Interorder transfer of mycoplasma-like microorganisms between Drosophila paulistorum and Ephestia kuehniella: Tissues,dosages, and effects

Testis and head extracts of sterile male intersemispecific hybrid Drosophila paulistorum are pathogenic when injected into Ephestia kuehniella larvae. The time and frequency of death of the recipients is a function of the extract concentration. Extracts of Ephestia recipients are pathogenic and will kill E. kuehniella larvae and D. paulistorum adults. Larval Drosophila recipients of these extracts survive through pupation. A majority of these recipients fail to eclose. Those animals which do survive to the adult stage and which are fertile demonstrate the same pattern of sterility among their progeny as is found in D. paulistorum hybrids and recipients of D. paulistorum extracts. The results indicate that the pathogenicity of the extracts is due to the mycoplasma-like microorganisms which are responsible for the male intersemispecific hybrid sterility in D. paulistorum. The mycoplasma-like microorganisms grow rapidly in E. kuehniella hosts, with a division time of approximately 1.8 hr, and they retain their host specificity for the semispecies of D. paulistorum.     

An electron microscopic study of the etiology of hybrid sterility in Drosophila paulistorum

Crosses between the semispecies of the Drosophila paulistorum complex produce fertile female but sterile male hybrids. An hypothesis is put forward that the hybrid sterility is in this case a result of discordance between a cytoplasmic symbiont and the genotype of the host. An ultrastructural analysis has been made of the testes of sterile male hybrids between the Andean and the Amazonian, and also other semispecies. Spermatid bundles undergo degenerative changes resulting in the loss of the axial filament complex and of associated mitochondrial derivatives. Numerous single or multiply clustered elements closely resembling Mycoplasma are observed in association with the degenerating spermatid bundles. Similar inclusions are observed also intruding into the wall of the distal parts of the testes and/or vasa deferentia. Some Mycoplasma-like bodies are observed also within the developing spermatids. These organs may be crowded with degenerating bundles and clusters of the Mycoplasma-like bodies. Each body is enclosed in a membrane, and may show a central reticular network and peripheral ribosome-like granules. The testes of the fertile males of the parental stocks reveal the presence of similar Mycoplasma-like inclusions, but not in such profusion.Dedicated to Professor Theodosius Dobzhansky on the occasion of his seventieth birthday, and in gratitude for our introduction to Drosophila paulistorum.     

Embryonic pole cells and mycoplasmalike symbionts in Drosophila paulistorum

Mycoplasmalike intracellular symbionts have been located in the pole cells of Drosophila paulistorum embryos. These cells are destined to form the germ cells of both sexes. The symbionts had been previously localized in larval and adult developing and mature ovaries and testes. It is via the egg cytoplasm that these microorganisms are transmitted between generations to apparently cause an infectious and hereditary hybrid male sterility.     

Taxonomic boundaries,phylogenetic relationships and biogeography of the <Emphasis Type="Italic">Drosophila willistoni</Emphasis> subgroup (Diptera: Drosophilidae)

The Drosophila willistoni subgroup represents a complex with varying taxonomic levels. It encompasses D. willistoni and its five sibling species: D. equinoxialis, D. insularis, D. paulistorum, D. pavlovskiana and D. tropicalis. Of these, D. equinoxialis, D. tropicalis and D. willistoni present differentiation at subspecific level, whereas D. paulistorum represents a superspecies, formed by six semispecies. Despite this taxonomic and evolutionary complexity, many of these semi and subspecific taxa have not yet had their phylogenetic status tested in an explicitly molecular study. Aiming to contribute to the understanding of the evolution of this challenging group, we analyzed nucleotide sequences from two mitochondrial and four nuclear datasets, both individually and simultaneously, through different phylogenetic methods. High levels of incongruence were detected among partitions, especially concerning the mitochondrial sequences. As this incongruence was found to be statistically significant and robust to the use of different models and approaches, and basically restricted to mitochondrial loci, we suggest that it may stem mainly from hybridization-mediated asymmetrical introgression. Despite this, our nuclear data finally led to a phylogenetic hypothesis which further refines several aspects related to the willistoni subgroup phylogeny. In this respect, D. insularis, D. tropicalis, D. willistoni and D. equinoxialis successively branched off from the willistoni subgroup main stem, which recently subdivided to produce D. paulistorum and D. pavlovskiana. As regards the semispecies evolution, we found evidence of a recent diversification, which highly influenced the obtained results due to the associated small levels of genetic differentiation, further worsened by the possibly associated incompletely sorted ancestral polymorphisms and by the possibility of introgression. This study also raises the question of whether these semispecies are monophyletic at all. This reasoning is particularly interesting when one considers that similar levels of reproductive isolation could be attained through infection with different Wolbachia strains.     

