Immature Cysts Research Articles

Energy metabolism and genetic information processing mark major transitions in the life history of Scrippsiella acuminata (Dinophyceae)

Many dinoflagellates perform sexual reproduction and form cysts as a life history strategy to survive adverse environmental conditions and seed annual harmful algal blooms (HABs). The molecular mechanisms underpinning the life stage transitions can provide clues about how key environmental factors induce encystment and initiation of a HAB but are still poorly understood. Here, we conducted an integrated physiological and transcriptomic study to unravel the mechanisms in Scrippsiella acuminata. We established a culture from a bloom, induced cyst formation, and divided the process into four life stages. Transcriptomic analysis of these stages revealed 19,900 differentially expressed genes (DEGs). The expression of genes related to photosynthesis was significantly up-regulated from vegetative stage to immature cyst stage, consistent with the marked increase in cell contents of energy-storing macromolecules (carbohydrates and lipids). When proceeding to resting cysts, most photosynthesis genes were down-regulated while “genetic information processing” related genes were up-regulated. Comparing germinating cysts with resting cysts revealed 100 DEGs involved in energy metabolism, indicating a high energy requirement of germination. In addition, the transition from germinating cysts to vegetative cells featured up-regulation of photosynthesis. Our results demonstrate that energy storage and consumption play a pivotal role in cyst formation and germination respectively and genetic information processing is crucial in cyst dormancy.

Simple, once-off mapping of various, recurrent immunostaining patterns of proliferating cell nuclear antigen in spermatogonia at the immature pole of the testis of adult wild-caught blue shark, Prionace glauca: Correlations with changes in testicular status.

This study was a single time-point mapping of various immunostaining patterns revealed with the proliferating cell nuclear antigen (PCNA) PC10 antibody in spermatogonia at the immature pole of the testis of the Blue shark (Prionace glauca). Scattered in the stroma of the germinal ridge that demarcates the immature pole's outer boundary were nests of variously immunoreactive A-spermatogonia, each flanked by a fusiform cell. Spermatocysts were assembled from niche-derived stromal cells, displaced A-progenitors, and their progeny, which showed one of two main immunostaining patterns (i.e., an uneven light brown/globular and homogeneous dark [hod] brown appearance). The testes of wild-caught Prionace showed two conditions, namely, extensive multinucleate cell death (MNC) near the mitosis-meiosis transition or an early recovery phase from the latter showing vacuolated areas. Both the proportion of cysts with immature Bhod -spermatogonia and the frequency of mitotic figures in such cysts in the early recovery testis condition were significantly higher than the comparable parameters in MNC testis condition. Moreover, the post-MNC recovery phase revealed a decrease in the proportion of immature cysts with uneven light brown/globular-like spermatogonia. The protracted spread of a cell cycle signal in an anatomically discrete, syncytially connected spermatogonial clone manifests as different PCNA immunoreactivities.

PARASITIC EGGS, CYSTS AND LARVAE OF SOME FRUITS SOLD AROUND DUTSIN-MA METROPOLIS, KATSINA STATE, NIGERIA

Several parasitic infections are associated with poor personal hygiene and environmental sanitation resulting in fruits containing eggs, cysts or larva of parasites. A survey of some fruits sold around Dutsin-ma metropolis in Katsina was carried out to identify the eggs, cyst and larva present on them. A total of 180 fruit pieces were examined using standard wet mount procedure and Kinyoun acid fast stain to detect presence of parasites. The percentage of fruits found with eggs, cysts or larvae of six parasites identified were eggs of hookworm (16.42%), Ascaris lumbricoides eggs (24.30%), Trichuris trichuira eggs (8.62%), Strongyloides stercoralis larvae (6.64%), immature cyst of Entamoeba histolytica (31.62%) and eggs of Taenia species (12.4%) respectively. Garden eggs had the highest percentage with parasites’ ova, cysts or larva (60.3%) followed by water melon (21.4%) and cucumber (12.12%), mangoes (10%), carrots (4.8%) and oranges (0%). The chi-square test showed significant (p<0.05) differences in number of fruits with parasitic infection. It is very important to encourage proper washing of fresh and raw fruits before they are sold or eaten which will thereby prevent transmission either at point of sell or consumption of fruits which infect via the oral route

Protein Network Studies on PCOS Biomarkers With S100A8, Druggability Assessment, and RNA Aptamer Designing to Control Its Cyst Migration Effect.

