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Genome dynamics in Bacillus megaterium

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Title: Genome dynamics in Bacillus megaterium


1
Genome dynamics in Bacillus megaterium
What genomic sequencing tells us about the
genetic forces that shape Bacillus genomes
  • October 29, 2009
  • Dept. of Biological Sciences
  • NIU

2
The Genus Bacillus
  • Gram-positive, aerobic endospore-forming
    rod-shaped bacteria
  • Normal habitat the soil (plus lots of other
    places)
  • Mostly mesophilic, but some grow as low as 0and
    as high as 65.
  • Pathogens B. anthracis and B. cereus
  • Industrial uses enzyme production, Bt
    insecticidal corn
  • Endospores very resistant to heat and chemicals

3
Relatives among the Firmicutes
4
A Bit of History
  • Bacillus subtilis, originally named Vibrio
    subtilis, by Christian Gottfried Ehrenberg in
    1835. He was the first to use the name
    bacteria.
  • Ferdinand Cohn (1872) renamed the species
    Bacillus subtilis, as part of his description of
    bacteria by their shape (bacillus little
    stick).
  • --He is also responsible for bacteria being
    considered plants and not animals
  • Robert Koch first showed that a specific
    bacterium caused a specific disease B. anthracis
    and anthrax. (1876)
  • B. megaterium was first described by Heinrich
    Anton de Bary in 1884.

5
Bacilluss Position in the Tree of Life
  • Anything called Bacillus in the 1800s would
    now be a member of the Firmicutes (strong
    skin), a phylum that contains the Gram-positive
    low GC bacteria.
  • An alternative model, based on indels in
    universal genes, puts the Firmicutes near the
    root of the tree.

6
Bacillus Taxonomy
  • Bacillus is a very old genus name, and it has
    been split several times.
  • Bergeys Manual of Systematic Bacteriology, first
    edition (1986) lists 32 valid species, with about
    an equal number of synonyms.
  • Based on morphology, biochemistry, some DNA-DNA
    hybridization, numerical taxonomy
  • Carl Woese introduced the use of 16S rRNA
    sequences for phylogeny in 1977.
  • Bergeys Manual second edition (2004) splits the
    Bacillus genus into 4 families, with 37 genera in
    the Bacillaceae. Over 200 species.
  • Bacillus is still a genus, and still contains
    both B. subtilis and B. megaterium.
  • As in other taxa, a common phenotype is well
    correlated with a common genotype

7
Ash et al. (1991) Lett. Appl. Microbiol.
13202-206.
8
Genome Sequencing
  • Strain QM B1551, containing 7 plasmids
  • NSF Grant, to Pat Vary and Jacques Ravel
  • Most lab work done at TIGR/U. Maryland
  • NIUs role annotating the 6000 genes
  • Joined forces with Dieter Jahns group at the
    Technische Universität in Braunschweig, Germany,
    who were sequencing the DSM 319 plasmidless
    strain
  • In addition, there are about 20 other fully
    sequenced genomes from Bacillus and related
    genera
  • DSM319 has no plasmids, but at least 70 genes on
    the QM plasmids have good homologues on the DSM
    chromosome (purple ring near the middle)

9
Common Features, Genetic Forces
Assuming that all Bacillus species descended from
a common ancestor, what is similar and different
between them, and why?
  • Genetic Forces
  • Vertical descent
  • Background substitution and indel mutations
  • Horizontal gene transfer (about 10 different
    genes between QM and DSM)
  • Intragenomic recombination
  • Homogenization of rRNA operons, presumably by
    gene conversion
  • Common Features
  • Morphological and biochemical characteristics
  • 16S rRNA genes
  • A group of common protein-coding genes
  • Chromosomal synteny
  • rRNA operons

10
16S Variation, Phylogeny, and Species
Identification
  • B. megaterium has 11 rRNA (rrn) operons on the
    chromosome in both sequenced strains, in the same
    genomic positions.
  • QM also has an rrn operon on plasmid pBM400,
    which is not found in DSM.
  • The 16S genes in B. megaterium are 1540 bp long
    and very similar, but not identical.
  • Gene conversion is thought to homogenize rRNA
    operons
  • Recombination between rrn operons leads to
    deletions
  • The question addressed here what effect does 16S
    variation within the genome have on phylogeny and
    species identification?

