Baseline analysis of Mycoplasma mycoides subsp. mycoides antigens as targets for a DIVA assay for use with a subunit vaccine for contagious bovine pleuropneumonia.


Journal

BMC veterinary research
ISSN: 1746-6148
Titre abrégé: BMC Vet Res
Pays: England
ID NLM: 101249759

Informations de publication

Date de publication:
10 Jul 2020
Historique:
received: 27 02 2020
accepted: 02 07 2020
entrez: 12 7 2020
pubmed: 12 7 2020
medline: 9 3 2021
Statut: epublish

Résumé

Mycoplasma mycoides subsp. mycoides (Mmm) is the causative agent of contagious bovine pleuropneumonia in cattle. A prototype subunit vaccine is being developed, however, there is currently no diagnostic test that can differentiate between infected cattle and those vaccinated with the prototype subunit vaccine. This study characterized Mmm proteins to identify potential antigens for use in differentiating infected from vaccinated animals. Ten Mmm antigens expressed as recombinant proteins were tested in an indirect ELISA using experimental sera from control groups, infected, and vaccinated animals. Data were imported into R software for analysis and drawing of the box and scatter plots while Cohen's Kappa assessed the level of agreement between the Mmm antigens. Two vaccine antigens (MSC_0499 and MSC_0776) were superior in detecting antibodies in sera of animals vaccinated with the subunit vaccines while two non-vaccine antigens (MSC_0636 and LppB) detected antibodies in sera of infected animals showing all clinical stages of the disease. Sensitivity and specificity of above 87.5% were achieved when the MSC_0499 and MSC_0636 antigens were tested on sera from vaccinated and infected animals. The MSC_0499 and MSC_0776 antigens were the most promising for detecting vaccinated animals, while MSC_0636 and LppB were the best targets to identify infected animals. Further testing of sera from vaccinated and infected animals collected at different time intervals in the field should help establish how useful a diagnostic test based on a cocktail of these proteins would be.

Sections du résumé

BACKGROUND BACKGROUND
Mycoplasma mycoides subsp. mycoides (Mmm) is the causative agent of contagious bovine pleuropneumonia in cattle. A prototype subunit vaccine is being developed, however, there is currently no diagnostic test that can differentiate between infected cattle and those vaccinated with the prototype subunit vaccine. This study characterized Mmm proteins to identify potential antigens for use in differentiating infected from vaccinated animals.
RESULTS RESULTS
Ten Mmm antigens expressed as recombinant proteins were tested in an indirect ELISA using experimental sera from control groups, infected, and vaccinated animals. Data were imported into R software for analysis and drawing of the box and scatter plots while Cohen's Kappa assessed the level of agreement between the Mmm antigens. Two vaccine antigens (MSC_0499 and MSC_0776) were superior in detecting antibodies in sera of animals vaccinated with the subunit vaccines while two non-vaccine antigens (MSC_0636 and LppB) detected antibodies in sera of infected animals showing all clinical stages of the disease. Sensitivity and specificity of above 87.5% were achieved when the MSC_0499 and MSC_0636 antigens were tested on sera from vaccinated and infected animals.
CONCLUSIONS CONCLUSIONS
The MSC_0499 and MSC_0776 antigens were the most promising for detecting vaccinated animals, while MSC_0636 and LppB were the best targets to identify infected animals. Further testing of sera from vaccinated and infected animals collected at different time intervals in the field should help establish how useful a diagnostic test based on a cocktail of these proteins would be.

Identifiants

pubmed: 32650780
doi: 10.1186/s12917-020-02453-w
pii: 10.1186/s12917-020-02453-w
pmc: PMC7350692
doi:

Substances chimiques

Antibodies, Bacterial 0
Antigens, Bacterial 0
Bacterial Vaccines 0
Vaccines, Subunit 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

236

Subventions

Organisme : Canadian International Food Security Research Fund (CIFSRF); VACNADA; African Biosciences Challenge Fund
ID : 107849; DCI-FOOD/2009/226-469

