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Citation Information : Polish Journal of Microbiology. Volume 67, Issue 1, Pages 49-58, DOI: https://doi.org/10.5604/01.3001.0011.6142
License : (CC-BY-NC-ND-4.0)
Received Date : 14-May-2017 / Accepted: 31-August-2017 / Published Online: 09-March-2018
Rhizobacteria are an active part of microbial population in the rhizosphere of plants. In this study, twenty rhizobacteria were isolated from the rhizosphere of a perennial grass,
Rhizobacteria can promote plant growth directly or indirectly and are found in rhizosphere in association with plant roots. A great number of bacteria have been reported for their plant growth promoting abilities such as Bacillus, Azotobacter, Pseudomonas, Klebsiella, Alcaligenes, Arthrobacter, Serratia, Burkholderia, Azospirillum, Enterobacter and Rhizobium (Kumar et al., 2012). Rhizosphere has been defined as the soil volume that is directly influenced by presence of roots of living plants. The rhizosphere thus supports an active microbial population (Ahmad et al., 2008). A number of studies have revealed that due to the presence of rhizodeposits and root exudates, the soil environment of root system is a favorable place of microbial abundance and activity (Hartmann et al., 2008; Smalla et al., 2006). Rhizobacteria are of great interest for their applications as biofertilizers or pesticides in agriculture and for phytoremediation. The plant growth promoting rhizobacteria (PGPR) can enhance plant growth and yield, and reduce chances of pathogen infection and biotic or abiotic plant stresses (Lugtenberg and Kamilova, 2009; van Loon and Bakker, 2006). In a number of cases, the required effects of PGPR are not attained in the field probably due to insufficient rhizosphere or plant colonization required for revealing beneficial effects (Lugtenberg et al., 2001), and the lack of thorough understanding of the mechanisms responsible to promote plant growth.
Haloxylon salicornicum (vernacular name: Lana or Khar) belongs to Chenopodiaceae family and is found in Cholistan desert of Pakistan as a common shrub (Shafi et al., 2002). It is much branched, erect leafless and woody at base perennial shrub. Its stem and branches are pale yellow, flowers and fruits are not found, and joints produce into two short triangular points in the form of leaves and are woolly within. The plant is used as fodder for domestic animals and is mostly grazed by camels. It has high salt contents and therefore, better to retrieve the desert soil. The extract of this plant is used for washing clothes (Arshad et al., 2002). The plant has medicinal importance and is taken as tea by women who are experiencing problems during pregnancy and to relieve dysmenorrhea (Saleem et al., 2013). Because of its unique characteristics, this plant is expected to host biotechnologically important microbes in its rhizosphere.
Ribosomal RNA sequences especially 16S rRNA are the most important targets for bacterial identification to study evolution, ecology and to determine phylogenetic relationships among various taxa. These sequences also serve for the exploration of bacterial diversity present in an environment and quantification of relative abundance of taxa of different ranks (Hugenholtz et al., 1998). The16S rRNA gene is suitable for bacterial identification because it allows studying phylogenetic relationships among distant taxa. The gene of 16S rRNA is functionally indispensable part of the core gene set (Daubin et al., 2003) that promotes its importance for studying phylogenetic relationships. It is subject to variations, especially in the variable regions, and allows enough diversification for bacterial classification. The suitable PCR primers have been enabled due to the presence of conserved regions in 16S rRNA gene to study different taxa at various taxonomic levels that range from individual bacterial strains to whole phyla (Head et al., 1998).
The current study was carried out to isolate some thermophilic bacterial strains from the rhizospheric soil of H. salicornicum of Cholistan desert. Morphological and biochemical properties of the isolated bacteria are reported. The 16S rRNA gene was amplified to identify these bacterial isolates and to study their phylogenetic relationships with other strains.
Study area. Cholistan desert spreads over an area of 26,000 km2 and is situated in Southern Punjab of Pakistan. It is located between 27°42´ and 29°45´ N latitude and 69°52´ and 75°24´ E longitude (Wariss et al., 2013). It is sandy and hot desert with mean annual rainfall of 100–150 mm. The rain usually falls during the period of monsoon, spring and winter seasons. The temperature reaches above 50°C in summer (Jamil et al., 2013). The inconsistent rainfall promotes only spiny, leafless, small and grazed shrubs in addition to some trees. The soils of this desert are mostly alkaline, saline, gypsiferous and often dunned (Akbar et al., 1996).
