Jennifer L. Cain , Leonor Sicalo Gianechini , Abigail L. Vetter , Sarah M. Davis , Leah N. Britton , Jennifer L. Myka , Paul Slusarewicz
{"title":"绵羊粪便样本中血包虫病虫卵的快速自动定量。","authors":"Jennifer L. Cain , Leonor Sicalo Gianechini , Abigail L. Vetter , Sarah M. Davis , Leah N. Britton , Jennifer L. Myka , Paul Slusarewicz","doi":"10.1016/j.ijpara.2023.07.003","DOIUrl":null,"url":null,"abstract":"<div><p><em>Haemonchus contortus</em> is one of the most pathogenic nematodes affecting small ruminants globally and is responsible for large economic losses in the sheep and goat industry. Anthelmintic resistance is rampant in this parasite and thus parasite control programs must account for drug efficacy on individual farms and, sometimes, whether <em>H. contortus</em> is the most prevalent trichostrongylid. Historically, coproculture has been the main way to determine the prevalence of <em>H. contortus</em> in faecal samples due to the inability to morphologically differentiate between trichostrongylid egg types, but this process requires a skilled technician and takes multiple days to complete. Fluoresceinated peanut agglutinin (PNA) has been shown to specifically bind <em>H. contortus</em> and thus differentiate eggs based on whether they fluoresce, but this method has not been widely adopted. The Parasight<sup>TM</sup> System (PS) fluorescently stains helminth eggs in order to identify and quantify them, and the <em>H. contortus</em> PNA staining method was therefore adapted to this platform using methodology requiring only 20 min to obtain results. In this study, 74 fecal samples were collected from sheep and analyzed for PNA-stained <em>H. contortus,</em> using both PS and manual fluorescence microscopy. The percentage of <em>H. contortus</em> was determined based on standard total strongylid counts with PS or brightfield microscopy. Additionally, 15 samples were processed for coproculture with larval identification, and analyzed with both manual and automated PNA methods. All methods were compared using the coefficient of determination (R<sup>2</sup>) and the Lin’s concordance correlation coefficient (ρc). Parasight<sup>TM</sup> and manual PNA percent <em>H. contortus</em> results were highly correlated with R<sup>2</sup> = 0.8436 and ρc = 0.9100 for all 74 fecal samples. Coproculture versus PS percent <em>H. contortus</em> were also highly correlated with R<sup>2</sup> = 0.8245 and ρc = 0.8605. Overall, this system provides a rapid and convenient method for determining the percentage of <em>H. contortus</em> in sheep and goat fecal samples without requiring specialized training.</p></div>","PeriodicalId":13725,"journal":{"name":"International journal for parasitology","volume":"54 1","pages":"Pages 47-53"},"PeriodicalIF":3.7000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Rapid, automated quantification of Haemonchus contortus ova in sheep faecal samples\",\"authors\":\"Jennifer L. Cain , Leonor Sicalo Gianechini , Abigail L. Vetter , Sarah M. Davis , Leah N. Britton , Jennifer L. Myka , Paul Slusarewicz\",\"doi\":\"10.1016/j.ijpara.2023.07.003\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><em>Haemonchus contortus</em> is one of the most pathogenic nematodes affecting small ruminants globally and is responsible for large economic losses in the sheep and goat industry. Anthelmintic resistance is rampant in this parasite and thus parasite control programs must account for drug efficacy on individual farms and, sometimes, whether <em>H. contortus</em> is the most prevalent trichostrongylid. Historically, coproculture has been the main way to determine the prevalence of <em>H. contortus</em> in faecal samples due to the inability to morphologically differentiate between trichostrongylid egg types, but this process requires a skilled technician and takes multiple days to complete. Fluoresceinated peanut agglutinin (PNA) has been shown to specifically bind <em>H. contortus</em> and thus differentiate eggs based on whether they fluoresce, but this method has not been widely adopted. The Parasight<sup>TM</sup> System (PS) fluorescently stains helminth eggs in order to identify and quantify them, and the <em>H. contortus</em> PNA staining method was therefore adapted to this platform using methodology requiring only 20 min to obtain results. In this study, 74 fecal samples were collected from sheep and analyzed for PNA-stained <em>H. contortus,</em> using both PS and manual fluorescence microscopy. The percentage of <em>H. contortus</em> was determined based on standard total strongylid counts with PS or brightfield microscopy. Additionally, 15 samples were processed for coproculture with larval identification, and analyzed with both manual and automated PNA methods. All methods were compared using the coefficient of determination (R<sup>2</sup>) and the Lin’s concordance correlation coefficient (ρc). Parasight<sup>TM</sup> and manual PNA percent <em>H. contortus</em> results were highly correlated with R<sup>2</sup> = 0.8436 and ρc = 0.9100 for all 74 fecal samples. Coproculture versus PS percent <em>H. contortus</em> were also highly correlated with R<sup>2</sup> = 0.8245 and ρc = 0.8605. Overall, this system provides a rapid and convenient method for determining the percentage of <em>H. contortus</em> in sheep and goat fecal samples without requiring specialized training.</p></div>\",\"PeriodicalId\":13725,\"journal\":{\"name\":\"International journal for parasitology\",\"volume\":\"54 1\",\"pages\":\"Pages 47-53\"},\"PeriodicalIF\":3.7000,\"publicationDate\":\"2024-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International journal for parasitology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0020751923001716\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PARASITOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International journal for parasitology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0020751923001716","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PARASITOLOGY","Score":null,"Total":0}
Rapid, automated quantification of Haemonchus contortus ova in sheep faecal samples
Haemonchus contortus is one of the most pathogenic nematodes affecting small ruminants globally and is responsible for large economic losses in the sheep and goat industry. Anthelmintic resistance is rampant in this parasite and thus parasite control programs must account for drug efficacy on individual farms and, sometimes, whether H. contortus is the most prevalent trichostrongylid. Historically, coproculture has been the main way to determine the prevalence of H. contortus in faecal samples due to the inability to morphologically differentiate between trichostrongylid egg types, but this process requires a skilled technician and takes multiple days to complete. Fluoresceinated peanut agglutinin (PNA) has been shown to specifically bind H. contortus and thus differentiate eggs based on whether they fluoresce, but this method has not been widely adopted. The ParasightTM System (PS) fluorescently stains helminth eggs in order to identify and quantify them, and the H. contortus PNA staining method was therefore adapted to this platform using methodology requiring only 20 min to obtain results. In this study, 74 fecal samples were collected from sheep and analyzed for PNA-stained H. contortus, using both PS and manual fluorescence microscopy. The percentage of H. contortus was determined based on standard total strongylid counts with PS or brightfield microscopy. Additionally, 15 samples were processed for coproculture with larval identification, and analyzed with both manual and automated PNA methods. All methods were compared using the coefficient of determination (R2) and the Lin’s concordance correlation coefficient (ρc). ParasightTM and manual PNA percent H. contortus results were highly correlated with R2 = 0.8436 and ρc = 0.9100 for all 74 fecal samples. Coproculture versus PS percent H. contortus were also highly correlated with R2 = 0.8245 and ρc = 0.8605. Overall, this system provides a rapid and convenient method for determining the percentage of H. contortus in sheep and goat fecal samples without requiring specialized training.
期刊介绍:
International Journal for Parasitology offers authors the option to sponsor nonsubscriber access to their articles on Elsevier electronic publishing platforms. For more information please view our Sponsored Articles page. The International Journal for Parasitology publishes the results of original research in all aspects of basic and applied parasitology, including all the fields covered by its Specialist Editors, and ranging from parasites and host-parasite relationships of intrinsic biological interest to those of social and economic importance in human and veterinary medicine and agriculture.