The prevalence of polycystic ovary syndrome (PCOS) has been gradually increasing among adult females worldwide. Laparoscopy drilling on ovary is the only available temporary solution with a high incidence of reoccurrence. S100A8 with S100A9 complex is believed to facilitate the cyst migration in PCOS condition. The high evident protein interaction network studies between PCOS biomarkers, cancer invasion markers, and the interactors of S100A8 confirm that this protein has strong interaction with other selective PCOS biomarkers, which may be associative in the immature cyst invasion process. Through the network studies, intensive structural and pathway analysis, S100A8 is identified as a targetable protein. In this research, the non-SELEX in silico method is adapted to construct RNA Library based on the consensus DNA sequence of Glucocorticoid Response Element (GRE) and screened the best nucleotide fragments which are bound within the active sites of the target protein. Selected sequences are joined as a single strand and screened the one which competitively binds with minimal energy. In vitro follow-up of this computational research, the designed RNA aptamer was used to infect the MCF7 cell line through Lipofectamine 2000 mediated delivery to study the anti-cell migration effect. Wound Scratch assay confirms that the synthesized 18-mer oligo has significant inhibition activity toward tumor cell migration at the cellular level.

A hyperendemic focus of porcine cystic echinococcosis in the Banke District of Nepal

Detailed post mortem analyses of 68 free-ranging, slaughter-age pigs from two sites in the Banke District of Nepal identified 36% as being infected with Echinococcus granulosus. The cysts ranged from infertile, immature cysts a few millimetres in diameter to fertile cysts >10 cm in diameter. PCR RFLP and DNA sequencing identified the cysts as being E. granulosus sensu stricto. The Banke district has recently been identified as having a high prevalence of porcine cysticercosis. These data suggest that cestode zoonoses in this, and possibly other parts of Nepal may be a serious concern for human health. An assessment of the level of human cystic echinococcosis and neurocysticercosis, in the region is warranted and the introduction of control measures are required to limit the parasites’ transmission.

Lactoferrin and lactoferricin endocytosis halt Giardia cell growth and prevent infective cyst production

Lactoferrin (LF) is an 80 KDa iron-binding glycoprotein that plays a significant role in the innate immune system and is considered to be an important microbicide molecule. It has been suggested to be effective in the treatment of giardiasis, an intestinal disease caused by the protozoan parasite G. lamblia. However, the molecular mechanisms by which LF exerts its effect on this parasite are unknown. Most of the microbicidal activity of human or bovine LF (hLF or bLF) has been associated with the N-terminal region of the mature LF - lactoferricin (LFcin). LFcin is produced by pepsin cleavage of the native protein in vitro and likely in vivo. In this work, we analyse the participation of the endocytic machinery of G. lamblia in the internalization of bLF and bLFcin and their effects on cell homeostasis. Our results show that, when bLF or bLFcin are internalized by receptor-mediated endocytosis, cell growth stops, and morphological changes are produced in the trophozoites, which ultimately will produce immature cysts. Our findings contribute to disclose the fine mechanism by which bLF and bLFcin may function as an antigiardial molecule and why they have therapeutic potential to eradicate giardiasis.

Multiple Sources for Sertoli Cells and Two Sertoli Phenotypes in the Adult Elasmobranch Testis: Insight from Two Species Belonging to Different Orders.

Findings presented here for the chondrichthyans Prionace glauca and Isurus oxyrinchus show that the assembly of the spermatocyst and it's attached collecting duct are seamlessly connected developmental phenomena. The cyst's somatic cell component (i.e., Sertoli cells, SCs) and the duct's constituent cells derive both from a common precursor cell type (typically a large oblong cell) found among the A-spermatogonia in the folliculogenic region. Novel findings show that the co-developing collecting duct itself serves also as a source of either normal-looking or basophilic atypical SCs (aSCs), depending on whether the duct-cyst transition remains mitotically active and open, or is sealed. The aSCs arise from accumulating slender basophilic cells at the duct-cyst interface after which the newly formed cyst is sealed. Quantitative analysis of the latter in P. glauca revealed a correlation between the appearance of this aSC in immature cysts and the degenerated testicular condition that displays a gradient of multinucleate cell (MNC) death among spermatogonial cysts. Findings seem to implicate these aSCs in the life-death balance in mature spermatogonial cohorts downstream in the spermatogenic sequence, rather than in newly formed cysts that exhibit low rates of apoptosis. Photomicrographs of developing spermatogonial cysts showing several aSCs interspersed among cytoplasmically linked spermatogonia that are proliferating or have died, seem to suggest that these small SCs may be involved in confining MNC death to a given cyst region under conditions of subthreshold levels of apoptosis such as to ensure cyst recovery in immature spermatogonial cysts. Anat Rec, 301:1944-1954, 2018. © 2018 Wiley Periodicals, Inc.

