scholarly journals Control of mating plug expelling and sperm storage in Drosophila: A gynandromorph- and mutation-based dissection

2019 ◽  
Vol 70 (4) ◽  
pp. 301-311
Author(s):  
János Szabad ◽  
Jing Peng ◽  
Eric Kubli
Keyword(s):  
Egg Production ◽  
Ventral Nerve Cord ◽  
Sperm Storage ◽  
Female Sterility ◽  
Wild Type ◽  
Thoracic Region ◽  
Mating Plug ◽  
Egg Deposition ◽  
Storage Organs ◽  
Reproductive Apparatus

Introduction In this study, we analyzed gynandromorphs with female terminalia, to dissect mating-related female behaviors in Drosophila. Materials and methods We used gynandromorphs, experimentally modified wild-type (Oregon-R) females, and mutant females that lacked different components of the female reproductive apparatus. Results Many of the gynandromorphs mated but did not expel the mating plug (MP). Some of these – with thousands of sperm in the uterus – failed to take up sperm into the storage organs. There were gynandromorphs that stored plenty of sperm but failed to release them to fertilize eggs. Expelling the MP, sperm uptake into the storage organs, and the release of stored sperm along egg production are separate steps occurring during Drosophila female fertility. Cuticle landmarks of the gynandromorphs revealed that while the nerve foci that control MP expelling and also those that control sperm uptake reside in the abdominal, the sperm release foci derive from the thoracic region of the blastoderm. Discussion and conclusion The gynandromorph study is confirmed by analyses of (a) mutations that cause female sterility: Fs(3)Avar (preventing egg deposition), Tm2gs (removing germline cells), and iab-4DB (eliminating gonad formation) and (b) by experimentally manipulated wild-type females: decapitated or cut through ventral nerve cord.

The Effects of the sphragis on male and female genitalia in Acraea (Nymphalidae) butterflies

2020 ◽  
Vol 22 ◽  
Author(s):  
Shannon L Summers ◽  
Akito Y Kawahara ◽  
Ana P. S. Carvalho
Keyword(s):  
Interspecific Variation ◽  
Sperm Storage ◽  
Male Mating ◽  
Museum Collections ◽  
Storage Organ ◽  
Mating Plug ◽  
Males And Females ◽  
Comparison And Analysis ◽  
Imagej Software ◽  
Sexually Antagonistic Coevolution

Male mating plugs have been used in many species to prevent female re-mating and sperm competition. One of the most extreme examples of a mating plug is the sphragis, which is a large, complex and externalized plug found only in butterflies. This structure is found in many species in the genus Acraea (Nymphalidae) and provides an opportunity for investigation of the effects of the sphragis on the morphology of the genitalia, which is poorly understood. This study aims to understand morphological interspecific variation in the genitalia of Acraea butterflies. Using specimens from museum collections, abdomen dissections were conducted on 19 species of Acraea: 9 sphragis bearing and 10 non-sphragis bearing species. Genitalia imaging was performed for easier comparison and analysis and measurements of genitalia structures was done using ImageJ software. Some distinguishing morphological features in the females were found. The most obvious difference is the larger and more externalized copulatory opening in sphragis bearing species, with varying degrees of external projections. Females of the sphragis bearing species also tend to have a shorter ductus (the structure that connects the copulatory opening with the sperm storage organ) than those without the sphragis. These differences may be due to a sexually antagonistic coevolution between the males and females, where the females evolve larger and more difficult to plug copulatory openings and the males attempt to prevent re-mating with the sphragis.

scholarly journals Expression of Mst89B and CG31287 is Needed for Effective Sperm Storage and Egg Fertilization in Drosophila

