Inviting an author to review:
Find an author and click ‘Invite to review selected article’ near their name.
Search for authorsSearch for similar articles
17
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Assessing allergenic fungi in house dust by floor wipe sampling and quantitative PCR

      research-article
      1 , 2 , 3 , 4 , 1
      Indoor Air
      Blackwell Publishing Ltd
      Fungi, House dust, Wipe sampling method, qPCR, Asthma, Allergy

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Abstract  In the present study, we modified an existing surface wipe sampling method for lead and other heavy metals to create a protocol to collect fungi in floor dust followed by real‐time quantitative PCR (qPCR)‐based detection. We desired minimal inconvenience for participants in residential indoor environmental quality and health studies. Accuracy, precision, and method detection limits (MDLs) were investigated. Overall, MDLs ranged from 0.6 to 25 cell/cm 2 on sampled floors. Overall measurement precisions expressed as the coefficient of variation because of sample processing and qPCR ranged 6–63%. Median and maximum fungal concentrations in house dust in study homes in Visalia, Tulare County, California, were 110 and 2500 cell/cm 2, respectively, with universal fungal primers (allergenic and nonallergenic species). The field study indicated samplings in multiple seasons were necessary to characterize representative whole‐year fungal concentrations in residential microenvironments. This was because significant temporal variations were observed within study homes. Combined field and laboratory results suggested this modified new wipe sampling method, in conjunction with growth‐independent qPCR, shows potential to improve human exposure and health studies for fungal pathogens and allergens in dust in homes of susceptible, vulnerable population subgroups.

          Practical Implications

          Fungi are ubiquitous in indoor and outdoor environments, and many fungi are known to cause allergic reactions and exacerbate asthma attacks. This study established—by modifying an existing—a wipe sampling method to collect fungi in floor dust followed by real‐time quantitative PCR (qPCR)‐based detection methodologies. Results from this combined laboratory and field assessment suggested the methodology’s potential to inform larger human exposure studies for fungal pathogens and allergens in house dust as well as epidemiologic studies of children with asthma and older adults with chronic respiratory diseases.

          Related collections

          Most cited references30

          • Record: found
          • Abstract: found
          • Article: not found

          Aspergillosis case-fatality rate: systematic review of the literature.

          To update the case-fatality rate (CFR) associated with invasive aspergillosis according to underlying conditions, site of infection, and antifungal therapy, data were systematically reviewed and pooled from clinical trials, cohort or case-control studies, and case series of >/=10 patients with definite or probable aspergillosis. Subjects were 1941 patients described in studies published after 1995 that provided sufficient outcome data; cases included were identified by MEDLINE and EMBASE searches. The main outcome measure was the CFR. Fifty of 222 studies met the inclusion criteria. The overall CFR was 58%, and the CFR was highest for bone marrow transplant recipients (86.7%) and for patients with central nervous system or disseminated aspergillosis (88.1%). Amphotericin B deoxycholate and lipid formulations of amphotericin B failed to prevent death in one-half to two-thirds of patients. Mortality is high despite improvements in diagnosis and despite the advent of newer formulations of amphotericin B. Underlying patient conditions and the site of infection remain important prognostic factors.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Indoor fungal composition is geographically patterned and more diverse in temperate zones than in the tropics.

            Fungi are ubiquitous components of indoor human environments, where most contact between humans and microbes occurs. The majority of these organisms apparently play a neutral role, but some are detrimental to human lifestyles and health. Recent studies that used culture-independent sampling methods demonstrated a high diversity of indoor fungi distinct from that of outdoor environments. Others have shown temporal fluctuations of fungal assemblages in human environments and modest correlations with human activity, but global-scale patterns have not been examined, despite the manifest significance of biogeography in other microbial systems. Here we present a global survey of fungi from indoor environments (n = 72), using both taxonomic and phylogeny-informative molecular markers to determine whether global or local indoor factors determine indoor fungal composition. Contrary to common ecological patterns, we show that fungal diversity is significantly higher in temperate zones than in the tropics, with distance from the equator being the best predictor of phylogenetic community similarity. Fungal composition is significantly auto-correlated at the national and hemispheric spatial scales. Remarkably, building function has no significant effect on indoor fungal composition, despite stark contrasts between architecture and materials of some buildings in close proximity. Distribution of individual taxa is significantly range- and latitude-limited compared with a null model of randomized distribution. Our results suggest that factors driving fungal composition are primarily global rather than mediated by building design or function.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Pulmonary aspergillosis in patients with chronic obstructive pulmonary disease: incidence, risk factors, and outcome.