Effect of 2, 6-Dichlorobenzonitrile on Amoebicidal Activity of Multipurpose Contact Lens Disinfecting Solutions.

Multipurpose contact lens disinfecting solutions (MPDS) are widely used to cleanse and disinfect microorganisms. However, disinfection efficacy of these MPDS against Acanthamoeba cyst remain insufficient. 2, 6-dichlorobenzonitrile (DCB), a cellulose synthesis inhibitor, is capable of increasing the amoebical effect against Acanthamoeba by inhibiting its encystation. In this study, we investigated the possibility of DCB as a disinfecting agent to improve the amoebicidal activity of MPDS against Acanthamoeba cyst. Eight commercial MPDS (from a to h) were assessed, all of which displayed insufficient amoebicidal activity against the mature cysts. Solution e, f, and h showed strong amoebicidal effect on the immature cysts. Amoebicidal efficacy against mature cysts remained inadequate even when the 8 MPDS were combined with 100 μM DCB. However, 4 kinds of MPDS (solution d, e, f, and h) including 100 μM DCB demonstrated strong amoebicidal activity against the immature cysts. The amoebicidal activity of solution d was increased by addition of DCB. Cytotoxicity was absent in human corneal epithelial cells treated with either DCB or mixture of DCB with MPDS. These results suggested that DCB can enhance the amoebicical activity of MPDS against Acanthamoeba immature cyst in vitro.

Chloroquine as a possible disinfection adjunct of disinfection solutions against Acanthamoeba

Acanthamoeba keratitis is commonly encountered by contact lens wearers. Contact lens solution plays an important role in the safe use of contact lenses. The most popular products for disinfecting lenses are multipurpose disinfecting solutions (MPDS). However, almost all MPDS retailed in Korea are ineffective in killing Acanthamoeba. The objective of this study was to determine the possibility of using autophagy inhibitor chloroquine as a disinfecting agent to improve the amoebicidal activity of MPDS against Acanthamoeba, especially the cyst. Amoebicidal effects of eight different MPDSs combined with chloroquine (CQ), an autophagy inhibitor, and their cytotoxicities to human corneal epithelium cells were determined. Almost all MPDS showed strong amoebicidal effect on trophozoites after 8 h of exposure. However, they showed inadequate amoebicidal effect on cysts even after 24 h of exposure. MPDSs combined with 100 μM CQ increased their amoebicidal effects on immature cyst by inhibiting formation of mature cysts. Incubation with 100 μM CQ for 30 min did not have cytotoxicity to human corneal epithelial cells.

Differential expressions of an Hsp70 gene in the dinoflagellate Akashiwo sanguinea in response to temperature stress and transition of life cycle and its implications

The unarmoured dinoflagellate Akashiwo sanguinea is a cosmopolitan species frequently causing harmful algal blooms in temperate to tropical estuaries and marine coasts. While resting cyst production and wide temperature tolerance have been well documented as two adaptive strategies for HAB-forming dinoflagellates, little attention has been paid to the molecular mechanisms, such as the functional genes and their expressions relevant to these ecological processes. Here, the cloning of the gene Hsp70, a gene putatively involved in the process of temperature stress responses, in A. sanguinea and its differential expressions in response to temperature stress and transition of life cycle stages were reported. Based on homologous cloning and the rapid amplification of cDNA ends (RACE), the full-length cDNA sequence (2171 bp) of an Hsp70 gene from A. sanguinea (AsHsp70) was obtained (Accession No. KJ755185), with an open reading frame of 1950 bp. The deduced 649 amino acids (aa) possessed an ATPase domain of 399 aa, a substrate peptide binding domain of 124 aa and a C-terminus domain of 126 aa. The highly conserved motifs of Hsp70 family identified in AsHsp70 suggest conservative function of Hsp70. Real-time quantitative PCR revealed that AsHsp70 expression (20°C-maintained) was dramatically up-regulated by both low (15°C, 10°C, 5°C) and high (25°C, 30°C) temperature shocks. Rapid and significant increase of AsHsp70 expression could be detected within 10min after exposure to lower temperature stress (10°C). Compared with the stepwise increases or decreases in temperature (±5°C each step), one-step shocks (±10°C) elicited markedly higher AsHsp70 transcripts. In addition, AsHsp70 transcription varied with growth stage and life cycle, peaking in immature cysts undergoing morphogenesis and returning to lower levels in cysts when morphogenesis was completed. The results together strongly suggest that A. sanguinea is more tolerant to gradual than drastic temperature stress and that AsHsp70 may be involved in the adaptation of A. sanguinea to varying temperatures. It is also suggested that Hsp70 might play roles in the encystment of dinoflagellates, which, however, needs more solid evidence for confirmation.