11
Differences between 16S genes with B. megaterium
  • Seven identical 16S genes the rrnE, rrnF, and
    rrnI genes in QM and the rrnA, rrnB, rrnF, and
    rrnK alleles in DSM.
  • Also, the rrnA and rrnB alleles in QM were
    identical to each other
  • Note the lack of clear vertical descent in this
    pattern
  • Total of 20 sites with polymorphisms.
  • All but 4 are unique to a single operon
  • All but one shared polymorphism are found in both
    QM and DSM
  • Positions 461 and 474 are probably a stem-loop
  • all genes with an A at 461 have a T at 474, and
    all lines with a G at 461 have a C at 474.

12
Mismatch Differences in Completely Sequenced
Genomes
13
Differences in Completely Sequenced Genomes
  • Maximum differences within any genome 16 (B.
    clausii)
  • My basic argument there is no point in having
    two different species which are less different
    than 16S genes within the same genome.
  • Among the cereus group genomes, there are fewer
    differences between genes in B. cereus, B.
    anthracis, and B. thurengiensis, than there are
    between genes in the same genome.
  • Also, B. weihenstephanesis has only very few
    differences from these
  • B. subtilis and B. amyloliquifaciens are also
    very similar.
  • Effects on phylogeny pick a random 16S gene from
    each genome, align, count differences, do a
    neighbor-joining tree. 1000 reps.

14
Neighbor-Joining Trees with Completely Sequenced
Genomes
  • Different choices of which 16S genes to use leads
    to different phylogenies, both at the
    species/subspecies level and at higher levels.
  • The variable nodes in the cereus group and the
    halodurans/clausii group are independent. Thus,
    these three tree represent 9 variants.

15
Defining B. megaterium and distinguishing it from
other species, using 16S
  • Comparison of B. megaterium isolates from Genbank
    to QM-rrnA
  • A total of 185 isolates that were gt1390 bp (i.e.
    gt 90 of full length) and had fewer than 10
    ambiguity characters were aligned with QM_rrnA,
    and the number of variant positions were counted.
  • 70 have 9 or fewer differences
  • 86 have 20 or fewer differences
  • 95 have 46 or fewer differences.
  • Most isolates seem to fall into a single group,
    but there may be some significantly different
    subtypes in B. megaterium.
  • Or, new species may be defined

16
Positions of Nucleotide Variants in Genbank
Isolates
  • 43 of the 1540 nucleotide positions in the 16S
    gene have at least one variant in the B.
    megaterium strains from Genbank.
  • Most of the variation occurs at the ends of the
    16S gene. This is also the region where missing
    data is most common.
  • PCR primers for 16S need to be internal to the
    gene
  • The variant positions in the middle were seen in
    QM and DSM the paired 461/474 positions, and
    1140. There are no major polymorphisms outside
    the end regions that are not seen in QM and DSM.

17
Closely Related Species
  • How easy is it to distinguish between B.
    megaterium and closely related species?
  • What species are closely related to B.
    megaterium? Different phylogenetic trees give
    different answers.
  • All of the species on the next slides appear to
    be more similar to B. megaterium than members of
    the cereus group on at least one phylogenetic
    tree.
  • All are in genus Bacillus except Lysinibacillus
    sphaericus.
  • Total of 344 strains used

18
Number of Differences from QM-rrnA for Different
Species
  • Except for B. flexus and one B. simplex isolate,
    all strains are well-differentiated from B.
    megaterium with a minimum of 58 differences.
  • B. flexus overlaps the B. megaterium distribution
    heavily. The average B. flexus isolaate had 29.4
    differences from QM_rrnA, with some isolates
    indistinguishable. Type strain differs at 16
    positions the B. megaterium type strain differs
    at 4 positions.
  • The average B. simplex isolate had 79.4
    differences from B. megaterium the one
    exceptional strain had 17 differences (maybe its
    a mis-labeling)

