Failure to vaccinate lambs against Haemonchus contortus with functional metabolic antigens identified by immunoelectrophoresis.

Metabolic products from Haemonchus contortus larvae cultured in vitro from the infective third to fourth stage were collected and concentrated. Chromatographic and immunoelectrophoretic analyses were made to study the numbers and activity of antigens in the metabolic products derived from the in vitro cultured larvae. Three-month-old lambs were given a series of injections of metabolic antigens with and without adjuvant at dose rates of 0·05, 0·5 and 5·0 mg antigen protein per injection. These animals and saline injected controls were each challenged with 3000 H. contortus infective larvae after the last antigen injection and killed 35 days later. No difference was seen in the faecal worm egg counts or the differential worm counts among the vaccinated and control animals. The antigen preparation of worm metabolic products conferred no resistance to challenge infection with the parasite.     

Porphyrins in the perienteric fluid of Ascaris lumbricoides.

Cain G. D. and Bassow F. 1976. Porphyrins in the perienteric fluid of Ascaris lumbricoides. International Journal for Parasitology6: 79–82. Porphyrins in the perienteric fluid of adult female A. lumbricoides were esterified in methanolic H₂SO₄, extracted in chloroform, separated by thin-layer chromatography, and identified spectrophotometrically before and after conversion to their zinc and copper chelates. Protoporphyrin IX was the major component, comprising 95·4% of the total; the remaining 4·6 % was coproporphyrin III. Uroporphyrin was not detected; no porphyrins were recovered from other worm tissues. Fluid from worms with light and dark colored guts varied in protoporphyrin content from 0·58 to 4·08 nmoles/ml, respectively, but fluid from both groups contained similar molar ratios of protoporphyrin, coproporphyrin and heme.     

The relationship of abnormal mucosal microtopography with distribution of Trichostrongylus colubriformis in the small intestines of lambs

The relationship of abnormal mucosal microtopography with distribution of Trichostrongylus colubriformis in the small intestines of lambs. International Journal for Parasitology4: 153–163. The distribution of T. colubriformis was studied by counting worms in sequential 1-m segments from the guts of 14 infected lambs. Mucosal morphology was described at corresponding 1-m intervals and compared with similar samples from uninfected controls. A mean of 90 per cent of worms was recovered in the first 6 metres of gut. Maximum worm counts occurred in the first (eight lambs) second (three lambs) or third (three lambs) metre. Less than 0·8 per cent of worms were found in the abomasa of five lambs. Flat mucosae or abnormal surface patterns were seen frequently in the anterior small intestine of infected lambs. Degree of mucosal abnormality was positively associated with magnitude of worm numbers/m, and negatively correlated with distance of the sample from the pylorus, by analysis of partial correlation of worm numbers/m, mucosal type score, and distance from the pylorus. Mucosae from areas with > 4000 worms/m tended to have significantly shorter villi than intestine of control lambs. Factors influencing worm distribution and pattern of establishment are discussed, as is the association of extreme villus atrophy with poor performance by infected lambs.     

In vitro culture of Trichobilharzia ocellata

Cercariae and schistosomula of Trichobilharzia ocellata were cultured to the organogeny stage in vitro in a medium based on Earle's saline (gassed with 5% CO₂ in air) and containing lactalbumen hydrolysate and duck or chicken serum together with homologous red cells. Similar results were obtained irrespective of whether cercariae, schistosomula recovered from the skin of ducklings or chickens, or schistosomula recovered after cercariae had penetrated gelatine membranes were used to initiate cultures. A lipid coat developed around the body of each worm during the first 2–3 days in vitro, but subsequently it became dislodged. The worms ingested red cells, and the caeca became dark with haematin after a few days but by day 10 they were generally translucent. Maximum development was achieved at day 12; by this time males had attained a length of 2·1 mm and females 1·4 mm. Worms cultured for 7 and 9 days were injected into the leg veins of ducks and patent infections were established.     

Further studies of the effect of L-canavanine on the tobacco hornworm, Manduca sexta.

