, Ctr Adv Computat Solut, Christchurch, New Zealand
[4] Broad Inst MIT & Harvard, Cambridge, MA USA
[5] Coconut Res Inst Sri Lanka, Lunuwila, Sri Lanka
来源:
关键词:
PSEUDOMONAS-FLUORESCENS STRAINS;
NEMATODE MELOIDOGYNE-INCOGNITA;
SOLANI DAMPING-OFF;
SYSTEMIC RESISTANCE;
TOMATO PLANTS;
BIOCONTROL;
RHIZOSPHERE;
BACTERIA;
MAIZE;
PROTECTION;
D O I:
10.1371/journal.pone.0193119
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Bacillus amyloliquefaciens QST713 and B. firmus I-1582 are bacterial strains which are used as active ingredients of commercially-available soil application and seed treatment products Serenade (R) and VOTiVO (R), respectively. These bacteria colonize plant roots promoting plant growth and offering protection against pathogens/pests. The objective of this study was to develop a qPCR protocol to quantitate the dynamics of root colonization by these two strains under field conditions. Primers and TaqMan (R) probes were designed based on genome comparisons of the two strains with publicly-available and unpublished bacterial genomes of the same species. An optimized qPCR protocol was developed to quantify bacterial colonization of corn roots after seed treatment. Treated corn seeds were planted in non-sterile soil in the greenhouse and grown for 28 days. Specific detection of bacteria was quantified weekly, and showed stable colonization between similar to 104-10(5) CFU/g during the experimental period for both bacteria, and the protocol detected as low as 10(3) CFU/g bacteria on roots. In a separate experiment, streptomycin-resistant QST713 and rifampicin-resistant I-1582 strains were used to compare dilution-plating on TSA with the newly developed qPCR method. Results also indicated that the presence of natural microflora and another inoculated strain does not affect root colonization of either one of these strains. The same qPCR protocol was used to quantitate root colonization by QST713 and I-1582 in two corn and two soybean varieties grown in the field. Both bacteria were quantitated up to two weeks after seeds were planted in the field and there were no significant differences in root colonization in either bacteria strain among varieties. Results presented here confirm that the developed qPCR protocol can be successfully used to understand dynamics of root colonization by these bacteria in plants growing in growth chamber, greenhouse and the field.
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页数:19
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