Background

Biol Direct

Biology Direct

1745-6150

BioMed Central

London

PMC1562361

1562361

16872524

1745-6150-1-21

16872524

10.1186/1745-6150-1-21

Research

Phylogeographic support for horizontal gene transfer involving sympatric bruchid species

Alvarez

Nadir

1 2 nadir.alvarez@unine.ch Benrey

Betty

1 betty.benrey@unine.ch Hossaert-McKey

Martine

2 martine.hossaert@cefe.cnrs.fr Grill

Andrea

1 andrea.grill@unine.ch McKey

Doyle

2 doyle.mckey@cefe.cnrs.fr Galtier

Nicolas

3 galtier@univ-montp2.fr

1Laboratoire d'Entomologie Evolutive, Université de Neuchâtel, 11 rue Emile-Argand, 2007 Neuchâtel, Switzerland 2Centre d'Ecologie Fonctionnelle et Evolutive, CNRS, 1919 route de Mende, 34293 Montpellier Cedex 5, France 3Laboratoire Génome Populations Interactions Adaptation, CNRS, Place Eugène Bataillon, 34095 Montpellier Cedex 5, France

2006

27 7 2006

1 21 21

24 7 2006 27 7 2006

2006

Alvarez et al; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Background

We report on the probable horizontal transfer of a mitochondrial gene, cytb, between species of Neotropical bruchid beetles, in a zone where these species are sympatric.

The bruchid beetles Acanthoscelides obtectus, A. obvelatus, A. argillaceus and Zabrotes subfasciatus develop on various bean species in Mexico. Whereas A. obtectus and A. obvelatus develop on Phaseolus vulgaris in the Mexican Altiplano, A. argillaceus feeds on P. lunatus in the Pacific coast. The generalist Z. subfasciatus feeds on both bean species, and is sympatric with A. obtectus and A. obvelatus in the Mexican Altiplano, and with A. argillaceus in the Pacific coast. In order to assess the phylogenetic position of these four species, we amplified and sequenced one nuclear (28S rRNA) and two mitochondrial (cytb, COI) genes.

Results

Whereas species were well segregated in topologies obtained for COI and 28S rRNA, an unexpected pattern was obtained in the cytb phylogenetic tree. In this tree, individuals from A. obtectus and A. obvelatus, as well as Z. subfasciatus individuals from the Mexican Altiplano, clustered together in a unique little variable monophyletic unit. In contrast, A. argillaceus and Z. subfasciatus individuals from the Pacific coast clustered in two separated clades, identically to the pattern obtained for COI and 28S rRNA. An additional analysis showed that Z. subfasciatus individuals from the Mexican Altiplano also possessed the cytb gene present in individuals of this species from the Pacific coast. Zabrotes subfasciatus individuals from the Mexican Altiplano thus demonstrated two cytb genes, an "original" one and an "infectious" one, showing 25% of nucleotide divergence. The "infectious" cytb gene seems to be under purifying selection and to be expressed in mitochondria.

Conclusion

The high degree of incongruence of the cytb tree with patterns for other genes is discussed in the light of three hypotheses: experimental contamination, hybridization, and pseudogenisation. However, none of these seem able to explain the patterns observed. A fourth hypothesis, involving recent horizontal gene transfer (HGT) between A. obtectus and A. obvelatus, and from one of these species to Z. subfasciatus in the Mexican Altiplano, seems the only plausible explanation. The HGT between our study species seems to have occurred recently, and only in a zone where the three beetles are sympatric and share common host plants. This suggests that transfer could have been effected by some external vector such as a eukaryotic or viral parasite, which might still host the transferred fragment.

Reviewers

This article was reviewed by Eric Bapteste, Adam Eyre-Walker and Alexey Kondrashov.

Open peer review

Reviewed by Eric Bapteste, Adam Eyre-Walker and Alexey Kondrashov. For the full reviews, please go to the Reviewers' comments section.

Background

The traditional view of evolution supports that DNA is transferred vertically from parent to offspring. Hybridization and genetic transfer between different species is usually strongly limited. However, exceptions to this rule, i.e. the horizontal transmission of genetic material between distantly related organisms (HGT), are increasingly recognized as an important process of evolution in prokaryotes [1-4]. In eukaryotes, however, reported cases of between-species genetic exchanges not involving hybridization have been essentially limited to noncoding or parasitic transposons or virus sequences. Exceptions to this are a few instances of horizontal transfer of selected genes between prokaryotes and eukaryotes (e. g., [5-7]) and two reports suggesting lateral transfer of mitochondrial genes between genetically distant land plant groups [8,9]. No instance of HGT in animals has been reported up to now.

In a recent paper, Martin [10] discusses the relevance of the HGT hypothesis in eukaryotes, focusing on land plants, and stresses the need for corroborating studies in other eukaryote groups. However, he addresses the necessity of careful interpretation of HGT data, and points to the requirement of first discussing such data in the light of standard theories of vertical inheritance of genes.

Our study investigates the phylogenetic relationships between four Neotropical bruchid beetles (Coleoptera, Bruchidae), namely Acanthoscelides obtectus Say, A. obvelatus Bridwell, A. argillaceus Sharp, and Zabrotes subfasciatus Boheman. These beetles develop on seeds of several bean species (genus Phaseolus): Acanthoscelides obtectus and A. obvelatus feed on the common bean (P. vulgaris L. group), A. argillaceus on the Lima bean (P. lunatus L. group), and Z. subfasciatus on both. As A. obtectus,A. obvelatus and Z. subfasciatus can develop on beans of the same species, they are often sympatric in wild or cultivated common beanpopulations. We sampled individuals from these three species in the southern part of the Mexican Altiplano, one such zone of sympatric occurrence of A. obtectus,A. obvelatus and Z. subfasciatus (Figure 1). Although the geographic range of A. argillaceus overlaps with those of its two congeners, it is rarely found in the same habitat, because of its distinct host plant. Acanthoscelides argillaceus and the generalist Z. subfasciatus, however, commonly co-occur in wild Lima bean populations [11]. This is the case in the Pacific coast of Mexico (Figure 1), where individuals from these two species were sampled.