              We describe a large series of patients with chronic obstructive pulmonary disease (COPD) and probable invasive pulmonary aspergillosis (IPA), and the risk factors and incidence of the disease in patients with isolation of Aspergillus from lower respiratory tract samples. From 2000 to 2007, we retrospectively studied all patients admitted with COPD and isolation of Aspergillus (239; 16.3/1000 admissions). Multivariate logistic regression and survival curves were used. Fifty-three patients had probable IPA (3.6 cases of IPA per 1000 COPD admissions). IPA affects at least 22.1% of patients with COPD and isolation of Aspergillus in culture. In 33 of the 53 patients with probable IPA, serum galactomannan was determined; in 14 (42.4%) of these, the result was positive. Five variables were independent predictors of IPA with statistical significance: admission to the intensive-care unit, chronic heart failure, antibiotic treatment received in the 3 months prior to admission, the accumulated dosage of corticosteroids equivalent to >700 mg prednisone received in the 3 months prior to admission, and the similar accumulated dosage of corticosteroids received from admission to the first clinical isolation of Aspergillus. Multivariate analysis gave an area under the curve of 0.925 (95% CI 0.888-0.962; p <0.001). The overall mean survival of the cohort was 64.1% (28.3% for IPA patients and 75.2% for non-IPA patients). The median number of days of survival was 48 (95% CI 33.07-62.92). However, we found statistically significant differences between patients with IPA (29 days; 95% CI 20.59-37.40) and patients without IPA (86 days; 95% CI 61.13-110.86) (log rank, p <0.001).
                Bookmark

                Author and article information

                Journal
                Indoor Air
                Indoor Air
                10.1111/(ISSN)1600-0668
                INA
                Indoor Air
                Blackwell Publishing Ltd (Oxford, UK )
                0905-6947
                1600-0668
                09 August 2011
                December 2011
                : 21
                : 6 ( doiID: 10.1111/ina.2011.21.issue-6 )
                : 521-530
                Affiliations
                [ 1 ]Department of Chemical and Environmental Engineering, Yale University, New Haven, CT, USA
                [ 2 ]Japan Society for the Promotion of Science, Ichiban‐Cho 8, Chiyoda‐Ku, Tokyo, Japan
                [ 3 ]Department of Environmental and Occupational Health and the Center for School and Community‐Based Research and Education, University of Medicine and Dentistry of New Jersey (UMDNJ), School of Public Health (SPH), Piscataway, NJ, USA
                [ 4 ]Exposure Science Division, Environmental and Occupational Health Sciences Institute, UMDNJ‐Robert Wood Johnson Medical School and Rutgers University, Piscataway, NJ, USA
                Author notes
                [*]Derek G. Shendell
Assistant Professor, University of Medicine and Dentistry of New Jersey (UMDNJ)
School of Public Health (SPH)
683 Hoes Lane West
3rd Fl. SPH Bldg., P.O. Box 9
Piscataway, NJ 08854
USA
Tel.: +1 732 235 5409; +1 732 235 4988
Fax: +1 732 235 4004; +1 732 235 4960
e‐mail: shendedg@ 123456umdnj.edu
                Article
                INA732
                10.1111/j.1600-0668.2011.00732.x
                7201893
                21767317
                fef20056-6ce7-49ad-a1e8-bc5a3e814067
                © 2011 John Wiley & Sons A/S

                This article is being made freely available through PubMed Central as part of the COVID-19 public health emergency response. It can be used for unrestricted research re-use and analysis in any form or by any means with acknowledgement of the original source, for the duration of the public health emergency.

                History
                : 14 March 2011
                : 9 July 2011
                Page count
                Figures: 4, Tables: 5, Pages: 10
                Categories
                Original Articles
                Custom metadata
                2.0
                December 2011
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.8.0 mode:remove_FC converted:15.04.2020

                Health & Social care
                fungi,house dust,wipe sampling method,qpcr,asthma,allergy
                Health & Social care
                fungi, house dust, wipe sampling method, qpcr, asthma, allergy

                Comments

                Comment on this article

                scite_
                0
                0
                0
                0
                Smart Citations
                0
                0
                0
                0
                Citing PublicationsSupportingMentioningContrasting
                View Citations

                See how this article has been cited at scite.ai

                scite shows how a scientific paper has been cited by providing the context of the citation, a classification describing whether it supports, mentions, or contrasts the cited claim, and a label indicating in which section the citation was made.

                Similar content118

                Cited by12

                Most referenced authors320