Efficiency of Commercial Air Filters Against Marek''s Disease Virus

In a series of 10 replicate trials with susceptible chickens as indicators of the presence of virus in the air, filter B(1) (Dri Pak, American Air Filter Co.), which has a dust spot rating of 93 to 97%, and filter C (Astrocel), with a dioctyl phathalate aerosol rating of over 99%, completely removed Marek's disease virus (MDV) from highly contaminated air. However, air passed through filter B(2) (Duracel), with a dust spot rating of 34 to 45%, remained infectious. Thus, an air filter with a dust spot rating of over 93% will effectively remove MDV from the air. The smallest infectious particles in the air are estimated to be greater than 0.3 mum in diameter.     

Air Filters for Germ-free Isolators

A germ-free isolator must have a perfect bacterial filter. This paper describes a new, relatively inexpensive, stainless-steel filter frame, which is easily and quickly assembled and protects the enclosed filter material at all times. Resistance to the flow of air was less than 4 inches of water at an airflow of 30 ft³/min through the filter frame with 204 inches² of surface area and four, one-half inch thick pieces of fiberglass filter material. This filter performed satisfactorily in our gnotobiotic laboratory and was found to be consistently 100% efficient in removing an aerosol containing Serratia marcescens from an air stream under a variety of operating conditions.     

Efficiency of Commercial Air Filters Against Marek's Disease Virus

In a series of 10 replicate trials with susceptible chickens as indicators of the presence of virus in the air, filter B₁ (Dri Pak, American Air Filter Co.), which has a dust spot rating of 93 to 97%, and filter C (Astrocel), with a dioctyl phathalate aerosol rating of over 99%, completely removed Marek''s disease virus (MDV) from highly contaminated air. However, air passed through filter B₂ (Duracel), with a dust spot rating of 34 to 45%, remained infectious. Thus, an air filter with a dust spot rating of over 93% will effectively remove MDV from the air. The smallest infectious particles in the air are estimated to be greater than 0.3 μm in diameter.     

Fungal Colonization of Air Filters and Insulation in a Multi-Story Office Building: Production of Volatile Organics

Secondary air filters in the air-handling units on four floors of a multi-story office building with a history of fungal colonization of insulation within the air distribution system were examined for the presence of growing fungi and production of volatile organic compounds. Fungal mycelium and conidia of Cladosporium and Penicillium spp. were observed on insulation from all floors and both sides of the air filters from one floor. Lower concentrations of volatile organics were released from air filter medium colonized with fungi as compared with noncolonized filter medium. However, the volatiles from the colonized filter medium included fungal metabolites such as acetone and a carbonyl sulfide-like compound that were not released from noncolonized filter medium. The growth of fungi in air distribution systems may affect the content of volatile organics in indoor air. Received: 2 June 1997 / Accepted: 13 June 1997     

A Method for the Removal from Membrane Filters of Micro-Organisms Filtered from Water and Air

S ummary : The micro-organisms in tap water were quantitatively (99%) retained by Oxoid membrane filters. The trapped organisms were extracted from the membrane filter by a simple washing process using glass beads or a magnetic stirrer. For counts on air, the membrane filter was considerably more efficient than an ammonium alginate filter in trapping bacteria, but both techniques were equally satisfactory for moulds.     

Evaluation of Filters for Removal of Bacteriophages from Air

Glass wool, nonabsorbent cotton, fiberglass filter medium, and a commercial absolute filter were tested for effectiveness in removing aerosolized bacterial viruses under low flow rate (1 ft(3)/min) and high flow rate (10 to 25 ft(3)/min) air-flow conditions. Special equipment was designed for measurement of filter efficiencies under the two air-flow conditions. Under low air-flow rate test conditions, glass wool was only 98.543 to 99.83% efficient, whereas cotton (five layers), fiberglass medium (three layers), and the commercial absolute filter were at least 99.900, 99.999, and 99.999 efficient, respectively. Glass wool and cotton were not used under higher air-flow conditions because they were difficult to assemble in leak-tight filters. The commercial absolute filter and fiberglass medium (three layers) were at least 99.990 and 99.999% efficient, respectively, under the higher air flow conditions. A stainless-steel filter of simple design and fitted with three layers of fiberglass medium was found to be greater than 99.999% efficient in removing high concentrations (20,000 to 70,000 plaque-forming units per cubic foot) of aerosolized bacteriophages from air moving at a low flow rate (1 ft(3)/min). Use of this filter on pressure-vacuum tanks in the fermentation industry is suggested. Several other uses of such a filter are proposed.     