Figure 1

Geographic origin of Acanthoscelides obtectus (), A. obvelatus (▽), A. argillaceus () and Zabrotes subfasciatus () individuals sampled. (a) Pacific coast populations; only one cytb gene is present in Z. subfasciatus populations (SJB, ELA). (b) Altiplano populations; two cytb genes are present in the same individual in some Z. subfasciatus (OCM, YAU, TLA); (c) population of origin of the Z. subfasciatus laboratory colony.

The genera Acanthoscelides and Zabrotes are morphologically very different [12], and are thought to have diverged during the Palaeocene (65 to 54.8 mya) or the Eocene (54.8 to 33.7 mya) [13], whereas the three Acanthoscelides species studied here belong to the same morphologically defined group within the genus and seem to have diverged during the Miocene (23.8 to 5.3 mya) [14,15]. To confirm the phylogenetic position of these four species in the context of host plant adaptation (see [16]), we performed amplification and sequencing of two mitochondrial genes and one nuclear gene.

Results

For each of the three studied genes, different models of evolution were selected by likelihood ratio tests: for COI, the Tamura-Nei model with a proportion of invariable sites and a gamma distribution was selected; for cytb, the Hasegawa-Kishino-Yano model with a gamma distribution was selected; for 28s rRNA, the Kimura 2-parameters model was selected. Topologies of phylogenetic trees were congruent for 28S rRNA and COI, and showed each species as a monophyletic group, the three Acanthoscelides species forming a distinct clade from Z. subfasciatus (see Figure 2a) (28S rRNA [accession numbers AY881176–AY881195, DQ152235–DQ152238]; COI [accession numbers AY881196–AY881214, AY881232, DQ152239–DQ152242]). COI genetic distances ranged from 0.273 to 0.324 substitutions per site between Acanthoscelides spp. and Zabrotes subfasciatus, and from 0.172 to 0.212 substitutions per site among Acanthoscelides species. According to a recent calibration of a beetle mitochondrial molecular clock [17], such genetic distances correspond to divergence times of 35–40 My between Acanthoscelides spp. and Zabrotes subfasciatus, and 20–25 My among Acanthoscelides species. These divergence times were confirmed by estimates obtained from mitochondrial 12S rRNA [16], and are fairly similar to the fossil record [13].

Figure 2

Phylogenetic patterns. a. Phylogenetic relationships between different populations of Acanthoscelides obtectus (), A. obvelatus (▽), A. argillaceus () and Zabrotes subfasciatus () for the mitochondrial COI gene. An identical topology is supported by 28S rRNA (not shown); b. Phylogenetic relationships between different populations of Acanthoscelides obtectus (), A. obvelatus (▽), A. argillaceus () and Zabrotes subfasciatus () for the cytb gene. Underlined individuals correspond to Z. subfasciatus populations from the Mexican Altiplano – some carry two cytb haplotypes. Stars (*) indicate Z. subfasciatus haplotypes identical to haplotypes from Acanthoscelides. "Z. subfasciatus CLNY" corresponds to an individual of the laboratory colony affected by HGT.

The analysis of cytb sequences, in contrast, revealed an unexpected pattern (see Figure 2b) (accession numbers AY422474–AY422479, AY422485–AY422488, AY881215–AY881232). First, individuals of A. obtectus and A. obvelatus were not separated in two distinct clades, but grouped into a single, little variable monophyletic unit, as would be expected for individuals belonging to the same species. A core clade containing 46 of the 50 sequenced individuals from the two species included 14 closely related haplotypes (maximal distance: 0.0084), some of them shared by the two species, others private to A. obtectus or A. obvelatus. In contrast, A. argillaceus individuals clustered in a separate clade, whose mean distance to the A. obtectus – A. obvelatus core clade was 0.143. Secondly, cytb data revealed a surprising discrepancy among the individuals of Z. subfasciatus. Whereas an expected 0.25 nucleotide divergence from Acanthoscelides spp. was found for the Z. subfasciatus individuals from the Pacific coast of Mexico, three Z. subfasciatus individuals from the Altiplano (coming from three different populations) showed a cytb sequence identical to the most common A. obtectus – A. obvelatus core clade haplotype.

PCR with specific primers and subsequent sequencing revealed that the three Altiplano Z. subfasciatus individuals surprisingly carried both cytb genes (Figure 2b), their own plus the one demonstrating an Acanthoscelides origin. The specific primers were then applied to other Z. subfasciatus individuals from the Altiplano and the Pacific coast. In the Altiplano, 20 individuals out of 70 were revealed to carry both cytb genes – while the remaining 50 only carried their own specific cytb – whereas in the Pacific coast, all the 40 sampled individuals were revealed to carry only their own cytb haplotype. The specific primers were then also applied to 25 individuals of a laboratory colony of Z. subfasciatus that had been maintained for 10 months in the Laboratory of Evolutionary Entomology at the University of Neuchâtel (Switzerland). The colony was founded using individuals from the Mexican Altiplano, i.e., potentially affected by the HGT. These individuals had not been in contact with any Acanthoscelides for about 5–10 generations. Three individuals out of the 25 were revealed to carry both cytb genes, while 22 showed only the Z. subfasciatus haplotype. The number of individuals sampled in each site and the number of individuals fitting the core clade haplotype are summarized in Table 2.

