Inactivation of S. epidermidis, B. subtilis, and E. coli bacteria bioaerosols deposited on a filter utilizing airborne silver nanoparticles

In the present study, a control methodology utilizing airborne silver nanoparticles is suggested and tested with respect to its potential to control Gram-positive Staphylococcus epidermidis and Bacillus subtilis, and Gram-negative Escherichia coli bacteria bioaerosols deposited on filters. As it is known that the Gram-negative bacteria are sensitive to airflow exposure, the main focus of this study for testing the airborne silver nanoparticles effect was the Gram-positive Staphylococcus epidermidis and Bacillus subtilis bacteria bioaerosols whereas Escherichia coli bioaerosols were utilized for comparison. Airborne bacteria and airborne silver nanoparticles were quantitatively generated in an experimental system. Bioaerosols deposited on the filter were exposed to airborne silver nanoparticles. The physical and biological properties of the airborne bacteria and airborne silver nanoparticles were measured via aerosol measurement devices. From the experimental results, it was demonstrated that this method utilizing airborne silver nanoparticles offers potential as a bioaerosol control methodology.     

Linking the conventional and emerging detection techniques for ambient bioaerosols: a review

Bioaerosols are biologically originated particles present in the atmosphere that can be formed from any process involving biological materials. They comprise of both living and non-living components including organisms, dispersal methods of organisms, and excretions. Bioaerosols such as airborne bacteria, fungal spores, pollen, and others possess diverse characteristics and effects. A large gap exists in the scientific understanding of the overall physical characteristics and measurement of bioaerosols. Consequently, this review aims to devise an appropriate approach to generate more scientific knowledge of bioaerosols. In addition to comparisons and discussions about the various factors affecting bioaerosols, sampling, handling, and the application of various devised analytical techniques, this review offers insight into the current state of bioaerosol research. The review focuses on instrumental and methodical strategies to understand bioaerosol measurement. Numerous studies have investigated conventional methods, advanced methods, and real-time methods that can be applied for bioaerosol monitoring. Each method is different in terms of working principle, characteristics, sensitivity, and efficiency. For the first time, this review explains and compares different methods of conventional, offline, online, and real-time detection methods of bioaerosols based on their working principles, sensitivity, and efficiency on a single platform. This will provide a clear concept and better options for selecting the appropriate method based on the research proposal. Furthermore, recent advances are summarized, and future outlooks are emphasized for bioaerosol identification and categorization. This study also encourages developing affordable and standardized methods to avoid the inter-laboratory and sampling variability to obtain a better understanding and comparison of bioaerosol measurements worldwide. Nevertheless, this work can assist researchers in selecting appropriate methods for bioaerosol measurement and investigation.

     

Using a bioaerosol personal sampler in combination with real-time PCR analysis for rapid detection of airborne viruses

We have recently developed a new personal sampler and demonstrated its feasibility for detection of viable airborne microorganisms including bacteria, fungi and viruses. To accelerate the time-consuming analytical procedure involving 2-5 days of biological testing, we employed a real-time PCR protocol in conjunction with the personal sampler for collection of airborne viruses. The advantage of this approach is that if the presence of a particular pathogen in the air is detected by the PCR, the remaining collecting liquid can be further analysed by more time-consuming biological methods to estimate the number of airborne infectious/live microorganisms. As sampling of bioaerosols in natural environments is likely to be associated with substantial contamination by a range of microorganisms commonly existing in an ambient air, an investigation of the specificity of detection by targeted PCR analysis is required. Here we present the results of the study on the detection of Influenza virus in the ambient air contaminated with high concentrations of bacteria and fungi using real-time PCR protocol. The combined sampling PCR detection method was found to be fully feasible for the rapid ( approximately 2.5 h) and highly specific (no cross-reactivity) identification of the labile airborne virus in the air containing elevated concentrations of other microorganisms.     