Références

Vet Microbiol. 1998 Feb 28;60(2-4):179-91
pubmed: 9646449
Genome Res. 2004 Feb;14(2):221-7
pubmed: 14762060
Stand Genomic Sci. 2015 Oct 29;10:89
pubmed: 26516405
Vaccine. 2014 May 23;32(25):3107-14
pubmed: 24462404
Trop Anim Health Prod. 2012 Aug;44(6):1233-8
pubmed: 22528527
Vet Immunol Immunopathol. 2015 Nov 15;168(1-2):103-10
pubmed: 26384697
Microbiology. 2008 Feb;154(Pt 2):539-549
pubmed: 18227258
Vet Immunol Immunopathol. 2016 Oct 1;178:64-9
pubmed: 27496744
Vet Microbiol. 2010 May 19;142(3-4):285-92
pubmed: 19900769
Microbiology. 2008 Aug;154(Pt 8):2427-2436
pubmed: 18667575
Vet Immunol Immunopathol. 2016 Mar;171:103-14
pubmed: 26964722
Ann N Y Acad Sci. 2000;916:364-9
pubmed: 11193648
Rev Sci Tech. 1996 Dec;15(4):1331-53
pubmed: 9527412
Mem Inst Oswaldo Cruz. 2016 Jul 4;111(8):501-4
pubmed: 27384081
Comp Immunol Microbiol Infect Dis. 2008 Mar;31(2-3):227-38
pubmed: 17706775
Clin Diagn Lab Immunol. 2000 Jul;7(4):588-95
pubmed: 10882657
Res Vet Sci. 2006 Dec;81(3):304-9
pubmed: 16624356
J Microbiol Methods. 2010 Jun;81(3):211-8
pubmed: 20381545
Rev Sci Tech. 2006 Dec;25(3):999-1011
pubmed: 17361766
Int J Syst Evol Microbiol. 2009 Jun;59(Pt 6):1353-8
pubmed: 19502315
J Bacteriol. 2012 Aug;194(16):4448-9
pubmed: 22843585
Oncotarget. 2017 Nov 02;9(47):28322-28336
pubmed: 29983863
Vet Res. 2011 Jun 12;42:77
pubmed: 21663697
BMC Microbiol. 2009 Oct 09;9:215
pubmed: 19818124
BMC Vet Res. 2019 Dec 12;15(1):451
pubmed: 31831071
Vaccine. 2017 Dec 4;35(48 Pt B):6604-6610
pubmed: 29079106
Vet Immunol Immunopathol. 2018 Mar;197:7-14
pubmed: 29475510
Vet Microbiol. 2002 Jan 23;84(3):195-205
pubmed: 11731172
Clin Vaccine Immunol. 2009 Nov;16(11):1665-74
pubmed: 19726613
ILAR J. 2006;47(1):5-14
pubmed: 16391426
Comp Immunol Microbiol Infect Dis. 2010 Jul;33(4):279-90
pubmed: 19187963
J Clin Microbiol. 2016 Jun;54(6):1557-1565
pubmed: 27053669
Vet J. 2015 Jan;203(1):79-84
pubmed: 25467991
ILAR J. 2002;43(4):244-58
pubmed: 12391400
Vet Immunol Immunopathol. 2016 Jan;169:63-7
pubmed: 26827840

Auteurs

Harrison O Lutta (HO)

Kenya Agricultural and Livestock Research Organization, Biotechnology Research Institute, P.O. Box 14733-00800, Nairobi, Kenya. holutta_006@yahoo.com.

David Odongo (D)

School of Biological Sciences, University of Nairobi, P.O. Box 30197-00100, Nairobi, Kenya.

Arshad Mather (A)

Agricultural Research Council - Onderstepoort Veterinary Research, Private Bag X5, Onderstepoort, Pretoria, 0110, South Africa.

Jose Perez-Casal (J)

Vaccine and Infectious Disease Organization-International Vaccine Centre (VIDO-InterVac), University of Saskatchewan, 120 Veterinary Rd, Saskatoon, SK, S7N 5E3, Canada.

Andrew Potter (A)

Vaccine and Infectious Disease Organization-International Vaccine Centre (VIDO-InterVac), University of Saskatchewan, 120 Veterinary Rd, Saskatoon, SK, S7N 5E3, Canada.

Volker Gerdts (V)

Vaccine and Infectious Disease Organization-International Vaccine Centre (VIDO-InterVac), University of Saskatchewan, 120 Veterinary Rd, Saskatoon, SK, S7N 5E3, Canada.

Emil M Berberov (EM)

Vaccine and Infectious Disease Organization-International Vaccine Centre (VIDO-InterVac), University of Saskatchewan, 120 Veterinary Rd, Saskatoon, SK, S7N 5E3, Canada.

Tracy Prysliak (T)

Vaccine and Infectious Disease Organization-International Vaccine Centre (VIDO-InterVac), University of Saskatchewan, 120 Veterinary Rd, Saskatoon, SK, S7N 5E3, Canada.

Martina Kyallo (M)

Biosciences eastern and central Africa-International Livestock Research Institute, Old Naivasha Road, P.O. Box 30709-00100, Nairobi, Kenya.

Alexander Kipronoh (A)

Kenya Agricultural and Livestock Research Organization, Veterinary Science Research Institute, P.O. Box 32-00902, Kikuyu, Kenya.

Moses Olum (M)

Kenya Agricultural and Livestock Research Organization, Veterinary Science Research Institute, P.O. Box 32-00902, Kikuyu, Kenya.

Roger Pelle (R)

Biosciences eastern and central Africa-International Livestock Research Institute, Old Naivasha Road, P.O. Box 30709-00100, Nairobi, Kenya.

Jan Naessens (J)

Biosciences eastern and central Africa-International Livestock Research Institute, Old Naivasha Road, P.O. Box 30709-00100, Nairobi, Kenya.

Articles similaires

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male
Humans Meals Time Factors Female Adult

Classifications MeSH