Collection of rhizospheric soil. Soil samples (5–10 g) from the rhizosphere of H. salicornicum growing in Cholistan were collected at various places in extreme summer (June and July), winter (December and January) and rainy seasons (August and September), mixed to get random samples. Samples were collected in sterile sealed plastic bags on dry ice using ethanol flamed spatula, preserved in properly labeled sterile plastic jars and stored in a dark and cool place. Some soil samples were also stored at 4°C and processed within a week for biochemical and molecular analyses.
Growth of cultivable bacteria in sterile normal saline/Ringer solution. Rhizospheric microbial suspension was made from the soil sample (1 g) including pieces of plant roots, about 3.5 cm in length, in 30 ml sterile ringer solution in a sterile cotton plugged 250 ml flask. After continuous swirling on shaker a homogeneous suspension was obtained that was used as stock to prepare serial dilutions.
The original suspension was serially diluted to get 6 dilutions ranging from 10–1 to 10–6. For bacterial growth, 100 μl of soil suspension (10–3 to 10–6 dilutions) was taken and poured/spread on LB agar plates. This step was followed by incubation of the plates at 30°C for 16–24 hrs. Several colonies were observed and colonies seen to be inhibiting the growth of another bacterial colony and having clear zone around (data not shown) were considered as antagonistic to each other and were isolated.
To get purified isolates, individual bacterial colonies grown on agar plates were picked and transferred to fresh LB agar plates. Repeated streaking and transfer was attempted to obtain pure strains. Following isolation, pure cultivable bacteria were stored as LB glycerol stocks (LB: glycerol, 50:50) at –70°C till further analysis.
For analyses, overnight LB broth cultures of bacterial isolates were grown using LB glycerol stocks as seed cultures.
Determination of antibacterial activity of the isolates. Disc diffusion method was used to evaluate the antibacterial potential of the isolates. Broth cultures of the isolates were grown for 16 hours at 50°C and 40 μl of the culture’s supernatant was applied on the filter paper discs (5 mm diameter) in installments of 10 μl. Discs were tested against 4 Gram-negative (Escherichia coli, Pseudomonas aeruginosa, Salmonella typhi, and Shigella sonnei) and 2 Gram-positive bacteria (Staphylococcus aureus and Bacillus subtilis).
Physical and biochemical analysis of cultivable bacteria. Colony and staining characteristics like gram staining, motility and cell morphology etc. of bacterial isolates were observed under the microscope. Biochemical analysis included tests for the production of amylase, acid, urease, gelatinase, catalase, protease, H2S and antibiotic production. Analysis was further extended to MR, VP, motility, and glucose, lactose and fructose fermentation tests. All analyses were carried out using standard reagents and following optimized procedures (Cappuccino and Sherman, 1999).
Extraction of genomic DNA from bacterial isolates. LB broth cultures of purified bacterial isolates were used for DNA isolation using standard protocol consisting of four stages including disruption, lysis, removal of proteins and contaminants, and finally recovery of DNA. In this study, SDS based method was employed (Vivantis, Kit. Catalogue No. GF-BA-100 preps) as suggested by the manufacturer.
Amplification of 16S rRNA gene. For the amplification of 16S rRNA gene of bacterial isolates, PCR conditions were optimized and reactions were carried out in a thermocycler (MY GENETm Model MG-96+). Universal forward and reverse primers specifically designed and reported for bacterial 16S rRNA genes in earlier studies (Porteous and Armstrong, 1993) were used for PCR amplification. Forward and reverse primers used in this study are shown below.
Sense primer: 5’-AACACATGCAAGTGGAAC-3’
Antisense primer: 5’-ACGGGCGGTGTGTACAAG-3’
Expected size of PCR amplicons using E. coli DNA was calculated to be 1357 bp. Each tube was loaded with 50 μl final volume of a solution containing 1 × PCR buffer, 1.5 mM MgCl2, 100 μM dNTPs mix, 0.3 μl of each primer (10 pmol), 1.25U of Taq DNA polymerase and an appropriate amount of chromosomal DNA. PCR amplifications were carried out as follows: initial denaturation at 94°C for 5 min, followed by 40 cycles each of 94°C for 30 s, 50°C for 60 s and 72°C for 60 s with a final extension step of 72°C for 10 min.