Cells ◽  
2021 ◽  
Vol 10 (2) ◽  
pp. 289
Author(s):  
Gurman Grewal ◽  
Bahar Patlar ◽  
Alberto Civetta
Keyword(s):  
Germ Line ◽  
Sperm Storage ◽  
Mature Sperm ◽  
Sperm Production ◽  
Cytogenetic Map ◽  
Egg Hatchability ◽  
Storage Organs ◽  
Competitive Success ◽  
Paternity Success ◽  
And Storage

In Drosophila, male reproductive fitness can be affected by any number of processes, ranging from development of gametes, transfer to and storage of mature sperm within the female sperm storage organs, and utilization of sperm for fertilization. We have previously identified the 89B cytogenetic map position of D. melanogaster as a hub for genes that effect male paternity success when disturbed. Here, we used RNA interference to test 11 genes that are highly expressed in the testes and located within the 89B region for their role in sperm competition and male fecundity when their expression is perturbed. Testes-specific knockdown (KD) of bor and CSN5 resulted in complete sterility, whereas KD of CG31287, Manf and Mst89B, showed a breakdown in sperm competitive success when second to mate (P2 < 0.5) and reduced fecundity in single matings. The low fecundity of Manf KD is explained by a significant reduction in the amount of mature sperm produced. KD of Mst89B and CG31287 does not affect sperm production, sperm transfer into the female bursa or storage within 30 min after mating. Instead, a significant reduction of sperm in female storage is observed 24 h after mating. Egg hatchability 24 h after mating is also drastically reduced for females mated to Mst89B or CG31287 KD males, and this reduction parallels the decrease in fecundity. We show that normal germ-line expression of Mst89B and CG31287 is needed for effective sperm usage and egg fertilization.

scholarly journals Functional morphology of immature mating in a widow spider

2021 ◽  
Vol 18 (1) ◽  
Author(s):  
Lenka Sentenská ◽  
Aileen Neumann ◽  
Yael Lubin ◽  
Gabriele Uhl
Keyword(s):  
Sperm Competition ◽  
Storage Conditions ◽  
Sperm Storage ◽  
Sperm Transfer ◽  
Costs And Benefits ◽  
Micro Computed Tomography ◽  
Mating Tactics ◽  
Adult Females ◽  
Storage Organs ◽  
Widow Spider

Abstract Background Mating generally occurs after individuals reach adulthood. In many arthropods including spiders, the adult stage is marked by a final moult after which the genitalia are fully developed and functional. In several widow spider species (genus Latrodectus), however, immature females may mate a few days before they moult to adulthood, i.e. in their late-subadult stage. While the “adult” mating typically results in cannibalism, males survive the “immature” mating. During both “immature” and “adult” matings, males leave parts of their paired copulatory organs within female genitalia, which may act as mating plugs. To study potential costs and benefits of the two mating tactics, we investigated female genital morphology of the brown widow spider, L. geometricus. Light microscopy, histology and micro-computed tomography of early-subadult, late-subadult and adult females were conducted to determine the overall pattern of genital maturation. We compared genitalia of mated late-subadult and adult females to reveal potential differences in the genitalic details that might indicate differential success in sperm transfer and different environments for sperm storage and sperm competition. Results We found that the paired sperm storage organs (spermathecae) and copulatory ducts are developed already in late-subadult females and host sperm after immature mating. However, the thickness of the spermathecal cuticle and the staining of the secretions inside differ significantly between the late-subadult and adult females. In late-subadult females mating plugs were found with higher probability in both spermathecae compared to adult females. Conclusions Sperm transfer in matings with late-subadult females follows the same route as in matings with adult females. The observed differences in the secretions inside the spermathecae of adult and late-subadult females likely reflect different storage conditions for the transferred sperm which may lead to a disadvantage under sperm competition if the subadult female later re-mates with another male. However, since males mating with late-subadult females typically transfer sperm to both spermathecae they might benefit from numerical sperm competition as well as from monopolizing access to the female sperm storage organs. The assessment of re-mating probability and relative paternity will clarify the costs and benefits of the two mating tactics in light of these findings.

