High throughput Luminex beads based multiplex assay for identification of six major bacterial pathogens of mastitis in dairy animals

被引:2
|
作者
Shrinet, Garima [1 ]
Chhabra, Rajesh [2 ]
Sharma, Archana [1 ]
Batra, Kanisht [3 ]
Talukdar, Saurabh Jyoti [2 ]
Maan, Sushila [3 ]
机构
[1] Lala Lajpat Rai Univ Vet & Anim Sci, Dept Vet Microbiol, Hisar, Haryana, India
[2] Lala Lajpat Rai Univ Vet & Anim Sci, Coll Cent Lab, Hisar, Haryana, India
[3] Lala Lajpat Rai Univ Vet & Anim Sci, Dept Anim Biotechnol, Hisar, Haryana, India
来源
FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY | 2023年 / 13卷
关键词
Luminex; mastitis; bovine; bacteria; high throughput; diagnosis; dairy; CHAIN-REACTION ASSAY; PCR ASSAY; FLUORESCENT IMMUNOASSAY; CLINICAL MASTITIS; INFECTION; MICROARRAY; ANTIBODIES; DETECT; FARMS;
D O I
10.3389/fcimb.2023.1125562
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
IntroductionBovine mastitis is caused by over 150 different microorganisms. Specific identification and quantification of multiple bacteria in a single milk sample becomes essential for rapid intervention. MethodsIn the present study a Luminex beads based multiplex assay emphasizing on the precise identification of six major bacterial pathogens of mastitis was developed. Assay was developed in two triplex sets, triplex 1 comprised of Streptococcus agalactiae, Streptococcus dysgalactiae and Streptococcus uberis while triplex 2 consisted of Staphylococcus aureus, E. coli and Klebsiella pneumoniae. ResultsThe analytical sensitivity was 10 6 copies per reaction mixture for all the six bacteria. A 100% analytical specificity was observed for simultaneous detection of these bacteria. Clinical milk samples from 100 bovine quarters were tested for validation. DiscussionThe analytical sensitivity was similar to the findings reported earlier in real time PCR multiplex assay targeting the DNA of the 11 most common bacterial species or groups in mastitis. The analytical specificity of the optimized assay was 100% similar to reported earlier for simultaneous detection of Mycoplasma spp. and for seven entric viruses of humans.The developed assay indicates a concept proof of a rapid, cost effective high throughput diagnostic tool for identification of major bacteria causing mastitis.
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