Polymorphic HSRs in chromosome 1 of the two semispecies Mus musculus musculus and M. m. domesticus have a common origin in an ancestral population

HSRs (homogeneously staining regions) are the cytological correlates of DNA amplification. In the house mouse, Mus musculus, many populations are polymorphic for the presence or absence of HSRs on chromosome 1. In the semispecies M. m. domesticus the amplified DNA is present within one HSR, whereas in M. m. musculus chromosomes 1 with two HSRs are found. Hybridization of HSR-specific probes to Southern blots of HSR-carrying genomic DNAs from different localities and semispecies revealed similar complex band patterns. the remaining variation is restricted to sequences with a low degree of amplification. Variation is higher between semispecies than within one semispecies. It is assumed that HSRs are derived from one original amplification event and that unequal recombination is the mechanism underlying the length variation of HSRs present today in both semispecies. Evidence from G-banding and in situ hybridization shows that the two HSRs of M. m. musculus originated from a single HSR by means of a paracentric inversion, where one break-point was located within the single HSR and the second outside the HSR. As a consequence of the paracentric inversion the two HSRs of M. m. musculus are permanently linked together. Since exchange of genes between the two semispecies is restricted to a narrow hybrid zone the amplification that gave rise to the HSR most probably occurred prior to the divergence into the semispecies M. m. domesticus and M. m. musculus about 1 million years ago.by D. Schweizer     

Combining morphology and molecular data to improve Drosophila paulistorum (Diptera,Drosophilidae) taxonomic status

The willistoni species subgroup has been the subject of several studies since the latter half of the past century and is considered a Neotropical model for evolutionary studies, given the many levels of reproductive isolation and different evolutionary stages occurring within them. Here we present for the first time a phylogenetic reconstruction combining morphological characters and molecular data obtained from 8 gene fragments (COI, COII, Cytb, Adh, Ddc, Hb, kl-3 and per). Some relationships were incongruent when comparing morphological and molecular data. Also, morphological data presented some unresolved polytomies, which could reflect the very recent divergence of the subgroup. The total evidence phylogenetic reconstruction presented well-supported relationships and summarized the results of all analyses. The diversification of the willistoni subgroup began about 7.3 Ma with the split of D. insularis while D.paulistorum complex has a much more recent diversification history, which began about 2.1 Ma and apparently has not completed the speciation process, since the average time to sister species separation is one million years, and some entities of the D. paulistorum complex diverge between 0.3 and 1 Ma. Based on the obtained data, we propose the categorization of the former “semispecies” of D. paulistorum as a subspecies and describe the subspecies D. paulistorum amazonian, D. paulistorum andeanbrazilian, D. paulistorum centroamerican, D. paulistorum interior, D. paulistorum orinocan and D. paulistorum transitional.     

Hybrid Dysgenesis in DROSOPHILA MELANOGASTER: Morphological and Cytological Studies of Ovarian Dysgenesis

A type of intraspecific hybrid sterility, between two strains of Drosophila melanogaster, referred to as GD (gonadal dysgenesis) sterility, is observed when females from a type of strain called M are crossed with males from a second type called P. Absence of egg-laying is characteristic of female GD sterility and its manifestation is conditional on high developmental temperatures. Morphological and cytological studies of GD sterile females are described. These individuals were normal in body size and external appearance. No defects in sperm storage were observed. Both adult and larval ovaries were drastically reduced in size in comparison with control ovaries. This ovarian dysgenesis was sometimes unilateral, but more frequently it was bilateral, particularly in females developing at the highest test temperature. The ovarioles of dysgenic ovaries contained no vitellaria; the germaria lacked any cells resembling the cystocyte clusters of normal ovaries. It is concluded that sterility results from an early blockage in ovarian development, rather than from atrophy of previously developed structures. Possible mechanisms for this developmental arrest are discussed.     