An analysis of cytb sequence variation within the A. obtectus – A. obvelatus core clade revealed no frameshift, and a low (0.106) ratio of non-synonymous to synonymous changes, significantly lower than 1 (likelihood ratio test: 2(ln [Likelihood(M1)]-ln [Likelihood(M2)]) = 47.5; χ²[1 df]: P < 10-4), indicating that this gene is under selection. Furthermore, these sequences included no mitochondrial stop codon, but typically five nuclear stop codons, strongly suggesting that this gene is replicated by a mitochondrion, and neither by a nuclear nor a bacterial machinery.

Discussion

The cytb pattern shown by A. obtectus, A. obvelatus and three Mexican Altiplano Z. subfasciatus individuals is highly incongruent with traditional taxonomy, and with the COI and 28S rRNA pattern. This is even more astonishing, considering that cytb and COI are supposedly genetically linked in the non-recombining mitochondrial genome.

Four hypotheses can be addressed to explain this unexpected result: (i) experimental contamination, (ii) hybridization, (iii) pseudogenisation and (iv) horizontal gene transfer.

Contamination hypothesis

All experiments were simultaneously conducted on many (>200) bruchid samples, including museum specimens with low amounts of DNA, by the same researcher in the same laboratory. Only the cytb PCR for Mexican Altiplano individuals yielded an additional, unexpected band. In Acanthoscelides, no individual from the Pacific Coast A. argillaceus carried the additional gene, although they were analyzed simultaneously with the A. obtectus and A. obvelatus samples. A putative laboratory contaminant would not only have affected the samples coming from the Mexican Altiplano but also individuals from other sites and particularly museum specimens, which contain very small amounts of DNA, given the fact that samples were randomized on the 96-well plates, both during DNA extraction and PCR reactions. Another strong argument against the contamination hypothesis is that several individuals of the core clade from both A. obtectus and A. obvelatus demonstrated private cytb haplotypes. These haplotypes cannot be the consequence of a contamination, since they were found only once (we sequenced all the amplified cytb fragments). In the case of a contamination, a single haplotype would be expected to occur in a large number of random samples, whereas our data show many related but distinct – and sometimes private – haplotypes found in a non-random subset of the samples. Sampling contamination (e.g., the presence of Acanthoscelides tissues in Z. subfasciatus samples) can also be excluded, since three Z. subfasciatus individuals sampled from the experimental colony showed the additional cytb PCR band. The experiments on colony individuals (DNA extraction, PCR) were conducted several weeks after the analysis of the wild samples, making any cross-experiment contamination impossible.

Hybridization hypothesis

Hybridization between Acanthoscelides species and Zabrotes subfasciatus is very unlikely. First, the split between the two genera dates back to around 40 mya (molecular clock data) to 60 mya (fossil record) ago. Moreover, they demonstrate a very high level of nucleotide divergence (25%). Usually, the degree of genetic divergence in documented cases of interspecific hybridization in insects never exceeds 5%-10% of nucleotide divergence for protein-encoding mitochondrial genes [18-20], which is much lower than the 25% divergence found between Acanthoscelides and Zabrotes. Secondly, hybridization appears functionally impossible, given the highly differentiated morphology, especially in the male genitalia. The lateral lobes of the male genitalia – which play the decisive role of pushing aside parts of the female genitalia to allow penetration by the median lobe, and which are known to be part of a specific lock/key system – are spectacularly different between the two genera. Borowiec [12] points out that the structure of the aedeagus is very different in Zabrotes and Acanthoscelides and highly specialized in both. The lateral lobes are particularly distinct, short and almost entirely fused in Zabrotes, but elongate and divided by a deep cleft almost to the base in Acanthoscelides. In the bruchid family, in which many cryptic species remain to be described, male genitalia are often the only character to distinguish between otherwise morphologically identical (but never hybridizing) sibling species. This clearly explains why any attempt to produce hybrid offspring between Acanthoscelides and Zabrotes failed (N. Alvarez, unpublished observations). Moreover, even in the two morphologically similar Acanthoscelides obtectus and A. obvelatus, no evidence of interspecific hybridization has been detected in natura, despite the genetic analysis (by means of diagnostic microsatellite loci) of hundreds of individuals from the two species, among which dozens originated from sympatric populations [15].

Pseudogene hypothesis

An additional surprise in our data is that the putatively transferred fragment appears to evolve under purifying selection. The rate of non-synonymous substitutions is significantly lower than expected under a model involving a non-selected gene, and there is no insertion or deletion in any cytb sequenced fragment. Moreover, the fragment seems to be expressed in a mitochondrion. Given that the gene is under purifying selection, it could hardly have been translated using the nuclear genetic code, since in that case, five codons would have been translated in stop-codons. These properties argue for an active gene, rather than a pseudogene. A pseudogene – which by definition can hardly ever be under purifying selection – would not show a bias to synonymous over non-synonymous mutations, and its sequence would most likely show nucleotide insertion or deletion. Furthermore, in the exceptional context of a selected pseudogene [21], the gene must not contain any stop codon when translated with the nuclear genetic code. The combined evidence suggests that genes from the core clade are (i) under purifying selection and are therefore not pseudogenes, and (ii) are translated in a mitochondrion.

Horizontal gene transfer hypothesis

Our data clearly argue against any standard explanation for the genetic pattern we observed. A horizontal transfer of the cytb gene between A. obtectus and A. obvelatus, and from one of these species to Z. subfasciatus, seems the most plausible hypothesis, even though the probability of such a mitochondrial genetic exchange between distinct eukaryote species is very low (but is invoked in a recent study in plants [8,9]). We assume that species polyphyly in the cytb core clade results from a relatively ancient HGT process having started at the time of the core clade ancestor or earlier. Alternatively, one may interpret this clade as resulting from a series of numerous, very recent HGT events. Under the latter hypothesis, the functional constraints we outlined in the last paragraph would have pre-dated HGT's, and would not guarantee that the transferred gene is active and expressed in a mitochondrion.