Extended Cyst Gastrostomy with Hydrogen Peroxide Irrigation Facilitates Endoscopic Pancreatic Necrosectomy

Figure: No Caption available.Purpose: Endoscopic cyst gastrostomy and pancreactic necrosectomy has emerged to be one of the main options for treatment of infected pancreatic pseudocyst or walled off pancreatic necrosis. One of the limitation of successful endoscopic drainage in these situations is the small size of the gastrostomy created (usually around 1 cm) and the large amount of necrotic material within the cyst/ abscess cavity. In this case series we describe our technique of creating large gastrostomy opening (2 cm) with hydrogen peroxide irrigation to facilitate abscess/cyst cavity drainage and hence improve the successfulness of the endoscopic intervention. Methods: This case series demonstrates our modified endoscopic ultrasound (EUS) guided cystgastrostomy technique using the following: 1) Creation of an extended cyst gastrostomy by gastrostomy dilation up to two either with: a) Single-stage dilation if the EUS showed no blood vessels within the puncture site and the CT scan demonstrates a mature cyst wall or b) Dilation of a pre-existing cyst gastrostomy in patients with gastric varices or immature cyst wall; 2) Direct endoscopic examination of the cavity with hydrogen peroxide irrigation to debride adherent nercotic tissue;3) Placement of two 10 French double pig tail stents to keep the gastrostomy tract open. Results: Four cases (2 male, 2 female) were included in this series. Mean age was 54.7 yrs. Three patients had walled-off pancreatic necrosis and one patient had pancreatic abscess after distal pancreatictomy. Resolution of the cyst or abscess cavity was achieved in all patients. No complication were reported. Conclusion: With our technique, patients required a single session or at maximum two-staged sessions of endoscopic pancreatic necrosectomy prior to resolution of the cyst/abscess cavity.

Acanthamoeba castellanii cysts: new ultrastructural findings

During Acanthamoeba castellanii trophozoite-cysts differentiation, four morphological stages were identified by scanning electron microscopy: trophozoite, precyst, immature cysts, and mature cysts. Fluorescence microscopy reveals the presence of small cumulus of actin in the cytoplasm of precysts after treatment with rhodamine phalloidin. By the contrary, in mature cysts, fluorescence was not observed. However, when excystation was induced, large fluorescent patches were present. By transmission electron microscopy, encysting amebas showed small cytoplasmic vesicles containing fibrillar material, surrounded by a narrow area of thin fibrils. Similar appearance was observed in pseudopods and phagocytic invaginations. In addition, large aggregates of rod-shape elements, similar to the chromatoid bodies, described in other amebas, were present in the cytoplasm. These cysts presented large areas with orange fluorescence after treatment with acridine orange.

Reproductive cycle and larval characteristics of the sponge Haliclona indistincta (Porifera: Demospongiae)

Haliclona indistincta has in some respects, a typical reproductive cycle for a marine haplosclerid sponge. We suggest that oocytes originate from archaeocytes and that spermatozoa originate from choanocytes. Oocytes were first seen in November and matured as eggs by May and June. Immature spermatic cysts were identified from February and mature cysts were present in May and June only. Of the individuals surveyed that had reproductive elements present (150/200), reproductive elements from a single sex were reported in over half of the specimens (59%) but there were also many hermaphrodites (41%). Embryos were first seen in June. Larvae were distributed throughout the mesohyl and were released from the end of June to the end of July. Three mobile larval stages and fusing of sibling larvae were observed. Post-settlement stages from early settlement to the development of oscula and excurrent canals are also shown. However, some elements of the larvae (uniform ciliation and no spicules at posterior pole) are not consistent with larvae from this genus.