A super lytic actinophage system as a pre-treatment in the isolation of non-streptomycete actinomycetes from soil

P.F. LONG AND G.E. AMPHLETT. 1996. An increase in the abundance and diversity of non-streptomycete actinomycetes isolated from soils was achieved after the number of streptomycetes was reduced by pre-incubating the soil with streptomycete-specific actinophage. This method is described as a super lytic actinophage system.     

Microorganisms of the Upper Atmosphere: I. Instrumentation for Isokinetic Air Sampling at Altitude

An aircraft-mounted air-sampling system for the collection of microorganisms from the upper air is described. The system is highly suitable for use in upper air sampling from an aircraft because (i) it is an isokinetic system, (ii) it is simple to operate, (iii) it employs a dry filter, (iv) the volume sampled can be easily determined, and (v) it operates efficiently at all altitudes and ambient temperatures.     

Restriction enzyme mapping of the DNA of Streptomyces bacteriophage B alpha and its deletion derivatives

Cleavage analysis of actinophage B alpha DNA was done with several restriction enzymes, and a restriction map of the DNA was determined. The DNA appeared to carry cohesive ends. Deletion mutants of actinophage B alpha were isolated by five cycles of treatment with 15 mM PPi. Both mutants had deletions of 2.5 of 1.8 megadaltons near one end of the genome, and one of them lost the single EcoRI cleavage site.     

Isolation of actinophage that attack some maduromycete actinomycetes

Abstract During the course of natural product screening, two actinomycete strains, designated 3828E and 3913E, were isolated from soil collected in the Phillipines and New Zealand, respectively. Strain 3828E released without induction an actinophage. The host isolate was chemotaxonomically identical to members of the revised genus Microtetraspora having both wall chemotype III, sugar pattern B and phospholipid pattern PIV. On the basis of cultural and morphological characteristics, the isolate was most similar to Microtetraspora salmonea . Strain 3913E shared the same chemotaxonomic characteristics as strain 3828E; however, morphological examination revealed the presence of spores arranged distinctively as pairs along aerial hyphae. On this basis, strain 3913E was classified as a member of the genus Microbispora . When re-infected into the soil it had been isolated from, actinophage were recovered that specifically attacked strain 3931E. The presence of phage from both maduromycetes was confirmed by transmission electron microscopy. Neither phage was able to attack a range of other actinomycetes. We believe this to be the first reported isolation of actinophage that attack species of the genera Microtetraspora and Microbispora .     

Biofiltration of Air: A Review

Abstract

In this paper we present a review of the existing air pollution control technologies (APCT), when used essentially for the elimination of volatile organic compounds (VOC). The biotechnologies referred to, bioscrubbers, biotrickling filters and biofilters, are also described. A more detailed review of biofiltration is proposed, presenting the most recent and latest developments achieved in the field of bioprocessing. In particular, the influence of the filter bed, the polluted air flowrates, the pollutants, the pressure drop, bed moisture content, temperature, nutrients, pH and the microorganisms are reviewed. Models of biofiltration are also presented.     

Fluorometric Method for Determining the Efficiency of Spun-Glass Air Filtration Media

The procedures and equipment needed to measure filtration efficiency by means of fluorescent aerosols are described. The filtration efficiency of individual lots of spun-glass air filtration medium or of entire air filtration systems employing such media was determined. Data relating to the comparative evaluation of spun-glass filter media by means of the fluorometric method described, as well as by conventional biological procedures, are presented.     

Air Filter Devices Including Nonwoven Meshes of Electrospun Recombinant Spider Silk Proteins

Based on the natural sequence of Araneus diadematus Fibroin 4 (ADF4), the recombinant spider silk protein eADF4(C16) has been engineered. This highly repetitive protein has a molecular weight of 48kDa and is soluble in different solvents (hexafluoroisopropanol (HFIP), formic acid and aqueous buffers). eADF4(C16) provides a high potential for various technical applications when processed into morphologies such as films, capsules, particles, hydrogels, coatings, fibers and nonwoven meshes. Due to their chemical stability and controlled morphology, the latter can be used to improve filter materials. In this protocol, we present a procedure to enhance the efficiency of different air filter devices, by deposition of nonwoven meshes of electrospun recombinant spider silk proteins. Electrospinning of eADF4(C16) dissolved in HFIP results in smooth fibers. Variation of the protein concentration (5-25% w/v) results in different fiber diameters (80-1,100 nm) and thus pore sizes of the nonwoven mesh.Post-treatment of eADF4(C16) electrospun from HFIP is necessary since the protein displays a predominantly α-helical secondary structure in freshly spun fibers, and therefore the fibers are water soluble. Subsequent treatment with ethanol vapor induces formation of water resistant, stable β-sheet structures, preserving the morphology of the silk fibers and meshes. Secondary structure analysis was performed using Fourier transform infrared spectroscopy (FTIR) and subsequent Fourier self-deconvolution (FSD).The primary goal was to improve the filter efficiency of existing filter substrates by adding silk nonwoven layers on top. To evaluate the influence of electrospinning duration and thus nonwoven layer thickness on the filter efficiency, we performed air permeability tests in combination with particle deposition measurements. The experiments were carried out according to standard protocols.     

