Evidence map›Paper›PMID 42436381›Full record

ArticleBMC genomic data2026

Genomic characterization of Mycoplasma bovis, Mannheimia haemolytica, and bovine viral diarrhea virus 1 from a bovine respiratory disease complex case.

Daniel W Nielsen, David J Holthausen, Anna K Goldkamp, Darrell O Bayles, Beate M Crossley, Harish Menghwar, Eduardo Casas, Rohana P Dassanayake

Abstract read
In one paragraph

Article in BMC genomic data, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Daniel W Nielsen *Ruminant Diseases and Immunology Research Unit, National Animal Disease Center, USDA, Agricultural Research Service, Ames, IA 50010, USA. daniel.nielsen@usda.gov.
David J Holthausen *Ruminant Diseases and Immunology Research Unit, National Animal Disease Center, USDA, Agricultural Research Service, Ames, IA 50010, USA. david.holthausen@usda.gov.ORCID https://orcid.org/0009-0006-2772-9485
Anna K GoldkampRuminant Diseases and Immunology Research Unit, National Animal Disease Center, USDA, Agricultural Research Service, Ames, IA 50010, USA.
Darrell O BaylesInfectious Bacterial Diseases Research Unit, National Animal Disease Center, USDA, Agricultural Research Service, Ames, IA 50010, USA.
Beate M CrossleyCalifornia Animal Health and Food Safety Laboratory, Medicine & Epidemiology, University of California, Davis, Davis, CA, 95616, USA.
Harish MenghwarRuminant Diseases and Immunology Research Unit, National Animal Disease Center, USDA, Agricultural Research Service, Ames, IA 50010, USA.
Eduardo CasasRuminant Diseases and Immunology Research Unit, National Animal Disease Center, USDA, Agricultural Research Service, Ames, IA 50010, USA.
Rohana P DassanayakeRuminant Diseases and Immunology Research Unit, National Animal Disease Center, USDA, Agricultural Research Service, Ames, IA 50010, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBovine respiratory disease (BRD) complex is a result of the interactions among pathogens, environmental factors, host factors, and management practices. Bacterial pathogens that contribute to BRD include Mycoplasma (Mycoplasmopsis) bovis, Mannheimia haemolytica, Pasteurella multocida, and Histophilus somni. Viral agents that contribute to BRD include bovine herpesvirus 1, bovine viral diarrhea virus (BVDV), bovine respiratory syncytial virus, parainfluenza-3 virus, bovine coronavirus, and influenza D virus.

resultsA case of BRD was submitted to the California Animal Health and Food Safety Laboratory for diagnostic evaluation. Bacterial and viral pathogens were isolated from a pneumonic lung sample including M. bovis, M. haemolytica, and BVDV. The DNAs/RNA of the pathogens were extracted, sequenced, analyzed, and compared to publicly available sequencing data. The genome of M. bovis was identified as a unique sequence type (ST299) with two novel alleles (gltX 28 and gpsA 32) and contained unique variable surface lipoproteins. However, the M. bovis genome also phylogenetically clustered with the M. bovis type strain PG45. The genome of M. haemolytica was similar to other publicly available M. haemolytica genomes, as it was assigned to sequence type 1 (ST1) and serotype 1. Finally, the genome of the isolated BVDV strain showed high similarity to the Singer (BVDV-1a) vaccine strain.

conclusionAs BRD is a complex, case studies in which the pathogens co-occur in the lung are important to report. Here, we report the complete genomes of three pathogens isolated from a single pneumonic lung sample. Notably, the M. bovis genome represents a unique sequence type. Future work should investigate the influence of the nine amino acid changes between the UCD-16 BVDV isolate and the Singer strain on disease pathogenesis.

Indexed as

Bovine Respiratory Disease ComplexDiarrhea Virus 1, Bovine ViralGenome, BacterialMannheimia haemolyticaMycoplasma bovisAnimalsCattlePhylogenyBovine respiratory disease (BRD)Bovine viral diarrhea virus (BVDV)Mannheimia haemolyticaMycoplasma bovis

Identifiers

PMID42436381
PMCPMC13644054

What Socratic holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.