Short-Term Temporal Variability in Airborne Bacterial and Fungal Populations

Airborne microorganisms have been studied for centuries, but the majority of this research has relied on cultivation-dependent surveys that may not capture all of the microbial diversity in the atmosphere. As a result, our understanding of airborne microbial ecology is limited despite the relevance of airborne microbes to human health, various ecosystem functions, and environmental quality. Cultivation-independent surveys of small-subunit rRNA genes were conducted in order to identify the types of airborne bacteria and fungi found at a single site (Boulder, CO) and the temporal variability in the microbial assemblages over an 8-day period. We found that the air samples were dominated by ascomycete fungi of the Hypocreales order and a diverse array of bacteria, including members of the proteobacterial and Cytophaga-Flavobacterium-Bacteroides groups that are commonly found in comparable culture-independent surveys of airborne bacteria. Bacterium/fungus ratios varied by 2 orders of magnitude over the sampling period, and we observed large shifts in the phylogenetic diversity of bacteria present in the air samples collected on different dates, shifts that were not likely to be related to local meteorological conditions. We observed more phylogenetic similarity between bacteria collected from geographically distant sites than between bacteria collected from the same site on different days. These results suggest that outdoor air may harbor similar types of bacteria regardless of location and that the short-term temporal variability in airborne bacterial assemblages can be very large.     

源于微生物的海鞘天然产物

海洋动物是具有生物活性海洋天然产物的重要来源。海鞘中含有丰富的微生物类群,如细菌、放线菌、真菌和蓝细菌。越来越多的直接或间接证据表明,一些从海鞘中分离的天然产物并不是海鞘本身产生的,而是由其共生微生物产生的。本文对近些年来的海鞘天然产物的微生物来源的研究方法进行综述,包括可培养细菌的分离、不可培养细菌的粗提物检测、宏基因组学、全基因组测序等直接方法,以及化合物结构比对的间接方法。通过对海鞘-微生物共生体中天然产物生物合成来源的研究,不仅可以从根本上解决动物药源的问题,而且可为研究海鞘与微生物共生关系提供有力证据。     

Assessing waste collectors' exposure to bioaerosols

Published studies on household wastecollectors' exposure to airborne biologicalagents (bioaerosols) do not indicate highexposures to these agents. However, thesestudies did not consider several factors. Theobjective of this study was to characterize theexposure of waste collectors to bioaerosols andto propose solutions to control exposures tothese agents.Personal exposures of waste collectors tobioaerosols (total bacteria, endotoxins andmolds) were measured for seven types ofcollection during the summer, which representsthe worst conditions. The effect of truckcleaning was also evaluated. Meanconcentrations of bacteria were all in theorder of 10³–10⁴ CFU/m³ of air. Theintervention threshold was exceeded forendotoxins during the collection of compostonce every two weeks in the country. Meanconcentrations varied from 8.5 to 100 endotoxinunits per cubic meter of air (EU/m³). Measuredmean concentrations of molds were between 8,300and 98,170 CFU/m³ of air. Also, the cleaningof an empty garbage truck does not improve thequality of the air. On the other hand, a dirtytruck is not a major source of bioaerosols.The sources of these bioaerosols are leachate,particularly if the waste in the truck is oforganic origin, as well as the garbage pailsthat contain this waste. Unnecessary exposuresto these sources should therefore be avoided. For bioaerosols, stringent personal hygienemeasures remain one of the best means ofprevention.     

A review of the emergence of antibiotic resistance in bioaerosols and its monitoring methods

Despite significant public health concerns regarding infectious diseases in air environments, potentially harmful microbiological indicators, such as antibiotic resistance genes (ARGs) in bioaerosols, have not received significant attention. Traditionally, bioaerosol studies have focused on the characterization of microbial communities; however, a more serious problem has recently arisen due to the presence of ARGs in bioaerosols, leading to an increased prevalence of horizontal gene transfer (HGT). This constitutes a process by which bacteria transfer genes to other environmental media and consequently cause infectious disease. Antibiotic resistance in water and soil environments has been extensively investigated in the past few years by applying advanced molecular and biotechnological methods. However, ARGs in bioaerosols have not received much attention. In addition, ARG and HGT profiling in air environments is greatly limited in field studies due to the absence of suitable methodological approaches. Therefore, this study comprehensively describes recent findings from published studies and some of the appropriate molecular and biotechnological methods for monitoring antibiotic resistance in bioaerosols. In addition, this review discusses the main knowledge gaps regarding current methodological issues and future research directions.