RFLP analysis of 16S rRNA amplicons using four cutter restriction enzymes. Five types of 4 base cutter restriction enzymes, RsaI, TaqI, HpaII, HinfI, and HhaI, were used in this study for RFLP of 16S rRNA gene PCR amplicons. The documented gels were labeled using 1 and 0 to indicate the presence/absence of band on gel. Data was transferred to excel sheet for preparation of dendrograms by PAST-3 software. Dendrograms helped to identify the pattern of similarity and dissimilarity within the group and among the other groups of rhizospheric soils bacteria.
Phylogenetic analysis of 16S rRNA genes. PCR amplified 16S rRNA genes of the isolates were selected based on dendrograms analyses. At least 2–3 members of each group were randomly selected and sequenced (Macrogen, South Korea). The sequences of 16S rRNA genes were assembled and analyzed using BLAST (Altschul et al., 1990). Along with our twenty sequences for 16S rRNA, twelve sequences of the most nearest relatives were also retrieved from GenBank for the comparison study. All the sequences were aligned using ClustalX and imported into the Bioedit program for manual alignment. Neighbor joining phylogenetic tree for 16S rRNA gene was constructed and the evolutionary analyses were conducted using MEGA7 (Kumar et al., 2016) with 100 bootstrap replicates. The evolutionary history was inferred using the Neighbor-Joining method (Saitou and Nei, 1987). The evolutionary distances were computed using the p-distance method (Nei and Kumar, 2000) and are in the units of the number of base differences per site. The analysis involved 33 nucleotide sequences. All positions containing gaps and missing data were eliminated. The final dataset consisted a total of 682 positions.
Determination of the antibacterial activity. Discs prepared using cultures of the isolated bacteria exhibited antibacterial activity against all tested microorganisms. Ampicillin was used as standard and tested at the concentration of 50 μg/disc. It is obvious from the results (Table I) that some isolates (HSHM1105, HSHM1109, HSHM1111, HSHM1118, HSHM1207, HSHM1212-HSHM1215, HSHM1219) were more effective against E. coli as compared to ampicillin. Isolates HSHM1103-1105, HSHM1117, HSHM1120, HSHM1202, HSHM1206, HSHM1208, HSHM1212, HSHM1214-1216, HSHM1219 were found to possess higher antibacterial potential against P. aeruginosa than the standard. Similarly, all isolates except HSHM1109, HSHM1110 and HSHM1216 exhibited a an antagonistic behavior against S. typhi higher than the standard. However, against S. sonnei 12 isolates (HSHM1111, HSHM1117, HSHM1118, HSHM1120, HSHM1201, HSHM1202, HSHM1206-1208, HSHM1213-1215) exhibited antibacterial activity higher than ampicillin. Multiple isolates were examined to be more active against S. aureus (HSHM1118, HSHM1120, HSHM1201, HSHM1207, HSHM1208, HSHM1212-1216, HSHM1219) and B. subtilis (HSHM1103, HSHM1104, HSHM1111, HSHM1118, HSHM1120, HSHM1202, HSHM1206-1208, HSHM1212, HSHM1214-1216, HSHM1219) as compared to ampicillin.
Phenotypic characterization of bacterial isolates. Total 20 rhizobacteria were isolated on agar plates from the rhizosphere of H. salicornicum. The bacterial isolates showed various phenotypic properties including different morphological traits, fermentable carbohydrates profiles and enzyme production patterns (Table II). In all cases, colonies were off-white, round and irregular after 15 and 24 hours, respectively. No chromogenesis and odor was observed in any bacterial isolate. All isolates were found to be gram-positive bacteria that belonged to bacilli class that is an extremely diverse group of bacteria. Production of urease, gelatinase, indole and hydrogen sulfide was not seen in these isolates. Catalase production and glucose fermentation were observed in all selected bacterial isolates.
Analysis of 16S rRNA sequences of isolates. The selected isolates showed varying percentage identity with different bacteria through nucleotide BLAST search of partial sequences (~ 1100 bp) of the 16S rRNA. Although, it has been suggested that RFLP can help differentiate bacterial strains up to species level (Dec et al., 2016), in the present study, phylogenetic trees developed on the basis of RFLP and base sequences exhibited some differences. This could be attributed to the number of restriction enzymes used for RFLP analyses.
