Mitchell C. Rowland, Lucas E. Graham, Callie Selby, Aaron J. Forga, Billy M. Hargis, Christine N. Vuong, Danielle Graham
{"title":"将解淀粉芽孢杆菌衍生的固态发酵产物应用于孵化柜环境以缓解孵化期微生物华的可行性","authors":"Mitchell C. Rowland, Lucas E. Graham, Callie Selby, Aaron J. Forga, Billy M. Hargis, Christine N. Vuong, Danielle Graham","doi":"10.1016/j.psj.2025.105190","DOIUrl":null,"url":null,"abstract":"<div><div>Formaldehyde has been used to control microbial contamination in commercial hatch cabinets. The purpose of the present study was to investigate the effects of spray application of <em>Bacillus amyloliquefaciens</em> solid state fermentation products on the microbial load in the hatch cabinet, pioneer colonization of the gastrointestinal tract (GIT), and early performance compared to formaldehyde fumigation. An environmental challenge model was used to simulate the microbial bloom to compare the application of two <em>B. amyloliquefaciens</em> strains (MCR002, MCR009) to formaldehyde fumigation. Groups included 1) non-challenged control (NC), 2) challenged with pathogen mix (PM) containing <em>Escherichia coli, Enterococcus faecalis,</em> and <em>Staphylococcus aureus</em> at DOE19, 3) PM + formaldehyde treated (PM+<em>F</em>), 4) PM + MCR002 (PM+MCR002), 5) PM + MCR009 (PM+MCR009), and 6) PM+MCR002+MCR009 (PM+Combo). All groups were evaluated in trial 1-3 except PM+Combo. Air samples were collected from the hatch cabinet environment on d20 of embryogenesis (DOE20) at ∼20, 50, 80 % hatch, and immediately prior to hatch pull at DOE21. GIT samples were collected for enumeration of relevant enteric bacteria at hatch (d0). Pen and feed weights were recorded at d0 and d7 for trial 1 and 2 and at d14 for trial 2 to assess BWG and FCR. In summary, there was a significant (<em>P</em> < 0.05) reduction in gram-negative bacterial recovery from the GIT for PM+<em>F</em>, PM+MCR002, and PM+MCR009 compared to PM while the two <em>B. amyloliquefaciens</em> treatments were similar to PM+<em>F</em>. Gram-negative bacteria and <em>Enterococcus</em> recovery from hatch cabinet air samples were significantly reduced in PM+<em>F</em> and PM+MCR002 compared to PM. No significant differences in performance were observed. Spray application of MCR002 or MCR009 alone shifted the microbial load in the hatch cabinet and in the GIT of chicks similar to PM + <em>F</em> without negatively affecting performance at d7 or 14. However, MCR002 was more effective. This suggests that MCR002 could be used to mitigate the microbial bloom during the hatching phase without impacting chick performance.</div></div>","PeriodicalId":20459,"journal":{"name":"Poultry Science","volume":"104 7","pages":"Article 105190"},"PeriodicalIF":3.8000,"publicationDate":"2025-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Feasibility of applying Bacillus amyloliquefaciens-derived solid state fermentation products into the hatch cabinet environment as a method to mitigate the microbial bloom during the hatching phase\",\"authors\":\"Mitchell C. Rowland, Lucas E. Graham, Callie Selby, Aaron J. Forga, Billy M. Hargis, Christine N. Vuong, Danielle Graham\",\"doi\":\"10.1016/j.psj.2025.105190\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Formaldehyde has been used to control microbial contamination in commercial hatch cabinets. The purpose of the present study was to investigate the effects of spray application of <em>Bacillus amyloliquefaciens</em> solid state fermentation products on the microbial load in the hatch cabinet, pioneer colonization of the gastrointestinal tract (GIT), and early performance compared to formaldehyde fumigation. An environmental challenge model was used to simulate the microbial bloom to compare the application of two <em>B. amyloliquefaciens</em> strains (MCR002, MCR009) to formaldehyde fumigation. Groups included 1) non-challenged control (NC), 2) challenged with pathogen mix (PM) containing <em>Escherichia coli, Enterococcus faecalis,</em> and <em>Staphylococcus aureus</em> at DOE19, 3) PM + formaldehyde treated (PM+<em>F</em>), 4) PM + MCR002 (PM+MCR002), 5) PM + MCR009 (PM+MCR009), and 6) PM+MCR002+MCR009 (PM+Combo). All groups were evaluated in trial 1-3 except PM+Combo. Air samples were collected from the hatch cabinet environment on d20 of embryogenesis (DOE20) at ∼20, 50, 80 % hatch, and immediately prior to hatch pull at DOE21. GIT samples were collected for enumeration of relevant enteric bacteria at hatch (d0). Pen and feed weights were recorded at d0 and d7 for trial 1 and 2 and at d14 for trial 2 to assess BWG and FCR. In summary, there was a significant (<em>P</em> < 0.05) reduction in gram-negative bacterial recovery from the GIT for PM+<em>F</em>, PM+MCR002, and PM+MCR009 compared to PM while the two <em>B. amyloliquefaciens</em> treatments were similar to PM+<em>F</em>. Gram-negative bacteria and <em>Enterococcus</em> recovery from hatch cabinet air samples were significantly reduced in PM+<em>F</em> and PM+MCR002 compared to PM. No significant differences in performance were observed. Spray application of MCR002 or MCR009 alone shifted the microbial load in the hatch cabinet and in the GIT of chicks similar to PM + <em>F</em> without negatively affecting performance at d7 or 14. However, MCR002 was more effective. This suggests that MCR002 could be used to mitigate the microbial bloom during the hatching phase without impacting chick performance.