The data available do not allow formal rejection of this latter hypothesis, under which the transferred pieces of DNA could even be nuclear pseudogenes. This hypothesis requires, however, a sudden, very recent increase of the HGT rate from zero to a very high value. This could be conceivable in the context of a rapid, infectious process (if, for instance, one specific strain of a parasite acquires the ability to switch species and invade the new niche), but in this case one would expect to see a single transferred haplotype (or a small number of them), whereas the intricate phylogeny of the core clade implies several events of HGT involving several distinct haplotypes.

Under either of these two hypotheses (one ancient HGT or several recent ones), the transfer from one species to another could possibly have been carried out by an external vector. Candidate vectors include viruses, prokaryotes such as Wolbachia or other endosymbiotic bacteria (a case of horizontal transfer of genes from Wolbachia to the nuclear genome of its host was recently reported in bruchids [22]) or even eukaryotes (e.g., intra- or extra-cellular parasites, endoparasitoïds). The location of the transferred cytb in the recipient species remains to be investigated. A parsimonious hypothesis is that the transferred cytb is still hosted by its vector. A eukaryotic parasite might have "domesticated" a bruchid mitochondrion (or at least some bruchid mitochondrial gene), carrying it on when switching to a new species. Such an hypothesis could explain the presence of two cytb genes in Z. subfasciatus individuals from the Altiplano, suggesting that one gene could be carried by a parasite, and the other could belong to the mitochondria of Z. subfasciatus itself. This could also be the case in A. obtectus or A. obvelatus, even though we could not yet demonstrate the existence of a second cytb gene in individuals belonging to the core clade.

If we consider that the vector may belong to a eukaryotic group (i) capable of mitochondrial recombination and (ii) showing a genetic code that uses the same mitochondrial stop-codons as those used by the mitochondria of invertebrates – these two conditions are for example filled by most unicellular eukaryotes – then the mitochondria carried by the parasite may have "included" the "bruchid"-cytb in its genome after recombination. Another interesting point is that the transferred gene replicates in Z. subfasciatus, since it survived ~5–10 generations in the laboratory.

Ecological context of HGT

As this HGT event has been detected only between individuals from the Altiplano where the three species co-occur and share the same host plant, it gives clues to the ecological context which may favor such a gene exchange. Indeed, the ecologically distinct A. argillaceus does not demonstrate a HGT pattern for cytb, despite its phylogenetic proximity to A. obtectus and A. obvelatus. This suggests that the probability of the occurrence of lateral gene transfer is partly controlled by the environment. The occurrence of HGT between bruchid species (i) presenting a high degree of phylogenetic divergence but (ii) sharing some dimensions of their ecological niche (e.g., their host plant) could indicate that ecology, as well as phylogeny, might play a role in the distribution of genetic variation across taxa.

Conclusion

Recent horizontal gene transfer (HGT) between A. obtectus and A. obvelatus, and from one of these species to Z. subfasciatus in the Mexican Altiplano, seems the most plausible hypothesis to explain the pattern we observed in our data for cytb. The transfer could have been effected by some external vector such as a eukaryotic parasite, which might still host the transferred fragment.

Obviously, additional molecular, cellular and tissular characterization would be of great relevance to the understanding of this intriguing system, of the exact length and structure of the apparently transferred fragment, and the nature of the genome hosting it. The contemporaneous nature of this putative HGT – it is still polymorphic in Z. subfasciatus at least – makes it a promising model for further investigation of the mechanisms underlying genetic exchanges between species

Methods

Individuals of A. obtectus, A. obvelatus, A. argillaceus, and Z. subfasciatus were sampled in the southern Mexican Altiplano. Coordinates of sampled sites are given in Table 1. We amplified and sequenced bi-directionally two mitochondrial genes – cytochrome oxidase I (COI) and cytochrome b (cytb) – and one nuclear gene – 28S ribosomal rRNA (28S rRNA) – from 6 to 25 individuals in each species, using universal primers (28S rRNA: 28ee and 28 mm; COI: C1-J-2183 and TL2-N-3014; cytb: CB-J-10933 and CB-N-11367 [23]). Total genomic DNA was extracted using DNeasy™ 96-well kit (QIAGEN). PCR amplifications were performed in a final volume of 10 μL, which contained 1 μL of extracted DNA, 1 μL of 25 mM MgCl2, 0.1 μL of 10 mM dNTPs, 1 μL of PCR buffer (Eurogentec), 1 unit of Taq DNA polymerase (Eurogentec Red Goldstar™), 0.5 μL of forward primer, and 0.5 μL of reverse primer. PCRs were performed separately for each primer pair on a PTC-200™ thermocycler using the following cycling conditions: initial denaturation at 92°C (1 min 30 s); 30 cycles of 92°C (30 s), annealing at 55°C (45 s), 72°C (1 min 30 s); final elongation at 72°C (10 min). Sequencing reaction was carried out using Applied Biosystems BygDye™ protocol. Products of the sequencing reactions were then analyzed on an ABI Prism 310 sequencer. Chromatograms were manually corrected using Chromas 2.23 (Technelysium Pty. Ltd., Helensvale, Australia) and further aligned using ClustalW 1.83 [24]. The best-fit substitution model was determined using Modeltest 3.06 [25] through hierarchical likelihood ratio tests. Phylogenetic trees were reconstructed by maximum likelihood using Treefinder [26]. Distances between groups were determined by distance methods using Mega 2.1 [27] with standard parameters (Kimura 2-parameters; gamma shape parameter = 0.5). Primers specific for cytb consensus haplotypes of A. obtectus and A. obvelatus, and for cytb haplotypes of Pacific coast Z. subfasciatus, respectively, were designed. Sequences of specific primers to the most common haplotype shared by A. obtectus and A. obvelatus are: TTGATAACGCAACCTTAACC (forward primer) and GATTAGCAGGAATGAAGTTG (reverse primer). Sequences of specific primers to Pacific-coast Z. subfasciatus cytb are: GAGATAATGCAACATTAACA (forward primer) and GGTTTGCGGGCGTAAAATTA (reverse primer). To test whether the sequenced cytb genes were under purifying selection (i.e., they were not the result of a nuclear mitochondrial pseudogene), we compared rates of synonymous and non-synonymous substitutions. Two models of codon evolution [28] were tested using PAML 3.14b [29]. In model M1, the ratio of non-synonymous to synonymous evolutionary rate (ω) was set to 1, as expected for a pseudogene. In model M2, the ratio was free to vary. A likelihood-ratio test was performed to compare the two models.