     

Monitoring airborne biotic contaminants in the indoor environment of pig and poultry confinement buildings

Given the growing concerns over human and animal health issues related to confined animal feeding operations, an in‐depth examination is required to monitor for airborne bacteria and associated antibiotic resistance genes. Our 16S rRNA‐based pyrosequencing revealed that the airborne microbial community skewed towards a higher abundance of Firmicutes (> 59.2%) and Bacteroidetes (4.2–31.4%) within the confinement buildings, while the office environment was predominated by Proteobacteria (55.2%). Furthermore, bioaerosols in the confinement buildings were sporadically associated with genera of potential pathogens, and these genera were more frequently observed in the bioaerosols of pig and layer hen confinement than the turkey confinement buildings and office environment. High abundances of tetracycline resistance genes (9.55 × 10² to 1.69 × 10⁶ copies ng^?1 DNA) were also detected in the bioaerosols sampled from confinement buildings. Bacterial lineages present in the poultry bioaerosols clustered apart from those present in the pig bioaerosols and among the different phases of pig production, suggesting that different livestock as well as production phase were associated with a distinct airborne microbial community. By understanding the diversity of biotic contaminants associated with the different confinement buildings, this study facilitates the implementation of better management strategies to minimize potential health impacts on both livestock and humans working in this environment.     

Detection of Legionella pneumophila in bioaerosols by polymerase chain reaction

Most studies focusing on detecting microorganisms in air by polymerase chain reaction (PCR) have used a liquid impinger to sample bioaerosols, mainly because a liquid sample is easy to be processed by PCR analysis. Nevertheless, the use of multiple-hole impactors for the analysis of bioaerosols by PCR has not been reported despite its great utility in culture analysis. In this study we have modified the impaction onto an agar surface sampling method to impaction onto a liquid medium using the MAS-100 air sampler (Merck) (single-stage multiple-hole impactor). To evaluate the recovery of airborne microorganisms of both sampling methods, a suspension containing Escherichia coli was artificially aerosolized and bioaerosols were collected onto Tergitol-7 agar and phosphate-buffered saline (PBS) with the MAS-100. A linear regression analysis of the results showed a strong positive correlation between both sampling methods (r = 0.99, slope 0.99, and y intercept 0.07). Afterwards, the method of impingement into a liquid medium was used to study airborne Legionella pneumophila by PCR. A total of 64 samples were taken at a wastewater treatment plant, a chemical plant, and an office building and analyzed by culture and PCR. Results showed that three samples were positive both by PCR and plate culture, and that nine samples negative by plate culture were positive by PCR, proving that L. pneumophila was present in bioaerosols from these three different environments. The results demonstrate the utility of this single-stage multiple-hole impactor for sampling bioaerosols, both by culture and by PCR.     

人为源微生物气溶胶的分布特征及风险研究进展

近年来,新型冠状病毒肺炎疫情全球肆虐,引起了公众对于微生物气溶胶潜在风险的极大关注,其中人为源微生物气溶胶潜在的健康危害逐步成为越来越多学者关注的热点之一。本文综述了近年来4类主要人为源微生物气溶胶的研究现状,比较了不同人为源微生物气溶胶的分布特征和微生物组成特性,并探究了影响微生物气溶胶特征的主要因素及其存在的潜在风险。结果表明,畜禽养殖场微生物气溶胶平均浓度最高,其次是污水处理厂和垃圾填埋场,医院最低。从微生物组成特性来说,不同人为源微生物气溶胶中微生物组成与其产生源密切相关;同时,其组成也受其所处环境条件影响。基于以上分析,本文进一步展望了未来人为源微生物气溶胶的主要研究方向,以期为微生物气溶胶控制标准的制定及控制技术的研发奠定基础。     

