The bronchopneumonia of calves represents a risk to national supply chain because it is an ecopathy and weakens the more intensive production systems. It is characterized by inflammatory changes in the bronchi, bronchioles, lung parenchyma, and pleura. It is a disease of multifactorial traits called Bovine Respiratory Disease (BRD). The association of infectious agents with host defense and management to which the animal is subjected leads to the emergence of major clinical manifestations of the disease. The clinical evolution of BRD can also have serious secondary changes such as pulmonary edema, sepsis, and pulmonary hypertension, or even be consequent to the involvement of other structures, such as in cases of myocarditis leading to congestive heart failure. Although this report refers to a non-experimental framework, the circumstances that caused the calf to be subjected to a protocol-specific respiratory assessment involving non-routine reviews has made it possible to associate circulatory and respiratory conditions, rarely considered in ruminant clinic. The focus of this report was pulmonary edema. Modern clinical vision requires of the veterinarian work with cost-benefit relation, so that the more accurate and the earlier the clinical diagnosis the less expensive the treatment.

Histophilus somni, a causative agent of the bovine respiratory disease complex, can also cause a variety of systemic disorders, including bronchopneumonia, myocarditis, pericarditis, arthritis, pleuritis, and infectious thrombotic meningoencephalitis. The purpose of this study was to determine if currently circulating strains differ from those of the 1980s by identifying genomic changes. Single nucleotide polymorphisms (SNPs) and insertion and deletion (INDEL) sites were examined by whole-genome sequencing in 12 samples, 6 old and 6 new. The 31 028 SNP/INDELs recorded were compared against the reference genome sequence of the pathogenic H. somni strain 2336. The distribution of about 75% of these SNPs within a specified gene differed between old and new isolates and did not follow any particular pattern. The other 25% clustered into 2 groups containing the same SNPs in various genes: group I included 5 old isolates and 1 new isolate; group II included 5 new isolates and 1 old isolate. For putative virulence genes there were more SNPs in group I compared with strain 2336, itself an older isolate, than in group II. Although only 25% of all the SNPs formed 2 clusters, the results suggest some genetic difference in various genes between old and new strains.

Encephalomyocarditis virus (EMCV) can infect many host species and cause acute myocarditis and sudden death in preweaned piglets. In this study, an EMCV strain (NJ08) was isolated from newborn pigs with clinical signs on a pig farm in mideastern China. It was identified by indirect immunofluorescence assay and reverse-transcription polymerase chain reaction. Experiments showed that the isolate could cause severe clinical symptoms and pathological changes in mice but no obvious clinical and pathological changes in commercial piglets. Complete genomic sequencing showed that the NJ08 strain was 78.3% to 100% identical with other isolates in regions coding for various proteins. Phylogenetic analysis showed that the NJ08 isolate belonged to subgroup Ia. This study confirmed that an EMCV isolate from pigs could be fatal to mice and provided new epidemiologic data on EMCV in China.