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DNA measurements and ploidy determination of different stages in the life cycle of Sarcocystis muris.

The DNA contents of different stages within the life cycle of Sarcocystis muris were measured cytophotometrically using DNA-specific Feulgen staining. Stages of gamogony were obtained by the transfer of isolated cyst merozoites into cat kidney-cell cultures. For calculation of absolute DNA contents, the amounts of DNA in the parasites were compared with those in chicken erythrocytes, which are known. The measurements revealed that all investigated stages of S. muris contained haploid DNA except the early zygotes, which were diploid. The further development of the zygotes started with a nuclear division, resulting in two daughter nuclei that again revealed haploid DNA values. The results confirm the existence of zygotic meiosis; thus, a haplo-homophasic life cycle is proposed for the Sarcosporidia.

Animals↗

The life cycle of Brachylaima ruminae n. sp. (Trematoda: Brachylaimidae), a parasite of rodents.

The life cycle of Brachylaima ruminae n.sp. (Trematoda: Brachylaimidae), a duodenal parasite of rodents on the Mediterranean island of Formentera (Spain) is elucidated. The new species follows a terrestrial triheteroxenous life cycle. Eggs passed in the faeces of the definitive host must be ingested by a specific first intermediate host, the land snail Rumina decollata. Branched cercariogenous sporocysts develop in the digestive gland. Microcercous cercariae come out through the terminal birth pores of the branches. Cercariae shed by the snail are terrestrial, crawling on humid substratum. They contact the second intermediate host, another land snail, principally the species R. decollata and less frequently slugs and Helicids. Cercariae enter via the excretory pore and kidney duct to their specific final location, the kidney. Unencysted metacercariae develop in the kidney (also, less frequently, in the pedal glands) to the mature, infective stage. Infective metacercariae infest the definitive host when ingested together with the snail.

Animals↗

Application of life-cycle assessment to type III environmental declarations.

The objective of this research is to develop a desirable type III environmental declaration format for the industrial consumer. A total of five different scenarios were chosen for the presentation of life-cycle assessment results in a format that meets the requirements of a type III environmental declaration. Life-cycle assessment of an electronic component was performed for this purpose. Environmentally significant impact categories and input/output items of a product system derived from the life-cycle assessment are presented in this format. Presenting these information concisely in a standardized format would accelerate the communication of environmental aspects of materials and components in a product supply chain. Thus the type III environmental declaration can be a useful instrument for the manufacturing of an ecoproduct.

Animals↗

Hosts, seasonal occurrence and life cycle of Rhipicentor nuttalli (Acari: Ixodidae).

There are only two species worldwide within the genus Rhipicentor, namely Rhipicentor bicornis and Rhipicentor nuttalli and both occur only in Africa. Rhipicentor nuttali has a widespread distribution in South Africa and the present investigation was initiated to elucidate its host preference, seasonality and life cycle. Rock elephant shrews, Elephantulus myurus were examined for ticks at four localities in the Free State Province, one in Gauteng Province and two in Limpopo Province, South Africa. Cape elephant shrews, Elephantulus edwardii were examined at two places in the Western Cape Province, and a single specimen of the bushveld elephant shrew, Elephantulus intufi was examined in central Namibia. Small mammals of other species were also examined at two of these localities. The majority of E. myurus at two sites in the Free State, at the locality in Gauteng and both sites in Limpopo Province were infested with larvae and/or nymphs of R. nuttalli, while the single E. edwardii examined at one site in the Western Cape Province and the single E. intufi examined in Namibia were infested with nymphs of this tick. Not one of the other small animals was infested. Although larvae and nymphs of R. nuttalli were present on E. myurus throughout the year, the former were generally most numerous during the period March to September, and the latter during May to October. The preferred hosts of the adults are domestic dogs, leopards, Panthera pardus and South African hedgehogs, Atelerix frontalis. Adult females engorged on Atelerix frontalis in 16-32 days and, after a preoviposition period of 2-4 days, produced approximately 170,00 eggs during the following 60-70 days. The average incubation period of the eggs was 59 days. Larvae engorged on E. myurus in 4-10 days and moulted to nymphs 12-20 days later. Nymphs required 11-15 days to engorge on E. myurus and moulted to adults 32-47 days later. Allowing 14 days for the exoskeletons and mouthparts of each of the three parasitic stages to harden before they can attach to a host, the life cycle took approximately 214 days to complete in the laboratory. The length of this period, considered in conjunction with the times of maximum seasonal occurrence of the immature stages, indicates that the life cycle probably takes a year to complete in the field.