Fifth instar Manduca sexta growth response to injected doses of canavanine was concentration-dependent over a range of 0·5 to 2·0 mg/g body weight. Twenty-four hr after injection of ¹⁴C-guanidinooxy-d,l-canavanine, M. sexta larvae incorporated approximately 3·6% of the labelled l-canavanine into protein of non-gut tissue. Adult M. sexta mortality was related to the level of injected canavanine over a range of 2 to 8 mg/g body weight. Injection of as little as 2 mg canavanine/g body weight caused hyperactivity in adult M. sexta. Arginine, able to negate the toxic effects of canavanine during larval growth, was only marginally capable of overcoming canavanine effects on larval-pupal ecdysis.     

Genetic studies of the lac repressor. IV. Mutagenic specificity in the lacI gene of Escherichia coli.

An extensive set of amber and ochre sites in the lacI gene has been characterized with respect to the base change required to generate the nonsense codon (Miller et al., 1977; Coulondre &; Miller, 1977). These mutations have been used to analyze the forward mutational spectrum of a series of mutagens in Escherichia coli. The sites induced by N′-methyl-N′-nitro-N-nitrosoguanidine, ethyl methanesulfonate, 4-nitroquinoline-1-oxide, and ultraviolet light, were examined, as well as those which arose spontaneously. Sites induced by the G · C → A · T transition were compared with those generated by 2-aminopurine mutagenesis. All together, more than 4000 independent occurrences of amber and ochre mutations were tabulated in order to define the respective mutagenic specificities. With the exception of the A · T → G · C change, all base substitutions lead to the generation of nonsense codons from wild-type. The A · T → G · C transition was monitored in a reversion system, in which the ochre to amber conversion (UAA → UAG) was scored, as well as the UAA → CAA reversion.Both NG³ and EMS were found to be highly specific for the G · C → A · T transition, less than 1% transversions appearing in either case. At between 1% and 5% the level of the G · C → A · T change, NG can stimulate the A · T → G · C transition. EMS stimulates the A · T → G · C transition at a significantly lower rate. NQO is also highly specific for G · C base-pairs, but approximately 10% of the changes found at these sites are transversions. Mutations found spontaneously or after irradiation with ultraviolet light showed none of the specificities found for EMS, NG or NQO. All transversions were detected in both cases. Moreover, a significant number of tandem double base changes were found to be induced by u.v. irradiation. Some of these have been verified directly by protein sequencing. The frequencies of occurrence of amber and ochre mutations arising from the G · C → A · T transition have been compared for different mutagens, revealing several striking hotspots. The implications of these findings with respect to the mechanism of mutagenesis and the application of different mutagens are discussed.     

Aspects of the nutrition of adult female Glossina morsitans during pregnancy

The adult female Glossina morsitans fed on goat takes, in terms of dry weight, approximately 37·6 mg of blood during a pregnancy period, and at least 84% of this dry blood comprises proteins. In this diet leucine is the most abundant, isoleucine and methionine contents are markedly small, while values for other amino acids differ and are intermediate. Shortly after pupariation the third instar larva produced by goat-fed females contains 67·3% water, 15·3% residual dry weight, 11·0% fat, and 6·4% puparium. The amount of each of the amino acids present in the larva and its puparium comprises a small proportion of that taken by the female fly during a pregnancy period. The fat content of the fully-fed larva is also very small compared with the total nutrient intake by the pregnant female. These results are discussed in terms of the nutrition of intra-uterine larva in relation to feeding by its female parent.     

Some physical properties of paramyosin from earthworms

Paramyosin was prepared from earthworms (Lumbricus terrestris) by two different methods that have been used in the past. Polyacrylamide gel electrophoresis in the presence of sodium dodecyl sulfate shows that the older method yields slightly degraded material (mostly β- and γ-paramyosin) while the newer method yields essentially intact, i.e., α-, paramyosin. Physical studies, particularly circular dichroism, light scattering, and sedimentation velocity show that the native molecule is a double α-helical coiled coil of molecular weight 200,000, length 1200 Å, and diameter 20 Å. These properties are the same as reported previously for molluscan paramyosin. Also like clam paramyosin, the worm protein molecule loses its helix content and dissociates into its two constituent polypeptide chains upon exposure to sufficient concentration of Gdn-HCl. Furthermore, the same partially denatured states can be reached from either native or completely denatured proteins, indicating that they are all equilibrium states. However, the Gdn · HCl-induced denaturation profile for the worm paramyosin is quite different from the clam. The helix content of worm paramyosin diminishes monophasically with increasing concentration of Gdn-HCl, showing that the molecule does not possess a region of special stability such as its clam analog boasts. This conclusion is supported by experiments on papain digestion of worm paramyosin, wherein no resistent core is seen.     