scholarly journals EVOLUTION OF MULTIPLE KINDS OF FEMALE SPERM-STORAGE ORGANS INDROSOPHILA

Evolution ◽  
1999 ◽  
Vol 53 (6) ◽  
pp. 1804-1822 ◽  
Author(s):  
Scott Pitnick ◽  
Therese Marrow ◽  
Greg S. Spicer
Keyword(s):  
Sperm Storage ◽  
Storage Organs

scholarly journals Virulence and Metabolic Characteristics of Salmonella enterica Serovar Enteritidis Strains with DifferentsefDVariants in Hens

2012 ◽  
Vol 78 (18) ◽  
pp. 6405-6412 ◽  
Author(s):  
Cesar A. Morales ◽  
Jean Guard ◽  
Roxana Sanchez-Ingunza ◽  
Devendra H. Shah ◽  
Mark Harrison
Keyword(s):  
Salmonella Enterica ◽  
Egg Production ◽  
The Body ◽  
Wild Type ◽  
Salmonella Enterica Serovar Enteritidis ◽  
Blood Calcium ◽  
Content Type ◽  
Metabolic Characteristics ◽  
Wide Range ◽  
Metabolic Properties

ABSTRACTSalmonella entericaserovar Enteritidis is one of a fewSalmonella entericaserotypes that has SEF14 fimbriae encoded by thesefoperon, which consists of 4 cotranscribed genes,sefABCD, regulated bysefR. A parental strain was used to construct asefDmutant and its complement, and all 3 strains were compared for gene expression, metabolic properties, and virulence characteristics in hens. Transcription ofsefDby wild type was suppressed at 42°C and absent for the mutant under conditions where the complemented mutant had 103times higher transcription. Growth of the complemented mutant was restricted in comparison to that of the mutant and wild type. Hens infected with the wild type and mutant showed decreased blood calcium and egg production, but infection with the complemented mutant did not. Thus, the absence ofsefDcorrelated with increased metabolic capacity and enhanced virulence of the pathogen. These results suggest that any contribution thatsefDmakes to egg contamination is either unknown or would be limited to early transmission from the environment to the host. Absence ofsefD, either through mutation or by suppression of transcription at the body temperature of the host, may contribute to the virulence ofSalmonella entericaby facilitating growth on a wide range of metabolites.

scholarly journals GENETIC ANALYSIS OF THREE DOMINANT FEMALE-STERILE MUTATIONS LOCATED ON THE X CHROMOSOME OF DROSOPHILA MELANOGASTER

Genetics ◽  
1983 ◽  
Vol 105 (2) ◽  
pp. 309-325
Author(s):  
D Busson ◽  
M Gans ◽  
K Komitopoulou ◽  
M Masson
Keyword(s):  
X Chromosome ◽  
Germ Line ◽  
Female Sterility ◽  
Recessive Mutation ◽  
Wild Type Allele ◽  
Wild Type ◽  
Allelic Series ◽  
Type Allele ◽  
Dominant Female ◽  
Female Germ Line

ABSTRACT Three dominant female-sterile mutations were isolated following ethyl methanesulfonate (EMS) mutagenesis. Females heterozygous for two of these mutations show atrophy of the ovaries and produce no eggs (ovoD  1) or few eggs (ovoD  2); females heterozygous for the third mutation, ovoD  3, lay flaccid eggs. All three mutations are germ line-dependent and map to the cytological region 4D-E on the X chromosome; they represent a single allelic series. Two doses of the wild-type allele restore fertility to females carrying ovoD  3 and ovoD  2, but females carrying ovoD  1 and three doses of the wild-type allele remain sterile. The three mutations are stable in males but are capable of reversion in females; reversion of the dominant mutations is accompanied by the appearance, in the same region, of a recessive mutation causing female sterility. We discuss the utility of these mutations as markers of clones induced in the female germ line by mitotic recombination as well as the nature of the mutations.

