Modification of the poliovirus capsid by ultraviolet light

1981 ◽  
Vol 27 (11) ◽  
pp. 1185-1193 ◽  
Author(s):  
John De Sena ◽  
Donald L. Jarvis

Ultraviolet (UV) irradiation of type I poliovirus resulted in a modified (M) particle that had lost infectivity, lacked ability to adsorb to HeLa cells, lacked VP4, and was reduced in S value. Additional irradiation resulted in the loss of VP2, further reduction in S value, and permeability of the capsid to RNAse, This particle (C) as well as M contain the genome. Acid pH (5.5–6.5) and sulfhydryl-reducing substances (dithiothreitol, reduced glutathione, and L-cysteine) inhibited UV-induced modification of the capsid. UV irradiation at alkaline pH (7.5–8.5) resulted in more extensive modification of the capsid than irradiation at neutral pH. Ionic compounds were found to inhibit the modifying reaction.

1977 ◽  
Vol 28 (1) ◽  
pp. 29-48
Author(s):  
K. Burg ◽  
A.R. Collins ◽  
R.T. Johnson

We have examined the effects of hydroxyurea on u.v.-irradiated Chinese hamster CHO-KI cells. Ultraviolet irradiation followed by incubation with hydroxyurea causes only slight disruption of DNA and chromosome structure in CHO-KI cells compared with HeLa cells. There is, however, a clear potentiation by hydroxyurea of the u.v. killing of CHO-KI cells, which is most pronounced at those points in the cycle which are reported to have small DNA precursor pools. This potentiation is reduced when DNA precursors are provided together with hydroxyurea. These data are discussed in terms of an uncoupling of excision and repair DNA synthesis.


2021 ◽  
Author(s):  
Sarka Klementova ◽  
Martina Poncarová ◽  
Helena Langhansová ◽  
Jaroslava Lieskovská ◽  
David Kahoun ◽  
...  

Abstract Photochemical degradation of fluoroquinolones ciprofloxacin, enrofloxacin and norfloxacin in aqueous solution under light conditions relevant to surface waters at neutral and alkaline pH was found to proceed readily with half-lives between 0.9 and 2.7 min. The products of photochemical degradation identified by HPLC-MS included defluorinated, hydroxylated, and decarboxylated structures as well as structures with opened cyclic structures. For all of the studied substances, the reaction pathways were influenced significantly by the pH of the reaction system, with more products formed at alkaline pH than at neutral pH: the ratios of products in neutral and alkaline pH were 16/26, 9/19, 15/23 for ciprofloxacin, enrofloxacin, and norfloxacin, respectively. The structures of photoproducts and pathways of photochemical degradation are proposed. The antibacterial activities of photoproduct mixtures tested on E. coli and S. epidermidis were significantly higher in comparison to parental antibiotics in the case of both ciprofloxacin and enrofloxacin with p-values less than 0.0001 in most cases. The effect of the photoproducts was shown to be dependent on the pH value of the original antibiotic solutions before photodegradation: for ciprofloxacin, antibacterial activity against E. coli was more notably pronounced with regard to neutral pH photoproducts, while a less significant, or in one case not significant, effect of pH was observed against S. epidermidis ; for norfloxacin, antibacterial activity against both E. coli and S. epidermidis were especially high with regard to alkaline pH photoproducts


1977 ◽  
Vol 55 (5) ◽  
pp. 1122-1134 ◽  
Author(s):  
J. G. Foulks ◽  
Florence A. Perry ◽  
P. Tsang