The effect of a juvenile hormone analogue on ecdysteroid titre during development and HnRNA formation in the moth,Ephestia cautella

The juvenile hormone analogue, methoprene was found to interfere with normal development of Ephestia in a manner dependent on age. Young embryos, prior to the stage of blastokinesis, and animals, shortly before and after pupation, were found to be the most sensitive to the compound. The JHA inhibited metamorphosis and produced giant larvae when it was given to immature larvae, however, when it was given to larvae 2–3 days prior to pupation or to young pupae it did not affect metamorphosis but prevented adult emergence. Comparison of the ecdysteroid titre determined in control and treated animals in the various developmental stages showed that JHA depressed the ecdysteroid titre totally only when it was given to young larvae and partially when it was applied shortly before pupation. It seems that the action of methoprene on ecdysone regulated systems and/or ecdysone producing systems in Ephestia appears to be mainly during the larval stage prior to the appearance of the small ecdysteroid peak and the formation of HnRNA in the transition period from larvae to pupae.     

Rapid evolution of courtship song pattern in Drosophila willistoni sibling species

Courtship behaviours may provide a more reliable means of identifying reproductively isolated taxa than traits such as morphology or many genetic markers. Here we describe the courtship songs of the Drosophila willistoni sibling species group, which consists of several species and subspecies. We find that song pattern is species-specific, despite significant differences among strains within species. D. paulistorum has the most variable song pattern, which reflects this species' traditional subdivision into semispecies. All the other species could be unambiguously identified by song. The major differences among these species was in the interpulse interval, as has been found in other studies of fly song. However, the interpulse intervals of the species studied here were often multimodal. This was partly due to the presence of multiple song types within the courtship repertoire, but it also reflected changes in interpulse interval within a song type by some males. Unusually, some species had distinctively patterned variation in interpulse interval. Song must have evolved rapidly within the species complex, probably due to sexual selection.     

Identification of the sibling species of the Drosophila willistoni subgroup through the electrophoretical mobility of acid phosphatase-1

The Drosophila willistoni group consists of 23 species of which six are sibling species and belong to the D. willistoni subgroup: D. willistoni, Drosophila equinoxialis, Drosophila tropicalis, Drosophila insularis, Drosophila pavlovskiana and Drosophila paulistorum. These sibling species are abundant in the Neotropical region and can hardly be differentiated by the usual taxonomic traits. Four of them (D. willistoni, D. equinoxialis, D. tropicalis and D. paulistorum) cover extensive geographic distribution areas overlapping in places while two of them are endemic (D. insularis and D. pavlovskiana). In this study, we presented a method for the identification of five sibling species of the D. willistoni subgroup based on the allozyme variation of acid phosphatase‐1 (Acph‐1) in acrylamide gel electrophoresis. Our work showed that Acph‐1 allozyme differences can be used for species‐diagnostic characterization. This method was shown to be a more efficient tool for species identification than others because it is both quicker and produces reliable results.     

Chromosomal Evolution of Sibling Species of the Drosophila willistoni Group. I. Chromosomal Arm IIR (Muller’s Element B)

The phylogenetic relationships among nine entities of Drosophila belonging to the D. willistoni subgroup were investigated by establishing the homologous chromosomal segments of IIR chromosome, Muller’s element B (equivalent to chromosome 2L of D. melanogaster). The sibling species of the D. willistoni group investigated include D. willistoni, D. tropicalis tropicalis, D. tropicalis cubana, D. equinoxialis, D. insularis and four semispecies of the D. paulistorum complex. The phylogenetic relationships were based on the existence of segments in different triads of species, which could only be produced by overlapping inversions. Polytene banding similarity maps and break points of inversions between species are presented. The implications of the chromosomal data for the phylogeny of the species and comparisons with molecular data are discussed. The aim of this study is to produce phylogenetic trees depicting accurately the sequence of natural events that have occurred in the evolution of these sibling species. Claudia Rohde, Ana Cristina Lauer Garcia: These authors contributed equally to this work     

Rapid sexual and genomic isolation in sympatric Drosophila without reproductive character displacement

