Abstract

Mastitis increases the activity of more than 20 enzymes in the glandular secretions of dairy cattle, including esterase. We hypothesized that milk esterase activity provides an inexpensive, rapid, and practical cow-side method for diagnosing subclinical mastitis (SCM). Our objective was therefore to determine the clinical utility of measuring esterase activity in quarter milk samples using Multistix® and PeriScreen™ strips to predict SCM. Quarter foremilk samples were collected from 115 dairy cows at dry-off and 92 fresh cows within 4-7 days post calving. Quarter somatic cell count (SCC) was measured using Delaval® cell counter with SCC≥200,000 cells/mL as the reference method for diagnosing SCM. Milk esterase activity was measured using Multistix® and PeriScreen™ strips. The area under the receiver operating curve (AUC), kappa coefficient (κ), and positive likelihood ratio (+LR) were calculated and P trace, the PeriScreen™ strip had an AUC=0.75, κ=0.32, and +LR=25.5 at dry-off, and AUC=0.66, κ=0.38, and +LR=∞ in fresh cows. At the optimal cut-point≥trace, the Multistix® strip had an AUC=0.71, κ=0.31, and +LR=4.2 at dry-off, and AUC=0.63, κ=0.31, and +LR=14.0 in fresh cows. The AUC,κ, and +LR values for the Multistix® and PeriScreen™ strips are considered suboptimal for a diagnostic test because clinically useful tests typically have an AUC >0.80,κ>0.6, or +LR>10. We therefore conclude that Multistix® and PeriScreen™ strips do not provide clinically useful cow-side tests for diagnosing SCM in lactating dairy cattle. List of abbreviations: SCC: Somatic cell count; IMI: Intramammary infection; SCM: Subclinical mastitis; PMNs: Polymorphonuclear cells; DCC: Delaval® cell counter; AUC: Area under the curve; ROC: Receiver operating characteristic curve; Se: Sensitivity; Sp: Specificity; Κ: kappa coefficient

Highlights

  • These enzymes include N-acetyl-D-glucosaminidase (NAG’ase), beta-glucuronidase, lactateMastitis leads to a variety of compositional dehydrogenase, alkaline phosphatase, aspartate changes in milk due to local inflammation, damage to aminotransferase, plasmin, catalase, elastase, and glandular tissue, increased leukocyte counts, and esterase (Kitchen, 1981; Zhao and Lacasse, 2008).serum components entering the milk due to increased Measurement of milk enzyme activity has permeability of the blood-milk barrier (Kitchen, potential as a screening test for subclinical mastitis1981; Pyörälä, 2003)

  • We have provided a preliminary report of the test performance of the PortaSCC® test elsewhere (Kandeel et al, 2017) and the focus of this study is to characterize the diagnostic performance of the Multistix® and PeriScreenTM strips in milk

  • Our objective was to characterize the ability of milk esterase activity measured by the Multistix® and PeriScreenTM strips to predict the presence of subclinical mastitis (SCM) and IMI in lactating dairy cattle at dry-off and freshening

Read more

Summary

Introduction

These enzymes include N-acetyl-D-glucosaminidase (NAG’ase), beta-glucuronidase, lactateMastitis leads to a variety of compositional dehydrogenase, alkaline phosphatase, aspartate changes in milk due to local inflammation, damage to aminotransferase, plasmin, catalase, elastase, and glandular tissue, increased leukocyte counts, and esterase (Kitchen, 1981; Zhao and Lacasse, 2008).serum components entering the milk due to increased Measurement of milk enzyme activity has permeability of the blood-milk barrier (Kitchen, potential as a screening test for subclinical mastitis1981; Pyörälä, 2003). Mastitis leads to a variety of compositional dehydrogenase, alkaline phosphatase, aspartate changes in milk due to local inflammation, damage to aminotransferase, plasmin, catalase, elastase, and glandular tissue, increased leukocyte counts, and esterase (Kitchen, 1981; Zhao and Lacasse, 2008). Serum components entering the milk due to increased Measurement of milk enzyme activity has permeability of the blood-milk barrier The. Leukocyte esterase reagent strips were developed initially as a semi-quantitative test for leukocytes in urine (St. John et al, 2006), and have been shown to be useful in other body fluids suc has peritoneal (Koulaouzidis et al, 2008), synovial (McNabb et al, 2017), cerebrospinal (Moosaet al., 1995) and bronchoalveolar lavage fluid (Jacobs et al, 2000) for detecting the presence of increased numbers of leukocytes (Mendler et al, 2010). The esterase reagent strip has several advantages over other point-of care tests including ease of use, low cost, and short test time

Objectives
Methods
Results
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call