The depressant effect of acidity on twitches and K contractures in frog skeletal muscle was greatly accentuated in the presence of organic anions, particularly anions such as butyrate, which also reduced these responses at neutral pH. Conversely, alkaline pH antagonized the depression of contractile responses by butyrate. Most of the effects of acid pH were rapid in onset and were accomplished without any change in membrane resting or action potentials, although depolarization developed in the presence of carboxylate anions when pH was reduced below 6.0. Simultaneous variation in pH and butyrate concentration showed that the undissociated acid exerted a prominent depressant effect only when its concentration reached 1–10 mM, and that the marked depressant action of butyrate at neutral pH was produced primarily by the dissociated anion. Similar experiments showed that the dissociated anion also was largely responsible for the enhanced depolarizing effect of acidity in media containing carboxylates. Acid-induced depolarization was not facilitated in media containing methane sulfonate, but in spite of its low pKa, this anion also increased the sensitivity of contractile responses to the depressant effects of acidity. Hence, the accentuation of the effects of organic anions by acid pH must be exerted on the sequence of membrane events which link excitation and contraction. The effect of acidity was greater when longer apolar hydrocarbon chains were attached to the anionic group for both the carboxylate and the sulfonate series of ions. These depressant effects may be produced by interference with the membrane-stabilizing actions of divalent cations, and may involve increased membrane fluidity.


1980 ◽  
Vol 26 (12) ◽  
pp. 1403-1407 ◽  
Author(s):  
Carolyn M. Sabatino ◽  
Siegfried Maier

The study was prompted by our inability to concentrate phages by a membrane adsorption method effective for polioviruses. Consequently two coliphages, WPK and T4, and F116 of Pseudomonas aeruginosa were tested for their resistance to acid (pH 5.2–3.2) and alkaline (pH 10–11.5) exposures. Only T4 proved acid resistant, allowing for acid adsorption, and only WPK was sufficiently alkaline resistant to allow for alkaline elution. Thus, the differential susceptibility of various phages precludes the use of the acid membrane adsorption–alkaline elution method as a general method for the concentration of phages from large volumes of water.


Blood ◽  
1995 ◽  
Vol 86 (11) ◽  
pp. 4331-4336 ◽  
Author(s):  
S Chin ◽  
B Williams ◽  
P Gottlieb ◽  
H Margolis-Nunno ◽  
E Ben-Hur ◽  
...  

The use of solvent/detergent mixtures and various forms of heat treatment to inactivate viruses has become widespread in the preparation of blood derivatives. Because viruses that lack lipid envelopes and/or are heat resistant, eg, hepatitis A virus (HAV) or parvovirus B19 may be present, the use of two methods of virus elimination that operate by different mechanisms has been advocated. We now report on short wavelength ultraviolet light (UVC) irradiation for virus inactivation and enhancement of its compatibility with proteins by quenchers of reactive oxygen species (ROS). Treatment of an antihemophilic factor (AHF) concentrate or whole plasma with 0.1 J/cm2 inactivated 10(5) to > or = 10(6) infectious doses (ID) of encephalomyocarditis virus (EMCV), HAV, bacteriophage M13, vesicular stomatitis virus (VSV), and porcine parvovirus. However, the recovery of factor VIII was 30% or lower on treatment of an AHF concentrate and 60% on treatment of plasma. Factor VIII recovery could be increased with little or no effect on virus kill by addition of rutin, a flavonoid known to quench both type I and type II ROS. On treatment of plasma in the presence of rutin, the recovery of several other coagulation factors was also enhanced by rutin addition and typically exceeded 75%. Electrophoretic analysis of treated AHF concentrate confirmed the advantage of rutin presence; UVC irradiation of plasma did not cause discernible changes in electrophoretic banding patterns, even in the absence of rutin. We conclude that addition of UVC treatment to existing processes used in the manufacture of blood derivatives will provide an added margin of safety, especially for nonenveloped or heat-stable viruses.


1997 ◽  
Vol 48 (5) ◽  
pp. 561 ◽  
Author(s):  
K. R. Helyar ◽  
B. R. Cullis ◽  
K. Furniss ◽  
G. D. Kohn ◽  
A. C. Taylor