Effect of temperature and photoperiod on the induction of diapause in the mite Metaseiulus occidentalis

Diapause in a predaceous mite, Metaseiulus occidentalis, from a Californian vineyard population is a photoperiodically induced, facultative, adult reproductive diapause in females. The laboratory-determined critical photophase at 19°C was estimated at 11·2 hr. At 16°C, the critical photophase under laboratory conditions was approximately 11·6 hr. Temperature influenced the photoresponse of M. occidentalis so that diapause was entirely averted at temperatures of 22, 25, and 30°C. Aestival diapause at higher temperatures and long photophases was lacking. Development was continuous under constant darkness at all the temperatures tested. Diapause termination in laboratory-reared mites occurred spontaneously under the inductive conditions. Under constant 19°C temperatures, females responded to photophases so that diapause was terminated most rapidly under a 16 hr photophase (in 18·6 days); the 12 and 8 hr photophases, at this temperature, were next in their effectiveness, with 27·9 and 73·0 days, respectively, required for termination.     

Cryopreservation of the promastigote form of Leishmania tropica var major at different cooling rates

Callow L. L. and Farrant J. 1973. Cryopreservation of the promastigote form of Leishmania tropica var major at different cooling rates. International Journal for Parasitology, 3: 77–88. An investigation of the optimal conditions for the preservation of Leishmania tropica var major by freezing was undertaken because it was important to obtain a high yield when the thawed organisms were cultured. As a prerequisite for comparing different conditions, assay methods were devised. One method was based on the reduced growth of promastigotes in diphasic medium that was found to follow inoculation of relatively few organisms. The other employed serial ten-fold dilutions of suspensions of organisms, and the inoculation of medium at each dilution stage. Viability was related to the time taken for flagellates to be found in the medium. A 1·0 m solution of glycerol in the flagellate suspension inhibited growth when diphasic medium was inoculated. This effect was removed by separating the organisms from the glycerol before inoculation, or by diluting the suspension approximately one hundred-fold. A similar inhibition was not observed for dimethylsulphoxide (DMSO). Glycerol (1·0 m), DMSO (1·5 m), polyvinylpyrrolidone (10% w/v) and sucrose (0·3 m) were not obviously detrimental to the organisms. Normal growth in diphasic medium resulted when these additives were removed after being in contact with organisms for 5 h in an ice bath. In freezing experiments, flagellates survived freezing and thawing while they were still in contact with their nutrient medium, and also after they had been separated, washed and resuspended in isotonic saline with 10 mm of glucose. The survival rate was much greater when either 1·5 m DMSO or 1·0 m glycerol was added. These additives were compared at one rate only, $\text{0·3°C}\text{min}$, and DMSO gave better protection. With 1·5 m DMSO, maximal survival was obtained at a cooling rate of $\text{1·9°C}\text{min}$. Relatively high rates of cooling, that is, over $\text{400°C}\text{min}$ were detrimental to the organisms.     

Utilization of body reserves for minim brood development by queens of the imported fire ant, Solenopsis invicta

Protein, glycogen, and lipid concentrations were followed in Solenopsis invicta queens, the imported fire ant, from egg deposition until the production of the first minim workers approximately 21 days later. During this time, the weight of the queens decreased from 14·7 to 7·5 mg. Immediately following egg deposition, total protein decreased by over 50 per cent for the first 6 days, then rose steadily for 9 days, then once again decreased markedly throughout the remainder of the study. Glycogen concentrations decreased rapidly from the 0·35 mg/ant found at oviposition until day 12. From this time until the end of the study, this polysaccharide remained constant at about 10 mg/ant. Lipid concentrations remained at 4·1 mg/ant for the first 9 days following oviposition, then steadily decreased to 2·3 mg/ant when the first minim workers were produced 12 days later.     

