16S Ribosomal DNA Characterization of Nitrogen-Fixing Bacteria Isolated from Banana (Musa spp.) and Pineapple (Ananas comosus (L.) Merril) (original) (raw)

Abstract

Nitrogen-fixing bacteria isolated from banana (Musa spp.) and pineapple (Ananas comosus (L.) Merril) were characterized by amplified 16S ribosomal DNA restriction analysis and 16S rRNA sequence analysis. Herbaspirillum seropedicae, Herbaspirillum rubrisubalbicans, Burkholderia brasilensis, and Burkholderia tropicalis were identified. Eight other types were placed in close proximity to these genera and other alpha and beta Proteobacteria.

Associative nitrogen-fixing bacteria such as Azospirillum brasilense, Herbaspirillum seropedicae, and Acetobacter diazotrophicus may benefit their host plants as N biofertilizers and plant growth promoters. The latter two organisms were the first nitrogen-fixing bacteria suggested to be endophytes (1, 4). Several new classified and as-yet-unclassified diazotrophic bacteria have been isolated from economically important mono- and dicotyledonous plants (3, 5), including banana and pineapple (17).

Thirty-eight nitrogen-fixing bacteria isolated from stems, leaves, roots, and fruits of pineapple and banana cultivars from Bahia (BA) and Rio de Janeiro (RJ) States, Brazil, including 14 isolates previously described (17), were analyzed following DNA sequencing and PCR-restriction fragment length polymorphism analysis of the 16S rRNA gene (amplified 16S ribosomal DNA restriction analysis [ARDRA]) to define their phylogenetic positions. Reference strains Z67, Z78, and M2 for H. seropedicae, M4 for Herbaspirillum rubrisubalbicans, M130 for Burkholderia brasilensis, and Ppe8 for Burkholderia tropicalis (1) were from our collection (Table 1). All strains were grown overnight in NFbHPN (8) medium at 30°C at 120 rpm, diluted (1:10), boiled for 5 min, and cooled on ice, and the DNA was amplified (7) in an OmniGene thermocycler from Hybaid Ltd., Teddington, United Kingdom. The primers used were Y1 (5′-TGGCTCAGAACGAACGCTGGCGGC-3′) (19) (positions 20 to 43 of the Escherichia coli 16S rRNA gene) and Y3 (5′-TACCTTGTTACGACTTCACCCCAGTC-3′) (J. P. W. Young, personal communication) (positions 1482 to 1507 of the E. coli 16S rRNA gene) (2), complementary to the ends of the 16S rDNA. The DNA templates extracted from all of the strains produced a single band of approximately 1,500 bp.

TABLE 1.

Characterization of nitrogen-fixing bacteria isolated from Musa spp. and Ananas comosus (L) Merril cultivated in Brazil, as revealed by ARDRA of Y1-Y3-amplified fragments and Y1-Y2 sequence of the 16S rDNA