This paper reports the effects of 6 wheat–annual pasture rotations over 18 years on soil N, organic C, P, and pH in a red earth soil at Wagga Wagga (35° 03′ S, 147° 21′E), in southern NSW. There were 3 cropping intensities (33, 50, 67%) with pastures dominated by subterranean clover (Trifolium subterraneum L. cv. Bacchus Marsh) and annual ryegrass (Lolium rigidum Gaud. cv. Wimmera). Rotations were long (6-year) or short (2- or 3-year). Initial soil N and organic C concentrations (0–10 cm) were low, 1300–1400 kg N/ha and 0·7–0·9 g organic C/100 g. The rate of increase of total N in the top 20 cm was the same on short and long rotations, and increased with the proportion of pasture in the rotation from 2·0 to 12·1 to 20·7 kg N/ha · year for pasture to crop ratios of 0·33, 0·50, and 0·67. Estimates of the amounts of N fixed and the measured accumulation of N per pasture year varied within the narrow ranges of 95–113 and 45–64 kg N/ha · pasture year. Organic C increased faster as the proportion of pasture in the rotation increased and there was no evidence that steady-state concentrations were achieved by Year 18. Estimates of the average amount of N leached below 30 cm varied in the range 22–29 kg N/ha · year. Analysis of the individual crop and pasture effects on soil N in the surface 10 cm indicated that net nitrate leaching was greatest in the second pasture year or in the first crop year following 1 year of pasture. A significant amount of N leached during the first 2 or 3 pasture years in a rotation was recovered by the first wheat crop or by the third and fourth year pastures. Second to fourth cereal crops depleted soil N by an amount similar to that removed in the grain. Average grain N% for the rotation treatments was closely described (R2 = 0·96) as a function of the length of the pasture phase, the pasture to crop ratio, and the interaction pasture to crop ratio number of preceding wheat crops. In the top 30 cm the pH changed at a rate near –0·04 units/year on all treatments, equivalent to addition of 2·3–2·8 kmol H+/ha · year. The acid addition rate, and hence the long-term lime requirement (50 kg lime/kmol H+), did not vary with pasture to crop ratio or with the length of the rotation. The proportion of the acid added to the top 30 cm of soil that was contributed from the N cycle (nitrification followed by nitrate loss by leaching below 30 cm or by run-off) was 0·65 for rotations with 67% pasture and 0·80 for rotations with 33% pasture. Carbon cycle acids, produced during organic matter accumulation and the synthesis of products that were subsequently removed, accounted for the remainder. Individual crop and pasture effects on soil pH were near the overall mean of –0·04 units except in years preceding and following the transition from pasture to cereal phases of the rotations. In cereal-dominated rotations the last pasture year was strongly acid (pH decrease 0·13–0·17) and the following cereal year was alkaline (pH increase 0·05–0·08). In pasture-dominated rotations the effects were reversed, the last pasture being alkaline (pH increase 0·07–0·12) and the following cereal being acid (pH decrease 0·13–0·19). In the 50% rotations, effects were intermediate. Organic and inorganic forms of soil P in the surface 10 cm increased linearly with time, accounting for 38% of the applied fertiliser P. Of the applied P, 88% was accounted for by the sum of P accumulated in the surface 20 cm of soil and by removal in products and waste products. The remainder may have been lost by erosion or accumulated in forms resistant to extraction by 0·1 M H2SO4 after ignition at 550°C. There was a slightly greater rate of increase of organic P as the proportion of pasture in the rotation increased. The annual addition of 11·8 kg P/ha·year marginally exceeded the amount required to maintain the available P concentration.


1968 ◽  
Vol 21 (4) ◽  
pp. 821 ◽  
Author(s):  
Anne FW oodlock ◽  
BS Harrap

In the acid pH region, the relative effects of various salts on the thermal stability of the collagen helix are quite different from their effects at neutral pH. The magnitude of the decrease in thermal stability brought about by the salts studied depends mainly on the nature and concentration of the anion and very little on the nature of the cation, whereas at neutral pH the nature of both anions and cations affects the collagen helix stability, the effects of the two ions being roughly additive. The magnitude of the effect of salts at acid pH is much greater than that at neutral pH whereas for a non-ionized denaturant, urea, the magnitudes at both neutral and acid pH are similar. The data are discussed in terms of possible interactions between salts and the positively charged protein with particular consideration of the effects of salts on the pKa of protein carboxyl groups.


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