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Microbiol."],"abstract":"<jats:p>Antibiotic resistance genes (ARGs) and antibiotic-resistant bacteria (ARB) in animal feces can be released into the atmosphere <jats:italic>via<\/jats:italic> aerosolization, posing a high health risk to farm workers. So far, little attention has been paid to the characterization of the aerosolization process. In this study, fecal and fine particulate matter (PM2.5) samples were collected from 20 animal farms involving swine, cattle, layers, and broilers, and the ARGs, ARB, and human pathogenic bacteria (HPB) were loaded in these two media. The results showed that approximately 70% of ARGs, 60% of ARBs, and 43% of HPBs were found to be preferential aerosolization. The bioaerosolization index (BI) of target 30 ARGs varied from 0.04 to 460.07, and the highest value was detected from <jats:italic>tetW<\/jats:italic>. The highest BI values of erythromycin- and tetracycline-resistant bacteria were for <jats:italic>Kocuria<\/jats:italic> (13119) and <jats:italic>Staphylococcus<\/jats:italic> (24746), respectively, and the distribution of BI in the two types of dominant ARB was similar. Regarding the bioaerosolization behavior of HPB, <jats:italic>Clostridium saccharolyticum<\/jats:italic> WM1 was the most easily aerosolized pathogen in swine and broiler farms, and <jats:italic>Brucella abortus<\/jats:italic> strain CNM 20040339 had the highest value in cattle and layer farms. Notably, the highest BI values for ARGs, ARB, and HPB were universally detected on chicken farms. Most ARGs, ARB, and HPB positively correlated with animal age, stocking density, and breeding area. Temperature and relative humidity have significant effects on the aerosolization behavior of targets, and the effects of these two parameters on the same target are usually opposite. The results of this study provide a basis for a better understanding of the contribution of animal feces to airborne ARGs and HPBs in farms, as well as for controlling the transport of the fecal microbiome to the environment through the aerosolization pathway.<\/jats:p>","DOI":"10.3389\/fmicb.2023.1175265","type":"journal-article","created":{"date-parts":[[2023,4,20]],"date-time":"2023-04-20T21:29:04Z","timestamp":1682026144000},"update-policy":"https:\/\/doi.org\/10.3389\/crossmark-policy","source":"Crossref","is-referenced-by-count":28,"title":["Aerosolization behavior of antimicrobial resistance in animal farms: a field study from feces to fine particulate matter"],"prefix":"10.3389","volume":"14","author":[{"given":"Huibo","family":"Xin","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Tianlei","family":"Qiu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yajie","family":"Guo","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Haoze","family":"Gao","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Liqiu","family":"Zhang","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Min","family":"Gao","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"1965","published-online":{"date-parts":[[2023,4,20]]},"reference":[{"key":"B1","doi-asserted-by":"publisher","first-page":"71","DOI":"10.1186\/s12917-022-03155-1","article-title":"Identification and molecular characterization of Brucella abortus and Brucella melitensis isolated from milk in cattle in azerbaijan","volume":"18","author":"Aliyev","year":"2022","journal-title":"BMC Vet. 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