</div></div>\",\"PeriodicalId\":20459,\"journal\":{\"name\":\"Poultry Science\",\"volume\":\"104 7\",\"pages\":\"Article 105190\"},\"PeriodicalIF\":3.8000,\"publicationDate\":\"2025-04-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Poultry Science\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0032579125004328\",\"RegionNum\":1,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"AGRICULTURE, DAIRY & ANIMAL SCIENCE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Poultry Science","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0032579125004328","RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"AGRICULTURE, DAIRY & ANIMAL SCIENCE","Score":null,"Total":0}
Feasibility of applying Bacillus amyloliquefaciens-derived solid state fermentation products into the hatch cabinet environment as a method to mitigate the microbial bloom during the hatching phase
Formaldehyde has been used to control microbial contamination in commercial hatch cabinets. The purpose of the present study was to investigate the effects of spray application of Bacillus amyloliquefaciens solid state fermentation products on the microbial load in the hatch cabinet, pioneer colonization of the gastrointestinal tract (GIT), and early performance compared to formaldehyde fumigation. An environmental challenge model was used to simulate the microbial bloom to compare the application of two B. amyloliquefaciens strains (MCR002, MCR009) to formaldehyde fumigation. Groups included 1) non-challenged control (NC), 2) challenged with pathogen mix (PM) containing Escherichia coli, Enterococcus faecalis, and Staphylococcus aureus at DOE19, 3) PM + formaldehyde treated (PM+F), 4) PM + MCR002 (PM+MCR002), 5) PM + MCR009 (PM+MCR009), and 6) PM+MCR002+MCR009 (PM+Combo). All groups were evaluated in trial 1-3 except PM+Combo. Air samples were collected from the hatch cabinet environment on d20 of embryogenesis (DOE20) at ∼20, 50, 80 % hatch, and immediately prior to hatch pull at DOE21. GIT samples were collected for enumeration of relevant enteric bacteria at hatch (d0). Pen and feed weights were recorded at d0 and d7 for trial 1 and 2 and at d14 for trial 2 to assess BWG and FCR. In summary, there was a significant (P < 0.05) reduction in gram-negative bacterial recovery from the GIT for PM+F, PM+MCR002, and PM+MCR009 compared to PM while the two B. amyloliquefaciens treatments were similar to PM+F. Gram-negative bacteria and Enterococcus recovery from hatch cabinet air samples were significantly reduced in PM+F and PM+MCR002 compared to PM. No significant differences in performance were observed. Spray application of MCR002 or MCR009 alone shifted the microbial load in the hatch cabinet and in the GIT of chicks similar to PM + F without negatively affecting performance at d7 or 14. However, MCR002 was more effective. This suggests that MCR002 could be used to mitigate the microbial bloom during the hatching phase without impacting chick performance.
期刊介绍:
First self-published in 1921, Poultry Science is an internationally renowned monthly journal, known as the authoritative source for a broad range of poultry information and high-caliber research. The journal plays a pivotal role in the dissemination of preeminent poultry-related knowledge across all disciplines. As of January 2020, Poultry Science will become an Open Access journal with no subscription charges, meaning authors who publish here can make their research immediately, permanently, and freely accessible worldwide while retaining copyright to their work. Papers submitted for publication after October 1, 2019 will be published as Open Access papers.
An international journal, Poultry Science publishes original papers, research notes, symposium papers, and reviews of basic science as applied to poultry. This authoritative source of poultry information is consistently ranked by ISI Impact Factor as one of the top 10 agriculture, dairy and animal science journals to deliver high-caliber research. Currently it is the highest-ranked (by Impact Factor and Eigenfactor) journal dedicated to publishing poultry research. Subject areas include breeding, genetics, education, production, management, environment, health, behavior, welfare, immunology, molecular biology, metabolism, nutrition, physiology, reproduction, processing, and products.