A core genome multilocus sequence typing (cgMLST) analysis of Mycoplasma bovis isolates.


Journal

Veterinary microbiology
ISSN: 1873-2542
Titre abrégé: Vet Microbiol
Pays: Netherlands
ID NLM: 7705469

Informations de publication

Date de publication:
Oct 2022
Historique:
received: 06 10 2021
revised: 02 08 2022
accepted: 03 08 2022
pubmed: 21 8 2022
medline: 14 9 2022
entrez: 20 8 2022
Statut: ppublish

Résumé

Mycoplasma bovis (M. bovis) is an emerging major bovine pathogen, causing economic losses worldwide in the dairy and beef industry. Whole-genome sequencing (WGS) now allows high resolution for tracing clonal populations. Based on WGS, we developed the core genome multilocus sequence typing (cgMLST) scheme and applied it onto 151 genomes of clonal and non-clonal strains of M. bovis isolated from China, Australia, Israel, Denmark, Canada, and the USA. We used the complete genome of M. bovis PG45 as the reference genome. The pairwise genome comparison of these 151 genome sequences resulted in 478 cgMLST gene targets present in > 99.0 % clonal and non-clonal isolates with 100 % overlap and > 90 % sequence similarity. A total of 478 core genes were retained as cgMLST target genes of which an average of 90.4-99 % were present in 151 M. bovis genomes, while M. agalactiae (PG2) had 17.0 % and M. mycoides subsp. capri (PG3), M. ovipneumoniae (Y98), and M. arginine resulted in 0.0 % of good targets. When tested against the clonal and non-clonal strains, we found cgMLST clusters were congruent with the MLST-defined clonal groups, which had various degrees of diversity at the whole-genome level. Notably, cgMLST could distinguish between clonal and epidemiologically unrelated strains of the same clonal group, which could not be achieved using traditional MLST schemes. Our results showed that ninety-two M. bovis genomes from clonal group isolates had > 10 allele differences and unambiguously differentiated from unrelated outgroup strains. Additionally, cgMLST revealed that there might be several sub-clones of the emerging ST-52 clone. The cgMLST phylogenetic analysis results showed substantial agreement with geographical and temporal information. cgMLST enables the use of next-generation sequencing technology to bovine mycoplasma epidemiology at both the local and global levels. In conclusion, the novel cgMLST scheme not only showed discrimination resolution highly as compared with MLST and SNP cgMLST in sub-typing but also indicated the capability to reveal more population structure characteristics than MLST.

Identifiants

pubmed: 35987183
pii: S0378-1135(22)00202-4
doi: 10.1016/j.vetmic.2022.109532
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

109532

Informations de copyright

Copyright © 2022 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of interest statement The authors declare that they have no competing interests.

Auteurs

Harish Menghwar (H)

Vaccine and Infectious Disease Organization (VIDO) University of Saskatchewan, 120 Veterinary Rd, Saskatoon, SK S7N 5E3, Canada. Electronic address: ham776@usask.ca.

Aizhen Guo (A)

The State Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan 430070, China; College of Veterinary Medicine, Huazhong Agricultural University, Wuhan 430070, China; Hubei International Scientific and Technological Cooperation Base of Veterinary Epidemiology, Huazhong Agricultural University, Wuhan 430070, China. Electronic address: aizhen@mail.hzau.edu.cn.

Yingyu Chen (Y)

The State Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan 430070, China; College of Veterinary Medicine, Huazhong Agricultural University, Wuhan 430070, China.

Inna Lysnyansky (I)

Mycoplasma Unit, Division of Avian Diseases, Kimron Veterinary Institute, POB 12, 50250 Beit Dagan, Israel.

Alysia M Parker (AM)

The University of Sydney, Sydney School of Veterinary Science, Camden, New South Wales 2570, Australia.

Tracy Prysliak (T)

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

Jose Perez-Casal (J)

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

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Classifications MeSH