19
Conclusions about 16S genes
  • Choosing different 16S genes from within genomes
    can affect the resulting phylogenetic trees.
  • The 16S genes within B. megaterium and other
    completely sequenced Bacillus genomes differ from
    each other by up to 16 positions.
  • Some species differ from other species at fewer
    positions than 16S genes differ within individual
    genomes.
  • Although most B. megaterium strains are very
    similar to QM and DSM, there are a few strains
    with very different 16S genes that may represent
    subtypes within B. megaterium, or which may
    ultimately be assigned to new species.
  • Most of the polymorphisms in the 16S genes are
    almost unique all of the widespread . megaterium
    polymorphisms are found in QM and DSM.
  • Most of the closely related species fall outside
    the range of variation seen within B. megaterium,
    but B. flexus is a major exception.
  • some isolates of B. flexus are indistinguishable
    from B. megaterium, and most fall within the same
    range of variation seen in B. megaterium

20
Common Genes and Synteny
  • Bacillus is a relatively well-sequenced genus,
    with 11 complete genomes publicly available (not
    including B. megaterium).
  • What genes are found in all Bacillus species, the
    core genome?
  • Where on the chromosome are the conserved genes?

21
Bacillus Core Genome
22
QM vs. DSM Genes
23
Between Species
24
Synteny Results
  • The syntenic region around the origin of
    replication is shared throughout the Bacillaceae,
    including the genera Bacillus, Geobacillus,
    Oceanobacillus, and Anoxybacillus.
  • 99 of the 2000 core genes are in the syntenic
    region.
  • Next rRNA operons and adjacent genes concrete
    examples of conserved synteny.

25
rRNA operons (rrn)
  • There are 11 rRNA operons on the B. megaterium
    chromosomes, plus one on plasmid pBM400 in the QM
    strain.
  • Other Bacillus species have 8-15 rrn operons
  • The rrn operons are in the conserved synteny
    region.
  • Only in Bacillus and relatives
  • rrn operons are all on the leading DNA strand
    transcribed in the same direction as the
    replication fork moves.
  • Most Bacillus rrn operons are on the right
    replichore, near the origin of replication

26
From Stewart and Cavanaugh, 2007, J. Mol.
Evol. 6544-67
27
Common Sites
  • Nearly all the rrn operons in the Bacillaceae can
    be found between sets of common flanking genes.
  • Sometimes with DNA insertions separating the rrn
    locus from one side
  • A few unique rrn operons, including 2 in B.
    megaterium
  • Not in Paenibacillus

A DNA repair protein recF B DNA gyrase, subunit
B C DNA gyrase, subunit A D
inosine-5'-monophosphate dehydrogenase E
D-alanyl-D-alanine carboxypeptidase. F glutamine
amidotransferase, synthase subunit
28
rrn operons in Bacillaceaae are in specific sites
29
Variations
  • Seven sites on the right replichore, plus one on
    the left replichore.
  • Also, a site shared within the cereus group, and
    two sites shared in Geobacillus and
    Anoxybacillus.
  • Individual rrn sites can contain 0-5 rrn operons.
  • Some sites are empty the flanking genes are
    adjacent, with no rrn operon between
  • A few sites are missing the flanking genes are
    not present in the genome or are dispersed to
    very different locations.
  • Tandem duplications of rrn operons are common
  • Several variations caused by apparent
    intragenomic recombination

30
Tandem Duplication Copy Number
31
Intragenomic Recombination at rrn Sites
  • rrn operons are almost identical, among the very
    few repeated sequences in bacterial genomes
  • A second example insertion sequences (IS) ,
    which are mobile genetic elements found in many
    genomes (very few in B. megaterium ).
  • The presence of highly conserved genes and the
    consequences of intragenomic recombination in a
    circular genome constrains genome rearrangements.
  • The arrangement of rrn operons and their sites
    can be understood as the result of three forces
  • intragenomic recombination between rrn operons,
  • insertions/deletions of blocks of protein-coding
    genes,
  • recombination events within tandem arrays of rrn
    operons.