Animals↗

Developmental changes in the molecular forms of acetylcholinesterase during the life cycle of the lamprey Petromyzon marinus.

1. We have determined the molecular forms of acetylcholinesterase (AChE) present in the skeletal muscle of the lamprey during the adult parasitic stage of its life cycle. AChE was found primarily in the globular G4 form, as well as in the asymmetric forms A4, A8 and A12. 2. We compare the complement of molecular forms present in skeletal muscle during the larval, parasitic, and spawning stages of the lamprey life cycle. The larval form, the ammocoete, contains elevated amounts of G1 and G2. However, the most striking change that we observed was in the proportion of asymmetric forms of AChE present: 5% in the ammocoete, 28% in the parasite and 9% in the spawner. 3. We speculate that these differences may be related to the physiological states of the lamprey during the various stages of its life cycle.

Acetylcholinesterase↗

Lysosomal response of earthworm (Eisenia fetida) coelomocytes to the fungicide copper oxychloride and relation to life-cycle parameters.

Juvenile specimens of the earthworm species Eisenia fetida Savigny, 1826, were exposed in the laboratory to a range of concentrations of the fungicide copper oxychloride. After an eight-week exposure period, the neutral-red retention (NRR) times were measured in the coelomocytes of all the worms that had matured. Life-cycle traits (survival, biomass change, cocoon production, cocoon mass, hatching of cocoons, number of hatchlings) were also monitored. Dose-related effects on NRR times, maturation, growth, and reproduction parameters were determined (one-way analysis of variance, p < 0.05). The lowest effect concentration for substrate copper (Cu) measured for the NRR time was 8.9 mg/kg (dry wt). Growth was severely affected at the highest exposure concentration (330 mg/kg substrate dry wt), at which no worms matured and no NRR times could be measured. Negative linear correlations (p < 0.05) were apparent between the NRR times and substrate and body Cu concentrations. Positive linear relationships were found between the NRR times and some life-cycle parameters (p < 0.05). This study showed that the NRR assay can indicate toxic stress due to Cu exposure at an early stage, and that NRR times can be linked to effects on certain life-cycle traits.

Animals↗

Life cycle patterns and their genetic control: an attempt to reconcile evolutionary and mechanistic speculation.

A model is proposed which implicates molecular recognition systems as the major controlling factors in life cycle expression. It is envisaged that such systems are important in immune functioning and catabolic, metabolic molecule recognition at both inter- and intra-cellular level. These recognition systems have the following characteristics: 1) Specific recognition molecules (recognisers), e.g. vertebrate antibodies, invertebrate agglutinins and plant agglutinins may recognise specific substances, e.g. antigens, catabolic and metabolic molecules. 2) The range of possible recognisable substances is very wide and variable. 3) The recognisers may themselves be recognised by other recognisers. 4) Recognisers are usually produced in large amounts only on presentation of the appropriate recognisable molecule. 5) The progressive introduction of new recognisable molecules increases the recogniser interaction, this interaction causing depression of some recogniser types (immune depression) and facilitation of other types among which may be recognisers specific for self components (e.g. auto-immunity). 6) Low juvenile viability is associated with a restricted range of available recognisers, high adult viability with increasing recogniser range and some auto-immunity/immune depression, senescence with a wide range of available recognisers and extensive auto-immunity/immune depression. Life cycle patterns and their control are discussed. It is suggested control mechanisms may include: 1) Dietary restriction and in some periods complete nutritional abstinence. 2) Specific recogniser depression, genes implicated here are the various antigens (species and polymorphic) found on cell surfaces, in the serum and in various body fluids of vertebrates, e.g. ABO, MNSs, P, Rh, Le and other blood groups, the ABO and Le secretor antigens and the HL-A antigens. In addition the immune response and mixed lymphocyte culture loci are implicated. Finally life cycle control is discussed with relation to sexual selection.

Aging↗

A study on the life-cycle and epidemiology of Pseudanoplocephala crawfordi Baylis, 1927.

A study of the life-cycle and epidemiology of Pseudanoplocephala crawfordi Baylis, 1927 is reported. Intermediate hosts are Tenebrio obscurus, T. molitor, Carpophilus dimidiatus and Tribolium castaneum. The first three species are new host records. Development in the intermediate host takes 1-1.5 months. The completion of the life-cycle takes 2-2.5 months. Surveys of intermediate hosts, pigs, humans and rats were carried out. In Rattus norvegicus, the prevalence was as high as 22%. Epidemiological factors and suggestions for control measures are discussed.