Reviewers' comments Reviewer's report 1 Eric Bapteste, Dalhousie University, Halifax, Canada

This paper presents potentially interesting data and a possibly compelling result – lateral gene transfers of genes between animal species-, that if confirmed, would certainly deserve to be reported to a broad audience of readers. Yet, a great deal of caution is required before accepting the conclusion proposed here. In my view the present study is still too weak to support the conclusion.

Certainly, the authors reject several alternative hypotheses to explain the bizarre distribution of cytb genes in bruchids. For instance, the presence of two divergent copies of the cytb gene in Z. subfasciatus, one of them being very conserved in sequence and shared by a set of traditionally distantly related taxa, deserves some explanation. In that respect, the authors are right to attract our attention of this result. They exclude the possibility of contamination, hybridization events and the possibility that one of the copies is in fact a pseudogene. Importantly enough though, I feel that more work is needed to test their final proposition and to conclude in favour of the lateral transfer of the gene between animals, based on the sole evidence presented here. Some more in depth analyses should be performed in order to test their claim and to propose a more precise interpretation of the data. Typically, questions about the mechanism of acquisition of this second copy of cytb should be at the heart of such future studies. Nevertheless, some quick adjustments could be incorporated into a moderately revised version of this manuscript.

It might be of some help in deciding if it is premature or legitimate to quote this study as a case of lateral gene transfer in animals if the authors could answer some of the questions below.

1. Is it really impossible that an endoparasite is a source of a contamination, that the relatively conserved cytb gene shared by the three species is not of bruchid origin and that the observations may be partly artefactual?

If these species hosted a population of closely related endoparasite, could not two cytb sequences be amplified from these organisms? In this case, we would get the sequences of the population of endoparasites (presenting thus some distinct but related haplotypes) and the one for the bruchid? What does a blast of this additional copy teach us: who are the closest completely sequenced relatives having homologues to this additional sequence? Including these data in a broader phylogenetic tree via a broader cytb alignment would certainly be a very important additional result to present to the readers. Are these bruchid sequences still monophyletic when a larger taxonomic sample is investigated and, if not, where do these gene copies branch in the tree? How much evidence support that these two sequences are carried in the genome of the bruchid (i.e. in the mitochondrial DNA of the species as the result of an actual transfer)?

Response from authors

The hypothesis of an endoparasite carrying the unusual cytb sequences deserves some attention. These sequences, however, are undoubtedly of bruchid origin, since a blast search of Genbank using the additional copy shows that the closest sequences outside Acanthoscelides or Zabrotes are carried by four bruchids, two Bruchus (B. signaticornis [AY390728.1], B. tristiculus [AY390729.1]) and two Bruchidius (B. saudicus [AY625444.1], B. rubicundus [AY625443.1]), all of them found exclusively in the Old World, and therefore unikely to have been in contact with Acanthoscelides and/or Zabrotes since 90 Mya. Moreover, the first 50 blast hits are all distributed amongst the bruchid family, both in New World genera (i.e. Acanthoscelides and Zabrotes) and in Old World genera (i.e. Bruchus, Bruchidius, Tuberculobruchus, Conicobruchus, Palaeoacanthoscelides and Callosobruchus). More distant sequences are found in species within the superfamily Chrysomeloidea, which comprises bruchids (e.g. Anophophora), or within more distantly related beetles (e.g. Blackburnia) or crickets (e.g. Gryllus). We therefore believe that presenting a broader phylogenetic tree including sequences from these more distantly-related species would not add useful information, since the additional cytb copy is typical of bruchids, and since the root of the tree is obviously in the Zabrotes lineage. Nevertheless, we certainly admit that we cannot be sure by which genome the additional gene is carried; It might be hosted by a eukaryote endoparasite, or by a prokaryotic or viral genome, although we present some evidence for mitochondrial translation. We hope to be able to address this question in a middle-term perspective.

2. Could insect species of the outgroup carry as well more than one cytb copy?

If we admit that the bruchid carries two copies and that this is not contamination, and if it carries them within its mitochondria, the scenario of a transfer is appealing, except if the presence of two copies is a "normal" condition for those insects. Without the study of the genetic composition of the outgroup, it is not clear to me if the apparently original situation of the Z. subfasciatus individuals (with two copies of cytb present in the Altiplano) is ancestral (vertically inherited) or derived (laterally acquired).

Could it be the case that the outgroup of these species actually already contained two copies of this gene? Are there precedents of related organisms with two cytb genes? Could it be tested by studying the composition of some completely sequenced mitochondrial genomes? Could then the present result be explained either (i) by a much more ancient lateral gene transfer (somewhere at the base of the bruchids, in which case the scenarios should try to explain this ancient phenomenon) or if not, eventually (ii) by some complex scenarios of independent genes losses to explain the patchy distribution of cytb in current bruchid populations?

