On-farm colorimetric detection of Pasteurella multocida, Mannheimia haemolytica, and Histophilus somni in crude bovine nasal samples

被引:31
作者
Pascual-Garrigos, Ana [1 ,2 ,3 ]
Maruthamuthu, Murali Kannan [1 ,3 ]
Ault, Aaron [4 ]
Davidson, Josiah Levi [1 ,3 ]
Rudakov, Grigorii [1 ,3 ,5 ]
Pillai, Deepti [6 ]
Koziol, Jennifer [7 ]
Schoonmaker, Jon P. [8 ]
Johnson, Timothy [8 ]
Verma, Mohit S. [1 ,3 ,5 ]
机构
[1] Purdue Univ, Dept Agr & Biol Engn, 225 S Univ St, W Lafayette, IN 47907 USA
[2] Purdue Univ, Dept Biochem, 175 South Univ St, W Lafayette, IN 47906 USA
[3] Purdue Univ, Birck Nanotechnol Ctr, 1205 W State St, W Lafayette, IN 47907 USA
[4] Purdue Univ, Sch Elect & Comp Engn, 465 Northwestern Ave, W Lafayette, IN 47907 USA
[5] Purdue Univ, Weldon Sch Biomed Engn, 206 South Martin Jischke Dr, W Lafayette, IN 47907 USA
[6] Purdue Univ, Dept Comparat Pathobiol, 625 Harrison St, W Lafayette, IN 47907 USA
[7] Texas Tech Univ, Sch Vet Med, 7671 Evans Dr, Amarillo, TX 79106 USA
[8] Purdue Univ, Dept Anim Sci, 270 S Russell St, W Lafayette, IN 47907 USA
基金
美国食品与农业研究所;
关键词
diagnostics; bovine respiratory disease; loop-mediated isothermal amplification; pen-side; MEDIATED ISOTHERMAL AMPLIFICATION; RAPID DETECTION; RESPIRATORY-DISEASE;
D O I
10.1186/s13567-021-00997-9
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
This work modifies a loop-mediated isothermal amplification (LAMP) assay to detect the bovine respiratory disease (BRD) bacterial pathogens Pasteurella multocida, Mannheimia haemolytica, and Histophilus somni in a colorimetric format on a farm. BRD causes a significant health and economic burden worldwide that partially stems from the challenges involved in determining the pathogens causing the disease. Methods such as polymerase chain reaction (PCR) have the potential to identify the causative pathogens but require lab equipment and extensive sample processing making the process lengthy and expensive. To combat this limitation, LAMP allows accurate pathogen detection in unprocessed samples by the naked eye allowing for potentially faster and more precise diagnostics on the farm. The assay developed here offers 66.7-100% analytical sensitivity, and 100% analytical specificity (using contrived samples) while providing 60-100% concordance with PCR results when tested on five steers in a feedlot. The use of a consumer-grade water bath enabled on-farm execution by collecting a nasal swab from cattle and provided a colorimetric result within 60 min. Such an assay holds the potential to provide rapid pen-side diagnostics to cattle producers and veterinarians.
引用
收藏
页数:12
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