Animals↗

High glucose accelerates the life cycle of the in vivo exposed mesothelium.

BACKGROUND: Mouse mesothelium exposed in vivo for 30 days to high glucose solutions develop morphological changes that characterize a population of cells near the end of their life span. METHODS: The present study was designed to explore, in mesothelial cell imprints, whether these changes could derive from an early acceleration of the cell population life cycle in mice exposed for periods of up to 30 days to a 4.25% glucose fluid (236 mmol/L/L) prepared in Hank's balanced salt solution (HBSS). Three critical points of the cell's life cycle were evaluated: the G1 checkpoint [proliferating cell nuclear antigen (PCNA) expression], DNA synthesis ((3)H-thymidine incorporation), and the prevalence of mitosis. RESULTS: Cell populations exposed to a high glucose concentration showed an initial acceleration of their life cycle, as sustained by a peak of mitosis at two hours, an early increase of DNA incorporation sustained during the first 24 hours, as well as a top level of PCNA expression after three to four hours. These significantly higher values, compared with the control animals treated with HBSS, collapsed after 24 hours and were nil after 30 days of exposure. CONCLUSIONS: Exposure to a high glucose concentration induced an early and short-lived acceleration of the mesothelial cell cycle, and with a longer exposure this was followed by a depletion of the growth capabilities of the exposed monolayer.

Animals↗

The life cycle of Clinostomum complanatum Rudolphi, 1814 (Digenea, Clinostomidae) on the floodplain of the high Paraná river, Brazil.

The life cycle of the digenetic trematode Clinostomum complanatum was studied on the floodplain of the high Paraná river, Brazil. Sampling was done between June 1999 and June 2000. The mollusc Biomphalaria peregrina was the first intermediate host with a prevalence of infection of 0.75%. The fish Loricariichthys platymetopon, Hoplosternum littorale, Parauchenipterus galeatus, Hoplias malabaricus and Loricaria sp. were second intermediate hosts, with the prevalence varying from 2.45% ( H. malabaricus) to 60.8% ( L. platymetopon). The birds Ardea cocoi, Phalacrocorax brasilianus, Egretta alba and Egretta thula were definitive hosts, with the prevalence ranging between 5.5% ( E. thula) and 95% ( A. cocoi). The high prevalences in birds, especially in A. cocoi, suggest some kind of mechanism facilitating the predation of infected fish. The importance of the various hosts is discussed, and it is concluded that the floodplain of the high Paraná river has suitable conditions for the maintenance of the life cycle of C. complanatum.

Animals↗

Some aspects of the life cycle of the tick Ixodes pilosus under laboratory conditions.

Some aspects of the life cycle of the tick Ixodes pilosus were studied under laboratory conditions. The preoviposition period was 7,2 +/- 0,6 d. Maximum egg production was on Day 4 after oviposition commenced, with total egg production of 2,395 +/- 128,7 eggs per female. The mean feeding time of larvae was 3,3 +/- 0,1 d. The life cycle could not be completed due to the specific requirements of this species.

Animals↗

[Features of the life cycles of Pterostichus montanus (Motschulsky, 1844) and Carabus loschnikovi (Fischer-Waldheim, 1822) (Coleoptera, Carabidae) in conditions of the mountain taiga belt in the Eastern Sayan].

We studied the seasonal dynamics and demographic structure of abundant ground beetle species from the mountain taiga belt in the Eastern Sayan. Data on the dynamics of the sexual and age structure of the populations as well as on the reproductive capacity of females in the biotopes on the slopes with different exposure and height were obtained. Life cycles with one- and two-year development were revealed for the ground beetles typical for the mountain taiga belt. As an example, data on the life cycles of Pterostichus montanus (Motschulsky, 1844) with one-year spring development and Carabus loschnikovi (Fischer-Waldheim, 1822) with two-year polyvariant multiseasonal development are given for the first time. Two strategies were revealed in the life cycles of ground beetles under alpine conditions: an accelerated population development in spring one-year species and a two-year development with pronounced polyvariance in two intrapopulation groups of ground beetles of the Carabus genus. The seasonal dynamics of the activity and reproduction periods proved to vary for these species on the slopes along the height gradient.