Response from authors

In our opinion, the polymorphic nature of this character (i.e. both the ecological/phylogeographic pattern of the distribution of the additional copy and the rare status of Zabrotes individuals carrying the two copies within sites) argues for a relatively recent event (i.e., more recent than the basal divergence of all the beetles studied here, as suggested by the reviewer). Even admitting that the outgroup carried two independent copies – that would, for instance, have two distinct functions and be indispensable to these bruchids – a vertical scenario could not have led to such a low (0–1%) divergence between the original Acanthoscelides copy and one of those carried by some Zabrotes subfasciatus indivudals, knowing that the two species have diverged during more than 50 Mya [13,30]. Alternatively, one would have to invoke a very bizarre pattern of gene conversion. We believe that sequence identity in this relatively rapidly-evolving mtDNA gene tends to favour the hypothesis of a relatively recent horizontal transfer over the hypothesis of an ancient divergence of the two copies, followed by vertical double inheritance of both copies.

3. Can one deduce anything about the mechanisms of recombination that inserted the new copy, if they are all within the mitochondrial bruchid genome?

If there is only one type of mitochondria in the bruchids, and if this mitochondria carries the two gene copies, it seems at first sight that the presence of two cytb copies in Z. subfasciatus rules out the hypothesis of a legitimate recombination to transfer this gene. Such a mechanism would likely have led to the replacement of one former cytb copy by another one, resulting in one copy per species. Could the opposite observation suggest then that the additional cytb was transferred in kind of a hitch-hiking process, due to the insertion of one (or more) other markers in the mitochondrial DNA, which could have themselves happened by homologous recombination? In this case the HGT event would be even larger, and would concern several markers. By contrast, for the species presenting only one copy of cytb, could we study the location of this single copy with more precision? A (partial) study of the genetic composition of the mitchondrial genome of these bruchids, typically of the genes bordering the cytb gene, could be very informative here. They may or may not have retained evidence of recombination or synteny. Would it be possible to characterise the genetic context of the cytb genes and test their conservation in later studies to decide if there was one or several instance of LGT and what was their mechanism? Alternatively, could the cytb copy be jumping using transposases? Do we have any evidence for/against the implication of transposons in this story?

Response from authors

We agree that sequencing the full mitochondrial genome(s) of bruchid individuals carrying two cytochrome b copies would help understanding further what happened and how. Unfortunately these data are lacking, and are not so easy to collect, given the relatively high level of sequence similarity between the two copies, the lack of knowledge of the genomic structure, and the scarcity of living individuals with two copies – a new round of field sampling is probably required. Sequencing the full mitochondrial genome(s) would also help us in understanding why a "double-pattern" is lacking for other cytb -linked genes such as COI, which seem to be consistent with the scenario supported by nuclear genes and classical taxonomy.

4. About the nature of the most likely vector: virus, endoparasite or... even an host reservoir?

I was interested by the different hypotheses presented in this paper regarding the vector of the possible lateral transfer. Viruses and endoparasites might be good candidates indeed, although I was wondering if a third possibility, inspired by the "you are what you eat theory" (see. W.F. Doolittle, 1998), could not be raised as well. Since these bruchid species share a host, could not their host have provided them the additional cytb copy?

Response from authors

See our response to question 1.

5. Ecological scenarios and the interest of harbouring two cytb copies to survive in the Altiplano.

I may have misunderstood, but I believe that the authors suggest that the persistence of two copies (or at least the swapping of cytb genes) could serve the purpose of an endoparasite. My naïve question is: could not it serve the purpose of the bruchids themselves? Could not they benefit in the Altiplano from such a genomic make up? Do we have any way to investigate the biochemistry/activity of these two divergent copies in more depth that would suggest to us that even if they are related their function is only partially overlapping?

Response from authors

This is an interesting hypothesis. Developing the capacity for research on functional mito-genomics in these non-model animals can only be a very long-term perspective, however.

Reviewer's report 2 Adam Eyre-Walker, University of Sussex, Centre for the Study of Evolution & School of Biological Sciences, Brighton, United Kingdom

This is an interesting paper which describes what I believe is one of those observations which almost defies rational explanation, although the observation does appear to be real.

Response from authors

We fully agree with this statement.

In this paper the authors describe a phylogenetic analysis of bruchid beetles from Mexico. They show that for one nuclear and one mitochondrial gene, the species are moderately divergent and phylogenetically well resolved – i.e. each species is monophyletic with high bootstrap support. However, for another mitochondrial gene the pattern is very different; two of the species have an almost identical cytb gene which is also shared by some members of the most divergent of the beetle species. All individuals which share this cytb sequence come from the same geographical area and live on the same host plant. Intriguingly, those individuals of the species Z. subfasciatus, which have the shared cytb gene, also have a cytb gene which is similar to Z. subfasciatus individuals from elsewhere in Mexico; this other cytb sequence is as divergent as one might expect given how distantly related this species is to the others.

So how do we explain this bizarre pattern? The authors consider a number of alternatives including contamination, hybridisation and pseudogenisation, none of which seems likely. This leaves horizontal gene transfer as possibly the only other explanation. They suggest that maybe some eukaryotic vector has transferred the cytb gene between different species. However, two questions remain. Why has only a part of the mitochondrial DNA been transferred? Individuals from different species share similar cytb sequences but have very different mitochondrial COI sequences.

Response from authors

See our response to Reviewer 1 (question 3).

And why don't all species which have this particular cytb sequence also have their own original cytb sequence, as individuals of Z. subfasciatus appear to have. One can explain these patterns but the explanations are not simple.

Response from authors

This question highlights one limitation of the PCR-only experimental strategy we had in this work. PCR can miss existing gene copies, so that we cannot make sure whether Acanthoscelides individuals from the "core clade" carrying the apparently mobile cytb sequence do or do not carry an additional, "private" copy (especially knowing that the mobile copy is probably of Acanthoscelides origin). Given the phylogenetic proximity between these two species, we did not succeed in designing specific primers. Again, full-genome data would clarify these questions but are lacking.

Reviewer's report 3 Alexey Kondrashov, National Institutes of Health, Bethesda, Maryland, United States

The authors claim that they discovered a case of rather recent lateral gene transfer between mitochondrial genomes of moderately related beetles. While the claim is striking, I see no obvious holes in the data and reasoning and, thus, tend to believe it.