Species and straina Host Cultivar Tissue Geographic origin Restriction patternb Type
ARDRAc Y1-Y2 sequenced
H. seropedicae
Z67 aaaa 1 I
Z78 aaaa 1 NEf
M2 aaaa 1 NE
BA153 Banana Marmelo Fruit Itaguaí, RJ aaaa 1 1
X8 NDe ND ND ND aaaa 1 II
H. rubrisubalbicans
M4 baaa 2 III
AB7 Pineapple Alenquer Leaf Cruz das Almas, BA baaa 2 I
BA10 Banana Butuhan Stem Cruz das Almas, BA baaa 2 I
BA11 Banana Butuhan Leaf Cruz das Almas, BA baaa 2 I
BA12 Banana Yangambi Root Cruz das Almas, BA baaa 2 I
BA14 Banana Yangambi Stem Cruz das Almas, BA baaa 2 I
BA15 Banana Prata Anã Root Cruz das Almas, BA baaa 2 I
BA16 Banana Prata Anã Stem Cruz das Almas, BA baaa 2 I
BA17 Banana Butuhan Stem Cruz das Almas, BA baaa 2 NE
BA134 Banana Maçã Stem Itaguaí, RJ baaa 2 I
BA149 Banana Maçã Leaf Itaguaí, RJ baaa 2 NE
BA161 Banana Maçã Root Itaguaí, RJ baaa 2 I
B. brasilensis
M130 cbbb 3 IV
BA124 Banana Prata Manteiga Stem Macaé, RJ cbbb 3 NE
B. tropicalis
Ppe8 dccb 4 V
AB98 Pineapple Pérola Fruit Macaé, RJ dccb 4 V
AB147 Pineapple Smooth cayenne Stem Quissamã, RJ dccb 4 V
Unknown
O1 Banana Yangambi ND Cruz das Almas, BA geed 5 VI
BA22 Banana Prata Anã Leaf Cruz das Almas, BA geed 5 VI
BA23 Banana Yangambi Stem Cruz das Almas, BA geed 5 VI
BA25 Banana Prata Anã Stem Cruz das Almas, BA geed 5 NE
BA27 Banana Yangambi Leaf Cruz das Almas, BA geed 5 VI
BA88 Banana Maçã Leaf Itaguaí, RJ geed 5 NE
BA104 Banana Prata Anã Stem Itaguaí, RJ geed 5 NE
BA106 Banana Maçã Leaf Itaguaí, RJ geed 5 NE
BA128 Banana Prata Fruit Itaguaí, RJ geed 5 NE
BA136 Banana Prata Leaf Itaguaí, RJ geed 5 VI
AB117 Pineapple Smooth Cayenne Root Quissamã, RJ gfcc 6 VII
AB120 Pineapple Pérola Stem Macaé, RJ gfcc 6 VII
BA123 Banana Prata Manteiga Root Macaé, RJ dgce 7 VIII
BA126 Banana D'água Root Itaguaí, RJ dgce 7 VIII
AB48 Pineapple Perolera Root Cruz das Almas, BA ghcc 8 IX
AB71 Pineapple Perolera Stem Cruz das Almas, BA ghcc 8 IX
AB119 Pineapple Pérola Leaf Macaé, RJ dibb 9 NE
Ala ND ND ND ND fddc 10 X
BA131 Banana D'água Leaf Itaguaí, RJ bjf– 11 XI
A2a ND ND ND ND eddc 12 NE
A3b ND ND ND ND eddc 12 NE
A8b ND ND ND ND eddc 12 NE

Y1-Y3 PCR products (10 μl) were digested with _Alu_I, _Hae_III, _Hin_fI, or _Rsa_I (5 U) as specified by Life Technologies, and the fragments were separated on a 2.5% agarose gel and stained with ethidium bromide (0.5 μg/ml). Three to seven fragments and 5 to 10 unique restriction patterns were produced by each endonuclease.

A combination of the restriction digests produced 12 unique banding patterns or ARDRA types (Table 1). Isolates BA153 and X8 shared the same pattern as H. seropedicae type strains Z67, Z78, and M2. Isolates AB7, BA10, BA11, BA12, BA14, BA15, BA16, BA17, BA134, BA149, and BA161 had the same pattern as H. rubrisubalbicans strain M4. Isolate BA124 showed the same pattern as B. brasilensis strain M130. Finally, AB98 and AB147 had the same pattern as B. tropicalis strain Ppe8. The remaining 22 isolates produced eight new ARDRA types, types 5 to 12.

Restriction analysis with endonucleases _Alu_I and _Hae_III was sufficient to allocate the strains into the 12 types. Moreover, _Hae_III alone was capable of resolving the most types (10 types), followed by _Alu_I (7 types), and _Hin_fI and _Rsa_I (5 types) (Table 1).

ARDRA types 1 (H. seropedicae) and 2 (H. rubrisubalbicans) shared all but one DNA fragment in the _Alu_I restriction pattern. Types 10 and 12 were differentiated by only two _Alu_I restriction fragments, and types 6 and 8 were differentiated only by the _Hae_III restriction pattern. A dendrogram, constructed from restriction patterns by using the TreeCon program (15), illustrated these tight relationships and showed three major clusters (Fig. 1). The first was formed by types 1 and 2 and included H. seropedicae and the H. rubrisubalbicans reference strains, the second was formed by types 3 to 9 and included Burkholderia reference strains M130 (type 3) and Ppe8 (type 4), and the third was formed by types 10 to 12 and was distant from the other two. Type 5 was separated from the other types in the cluster formed by types 3 to 9 and separated the Burkholderia and Herbaspirillum clusters (Fig. 1).

FIG. 1.

FIG. 1

Dendrogram inferred from _Alu_I, _Hae_III, _Hin_fI, and _Rsa_I restriction pattern data from Y1-Y3 16S rDNA PCR-amplified fragments obtained for the types shown in Table 1. Distances were calculated for all pairwise patterns with Nei-Li coefficient (9), and the dendrogram was established by the unweighted pair-group method with arithmetic average (12).