The rapid evolution of sexual isolation in sympatry has long been associated with reinforcement (i.e., selection to avoid maladaptive hybridization). However, there are many species pairs in sympatry that have evolved rapid sexual isolation without known costs to hybridization. A major unresolved question is what evolutionary processes are involved in driving rapid speciation in such cases. Here, we focus on one such system; the Drosophila athabasca species complex, which is composed of three partially sympatric and interfertile semispecies: WN, EA, and EB. To study speciation in this species complex, we assayed sexual and genomic isolation within and between these semispecies in both sympatric and allopatric populations. First, we found no evidence of reproductive character displacement (RCD) in sympatric zones compared to distant allopatry. Instead, semispecies were virtually completely sexually isolated from each other across their entire ranges. Moreover, using spatial approaches and coalescent demographic simulations, we detected either zero or only weak heterospecific gene flow in sympatry. In contrast, within each semispecies we found only random mating and little population genetic structure, except between highly geographically distant populations. Finally, we determined that speciation in this system is at least an order of magnitude older than previously assumed, with WN diverging first, around 200K years ago, and EA and EB diverging 100K years ago. In total, these results suggest that these semispecies should be given full species status and we adopt new nomenclature: WN—D. athabasca, EA—D. mahican, and EB—D. lenape. While the lack of RCD in sympatry and interfertility do not support reinforcement, we discuss what additional evidence is needed to further decipher the mechanisms that caused rapid speciation in this species complex.     

A stereological analysis of developing egg chambers in Ephestia kuhniella

A polytrophic ovariole of the flour moth, Ephestia kuhniella, is composed of a linear series of increasingly mature egg chambers, each consisting of an oocyte, an interconnected cluster of seven nurse cells, and a covering layer of follicle cells. This study describes changes in the volume of each component as a function of the position of the egg chamber in the ovariole. Analysis of the growth curve of the Ephestia oocyte yields two possible correlations between accelerated oocyte growth and ultrastructural events enhancing the supply of yolk materials to the oocyte: the first is the initiation of yolk synthesis by the follicle cell layer and its transfer to the oocyte, and the second is the formation of channels between the follicle cells allowing hemolymph to gain access to the oocyte. An Ephestia oocyte increases in volume from approximately 2.5 × 10³ μm³ to approximately 2.0 × 10⁷ μm³ over an average series of 58 egg chambers.     

A candidate male-fertility female-fertility gene tagged by the soybean endogenous transposon, Tgm9

In soybean, the W4 gene encoding dihydroflavonol-4-reductase controls anthocyanin pigment biosynthesis in flowers. The mutant allele, w4-m, is characterized by variegated flowers and was evolved from the insertion of an endogenous transposable element, Tgm9, in intron II of the W4 gene. In the w4-m mutant line, reversion of the unstable allele from variegated to normal purple flower in revertants would indicate Tgm9’s excision accompanied by its insertion into a second locus. We identified a male-sterile, female-sterile mutant from such germinal revertant bearing purple flowers. The objectives of our investigation were to map the sterility locus, identify candidate genes for the male-fertile, female-fertile phenotype, and then determine if sterility is associated with the insertion of Tgm9 in the sterility locus. We used bulked segregant analysis to map the locus to molecular linkage group J (chromosome 16). Fine mapping enabled us to flank the locus to a 62-kb region that contains only five predicted genes. One of the genes in that region, Glyma16g07850.1, codes for a helicase. A rice homolog of this gene has been shown to control crossing over and fertility phenotype. Thus, Glyma16g07850.1 is most likely the gene regulating the male and female fertility phenotype in soybean. DNA blot analysis of the segregating individuals for Tgm9 showed perfect association between sterility and the presence of the transposon. Most likely, the sterility mutation was caused by the insertion of Tgm9. The transposable element should facilitate identification of the male- and female-fertility gene. Characterization of the fertility gene will provide vital molecular insight on the reproductive biology of soybean and other plants.     

