TY - JOUR
T1 - Impact of oil contamination and biostimulation on the diversity of indigenous bacterial communities in soil microcosms
AU - Evans, Flavia F.
AU - Rosado, Alexandre S.
AU - Sebastián, Gina V.
AU - Casella, Renata
AU - Machado, Pedro L.O.A.
AU - Holmström, Carola
AU - Kjelleberg, Staffan
AU - Van Elsas, Jan D.
AU - Seldin, Lucy
N1 - Generated from Scopus record by KAUST IRTS on 2021-02-16
PY - 2004/8/1
Y1 - 2004/8/1
N2 - The aim of this study was to analyse the effect of oil contamination and biostimulation (soil pH raise, and nitrogen, phosphate and sulphur addition) on the diversity of a bacterial community of an acidic Cambisol under Atlantic Forest. The experiment was based on the enumeration of bacterial populations and hydrocarbon degraders in microcosms through the use of conventional plating techniques and molecular fingerprinting of samples directly from the environment. PCR followed by denaturing gradient gel electrophoresis (DGGE) was used to generate microbial community fingerprints employing 16S rRNA gene as molecular marker. Biostimulation led to increases of soil pH (to 7.0) and of the levels of phosphorus and K, Ca, and Mg. Oil contamination caused an increase in soil organic carbon (170-190% higher than control soil). Total bacterial counts were stable throughout the experiment, while MPN counts of hydrocarbon degraders showed an increase in the biostimulated and oil-contaminated soil samples. Molecular fingerprinting performed with 16S rRNA gene PCR and DGGE analysis revealed stable patterns along the 360 days of experiment, showing little change in oil-contaminated microcosms after 90 days. The DGGE patterns of the biostimulated samples showed severe changes due to decreases in the number of bands as compared to the control samples as from 15 days after addition of nutrients to the soil. Results obtained in the present study indicate that the addition of inorganic compounds to soil in conjunction with oil contamination has a greater impact on the bacterial community than oil contamination only. © 2004 Federation of European Microbiological Societies. Published by Elsevier B.V. All rights reserved.
AB - The aim of this study was to analyse the effect of oil contamination and biostimulation (soil pH raise, and nitrogen, phosphate and sulphur addition) on the diversity of a bacterial community of an acidic Cambisol under Atlantic Forest. The experiment was based on the enumeration of bacterial populations and hydrocarbon degraders in microcosms through the use of conventional plating techniques and molecular fingerprinting of samples directly from the environment. PCR followed by denaturing gradient gel electrophoresis (DGGE) was used to generate microbial community fingerprints employing 16S rRNA gene as molecular marker. Biostimulation led to increases of soil pH (to 7.0) and of the levels of phosphorus and K, Ca, and Mg. Oil contamination caused an increase in soil organic carbon (170-190% higher than control soil). Total bacterial counts were stable throughout the experiment, while MPN counts of hydrocarbon degraders showed an increase in the biostimulated and oil-contaminated soil samples. Molecular fingerprinting performed with 16S rRNA gene PCR and DGGE analysis revealed stable patterns along the 360 days of experiment, showing little change in oil-contaminated microcosms after 90 days. The DGGE patterns of the biostimulated samples showed severe changes due to decreases in the number of bands as compared to the control samples as from 15 days after addition of nutrients to the soil. Results obtained in the present study indicate that the addition of inorganic compounds to soil in conjunction with oil contamination has a greater impact on the bacterial community than oil contamination only. © 2004 Federation of European Microbiological Societies. Published by Elsevier B.V. All rights reserved.
UR - https://academic.oup.com/femsec/article-lookup/doi/10.1016/j.femsec.2004.04.007
UR - http://www.scopus.com/inward/record.url?scp=3142776638&partnerID=8YFLogxK
U2 - 10.1016/j.femsec.2004.04.007
DO - 10.1016/j.femsec.2004.04.007
M3 - Article
SN - 0168-6496
VL - 49
SP - 295
EP - 305
JO - FEMS Microbiology Ecology
JF - FEMS Microbiology Ecology
IS - 2
ER -