Fine structural changes in dark-light adaptation in relation to unit studies of an insect compound eye with a crustacean-like rhabdom

Structural changes in dark-light adaptation of the compound eye of the beetle Creophilus erythrocephalus, have been investigated by electron microscopy. Their functional consequences have been studied by means of intracellular electrophysiological recordings from retinula cells. In the dark-adapted state the intercellular spaces between the retinula cells swell considerably and produce a palisade of extracellular origin around the rhabdom. Units from dark-adapted eyes are approximately ten times more sensitive than those from light-adapted animals and have larger acceptance angles (7·037° ± 1·23 S.D. compared with 5·135° ± 0·99 S.D. for the light-adapted insect). A spikegenerating unit, inhibited by light, was found once. Although the rhabdom is of the ‘banded’ type, polarization sensitivity was found to be unexpectedly low: 2·31 ± 1·54 S.D. It is concluded that electrical coupling, useful for dim light conditions and eyes with tiny apertures, most likely appears to be the reason for the low average polarization sensitivity.     

Effect of dietary tetrapyrroles on gut pigmentation and perienteric fluid hemoglobin concentration in Ascaris lumbricoides

Ascaris lumbricoides was maintained for 46 days in three pigs fed diets enriched with different metalloporphyrins. Diets, host gut contents, and washed worm guts were differentially extracted for carotenoids, bile pigments, porphyrins and metalloporphyrins, and extracts were compared by spectrophotometric and qualitative chemical tests. Host gut contents from a control diet with no added porphyrin contained carotenoids and bilirubin; worms from this host contained bilirubin and an unidentified metalloporphyrin. An alfalfa-enriched diet yielded phaeophytin A in host gut contents, while worm gut tissue contained an unidentified metalloporphyrin different from the controls. Host gut contents and worms from a blood meal-enriched diet both contained protoheme IX; perienteric fluid concentration in these worms (0·211 mM) was five times that of the other groups. The presence of metalloporphyrins in guts of worms reared on linear tetrapyrroles suggests the ability to convert these compounds to heme.     

Dynamics of the pregnancy cycle in the tsetse Glossina morsitans

A normal pregnancy in tsetse involves the successful integration of larval development with maternal activity. At 25°C, ovulation in Glossina morsitans occurs 1 hr after the previous larviposition, the egg hatches on day 3·8 (1·57 mm length, 0·09 mg dry wt.), ecdysis to second instar occurs on day 4·9 (2·3 mm, 0·30 mg), the third instar cuticle is formed on day 6·8 (4·5 mm, 5·0 mg), and parturition occurs on day 9·0 (6·0 mm, 10·0 mg). Melanization of the in utero third instar follows a regular sequence over a 2 day period. Parturition follows a circadian pattern with a peak 9 hr after lights on (12 hr daily photophase). All instars receive nutriment from the female's milk gland. During early pregnancy the rate of milk synthesis is greater than rate of uptake by the larva, thus causing expansion of the secretory reservoirs. After day 6, the volume of the secretory reservoirs decreases, but as is indicated by nuclear volume and larval growth the rate of synthesis remains high until day 8. Feeding activity of the adult female is maximal on day 1, levels off at 60 per cent up to day 6, and then declines sharply towards the end of pregnancy. Oöcyte development proceeds in phase with larval development and thus minimizes a lag period between successive pregnancies.     

Asymmetry in forming 2-aminopurine . hydroxymethylcytosine heteroduplexes; A model giving misincorporation frequencies and rounds of DNA replication from base-pair populations in vivo

We present the first direct measurement of a transient mismatched base-pair in a 2-aminopurine-induced mutagenic pathway. We provide a model to calculate misincorporation rates in vivo from measured base-pair populations. The population of 2-aminopurine · hydroxymethylcytosine (AP · C²) base-pairs at a marker locus in T4 bacteriophage is measured as rII-r⁺ heteroduplex-heterozygotes in a modified single burst experiment after 2-aminopurine mutagenesis. This completes the determination of each of the base-pairs in the 2-aminopurine-induced A · T → G · C transition pathway for the marker rUV199. The observed AP · C population confirms a surprising model prediction that the probability of incorporating HMdCTP opposite a template 2-aminopurine is very large, approximately 2% per round of replication. AP induces A · T → G · C and G · C → A · T transitions at roughly the same rates. A quantitative comparison of 2-aminopurine-induced A · T → G · C and G · C → A · T transition pathways shows a marked asymmetry in the formation of AP · C base-pairs; the probability of forming AP · C base-pair intermediates in the A · T → G · C transition pathway is several orders of magnitude larger than in the G · C → A · T pathway. A set of analytic equations giving the population of each state of an allele undergoing 2-aminopurine mutagenesis (A · T, AP · T, AP · C and G · C) as a function of interstate (e.g. A · T → AP · T) and intrastate (e.g. A · T → A · T) transition rate constants and the number of rounds of replication is derived. The equations also demonstrate that a determination of $\text{AP}\text{·}\text{C}\text{G}\text{·}\text{C}$ base-pair ratios is a direct measure of the number of rounds of replication; thus the value of 0.35 AP · C per G · C base-pair as measured in this experiment reveals that there were eight to nine rounds of DNA replication during the mutagenesis treatment.     