Multiple Matings and Sperm Competition

2020 ◽  
pp. 332-363
Author(s):  
Carola Becker ◽  
Raymond T. Bauer
Keyword(s):  
Genetic Diversity ◽  
Sperm Competition ◽  
Mate Guarding ◽  
Sperm Storage ◽  
Internal Fertilization ◽  
Multiple Matings ◽  
Storage Organs ◽  
Anatomical Adaptations ◽  
Multi Level ◽  
Molecular Aspects

In polyandrous mating systems, females mate multiple times and males have evolved adaptations for sperm competition which increase the number and fitness of their offspring. Mate guarding is a widespread monopolization strategy in groups where female receptivity is temporally restricted and often associated with the molt. Precopulatory guarding occurs in branchipods, copepods, peracarids and decapods. Postcopulatory guarding is notable in numerous brachyurans with males protecting females until her exoskeleton has hardened. During copulation, male success in fertilization depends on an effective sperm transfer mechanism, the precise placement of ejaculates closest to where female gametes are fertilized. Male copulatory systems are highly diverse and strongly adapted to these tasks, especially the structures that interact with the female genital ducts. The elaborate tips of brachyuran gonopods are supposed to act in the displacement, possibly even in the removal of rival sperm masses; however, sperm removal is only evident in crayfish: males eat spermatophores previously deposited by other males. During copulation of several crustacean groups, males transfer secretions that harden and form a sealant. These sperm plugs, plaques and gel layers may protect their own sperm, prevent remating or seal off rival sperm from the site of fertilization. Several groups of isopods and decapods have internal insemination, elaborate sperm storage organs and some exhibit internal fertilization. The intensity of sperm competition increases with the latency between the processes of insemination and fertilization. This chapter gives on overview on mate guarding, male sealants and the anatomical adaptations to sperm competition in crustaceans. We also briefly discuss the consequences of multiple matings for the genetic diversity of broods, i.e., single vs. multiple paternities. There is still a lack of data for many crustacean groups. Moreover, it is often hard to assess how successful a male strategy to ensure paternity actually is as many studies focus on either the behavioral, anatomical, or molecular aspects, while comprehensive multi-level studies on crustacean sperm competition are virtually absent from the literature.

scholarly journals Destination of apyrene sperm following migration from the bursa copulatrix in the monandrous swallowtail butterfly Byasa alcinous

2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Tatsuro Konagaya ◽  
Naoto Idogawa ◽  
Mamoru Watanabe
Keyword(s):  
Sperm Storage ◽  
Bursa Copulatrix ◽  
Swallowtail Butterfly ◽  
Storage Organs ◽  
Apyrene Sperm ◽  
Eupyrene Sperm ◽  
Spermathecal Gland

AbstractMost male lepidopterans produce fertile eupyrene sperm and non-fertile apyrene sperm, both of which are transferred to the female in a spermatophore during mating. Apyrene sperm outnumbers eupyrene sperm and both sperm types migrate from the bursa copulatrix to the spermatheca after mating. While eupyrene sperm are maintained in the spermatheca until oviposition, the number of apyrene sperm decreases with time. It is unclear whether apyrene sperm disappear from all sperm storage organs in females because both sperm types are often observed in the spermathecal gland. To investigate this, the numbers of both sperm types were estimated in the spermatheca and spermathecal gland of female Byasa alcinous (a monandrous butterfly) 6, 12, 48, 96, and 192 h after mating terminated. Apyrene sperm arrived in the spermatheca earlier than eupyrene sperm; however, some eupyrene and apyrene sperm migrated to the spermathecal gland from the spermatheca at almost the same time. The number of apyrene sperm reached a peak 12 h after the termination of mating and then decreased with time in both the spermatheca and spermathecal gland. Our results suggest that the role of apyrene sperm might be completed early after arriving in the spermatheca of B. alcinous.

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