Field Evaluation of Personal Sampling Methods for Multiple Bioaerosols

Ambient bioaerosols are ubiquitous in the daily environment and can affect health in various ways. However, few studies have been conducted to comprehensively evaluate personal bioaerosol exposure in occupational and indoor environments because of the complex composition of bioaerosols and the lack of standardized sampling/analysis methods. We conducted a study to determine the most efficient collection/analysis method for the personal exposure assessment of multiple bioaerosols. The sampling efficiencies of three filters and four samplers were compared. According to our results, polycarbonate (PC) filters had the highest relative efficiency, particularly for bacteria. Side-by-side sampling was conducted to evaluate the three filter samplers (with PC filters) and the NIOSH Personal Bioaerosol Cyclone Sampler. According to the results, the Button Aerosol Sampler and the IOM Inhalable Dust Sampler had the highest relative efficiencies for fungi and bacteria, followed by the NIOSH sampler. Personal sampling was performed in a pig farm to assess occupational bioaerosol exposure and to evaluate the sampling/analysis methods. The Button and IOM samplers yielded a similar performance for personal bioaerosol sampling at the pig farm. However, the Button sampler is more likely to be clogged at high airborne dust concentrations because of its higher flow rate (4 L/min). Therefore, the IOM sampler is a more appropriate choice for performing personal sampling in environments with high dust levels. In summary, the Button and IOM samplers with PC filters are efficient sampling/analysis methods for the personal exposure assessment of multiple bioaerosols.     

Characterization of airborne bacteria at an underground subway station

The reliable detection of airborne biological threat agents depends on several factors, including the performance criteria of the detector and its operational environment. One step in improving the detector's performance is to increase our knowledge of the biological aerosol background in potential operational environments. Subway stations are enclosed public environments, which may be regarded as potential targets for incidents involving biological threat agents. In this study, the airborne bacterial community at a subway station in Norway was characterized (concentration level, diversity, and virulence- and survival-associated properties). In addition, a SASS 3100 high-volume air sampler and a matrix-assisted laser desorption ionization-time of flight mass spectrometry-based isolate screening procedure was used for these studies. The daytime level of airborne bacteria at the station was higher than the nighttime and outdoor levels, and the relative bacterial spore number was higher in outdoor air than at the station. The bacterial content, particle concentration, and size distribution were stable within each environment throughout the study (May to September 2010). The majority of the airborne bacteria belonged to the genera Bacillus, Micrococcus, and Staphylococcus, but a total of 37 different genera were identified in the air. These results suggest that anthropogenic sources are major contributors to airborne bacteria at subway stations and that such airborne communities could harbor virulence- and survival-associated properties of potential relevance for biological detection and surveillance, as well as for public health. Our findings also contribute to the development of realistic testing and evaluation schemes for biological detection/surveillance systems by providing information that can be used to mimic real-life operational airborne environments in controlled aerosol test chambers.     

Application of flow cytometry and fluorescent in situ hybridization for assessment of exposures to airborne bacteria.

Current limitations in the methodology for enumeration and identification of airborne bacteria compromise the precision and accuracy of bioaerosol exposure assessment. In this study, flow cytometry and fluorescent in situ hybridization (FISH) were evaluated for the assessment of exposures to airborne bacteria. Laboratory-generated two-component bioaerosols in exposures chambers and complex native bioaerosols in swine barns were sampled with two types of liquid impingers (all-glass impinger-30 and May 3-stage impinger). Aliquots of collection media were processed and enumerated by a standard culture technique, microscopy, or flow cytometry after nucleic acid staining with 4',6-diamidino-2-phenylindole (DAPI) and identified taxonomically by FISH. DAPI-labeled impinger samples yielded comparable estimates of bioaerosol concentrations when enumerated by microscopy or flow cytometry. The standard culture method underestimated bioaerosol concentrations by 2 orders of magnitude when compared to microscopy or flow cytometry. In the FISH method, aliquots of collection media were incubated with a probe universally complementary to eubacteria, a probe specific for several Pseudomonas species, and a probe complementary to eubacteria for detection of nonspecific binding. With these probes, FISH allowed quantitative identification of Pseudomonas aeruginosa and Escherichia coli bioaerosols in the exposure chamber without measurable nonspecific binding. Impinger samples from the swine barn demonstrated the efficacy of the FISH method for the identification of eubacteria in a complex organic dust. This work demonstrates the potential of emerging molecular techniques to complement traditional methods of bioaerosol exposure assessment.     