Cluster analysis of aminoacyl-tRNAs from mouse plasmacytomas correlates chromatographic profiles with myeloma protein similarity,clonal origin of tumor lines,and the neoplastic nature of the tissues

In order to test whether tRN A populations are correlated with (determined by or adapted to) the major proteins synthesized by tumor cells, RPC-5 Chromatographie profiles of aminoacyl-tRNAs from 11 mouse plasmacytomas and from normal adult mouse liver and brain were analyzed by the use of “dissimilarity indices” drawn from all possible pairs of tissues. Cluster analysis was then performed and dendrograms constructed. Although myeloma protein synthesis is only one of many proteins being synthesized by these malignant cells, a novel nonparametric statistical analysis of these dendrograms indicates that independently arising tumors have more similar profiles if their immunoglobulin light and heavy chains are very similar than if these chains are dissimilar (P < 0·015). Even more strikingly significant was the finding that drastic changes in myeloma protein synthesis such as loss of both heavy and light chain synthesis do not result in increased dissimilarity of aminoacyl-tRNA profiles (P < 0·00001). Unlike other eukaryotic systems such as sheep reticulocytes and silk worm silk gland which have been shown to adapt their tRNA populations to changes in protein synthesis, these plasmacytomas do not appear to do so.The novel use of statistical methods, esp. cluster analysis, to examine graphic displays of data may have useful applications in comparing other Chromatographie profiles, densitometric scans, etc.     

The effect of temperature of the rate of photosynthetic electron transfer in chloroplasts of chilling-sensitive and chilling-resistant plants

1. Photochemical activities as a function of temperature have been compared in chloroplasts isolated from chilling-sensitive (below approximately 12 °C) and chilling-resistant plants.2. An Arrhenius plot of the photoreduction of NADP⁺ from water by chloroplasts isolated from tomato (Lycopersicon esculentum var. Gross Lisse), a chilling-sensitive plant, shows a change in slope at about 12 °C. Between 25 and 14 °C the activation energy for this reaction is 8.3 kcal·mole^?1. Between 11 and 3 °C the activation energy increases to 22 kcal·mole^?1. Photoreduction of NADP⁺ by chloroplasts from another chilling-sensitive plant, bean (Phaseolus vulgaris var. brown beauty), shows an increase in activation energy from 5.9 to 17.5 kcal·mole^?1 below about 12 °C.3. The photoreduction of NADP⁺ by chloroplasts isolated from two chilling-resistant plants, lettuce (Lactuca sativa var. winter lake) and pea (Pisum sativum var. greenfeast), shows constant activation energies of 5.4 and 8.0 kcal·mole^?1, respectively, over the temperature range 3–25 °C.4. The effect of temperature on photosynthetic electron transfer in the chloroplasts of chilling-sensitive plants is localized in Photosystem I region of photosynthesis. Both the photoreduction of NADP⁺ from reduced 2,6-dichlorophenol-indophenol and the ferredoxin-NADP⁺ reductase (EC 1.6.99.4) activity of choroplasts of chilling-sensitive plants show increases in activation energies at approximately 12 °C whereas Photosystem II activity of chloroplasts of chilling-sensitive plants shows a constant activation energy over the temperature range 3–25 °C. The photoreduction of Diquat (1,1′-ethylene-2,2′-dipyridylium dibromide) from water by bean chloroplasts, however, does not show a change in activation energy over the same temperature range. The activation energies of each of these reactions in chilling-resistant plants is constant between 3 and 25 °C.5. The effect of temperature on the activation energy of these reactions in chloroplasts from chilling-sensitive plants is reversible.6. In chilling-sensitive plants, the increased activation energies below approximately 12 °C, with consequent decreased rates of reaction for the photoreduction of NADP⁺, would result in impaired photosynthetic activity at chilling temperatures. This could explain the changes in chloroplast structure and function when chilling-sensitive plants are exposed to chilling temperatures.     