The Y1-Y3 PCR products were purified using Nucleon QC (Amersham Pharmacia Biotech) and sequenced using dye terminator chemistry and an ABI PRISM 310 sequencer (Applied Biosystems). Primers Y1 and Y2 (5′-CCCACTGCTGCCTCCCGTAGGAGT-3′) (19) were used to sequence both strands of the variable region (approximately 300 bp) located at the 5′ end of the 16S rRNA gene. The length of the Y1-Y2 region varied from 286 to 290 bp for types I to IX (see below), as reported for beta Proteobacteria (11), and was 260 and 259 bp for types X and XI, respectively, as reported for alpha Proteobacteria (16, 19).

The 30 bacterial isolates examined were allocated into 11 different groups (types I to XI [Table 1]), with each group consisting of isolates with the identical sequence. These sequences defined types which agreed well with the ARDRA-defined types, showing no apparent polymorphism within the types. However, two disagreements were observed with Herbaspirillum types: ARDRA type 1 contained the sequence-defined types I and II, and ARDRA type 2 contained the sequence-defined types I and III. While reference strains of H. seropedicae and H. rubrisubalbicans had distinct ARDRA (types 1 and 2) and sequence (types I and III) types, 11 isolates had the same H. rubrisubalbicans ARDRA type while showing 100% sequence identity to H. seropedicae in the Y1-Y2 region (Table 1). These isolates failed to hybridize with an H. seropedicae 23S rDNA species-specific probe (17), and the present molecular data support that these may constitute a new Herbaspirillum cluster.

A phylogenetic tree was constructed using the type I to XI sequences plus 47 sequences of 16S rDNAs of alpha and beta Proteobacteria available in the GenBank database (Fig. 2). The sequences were aligned with the ClustalX program (13), and the phylogenetic tree was reconstructed with the TreeCon program (15). A close relationship of types I, II, and III (Table 1) to the Herbaspirillum cluster was evident (Fig. 2). High bootstrap values supported types IV, V, VII, VIII, and IX being clustered within the Burkholderia genus. Type VI clustered within the Comamonadaceae, a family that originated from the Pseudomonas rRNA group III (14), as Burkholderia originated from Pseudomonas rRNA group II (18), and which also contains phytopathogenic species. Finally, types X and XI clustered within the alpha Proteobacteria, the former close to Azospirillum lipoferum and the latter close to Ochrobactrum anthropi.

FIG. 2.

FIG. 2

Phylogenetic tree inferred for genotype sequences I to X and representative organisms of the alpha and beta subclasses of Proteobacteria available in the GenBank database (accession numbers are in parentheses). The Y1-Y2 region was used to reconstruct the tree by the neighbor-joining method (10) from distances calculated by the method of Jukes and Cantor (6). A bootstrap analysis with 100 repetitions was performed, and only values above 50 are shown. The sequence of E. coli (a member of the gamma subclass of Proteobacteria) was used to root the tree.

The 14 isolates described by Weber et al. (17) used in this work were originally assigned to six groups related to Herbaspirillum and Burkholderia. Isolates AB48, AB98, AB119, AB120, AB147, BA123, BA124, and BA126, originally present within the same morphological and physiological group as strain M130 of B. brasilensis (17), clustered into six ARDRA groups (types 3, 4, 6, 7, 8, and 9), with only isolate BA124 being related to strain M130 (Table 1). Isolates AB98 and AB147 were similar to B. tropicalis Ppe8, while isolates AB48, AB119, AB120, BA123, and BA126 clustered within the Burkholderia genus. Isolates BA22 and BA23 failed to hybridize to oligonucleotide probes specific for Azospirillum spp., Herbaspirillum spp., Burkholderia spp., and Acetobacter diazotrophicus (17). The present results showed that these two isolates and eight new isolates, sharing the same ARDRA type, were related to Comamonadaceae.

In this paper we redefined 14 isolates described by Weber et al. (17) and the 24 new isolates into 12 genotypes. The discovery of eight new nitrogen-fixing bacterial genotypes, in addition to H. seropedicae, H. rubrisubalbicans, B. brasilensis, and B. tropicalis, in a few bacterial isolates from banana and pineapple revealed the great diversity of nitrogen-fixing bacteria associated with these fruit crops.

Nucleotide sequence accession numbers.

The sequences of the Y1-Y2 region of the 16S rDNA have been deposited in the GenBank database under accession numbers AF164042 through AF164065 and AF213248.

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