Smooth and transparent
hydrophilic films showing excellent water
sliding properties were prepared by using a sol–gel solution
of 2-[methoxy (ethyleneoxy)10 propyl]trimethoxysilane and
tetraethoxysilane. The resulting hybrid films were statically hydrophilic
(static water contact angles (CAs) were in the range of 30–45°),
but water droplets (50 μL) could move smoothly on an inclined
surface (minimum sliding angle was 6°) without pinning or tailing
because of low CA hysteresis (5 ± 1°). Thanks to this hybrid
film formation on aluminum (Al) substrate, drainage performance during
condensation and frosting/defrosting markedly improved compared to
that on hydrophilic, bare Al, or hydrophobic monolayer-covered Al
substrates.
The immune response during the onset of coliform mastitis in vaccinated cows was investigated by measuring lactoferrin (LF), interleukin‐8 (IL‐8), and interleukin‐1β (IL‐1β) concentrations and somatic cell counts in 28 milk samples at the onset of acute coliform mastitis (ACM) and 73 milk samples at the onset of peracute coliform mastitis (PCM). Vaccinated ACM, unvaccinated ACM, and vaccinated PCM showed significantly higher values for LF and IL‐1β levels than unvaccinated PCM (p < .01). The IL‐8 concentration was lower in vaccinated PCM than in unvaccinated PCM (p < .05). There was no significant difference in somatic cell counts for each parameter. There were no significant differences in the parameters between vaccinated and unvaccinated ACM cows, or vaccinated ACM and PCM cows. From the above results, it is suggested that mastitis vaccination improved the early immune response, particularly at the onset of PCM, and played a large role in host defense against the initial infection.
The aim of this study was to evaluate the microbiota of normal milk in dairy cows and their relationship with host factors, such as the age of the cow (Age), somatic cell counts in milk (SCCs), and days in milk (DIM). We investigated 48 milk samples from 22 cows with no systemic or local clinical signs using MinION TM nanopore sequencing for a 16S rRNA gene amplicon. Bacterial richness was positively correlated with the DIM (p = 0.043), and both the Shannon-Wiener Index and Simpson's Index, which are metrics of alpha-diversity, were also significantly positively correlated with the SCC (p < 0.001). The composition ratios of both Actinobacteria at the phylum level and Kocuria spp. at the genus level in the milk microbiota were significantly correlated with the SCC (p < 0.001 and p < 0.001, respectively). In the beta-diversity test, the one-way analysis of similarities test showed a significant difference (p = 0.0051) between the low-and high-SCC groups. This study clarified that the composition of the normal milk microbiota in this herd was related to the SCC. It also raised the possibility of variations in bacterial genera in the normal milk microbiota between the low-and high-SCC groups.However, to clarify the actual condition of the milk microbiota and to elucidate the relationship with the SCC, it is necessary to perform further analyses taking into account not only the relative abundance, but also the absolute abundance of microbes.
Milk production loss after recovery from acute coliform mastitis causes major economic
losses for dairy industries. Declines in milk production and composition are caused by
multiple factors, including cow factors, microorganisms and treatments, but the influence
of each factor has not been determined. To investigate risk factors for milk loss after
treatment for acute coliform mastitis, multiple logistic regression analyses were
conducted in 53 clinical cases. Systemic administration of fluoroquinolone was
significantly associated with recovery of marketable milk production. The time to
slaughter was significantly shorter in cows with complete loss of quarter milk production
than in cows that produced marketable milk. In this study, we identified factors
associated with increased risk of milk production loss.
This study aimed to determine whether causative pathogens in mastitic milk can be determined by Gram staining after the centrifugation of milk. Gram staining was performed using unconcentrated and concentrated milk cells. Using this method, we found that the background of microscopic image of unconcentrated milk cells was complex and bacteria were difficult to detect. In contrast, the background of the smears in the concentrated milk cells was translucent, and bacterial and somatic cells were clearly visible. The sensitivity and specificity of the Gram staining of concentrated milk cells were 84.4% and 86.0% and 50.0% and 94.5% for the detection of gram-positive and gram-negative bacteria, respectively. The presented method provides a simple and inexpensive means of determining mastitis-causing pathogens.
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