Adaptation, Physiological↗

The life cycle of Eimeria dispersa Tyzzer 1929 from the turkey in gallinaceous birds.

The life cycle of a turkey strain of Eimeria dispersa was studied in chickens, Chukar partridge, Ring-necked pheasant, and Bobwhite quail. Endogenous development in partridge and quail differed from development in chickens and pheasant. In partridge and quail, mature 1st-, 2nd-, and 3rd-generation schizonts, macrogamets, and oocysts were found in tissue sections at an earlier time interval, mature 1st-generation schizonts were larger, and mature 1st-, 2nd-, and 3rd-generation schizonts contained a greater number of merozoites that were longer. The only apparent similarity among the 4 hosts was the size of mature 2nd- and 3rd-generation schizonts. The life cycle was completed in all 4 species of birds. The prepatent period was approximately 6 hr shorter in partridge and quail than in chickens and pheasant. Two partridge and 2 quail given 50,000 sporulated oocysts each shed a total of 23 million and 135 million oocysts, respectively, during 4-day interval. Two chickens and 2 pheasant given the same dosage shed a total of only 70,000 and 1 million oocysts, respectively, during the same interval. Oocysts from partridge and quail sporulated more quickly and were slightly larger than those from chickens and pheasant.

Animals↗

Study of the early steps of the Hepatitis B Virus life cycle.

Hepatitis B virus (HBV) is a human pathogen, causing the serious liver disease. Despite considerable advances in the understanding of the natural history of HBV disease, most of the early steps in the virus life cycle remain unclear. Virus attachment to permissive cells, fusion and penetration through cell membranes and subsequent genome release, are largely a mystery. Current knowledge on the early steps of HBV life cycle has mostly come from molecular cloning, expression of individual genes and studies of the infection of duck hepatitis B virus (DHBV) with duck primary duck hepatocytes. However, considering of the difference of the surface protein of HBV and DHBV both in the composition and sequence, the degree to which information from DHBV applies to human HBV attachment and entry may be limited. A major obstacle to the study HBV infection is the lack of a reliable and sensitive in vitro infection system. We have found that the digestion of HBV and woodchuck hepatitis virus (WHBV) by protease V8 led to the infection of HepG2 cell, a cell line generally is refractory for their infection [Lu et al. J Virol. 1996. 70. 2277-2285 . Lu et al. Virus Research. 2001. 73(1): 27-4].. Further studies showed that a serine protease inhibitor Kazal (SPIK) was over expressed in the HepG2 cells. Therefore, it is possible that to silence the over expressed SPIK and thus to reinstate the activity of indispensable cellular proteases can result in the restoration of the susceptibility of HepG2 cells for HBV infection. The establishing a stable cell line for study of the early steps of HBV life cycle by silencing of SPIK is discussed.

Journal Article↗

Life cycle analysis of mammalian cells. 3. The inhibition of division in Chinese hamster cells by puromycin and actinomycin.

Analysis of the effects of actinomycin and puromycin on the G(2) and mitotic parts of the life cycle in Chinese hamster ovary cells grown in suspension and synchronized by thymidine treatment has been carried out. Rates of division of partially synchronized cell populations were measured in the presence and absence of the drugs, and various controls were performed to test for absence of complex side effects. Actinomycin produces a block 1.9 hr before completion of division, while puromycin produces a block almost coinciding with the initiation of mitosis. Evidence is presented that the puromycin block may be a double one, inhibiting one kind of protein synthesis that virtually coincides with the beginning of mitosis and another that occurs about 8 min earlier. The data are interpreted in terms of the time interval between messenger formation and its associated protein synthesis in this region of the life cycle. The various events studied have been provisionally mapped in the G(2) and mitotic periods of the life cycle.

Animals↗

Molecular cloning of casein kinase II alpha subunit from Dictyostelium discoideum and its expression in the life cycle.