污水处理厂生物气溶胶抗生素抗性污染特征、来源及潜在风险

污水处理厂是抗生素抗性基因（antibiotic resistance genes,ARGs）和抗生素抗性细菌（antibiotic resistant bacteria,ARB）重要的源和汇,生物气溶胶是ARGs和ARB自污水处理厂向周边环境释放的关键载体。目前缺乏对污水处理厂生物气溶胶抗生素抗性污染特征、来源及潜在风险的系统性总结。本文从采样方法、检测方法、逸散特征、来源、潜在危害和风险评估等方面对污水处理厂抗生素抗性污染研究现状进行综述。惯性采样法和过滤法是常用的污水处理厂抗生素抗性生物气溶胶主要采集方法,而宏基因组测序、组装和分箱为其ARGs组成、可移动性和宿主提供了有效的检测方法,抗多药类、抗杆菌肽类、抗氨基糖苷类、抗四环素类、抗β-内酰胺类、抗磺胺类、抗大环内酯类和抗糖肽类等抗性基因在污水处理厂PM₁₀、PM_2.5和PM_1.0颗粒物中广泛检出。格栅间、生化反应池和污泥处理单元是污水处理厂PM₁₀、PM_2.5和PM_1.0负载ARGs和ARB的主要释放单元。污水处理厂不同粒径生物气溶胶中致病性ARB的存在增加了抗生素治疗的难度,而污水和污泥对ARGs和ARB的释放起到了重要的源的贡献。本文在研究内容、研究技术和控制策略等方面也提出了相关展望,以期为污水厂生物气溶胶抗生素抗性污染的监测和防护提供参考和借鉴。     

Temporal Variability of the Bioaerosol Background at a Subway Station: Concentration Level,Size Distribution,and Diversity of Airborne Bacteria

Naturally occurring bioaerosol environments may present a challenge to biological detection-identification-monitoring (BIODIM) systems aiming at rapid and reliable warning of bioterrorism incidents. One way to improve the operational performance of BIODIM systems is to increase our understanding of relevant bioaerosol backgrounds. Subway stations are enclosed public environments which may be regarded as potential bioterrorism targets. This study provides novel information concerning the temporal variability of the concentration level, size distribution, and diversity of airborne bacteria in a Norwegian subway station. Three different air samplers were used during a 72-h sampling campaign in February 2011. The results suggested that the airborne bacterial environment was stable between days and seasons, while the intraday variability was found to be substantial, although often following a consistent diurnal pattern. The bacterial levels ranged from not detected to 10³ CFU m⁻³ and generally showed increased levels during the daytime compared to the nighttime levels, as well as during rush hours compared to non-rush hours. The airborne bacterial levels showed rapid temporal variation (up to 270-fold) on some occasions, both consistent and inconsistent with the diurnal profile. Airborne bacterium-containing particles were distributed between different sizes for particles of >1.1 μm, although ∼50% were between 1.1 and 3.3 μm. Anthropogenic activities (mainly passengers) were demonstrated as major sources of airborne bacteria and predominantly contributed 1.1- to 3.3-μm bacterium-containing particles. Our findings contribute to the development of realistic testing and evaluation schemes for BIODIM equipment by providing information that may be used to simulate operational bioaerosol backgrounds during controlled aerosol chamber-based challenge tests with biological threat agents.     

A Metagenomic Framework for the Study of Airborne Microbial Communities

Understanding the microbial content of the air has important scientific, health, and economic implications. While studies have primarily characterized the taxonomic content of air samples by sequencing the 16S or 18S ribosomal RNA gene, direct analysis of the genomic content of airborne microorganisms has not been possible due to the extremely low density of biological material in airborne environments. We developed sampling and amplification methods to enable adequate DNA recovery to allow metagenomic profiling of air samples collected from indoor and outdoor environments. Air samples were collected from a large urban building, a medical center, a house, and a pier. Analyses of metagenomic data generated from these samples reveal airborne communities with a high degree of diversity and different genera abundance profiles. The identities of many of the taxonomic groups and protein families also allows for the identification of the likely sources of the sampled airborne bacteria.     