处理甲苯废气的生物滴滤池中微生物生态学研究

利用PCR-DGGE技术分析了处理甲苯废气的生物滴滤池生物多样性,结果表明:在运行过程中,随着生物滴滤池对甲苯去除能力的不断增加,填料当中的微生物种群也发生了明显的变化。在甲苯的选择压力下,随时间的迁延,微生物种类减少,优势种群的相对丰度增加,处于不同层面填料上的微生物分布也趋向于一致。     

Testing Air-Filtering Systems: I. Procedure for Testing High-Efficiency Air Filters on Exhaust Systems

A procedure was developed for evaluating high-efficiency filters mounted in exhaust ducts at the National Animal Disease Laboratory. An aerosol of the test organism, Escherichia coli B T₃ bacteriophage, was generated in a chamber attached to a ceiling exhaust register in concentrations of at least 1000 viable organisms per ft³ of air. Samples were collected from both the pre- and postfilter areas, and the number of organisms per ft³ of air was determined. The efficiency of the filter was calculated from these figures. A total of 269 high-efficiency filters were tested. Of these, 249 had efficiencies of 98% or greater. The remaining 20, with efficiencies of less than 98%, were repaired and retested. No filter was accepted with an efficiency of less than 98%.     

Delimitation of cohesive ends site (cos) of Streptomyces temperate bacteriophage R4.

The cohesive ends site (cos) of actinophage R4 was delimitated by assaying the in vivo packaging activity of cosmid derivatives in Streptomyces lividans. A region of 66 bp from -30 to +36 from the center of cohesive ends was required for the basal level of packaging activity. Two additional regions outside the basal sequences from -39 to -31 and from +37 to +97 were necessary for the high level of activity, defined as the accessory sequences. Direct- or inverted-repeat sequences were found within the delimitated region, which might be involved in the recognition by the terminase of actinophage R4.     

Distribution and Rate of Microbial Processes in an Ammonia-Loaded Air Filter Biofilm

The in situ activity and distribution of heterotrophic and nitrifying bacteria and their potential interactions were investigated in a full-scale, two-section, trickling filter designed for biological degradation of volatile organics and NH₃ in ventilation air from pig farms. The filter biofilm was investigated by microsensor analysis, fluorescence in situ hybridization, quantitative PCR, and batch incubation activity measurements. In situ aerobic activity showed a significant decrease through the filter, while the distribution of ammonia-oxidizing bacteria (AOB) was highly skewed toward the filter outlet. Nitrite oxidation was not detected during most of the experimental period, and the AOB activity therefore resulted in NO₂⁻, accumulation, with concentrations often exceeding 100 mM at the filter inlet. The restriction of AOB to the outlet section of the filter was explained by both competition with heterotrophic bacteria for O₂ and inhibition by the protonated form of NO₂⁻, HNO₂. Product inhibition of AOB growth could explain why this type of filter tends to emit air with a rather constant NH₃ concentration irrespective of variations in inlet concentration and airflow.Emissions of NH₃, odorous organic gasses, and dust from pig facilities cause significant problems for neighbors and the surrounding natural environment. In Denmark, swine production accounts for 34% of the total atmospheric NH₃ emission, of which 50% originates from pig house emissions (19). Furthermore, multiple volatile and very odorous organic compounds are emitted with animal house exhaust air and constitute a severe nuisance in residential areas (16, 31). While biofilters based on wood chips, compost, and peat have proven efficient in removing complex mixtures of volatile organic compounds (VOC) from piggery exhaust air, biotrickling filters have been shown to be efficient in both odor and NH₃ removal (30). In these filters, airborne VOC and NH₃ are taken up by an irrigated biofilm and oxidized by organoheterotrophic and nitrifying bacteria, respectively, resulting in the production of CO₂, NO₂⁻ or NO₃⁻, and microbial biomass (43). The nitrification process, which comprises the two-step oxidation of NH₃ via NO₂⁻ to NO₃⁻, is catalyzed by ammonia-oxidizing bacteria (AOB) and ammonia-oxidizing archaea and by nitrite-oxidizing bacteria (NOB), respectively (22, 23). However, in many biotrickling filters, NOB activity seems to be absent, resulting in NO₂⁻ being the end product of nitrification (29).Waste products often accumulate in biotrickling filters, as the water is recycled many times to minimize wastewater discharge. In particular, NO₂⁻ may accumulate to concentrations above 100 mM (29), resulting in high levels of free nitrous acid (FNA, or HNO₂), which is inhibitory to many microorganisms (2, 40, 50). As a result of an overall countercurrent air-water flow, FNA, VOC, and NH₃ concentrations are expected to decrease from the filter air inlet toward the outlet, potentially promoting a gradient of microbial processes and species distribution through the filter.Also, on a smaller scale, physical and chemical heterogeneity results in microgradients of substrates and O₂ within the biofilm that may affect the spatial distribution and rate of microbial processes. While considerable research effort has been given to the physicochemical aspects of filter optimization (11, 44), very little is known about the distribution, activity, and potential interactions of bacterial processes in the biofilm. Problems frequently arise, such as highly variable odor reduction, failed NH₃ removal, and filter clogging due to excess biofilm growth and slime excretion. Improved insight into the dynamics of the microbial activities may help control the biological processes in order to optimize and stabilize filter performance.In this study, the in situ activity and distribution of organoheterotrophic bacteria and AOB and the identity and NH₃ oxidation potential of the AOB were investigated in a two-section, full-scale biological air filter treating waste gas from a pig facility. Biofilms in different filter sections along a gradient of decreasing VOC and NH₃ load and NO₂⁻ accumulation were characterized. The goal was to attain a basic understanding of the microbial processes and thus filter function.     