Biosystematic and evolutionary statuses of two sympatric populations ofAphytis mytilaspidis [Hym.: Aphelinidae]

Studies on 2 sympatric morphologically identical populations ofAphytis mytilaspidis Le Baron frpm Greece were conducted on their mating behavior, reproductive isolation, hybridization in the laboratory, host preferences and adult survivorships at different temperatures. These studies revealed that the 2 populations were partially reproductively isolated and qualify at least for the rank of strong “semispecies” with respect to one another. Marked differences were also recorded in their host preferences and adult survivorships at different temperatures. Gene flow among these populations in nature is likely to occur only in one direction. Differences in host preference may further reduce gene flow by providing ecological reproductive isolation. Also hybrid sterility is indicated which if complete would prove these 2 forms to be sibling species. Based on the experimental evidence, an hypothesis is presented that these 2 populations represent a case of incipient if not complete sympatric speciation, with the presumed descendant population (R-69-120) possessing a broader host range and better adult longevity, in comparison to the proposed progenitor population (R-63-63-4).     

A Genetic Basis for a Postmeiotic X Versus Y Chromosome Intragenomic Conflict in the Mouse

Intragenomic conflicts arise when a genetic element favours its own transmission to the detriment of others. Conflicts over sex chromosome transmission are expected to have influenced genome structure, gene regulation, and speciation. In the mouse, the existence of an intragenomic conflict between X- and Y-linked multicopy genes has long been suggested but never demonstrated. The Y-encoded multicopy gene Sly has been shown to have a predominant role in the epigenetic repression of post meiotic sex chromatin (PMSC) and, as such, represses X and Y genes, among which are its X-linked homologs Slx and Slxl1. Here, we produced mice that are deficient for both Sly and Slx/Slxl1 and observed that Slx/Slxl1 has an opposite role to that of Sly, in that it stimulates XY gene expression in spermatids. Slx/Slxl1 deficiency rescues the sperm differentiation defects and near sterility caused by Sly deficiency and vice versa. Slx/Slxl1 deficiency also causes a sex ratio distortion towards the production of male offspring that is corrected by Sly deficiency. All in all, our data show that Slx/Slxl1 and Sly have antagonistic effects during sperm differentiation and are involved in a postmeiotic intragenomic conflict that causes segregation distortion and male sterility. This is undoubtedly what drove the massive gene amplification on the mouse X and Y chromosomes. It may also be at the basis of cases of F1 male hybrid sterility where the balance between Slx/Slxl1 and Sly copy number, and therefore expression, is disrupted. To the best of our knowledge, our work is the first demonstration of a competition occurring between X and Y related genes in mammals. It also provides a biological basis for the concept that intragenomic conflict is an important evolutionary force which impacts on gene expression, genome structure, and speciation.     

Infectious speciation revisited: impact of symbiont-depletion on female fitness and mating behavior of Drosophila paulistorum

The neotropical Drosophila paulistorum superspecies, consisting of at least six geographically overlapping but reproductively isolated semispecies, has been the object of extensive research since at least 1955, when it was initially trapped mid-evolution in flagrant statu nascendi. In this classic system females express strong premating isolation patterns against mates belonging to any other semispecies, and yet uncharacterized microbial reproductive tract symbionts were described triggering hybrid inviability and male sterility. Based on theoretical models and limited experimental data, prime candidates fostering symbiont-driven speciation in arthropods are intracellular bacteria belonging to the genus Wolbachia. They are maternally inherited symbionts of many arthropods capable of manipulating host reproductive biology for their own benefits. However, it is an ongoing debate as to whether or not reproductive symbionts are capable of driving host speciation in nature and if so, to what extent. Here we have reevaluated this classic case of infectious speciation by means of present day molecular approaches and artificial symbiont depletion experiments. We have isolated the α-proteobacteria Wolbachia as the maternally transmitted core endosymbionts of all D. paulistorum semispecies that have coevolved towards obligate mutualism with their respective native hosts. In hybrids, however, these mutualists transform into pathogens by overreplication causing embryonic inviability and male sterility. We show that experimental reduction in native Wolbachia titer causes alterations in sex ratio, fecundity, and mate discrimination. Our results indicate that formerly designated Mycoplasma-like organisms are most likely Wolbachia that have evolved by becoming essential mutualistic symbionts in their respective natural hosts; they have the potential to trigger pre- and postmating isolation. Furthermore, in light of our new findings, we revisit the concept of infectious speciation and discuss potential mechanisms that can restrict or promote symbiont-induced speciation at post- and prezygotic levels in nature and under artificial laboratory conditions.