Nearest relatives of selected bacteria isolated from rhizosphere of H. salicornicum are given (Table III) along with their percentage identity. Out of twenty nearest relative isolates, 14 isolates showed 91–99% identity with Brevibacillus borstelensis, 4 with Bacillus subtilis (97–98%) and 2 isolates with Bacillus licheniformis (94–99%). The partial nucleotide 16S rRNA gene sequences of all bacterial isolates were deposited in GenBank have been allotted accession numbers (Table III).
A neighbor-joining (NJ) phylogenetic tree was generated through aligning 16S rRNA sequences of the bacterial isolates examined in this study and their nearest relatives taken from GenBank, NCBI (Fig. 1) to study their evolutionary relationships and cladding pattern. Three main groups of bacteria were observed in this phylogeny on the basis of which bacteria fell in different clades. HS1219, HS1215, HS1214, HS1208, HS1202, HS1119, HS1118, HS1110, HS1201, HS1120, HS1103, HS1207, HS1105 and HS1109 grouped with B. borstelensis, showing their homology with other B. borstelensis species. Only two isolates, that is, HS1206 and HS1213 were found in the clade of B. licheniformis with ESR26 and PF4H_1 strains of B. licheniformis. Four isolates were identified as Bacillus subtilis species HS1111, HS1212, HS1104 and HS1216) but the interesting observation in this clade was the unusual branching of HS1111 that was not cladded with other species of B. subtilis. The nearest relative of HS1111 (accession number: DQ420172) was also found as a separate branch above HS1111 that was showing evolutionary divergence of both sequences from other B. subtilis species. Phenotypic characteristics showed that HS1111 is different from other B. subtilis species in terms of margin, elevation and opacity as it had branching filaments with positive values for colony elevation and opacity.
RFLP and phylogenetic analysis. RFLP analysis of the 20 selected bacterial isolates using 16S rRNA products identified 5 distinct patterns. Representative patterns are shown in Fig. 2. These patterns were found to be consistent and absolutely reproducible. Among 222 16S rRNA restriction fragments recorded, RsaI and HinfI each gave 20 shared fragments (18% of total), 16 fragments were unique among accessions (7.2%) and remaining 166 fragments were phylogenetically informative (74.7%). A dendrogram was constructed based on RFLP analysis of 16S rRNA gene of bacteria isolated from rhizosphere of H. salicornicum (Fig. 3). The RFLP dendrogram showed two main clades (labeled with letters A and B). Clade B has only five isolates, that is, HS1109, HS1119, HS1202, HS1208 (all have identity with B. borstelensis) and HS1213 (that has identity with B. licheniformis). Clade A was further divided into 2 subclades (labeled with a1 and a2). Only three isolates, that is, HS1214, HS1215 (had identity with B. borstelensis) and HS1216 (identity with B. subtilis) fell into subclades a2. Species of the same genera did not appear together in RFLP dendrograms revealing that identification of bacterial isolates on the basis of RFLP is not a reliable technique.
A number of plant-associated rhizobacteria are known for their role in promotion of plant growth and to increase plant resistance against different diseases and abiotic stresses. Cholistan desert has not been explored for its rhizobacterial diversity associated with its plants. Therefore, the present study represents the very first study of its kind that has been performed to isolate and identify rhizobacteria from a representative plant H. salicornicum from Cholistan desert, a desert having unique soil with high salinity and basic pH (Hameed et al., 2011). Based on biochemical characterization these isolates were found to be catalase positive and glucose fermentive; 19 were found positive for fructose fermentation and 11 were positive for amylase production. Amylase producers are more important industrially because bacterial enzymes are obtained in high yield and they possess high thermostability. A thermostable α-amylase from B. licheniformis has also been reported (Morgan and Priest, 1981).
Bacterial classification is accomplished when morphological and biochemical methods are used along with molecular methods of analysis. The amplified fragment length polymorphism (AFLP) technique of DNA fingerprinting has been shown to be useful for the identification of different bacterial species (Duim et al., 2001) but it is expensive and laborious. Another technique, whole-genome DNA-DNA hybridization allows identification of bacterial species but is not routinely used (Stackebrandt and Goebel, 1994). Community structures, metabolic function, composition and ecological roles are the characteristics of different microbial communities. The 16S rRNA gene has been employed to investigate environmental microbial diversity that does not require isolation and cultivation of bacteria to offer phylogenetic taxonomic classification. Because of heterogeneity of 16S phylogenetic marker among operons of same genome or lack of its resolution at species level, the use of this technique is often criticized but the technique is still believed to be a standard for bacterial identification (Pontes et al., 2007). The 16S rRNA based identification of bacteria has therefore come up as a potential and useful alternative.