32
Symmetrical Inversion Between Replichores
  • Anoxybacillus flavithermus

33
Double Crossover Re-orders Flanking Genes
  • B. pumilis

34
Double Crossover in Flanking tRNA Regions
  • B. amyloliquifaciens rrnE.
  • Resulted in loss of 2/3 of the 16S gene.
  • 23S and 5S OK
  • very little obvious homology on the right side.

35
Tandem Duplication Events Duplication by
Unequal Crossing Over
  • rrnD in Oceanobacillus iheyensis

36
Tandem Duplications in the cereus group rrnG site
  • Every deletion between adjacent rrn operons can
    be seen.
  • Deletion of genes between rrn 2 and rrn3
    (preserving one gene in the middle).
  • Region between rrn 3 and rrn 4 completely
    replaced.

37
Intragenomic Recombination Conclusions
  • Most rrn operons are found in the same sites in
    all Bacillus genomes
  • Differences in rrn operon number are mostly due
    to tandem duplications within these sites
  • Intragenomic recombination is well documented in
    Bacillus genomes
  • Anoxybacillus symmetric inversion across ori
  • B. pumilis double crossover involving 3 regions
  • Oceanobacillus rrnD CO between tandem copies
  • rrnD in other species at least 2 events
  • cereus group rrnG deletions between tandem
    copies (at least 4 different events)
  • cereus group rrnG replacement of inter-rrn
    region by presumed 2CO
  • cereus group rrnG deletion of inter-rrn region,
    leaving a central portion intact (2 deletions?).
  • B. amyloliquifaciens rrnE 2CO involving 3
    regions, with the central section having the COs
    150 bp apart
  • B. megaterium rrnBC 2CO involving 3 regions,
    with little homology at one end
  • Several other duplication/deletion events within
    tandem duplications

38
Some Events NOT Observed
  • The lack of certain events supports several
    current ideas.
  • to the extent that lack of evidence constitutes
    evidence.
  • Crossovers between rrn sites despite numerous CO
    events within rrnG in the cereus group, plus many
    other CO events
  • supports the idea that the flanking genes are
    necessary
  • Asymmetric CO across ori only one symmetric one
    observed, so evidence is not strong.
  • Supports the idea that symmetric replichores are
    selectively advantageous
  • Inversions within a replichore all rrn in all
    species are on the leading strand, in both
    replichores.
  • supports the idea that replication and rrn
    transcription must proceed in the same direction

39
Some Unsolved Questions
  • Replichore asymmetry
  • most of the rrn are in the right replichore
  • compositional bias between replichores
  • Mechanism of insertion/deletion/horizontal gene
    transfer
  • a big question. We are examining insertion sites
    for clues.
  • Is there a common phylogeny for the conserved
    synteny region in B. megaterium?
  • Finding and analyzing allegedly unique events
    (indels and recombinations)

40
DNA Composition shows replichore asymmetry
41
Simple vs. Compound Insertions
42
Thanks!
  • NIU Biology Dept.
  • Pat Vary
  • Janaka Edirisinghe
  • Kirthi Kumar Kutumbaka
  • Sandhya Balasubramanian
  • Jenn Hintzsche
  • Chris Braun
  • Denise Tombolato
  • Judy Luke
  • Scott Grayburn
  • NIU Computer Science Dept.
  • Stephen Snow
  • Reva Freedman
  • Minmei Hou
  • Argonne National Labs
  • Ross Overbeek
  • Gordon Pusch
  • Terry Disz
  • TIGR/U. Maryland
  • Jacques Ravel
  • Mark Eppinger
  • MJ Rosovitz
  • Technische U. Braunschweig
  • Dieter Jahn
  • Boyke Bunk
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