A very interesting observation is that Zabrotes subfasciatus is polymorphic by presence/absence of laterally acquired cytb gene. When this gene is present, it does not replace the original one and, instead, the two coexist within the same mitochondrial genome. This system opens a rare opportunity to study microevolutionary aspects of lateral gene transfer. It would be worthwhile to sequence complete mitochondrial genomes possessing two cytb genes (native and foreign).

Response from authors

See our response to Reviewer 1 (question 3).

Also, standard selective sweep analysis may tell us whether positive selection favors genomes with the extra, foreign cytb. A great system for further analysis of eukaryotic LGT.

Response from authors

This is an interesting suggestion. We analysed separately the sample of "core clade" haplotypes and found significantly (p <0.05) negative Tajima's D and Fu & Li's F*, which is indicative of a star-like genealogy compatible with the selective sweep (or founder event) hypothesis. Single-locus arguments for selective sweeps are generally weak, however, given the large number of factors potentially influencing the shape of genealogies.

Authors' contributions

NA carried out most of the molecular genetic studies and drafted the manuscript. BB and AG participated in the writing of the manuscript and revised the final version. MHM and DM contributed in the interpretation of the data and in the writing of the manuscript. Finally, NG supervised data analysis and participated substantially in interpretation of the data and writing of the manuscript. All authors read and approved the final manuscript.

Table 1

List of sampled sites.

Code	Site name	Geographic position	Sampled species	Latitude (°North)	Longitude (°West)	Altitude (m)
CLNY	(proceeding from Malinalco)	Altiplano	Z. subfasciatus	18°57'13.2"	99°30'08.9"	1935
COP	Copandaro	Altiplano	A. obvelatus	19°26'24.6"	101°45'35.5"	2087
ELA	Elabillal	Pacific coast	A. argillaceus Z. subfasciatus	18°00'27.0"	102°21'44.8"	28
HUI	Huitzilac	Altiplano	A. obvelatus	19°01'24.4"	99°16'23.3"	2544
OCM	Tilapa	Altiplano	Z. subfasciatus	19°11'24.5"	99°25'12.2"	1300
PAZ	Playa Azul	Pacific coast	A. argillaceus	17°59'20.8"	102°21'14.4"	21
SIL	San Ildefonso	Altiplano	A. obvelatus	19°22'19.8"	100°08'56.9"	2400
SJB	San Juan Bosco	Pacific coast	Z. subfasciatus	18°07'12.4"	102°08'24.9"	150
SJS	San Jose de los Laureles arriba	Altiplano	A. obtectus A. obvelatus	18°58'49.7"	99°00'05.0"	1855
SJC	San Jose de los Laureles abajo	Altiplano	A. obtectus	18°58'40.3"	98°58'20.0"	1730
SPT	San Pablo de Tejalpa	Altiplano	A. obtectus	18°52'59.8"	99°36'00.3"	1750
STL	Santa Lucia	Altiplano	A. obvelatus	18°52'12.5"	100°00'03.7"	1790
TEP	Tepoztlan	Altiplano	A. obtectus A. obvelatus	18°59'36.3"	99°07'15.7"	1931
TLA	Tlayecapan	Altiplano	A. obtectus Z. subfasciatus	18°57'20.0"	99°03'24.4"	1750
XOT	Xochitlan	Altiplano	A. obtectus	19°57'59.9"	97°39'02.0"	1450
YAU	Yautepec	Altiplano	Z. subfasciatus	18°45'31.9"	99°01'24.0"	1700

Table 2

Number of individuals collected in each site for each species and number of individuals fitting the "core clade" haplotype in each population. In Zabrotes subfasciatus populations, all individuals also fitted their own original cytb haplotype.

Species	Site	Geographic position	Nb of sampled individuals	Nb of individuals fitting the "core clade" haplotype
A. argillaceus	ELA	Pacific coast	6	0
	PAZ	Pacific coast	6	0

A. obtectus	SJC	Altiplano	10	10
	SJS	Altiplano	10	10
	SPT	Altiplano	10	10
	TEP	Altiplano	10	10
	TLA	Altiplano	10	10
	XOT	Altiplano	10	10

A. obvelatus	COP	Altiplano	10	10
	HUI	Altiplano	10	10
	SIL	Altiplano	10	10
	SJS	Altiplano	10	10
	STL	Altiplano	10	10
	TEP	Altiplano	10	10

Z. subfasciatus	CLNY	Altiplano	25	3
	OCM	Altiplano	8	4
	TLA	Altiplano	30	9
	YAU	Altiplano	7	4
	ELA	Pacific coast	20	0
	SJB	Pacific coast	20	0

Acknowledgements

We thank P. Jarne for his support during this study; E. Desmarais, P. Sourrouille and C. Debain for technical assistance; J. Romero, T. Shani and Y. Borcard for providing several Z. subfasciatus individuals; F. Kjellberg and P. David for critical reading of the manuscript; and A. Delgado-Salinas, J. Moreau and A. Aebi for discussion. Financial support was provided by the Swiss National Science Foundation (Project 3100.064821.01) and the Swiss Center of Competence in Research "Plant Survival".

Syvanen

Horizontal gene transfer: evidence and possible consequences

Ann Rev Genet 1994 28 237 261

7893125

Doolittle

Boucher

Nesbo

Douady

Andersson

Roger

How big is the iceberg of which organellar genes in nucleargenomes are but the tip?