Stress-Induced Pseudocyst Formation - A Newly Identified Mechanism of Protection against Organic Solvents in Acanthamoebae of the T4 Genotype

Differentiation into highly resistant double-walled cysts is a major mechanism allowing amphizoic acanthamoebae to survive under long-lasting, unfavourable environmental conditions. We found that relatively low concentrations of methanol, acetone or DMSO stimulate promptAcanthamoebadifferentiation into a rounded cyst-like stage with a single envelope. To address whether this rapid response differs from the encystment, time-dependent changes in cell surface characteristics and cyst-specific gene expression were monitored in encystating cells and cells differentiating under methanol treatment using microscopic, lectin-binding, PCR and resistance studies. In contrast to the encystment: (1) a single-layered amorphous mannose/glucose coat was the only envelope assembled on the surface of the solvent-treated cells, (2) the cyst-specific protein (CSP21) was not expressed, (3) the coat did not protect cells against acidic pH and (4) in solvent-free encystment medium, the coated cells did not assemble the double-layered wall, thus indicating that these cells were not immature cysts. These findings lead us to specify a terminal stage of rapidAcanthamoebadifferentiation elicited by acute organic solvent stress as "pseudocyst", and to suggest that encystation and pseudocyst formation are distinct stress responses. Moreover, the possibility exists that pseudocysts might form in response to certain contact lens solutions thus increasing resistance of acanthamoebae to disinfecting agents.

An Entamoeba cysteine peptidase specifically expressed during encystation

Protozoan parasites of the genus Entamoeba possess a considerable number of cysteine peptidases (CPs), the function of most of these molecules for amoeba biology needs to be established. In order to determine whether CPs may play a role during Entamoeba stage conversion from trophozoites into cysts and vice versa, expression of cp genes was analysed in the reptilian parasite Entamoeba invadens, a model organism for studying Entamoeba cyst development. By homology search, 28 papain-like cp genes were identified in public E. invadens genome databases. For eight of these genes the expression profiles during stage conversion was determined. By Northern blot analysis, transcripts for eicp-a9, -b7, -b8 and -c2, respectively, were detected neither in trophozoites or cysts nor at any of the point of times analysed during stage conversion. On the other hand, eicp-a5 is constitutively expressed during all developmental stages, whereas eicp-a3 and eicp-a11, respectively, are trophozoite-specific. Only eicp-b9 was found to be cyst-specific as it is expressed exclusively 18 to 28 h after cyst induction. Cyst-specific expression was confirmed by immunofluorescence microscopy of the corresponding protein EiCP-B9. In immature cysts, the molecule is located in structures that accumulate near the cyst wall, but which are uniformly distributed in mature cysts. The precise function of EiCP-B9 during Entamoeba encystation remains to be determined. However, colocalisation studies with an Entamoeba marker for autophagosomes suggest that EiCP-B9 is not associated with Entamoeba autophagy.

Encystment of Acanthamoeba During Incubation in Multipurpose Contact Lens Disinfectant Solutions and Experimental Formulations

Acanthamoeba keratitis (AK) is most commonly found in contact lens wearers with poor lens care hygiene. Recent reports have indicated an increase in cases of AK in the United States associated with the use of Complete MoisturePlus multipurpose solution. This association may not appear explainable by differences in Acanthamoeba kill rates among multipurpose solutions. In this study the physiologic response of Acanthamoeba trophozoites to incubation in various contact lens solutions was investigated. Acanthamoeba trophozoites were incubated in commercial and experimental solutions and the percentage encystment and viability determined in conjunction with microscopic analysis of cyst formation. Among commercial products, MoisturePlus solution induced encystment within 6 to 24 hr of incubation. Only immature cysts formed which failed to mature even after 5 days incubation in the solution although they remained viable. Experimental formulations of MoisturePlus solution, modified by omitting key ingredients, identified propylene glycol as the agent responsible for inducing encystment. However, tests of other commercial solutions containing propylene glycol produced reduced or no encystment. The presence of propylene glycol was shown to be the key factor in inducing Acanthamoeba encystment. However, the reduced or absence of encystment in other commercial solutions containing propylene glycol suggests additional factors, such the buffering system, may be involved in the phenomenon. How these observations relate to the solution's role in the reported association with AK is unclear. Nevertheless, it is recommended that all lens care products be tested for propensity to induce Acanthamoeba encystment and formulations containing propylene glycol may warrant special scrutiny.