废气生物处理设施排放的微生物气溶胶逸散特征、影响因素与暴露风险研究进展

生物处理技术因其具有高效、成本低廉、操作简便、清洁、无二次污染等特点,已被广泛应用于废气处理方面,但微生物气溶胶会作为二次污染物从废气处理设施排放到周围空气中。由于携带和传播有害微生物,微生物气溶胶对人体健康造成潜在危害和风险。废气生物处理设施既是微生物气溶胶的“汇”,也是微生物气溶胶的“源”。本文阐述了废气生物处理设施微生物气溶胶的逸散水平、群落结构和粒径分布特征,分析了其形成原因、主要来源、影响因素和暴露风险,为废气生物处理设施产生的微生物气溶胶的识别和控制技术研究提供科学依据和参考。     

Treatment of Fungal Bioaerosols by a High-Temperature,Short-Time Process in a Continuous-Flow System

Airborne fungi, termed fungal bioaerosols, have received attention due to the association with public health problems and the effects on living organisms in nature. There are growing concerns that fungal bioaerosols are relevant to the occurrence of allergies, opportunistic diseases in hospitals, and outbreaks of plant diseases. The search for ways of preventing and curing the harmful effects of fungal bioaerosols has created a high demand for the study and development of an efficient method of controlling bioaerosols. However, almost all modern microbiological studies and theories have focused on microorganisms in liquid and solid phases. We investigated the thermal heating effects on fungal bioaerosols in a continuous-flow environment. Although the thermal heating process has long been a traditional method of controlling microorganisms, the effect of a continuous high-temperature, short-time (HTST) process on airborne microorganisms has not been quantitatively investigated in terms of various aerosol properties. Our experimental results show that the geometric mean diameter of the tested fungal bioaerosols decreased when they were exposed to increases in the surrounding temperature. The HTST process produced a significant decline in the (1→3)-β-d-glucan concentration of fungal bioaerosols. More than 99% of the Aspergillus versicolor and Cladosporium cladosporioides bioaerosols lost their culturability in about 0.2 s when the surrounding temperature exceeded 350°C and 400°C, respectively. The instantaneous exposure to high temperature significantly changed the surface morphology of the fungal bioaerosols.Fungi are omnipresent in indoor and outdoor environments (2, 28, 39). Most fungi are dispersed through the release of spores into the air, a phenomenon known to be driven by two kinds of energy (17): the energy provided by the fungus itself and the energy provided by external sources, such as air currents, rain, gravity, or changes in temperature and nutritional sources. Of these various mechanisms of fungal particle release, dispersal by air currents is the most prevalent mechanism for indoor fungal particles (19, 31). These airborne fungal spores, termed fungal bioaerosols, are resistant to environmental stresses and are adapted to airborne transport.Fungal bioaerosols constitute the major component of ambient airborne microorganisms (23, 50, 51). Several studies have reported that the concentration of fungal bioaerosols is relevant to the occurrence of human diseases and public health problems associated with acute toxic effects, allergies (3, 18), and asthma (4, 5, 13, 48). Fungal bioaerosols are of particular concern in healthcare facilities, where they can cause major infectious complications as opportunistic pathogens in patients with an immunodeficiency (9). For instance, invasive mycoses can affect patients undergoing high-dose chemotherapy for hematological malignancies associated with a prolonged period of neutropenia; they can also affect solid-organ transplant recipients. Despite all diagnostic and therapeutic efforts, the outcome of an invasive fungal infection is often fatal (with a mortality rate of around 50% for aspergillosis) (37). The main fungal genera responsible for these infections are as follows: Aspergillus spp., Fusarium spp., Scedosporium spp., and Mucorales spp. (10, 12, 20). However, virtually any filamentous fungus can be a pathogen (22, 41). In the hospital environment, possible sources of airborne nosocomial infection include ventilation or air-conditioning systems, decaying organic material, dust, water, food, ornamental plants, and building materials in and around hospitals (1).One of the major bioaerosols of concern is (1→3)-β-d-glucans, which comprises up to 60% of the cell wall of most fungal organisms. The (1→3)-β-d-glucans are glucose polymers with a variable molecular weight and a degree of branching (49). The results of several studies about the exposure of subjects to airborne (1→3)-β-d-glucans suggest that these agents play a role in bioaerosol-induced inflammatory responses and resulting respiratory symptoms, such as a dry cough, phlegmy cough, hoarseness, and atopy (11, 44). In