Phil Trans R Soc Lond B 2003 358 39 57

12594917

10.1098/rstb.2002.1185

Jain

Rivera

Moore

Lake

Horizontal gene transfer in microbial genome evolution

Theor Popul Biol 2002 61 489 495

12167368

10.1006/tpbi.2002.1596

Rivera

Lake

The ring of life provides evidence for a genome fusion origin of eukaryotes

Nature 2004 431 152 155

15356622

10.1038/nature02848

Andersson

Sjogren

Davis

LAM

Martin Embley

Roger

Phylogenetic analyses of diplomonad genes reveal frequent lateral gene transfers affecting eukaryotes

Curr Biol 2003 13 94 104

12546782

10.1016/S0960-9822(03)00003-4

Mita

Morimyo

Okano

Koike

Nohata

Kawasaki

Kadono-Okuda

Yamamoto

Suzuki

Shimada

Goldsmith

Maeda

The construction of an EST database for Bombyx mori and its application

Proc Natl Acad Sci USA 2003 100 14121 14126

14614147

10.1073/pnas.2234984100

Goldsmith

Shimada

Abe

The genetics and genomics of the silkworm, Bombyx mori

Ann Rev Entomol 2005 50 71 100

15355234

10.1146/annurev.ento.50.071803.130456

Bergthorsson

Adams

Thomason

Palmer

Widespread horizontal transfer of mitochondrial genes in flowering plants

Nature 2003 424 197 201

12853958

10.1038/nature01743

Bergthorsson

Richardson

Young

Goertzen

Palmer

Massive horizontal transfer of mitochondrial genes fromdiverse land plant donors to the basal angiosperm Amborella

Proc Natl Acad Sci USA 2004 101 17747 17752

15598737

10.1073/pnas.0408336102

Martin

Lateral gene transfer and other possibilities

Heredity 2005 94 565 566

15798778

10.1038/sj.hdy.6800659

Delgado-Salinas

Bonet

Gepts

Gepts P Dordrecht

The wild relative of Phaseolus vulgaris in middle America

Genetic Resources of Phaseolus Beans 1988

The Netherlands: Kluwer Academic Publishers

163 184

Borowiec

The genera of seed-beetles (Coleoptera, Bruchidae)

Pol Pismo Entomol 1987 57 3 207

Farrell

"Inordinate fondness" explained: Why are there so many beetles?

Science 1998 281 555 559

9677197

10.1126/science.281.5376.555

Johnson

Ecosystematics of Acanthoscelides (Coleoptera: Bruchidae) of southern Mexico and Central America

Misc Publ Entomol Soc Am 1983 56 1 370

Alvarez

Hossaert-McKey

Rasplus

J-Y

McKey

Mercier

Soldati

Aebi

Shani

Benrey

Sibling species of bean bruchids: Morphological and phylogenetic studies among Acanthoscelides obtectus Say and A. obvelatus Bridwell

J Zool Syst Evol Res 2005 43 29 37

10.1111/j.1439-0469.2004.00286.x

Alvarez

Romero Napoles

Anton

K-W

Benrey

Hossaert-McKey

Phylogenetic relationships in the Neotropical bruchid genus Acanthoscelides Schilsky

J Zool Syst Evol Res 2006 44 63 74

10.1111/j.1439-0469.2005.00344.x

Gomez-Zurita

Juan

Petitpierre

The evolutionaryhistory of the genus Timarcha (Coleoptera, Chrysomelidae) inferred from mitochondrial COII gene and partial 16S rDNA sequences

Mol Phylogenet Evol 2000 14 304 317

10679162

10.1006/mpev.1999.0712

Orr

Porter

Mousseau

Dingle

Molecular and morphological evidence for hybridization between two ecologically distinct grasshoppers (Melanoplus sanguinepes &M. devastator) in California

Heredity 1994 72 42 54

Orr

The unexpected recovery of hybrids in a Drosophila species cross: A genetic analysis

Genet Res 1996 67 11 18

8919886

Willett

Ford

Harrison

Inferences about the origin of a field cricket hybrid zone from a mitochondrial DNA phylogeny

Heredity 1997 79 484 494

9369011

10.1038/sj.hdy.6882430

Hirotsune

Yoshida

Chen

Garrett

Sugiyama

Takahashi

Yagami

Wynshaw-Boris

Yoshiki

An expressed pseudogene regulates the messenger-RNA stability of its homologous coding gene

Nature 2003 423 91 96

12721631

10.1038/nature01535

Kondo

Nikoh

Ijichi

Shimada

Fukatsu

Genome fragment of Wolbachia endosymbiont transferred to X chromosome of host insect

P Natl Acad Sci USA 2002 99 14280 14285

10.1073/pnas.222228199

Simon

Frati

Beckenbach

Crespi

Liu

Flook

Evolution, weighting, and phylogenetic utility of mitochondrial gene-sequences and a compilation of conserved polymerase chain-reaction primers

Ann Entomol Soc Am 1994 87 651 701

Thompson

Higgins

Gibson

CLUSTAL W: Improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice

Nucl Acids Res 1994 22 4673 4680

7984417

Posada

Crandall

Modelstest: testing the model of DNA substitution

Bioinformatics 1998 14 17 818

10.1093/bioinformatics/14.9.817

Jobb

Von Haeseler

Strimmer

TREEFINDER: a powerful graphical analysis environment for molecular phylogenetics

BMC Evol Biol 2004 4 18

15222900

10.1186/1471-2148-4-18

Kumar

Tamura

Jakobsen

Nei

MEGA2: Molecular evolutionary genetics analysis software

Bioinformatics 2001 17 1244 1245

11751241

10.1093/bioinformatics/17.12.1244

Goldman

Yang

A codon-based model of nucleotide substitution for protein-coding DNA sequences

Mol Biol Evol 1994 11 725 736

7968486

Yang

PAML: a program package for phylogenetic analysis by maximum likelihood

Comput Appl Biosci 1997 13 555 556

9367129

Kergoat

Alvarez

Hossaert-McKey

Faure

Silvain

J-F

Parallels in the evolution of the two largest New and Old World seed-beetle genera (Coleoptera, Bruchidae)

Mol Ecol 2005 44 63 74