In the present studies, 14 Brevibacillus and 6 Bacillus (4 B. subtilis and 2 B. licheniformis) species were identified from rhizosphere of H. salicornicum. The isolate HS1111 depicted a divergence through different branching pattern in the phylogenetic tree because it didn’t clade with other strains of B. subtilis (Fig. 1). The importance of Bacillus species in plant growth promotion is widely accepted and a large number including B. subtilis have been reported for their bio-control because of the production of various antibiotics. Plant growth promotion is also supported through phytohormones production, phosphate solubilization and release of ammonia from nitrogenous organic matter (Hayat et al., 2010). B. subtilis and B. licheniformis are also reported for producing two important plant hormones, indole-3-acetic acid and indole-3-butyric acid (Lim and Kim, 2009). It has also been observed that the colonization of B. subtilis at root hairs of plants is accompanied with morphological changes of these root hairs (Huang et al., 2011). The PGPR strain of B. licheniformis has been found capable of survival under drought stress conditions and the PGPR treated plants, therefore, continue to accumulate plant growth when exposed to drought stress (Lim and Kim, 2013). In other studies, it is also revealed that B. licheniformis has great resistance against abiotic stress including drought stress (Cheng et al., 2007; Kloepper et al., 2007; Sziderics et al., 2007).
Bacillus species are aerobic endospore forming plant growth promoting rhizobacteria which are known to produce many valuable enzymes including proteases, amylases, laccase and lipases. In addition, the Bacillus species have potential to degrade complex carbohydrates including cellulose, xylulose and oligosaccharides like arabinogalactan, stachyose and raffinose (Ahmad et al., 2008; Amoa-Awua and Jakobsen, 1995; Larsen et al., 2014; Ouoba et al., 2003a; Ouoba et al., 2003b; Ouoba et al., 2003c; Ouoba et al., 2007; Reiss et al., 2011). Many Bacillus species have been identified to have antimicrobial potential. Antimicrobial potential of thermophilic bacterial species including Brevibacillus borstelensis and B. licheniformis has been documented against gram positive bacteria (Micrococcus luteus and Staphylococcus aureus) and gram negative bacteria including Pseudomonas aeruginosa, Escherichia coli and Klebsiella pneumonia (Muhammad et al., 2009). B. subtilis is capable of producing an amocaumacin-A like secondary metabolite that has antimicrobial potential against Candida albicans, Ustilago maydis, Cryptococcus neoformans, S. aureus and E. coli (Esikova et al., 2002; Shankarrao et al., 2014). B. borstelensis and B. licheniformis induce systemic resistance in plants and inhibit many phytopathogens (Kloepper et al., 2004; Sharma et al., 2014). Contrary to these positive effects, few studies have reported the pathogenic properties of B. licheniformis against humans (Salkinoja-Salonen et al., 1999). Moreover, Brevibacillus species have potential of degrading many toxic chemicals like Toluidine Blue dye and carbendazim, a known fungicide (Alhassani et al., 2007; Arya and Sharma, 2014; Mallick et al., 2014).
In conclusion, the morphological, biochemical and the molecular approaches described above present the first ever study carried out under given experimental conditions to identify and characterize 20 rhizobacteria from a representative plant of Cholistan desert. The phylogenetic significance of the presence of all bacilli from three species in the rhizosphere of one desert plant remains to be determined. Work is in progress on the molecular analysis of rhizobacteria from other plants of Cholistan desert in this regard. These bacteria on further characterization can be explored for the production of valuable molecules and can be manipulated to induce tolerance efficiently against both biotic and abiotic stress in economically important plants.
Availability of data and materials. Ribosomal DNA sequences are presented in the GenBank data as per accession numbers presented in Table II.
Conflict of interests
The authors declare that they have no financial or non-financial competing interests.
FHN was the PI and HEC grant recipient. M Ashraf, JR and MSC were the collaborators who contributed through sample identification, collection and analyses. M Aslam, RR and HM performed the bench work. SE, FHN, M Ashraf, M Aslam and JR were involved in the data analyses and manuscript writing. M Aslam and GM prepared the dendrograms and conducted the related analysis.
Neighbour-joining phylogenetic tree of the selected bacterial isolates. The tree was rooted with
Neighbour-joining phylogenetic tree of the selected bacterial isolates.
The tree was rooted with