addition, given that many epidemiological studies have reported that (1→3)-β-d-glucan has strong immuno-modulating effects (42, 47), (1→3)-β-d-glucan is an important parameter for exposure assessment by itself and as a surrogate component for fungi (16).To prevent the adverse health effects of fungal bioaerosols, we must ensure that control methods for airborne fungal spores are studied and developed. However, despite the necessity of controlling fungal bioaerosols, few studies have focused on such control mechanisms. The most common control methods are UV irradiation and electric ion emission. Given that UV irradiation is known to have a germicidal effect, several studies have examined how UV irradiation affects the viability of bioaerosols (35, 42). However, although UV irradiation can be easily applied by simply installing and turning on a UV lamp, the 254-nm-wavelength UV light produces ozone and radicals, which cause harmful effects to surrounding humans. Electric ion emission has also been studied as a means of controlling bioaerosols (21, 27). When the efficiency of the filter is increased, the efficacy of respiratory protection devices against bioaerosols can be enhanced. Although electric ions decrease the viability of airborne bacteria (25), the generation of the ions produces ozone, a pollutant, and also causes electric charges to accumulate on surrounding surfaces.Recently, heat treatment of indoor air using thermal processes has been considered a safe, effective, and environment-friendly method; it does not produce ozone or use ion or filter media. A thermal heating process has long been considered a suitable and reliable method for controlling microorganisms. Two types of heat are generally used, moist heat and dry heat. Moist heat utilizes steam under pressure, whereas dry heat involves high-temperature exposure without additional moisture. Several types of heat treatment are currently used for killing microorganisms. The treatments include incineration, Tyndallization, pasteurization, and autoclaving (32). However, most of these technologies were originally limited to controlling microorganisms in liquid or on material surfaces. In addition, they may not be adequate for controlling bioaerosols because the continuous surrounding environment of bioaerosols is significantly different from the conditions in liquid and on solid surfaces. Therefore, it is necessary to find adequate and practical conditions for controlling bioaerosols. Thus far, several investigations regarding the use of thermal processes against bioaerosols have been reported. Some of these studies have targeted airborne bacteria spores widely used as surrogates for biological warfare agents (8, 34), while others have focused on environmental parameters for the culture and survival of various vegetative cells (14, 29, 46). However, in these studies novel techniques for aerosols, such as measuring and analyzing aerosol particle size, distributions, and concentrations, were not utilized. In addition, to the best of our knowledge, there has been no study on the use of a thermal process for controlling fungal bioaerosols in continuous airflow. Fungal bioaerosols were found to be very resistant to a thermal environment in previous studies.In this study, we investigated the thermal heating effects on the physical, chemical, and biological properties of fungal bioaerosols using a high-temperature, short-time (HTST) sterilization process. The HTST process, a type of thermal heating process, is based on high-temperature stresses for very short periods. Although this thermal process has been used for the microbial decontamination of seeds and dried, powdered products, such as pharmaceuticals and heat-sensitive drink and food, it can be also applied to the control of an airborne microorganism in a continuous-flow system, such as a heating, ventilation, and air-conditioning system (15, 33, 38). When the fungal bioaerosol was passed through a thermal electric heating system, the fungal spores were exposed to various temperatures for short periods. Then, we examined the bioaerosol and aerosol characteristics, including aerosol size distribution, culturability, (1→3)-β-d-glucan production, and surface morphology, using a novel technique for sampling and measuring aerosols.     

海藻酸分解菌研究进展

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微生物气溶胶是悬浮于空气中粒径差异显著的生物粒子。污水处理、垃圾填埋等污水和固体废弃物的处理过程会产生大量的微生物气溶胶。近年来,随着对微生物气溶胶的不断认识,对其产生、逸散以及危害环境和人体的研究越来越多。在过去的150年,研究者们研发了多种微生物气溶胶采集技术和仪器设备,每种采集技术各有特点和适用条件。本文阐述沉降法、惯性采样法和过滤法3种典型微生物气溶胶采集技术的特点和原理,分析各种采样设备的适用性,为微生物气溶胶的采集和研究提供参考。