A Dictyostelium discoideum cDNA encoding an alpha-type subunit of casein kinase II was isolated, and its cDNA was used to study developmental expression of casein kinase II during the Dictyostelium life cycle. The 1.3-kb cDNA insert contained an open reading frame of 337 amino acids (M(r) 39,900). The deduced amino acid sequence has high homology with those of casein kinase II alpha subunits from other species. Genomic Southern blot analysis suggested that there is a single gene encoding casein kinase II alpha subunit in D. discoideum. Northern (RNA) blot analysis showed that the casein kinase II alpha-subunit gene is expressed constitutively as a 1.9-kb mRNA throughout vegetative growth and multicellular development. Casein kinase purified from normal vegetative cells contained a major protein band of approximately 36 kDa, which was recognized by antisera raised against rat testis casein kinase II. Comparison of the in vitro transcription/translation product of the alpha-subunit cDNA clone and the purified 36-kDa protein by partial proteolysis indicated that the isolated cDNA clone encodes the Dictyostelium casein kinase II alpha subunit. No protein corresponding to a beta subunit was detected in purified casein kinase. Immunoblot analysis using anti-rat casein kinase II sera showed that the alpha subunit of casein kinase II is expressed constitutively like its mRNA during the life cycle of D. discoideum. Casein kinase II activity measured by using a specific peptide substrate paralleled the level of alpha subunit detected by immunoblotting during the life cycle, with a maximum variation of approximately 2-fold. We were unable to obtain disruptants of the casein kinase II alpha gene, suggesting that there is a single casein kinase II alpha gene, which is essential for vegetative growth of D. discoideum.

Amino Acid Sequence↗

Inhibitory effects of (-)-epigallocatechin gallate on the life cycle of human immunodeficiency virus type 1 (HIV-1).

Epigallocatechin gallate (EGCg), the major tea catechin, is known as a potent anti-bacterial agent. In addition, anti-tumor promoting, anti-inflammatory, anti-oxidative and antiviral activities have been reported. In the present study, we investigated possible anti-human immunodeficiency virus type-1 (HIV-1) activity of EGCg and its mechanisms of action in the viral life cycle. EGCg impinges on each step of the HIV life cycle. Thus, destruction of the viral particles, viral attachment to cells, post-adsorption entry into cells, reverse transcription (RT), viral production from chronically-infected cells, and the level of expression of viral mRNA, were analyzed using T-lymphoid (H9) and monocytoid (THP-1) cell systems, and antiviral protease activity was measured using a cell-free assay. Inhibitory effects of EGCg on specific binding of the virions to the cellular surfaces and changes in the steady state viral regulation (mRNA expression) due to EGCg were not observed. However, EGCg had a destructive effect on the viral particles, and post-adsorption entry and RT in acutely infected monocytoid cells were significantly inhibited at concentrations of EGCg greater than 1 microM, and protease kinetics were suppressed at a concentration higher than 10 microM in the cell-free study. Viral production by THP-1 cells chronically-infected with HIV-1 was also inhibited in a dose-dependent manner and the inhibitory effect was enhanced by liposome modification of EGCg. As expected, increased viral mRNA production was observed in lipopolysaccharide (LPS)-activated chronically HIV-1-infected cells. This production was significantly inhibited by EGCg treatment of THP-1 cells. In contrast, production of HIV-1 viral mRNA in unstimulated or LPS-stimulated T-lymphoid cells (H9) was not inhibited by EGCg. Anti-HIV viral activity of EGCg may thus result from an interaction with several steps in the HIV-1 life cycle.

Anti-HIV Agents↗

Characterisation of complementary DNAs from the expressed sequence tag analysis of life cycle stages of Laminaria digitata (Phaeophyceae).

Laminariales (Phaeophyceae, Heterokonta) are characterised by a heteromorphic digenetic life cycle with a filamentous, microscopic gametophyte and a highly evolved, macroscopic sporophyte. With the ultimate goal of comparing gene expression in each life cycle stage, complementary DNA libraries were constructed from sporophytes and gametophytes of Laminaria digitata. A set of ca. 500 expressed sequence tags (EST) was generated from each life history phase, by single-run partial sequencing of randomly picked cDNA clones. Comparison of the EST deduced amino acid sequences with database protein sequences assigned a putative identity for 39% of the 412 gametophyte clones and 48% of the 493 sporophyte clones sequenced thus far. These data represent more than 152 different proteins now probably identified in L. digitata. Several of those newly identified proteins are of interest to our understanding of the molecular physiology of kelps, for example their carbon-concentrating mechanisms, cell wall biosynthesis and halogen metabolism. EST analysis also confirmed that genes with long 3'-UTRs are widespread in Laminariales and the study of 5'-UTRs allowed the identification of a Kozak consensus sequence, c(A/C)A(A/C)CAUGGc(G/T). Several potential developmentally regulated differences in gene expression are discussed.

Algal Proteins↗