A gelatin film procedure for the localization of proteolytic activity in Leucochloridiomorpha constantiae (Trematoda) adults

A gelatin film procedure was used to localize proteolytic activity in the lumen of the intestinal ceca of Leucochloridiomorpha constantiae (Trematoda) adults. Slides were coated with a 7·5% gelatin solution and then fixed in 10% neutral buffered formalin (NBF). Cryostat sections of isolated worms or those attached to the bursa of Fabricius of the domestic chick were affixed to the gelatin film. Experimental and control slides were incubated in a humid chamber for 30 min at 37·5 and 4°C, respectively. Slides were again fixed in NBF, and then stained for protein with mercuric bromphenol blue (MBB). In experimental slides, the lumen of the intestinal ceca was lysed and did not stain, whereas worm and host tissue and the gelatin were protein-positive. Control sections stained uniformly positive for protein. In this procedure tissue is retained on the slide and proteolytic activity can be correlated with a tissue site on the same slide.     

Further evidence and biological significance for non-random localization of the centromere on mammalian chromosomes

A further quantitative analysis of the localization of the centromere on chromosomes was made using 16,817 individual chromosomes obtained from 723 mammalian species. Centromeric position was expressed quantitatively by the size of short arms as per cent weight (S_w) relative to the X-containing haploid set. When the class interval of S_w was 0·1 instead of the previous 0·2 (Imai, 1975), the frequency distribution of S_w showed an uneven (W-shaped) pattern with two distinct antimodes lying at S_w 0·6 (reconfirmation) and 0·1 (new finding). Two hypotheses, that are not mutually exclusive, are proposed to explain the non-random distribution of centromere position. One is that there are three structurally different short arms consisting of (1) centromere, (2) constitutive heterochromatin (as determined by C-banding), and (3) euchromatin, each arm-type being approximately characterized by the size of short arms (S_w) as S_w < 0·1, 0·1 ? S_w ? 0·6 and S_w > 0·6. The other possibility is concerned with an “orthogenetical” change of chromosome morphologies. When the chromosomes with S_w < 0·1, 0·1 ? S_w ? 0·6 and S_w > 0·6 are denoted as telocentric (T), acrocentric (A), and meta-, submeta- and subtelocentric (M, SM & ST), it was suggested that the chromosome morphologies tend to change orthogenetically (in a statistical sense) from T to M, SM & ST via A-chromosomes by rearrangements such as tandem growth of constitutive heterochromatic, pericentric inversions, and centric fusions.     

Nematospiroides dubius: arrested development of larvae in immune mice.

When immune NIH mice were killed 10 days after a challenge infection with Nematospiroides dubius, approximately 10% of the inoculated larvae were recovered from the intestinal lumen, irrespective of the dose administered. When such mice were treated with cortisone from Day 10 for a period of 8 to 14 days and were subsequently killed for worm counts, it was found that they had significantly more worms than the immune control mice killed on Day 10. During the week following the beginning of treatment with cortisone there was little change in the low worm burdens in immune mice. However, 9 to 11 days after this treatment worm counts indicated that worms were accumulating in the intestinal lumen, and concurrently eggs were recorded in the feces of the mice. These observations indicated that a period of 9 to 11 days was required after the initiation of cortisone treatment on Day 10 for the worms in immune mice to complete their development to the adult lumen-dwelling stage. It is suggested that the larvae in the challenge infection became arrested early in their development in the intestinal wall and that growth resumed only after cortisone treatment. When treatment with cortisone was initiated later after challenge, it was still effective in reactivating arrested worms, but the lower worm recoveries in these mice indicated that the arrested larvae were being slowly rejected by the host. In subsequent experiments it was established that the arrested larvae of N. dubius were insusceptible to the activity of pyrantel embonate, an anthelmintic which is 99% effective against adult worms in the intestinal lumen. The mechanism whereby the larvae of N. dubius became arrested in immune mice and subsequently resumed their development after cortisone treatment is discussed.