Infection of plant-parasitic nematodes by Paecilomyces lilacinus and Monacrosporium lysipagum

Studying the mode of infection of a biocontrol agent is important in order to assess its efficiency. The mode and severity of infection of nematodes by a soil saprophyte Paecilomyces lilacinus (Thom) Samson and a knob-producing nematode trapping fungus Monacrosporium lysipagum (Drechsler) Subram were studied under laboratory conditions using microscopy. Infection of stationary stages of nematodes by P. lilacinus was studied with three plant-parasitic nematodes Meloidogyne javanica (Treub) Chitwood, Heterodera avenae Wollenweber and Radopholus similis (Cobb) Thorne. Paecilomyces lilacinus infected eggs, juveniles and females of M. javanica by direct hyphal penetration. The early developed eggs were more susceptible than the eggs containing fully developed juveniles. As observed by transmission electron microscopy, fungal hypha penetrated the M. javanica female cuticle directly. Paecilomyces lilacinus also infected immature cysts of H. avenae including eggs in the cysts and the eggs of R. similis. Trapping and subsequent killing of mobile stages of nematodes by M. lysipagum were studied with the above three nematodes. In addition, plant-parasitic nematodes Pratylenchus neglectus (Rensch) Chitwood and Oteifa and Ditylenchus dipsaci (Kuhn) Filipjev were tested with M. lysipagum. This fungus was shown to infect mobile stages of all the plant-parasitic nematodes. In general, juveniles except those of P. neglectus, were more susceptible to the attack than adults.

Apoptosis during spermatogenesis in the spotted ray Torpedo marmorata

This article is a cytological and molecular investigation on the occurrence of apoptosis during spermatogenesis in Torpedo, a cartilaginous fish characterised by a typical cystic testis. Using DNA fragmentation and Bak gene expression, it demonstrated that germ cells undergo apoptosis only at the stages of spermatocyte and spermatid, and degeneration also involves Sertoli but not Leydig cells. In immature cysts, this cellular process probably occurs when the ratio of germ cells to the only Sertoli cell (SC) forming the spermatoblast changes. Apoptosis also takes place in mature cysts after sperm release to eliminate most of the SCs. Few of them, however, become cytoplasts and probably continue secreting androgens so as to control the final events of spermatogenesis, i.e., passage of spermatozoa through the ductus deferentes. Finally, the present investigation demonstrated that, in Torpedo testis, Bak mRNA is expressed during spermatogenesis, thus suggesting that the mitochondrial pathway might be active. This observation in one of the oldest vertebrate classes indicates that, in all vertebrates, the apoptotic process during spermatogenesis is conserved, contributing to testicular homeostasis.

The distribution and proliferation of the intracellular bacteria Wolbachia during spermatogenesis in Drosophila.

Wolbachia is a cytoplasmically inherited alpha-proteobacterium found in a wide range of host arthropod and nematode taxa. Wolbachia infection in Drosophila is closely associated with the expression of a unique form of post-fertilization lethality termed cytoplasmic incompatibility (CI). This form of incompatibility is only expressed by infected males suggesting that Wolbachia exerts its effect during spermatogenesis. The growth and distribution of Wolbachia throughout sperm development in individual spermatocysts and elongating sperm bundles is described. Wolbachia growth within a developing cyst seems to begin during the pre-meiotic spermatocyte growth phase with the majority of bacteria accumulating during cyst elongation. Wolbachia are predominantly localized in the proximal end of the immature cyst, opposite the spermatid nuclei, and throughout development there appears little movement of Wolbachia between spermatids via the connecting cytoplasmic bridges. The overall number of new cysts infected as well as the number of spermatids/cysts infected seems to decrease with age and corresponds to the previously documented drop in CI with age. In contrast, in one CI expressing line of Drosophila melanogaster, fewer cysts are infected and a much greater degree of variation in numbers is observed between spermatids. Furthermore, the initiation and extent of the fastest period of Wolbachia growth in the D. melanogaster strain lags behind that of Drosophila simulans. The possible implications on the as yet unexplained mechanism of CI are discussed.

A comparison of cyst age and assay method of the efficacy of contact lens disinfectants againstAcanthamoeba

AIMS(i) To determine effect of Acanthamoeba cyst age, method of production, and (ii) to assay technique on the efficacy of multipurpose solutions (MPS) and hydrogen peroxide based contact lens disinfectants....