Chamber Bioaerosol Study: Outdoor Air and Human Occupants as Sources of Indoor Airborne Microbes

Human occupants are an important source of microbes in indoor environments. In this study, we used DNA sequencing of filter samples to assess the fungal and bacterial composition of air in an environmental chamber under different levels of occupancy, activity, and exposed or covered carpeting. In this office-like, mechanically ventilated environment, results showed a strong influence of outdoor-derived particles, with the indoor microbial composition tracking that of outdoor air for the 2-hour sampling periods. The number of occupants and their activity played a significant but smaller role influencing the composition of indoor bioaerosols. Human-associated taxa were observed but were not particularly abundant, except in the case of one fungus that appeared to be transported into the chamber on the clothing of a study participant. Overall, this study revealed a smaller signature of human body-associated taxa than had been expected based on recent studies of indoor microbiomes, suggesting that occupants may not exert a strong influence on bioaerosol microbial composition in a space that, like many offices, is well ventilated with air that is moderately filtered and moderately occupied.     

Evaluation of Membrane Filter Field Monitors for Microbiological Air Sampling

Due to area constraints encountered in assembly and testing areas of spacecraft, the membrane filter field monitor (MF) and the National Aeronautics and Space Administration-accepted Reyniers slit air sampler were compared for recovery of airborne microbial contamination. The intramural air in a microbiological laboratory area and a clean room environment used for the assembly and testing of the Apollo spacecraft was studied. A significantly higher number of microorganisms was recovered by the Reyniers sampler. A high degree of consistency between the two sampling methods was shown by a regression analysis, with a correlation coefficient of 0.93. The MF samplers detected 79% of the concentration measured by the Reyniers slit samplers. The types of microorganisms identified from both sampling methods were similar. Variables in the MF samplers, such as pore size, relative humidity, and flow rates, have been studied, but no effect was noted on recovery. The results show that the MF method could be used to estimate the number and types of microorganisms found in the air.     

Isolation and characterization of a temperate bacteriophage from Streptomyces galilaeus

A new temperate actinophage from Streptomyces galilaeus ATCC 31133 was purified after that strain was crossed with S. peucetius ATCC 29050. Sensitive hosts became lysogenized and yielded turbid plaques of 2 to 3 mm in diameter. Host-range analysis indicated that 16 of 27 Streptomyces strains tested were sensitive to infection on solid medium. S. lividans and S. coelicolor A3(2) were among those not infected by this new actinophage. The new actinophage, designated phi SPK1, belongs to the Bradley group B morphological type, the pH optimum for infection is 6.75 to 7.0, it is not efficiently induced by mitomycin C or UV irradiation, it has a circular chromosome of 35.8 +/- 0.5 kilobase pairs in length containing overlapping (cohesive) ends, and the G+C content of its DNA was calculated from the buoyant density of 1.7240 to be 69 mol%. The DNA of phage phi SPK1 was cleaved by the restriction endonucleases ApaI, AluII, EcoRI, PvuII, and SalI, but, in all cases except that with EcoRI, treatment yielded greater than 20 restriction fragments. No sites were detected for BamHI, BclI, BglII, ClaI, HindIII, MluI, PstI, SmaI, SphI, SstI, XbaI, or XhoI.