Early detection of intramammary infection (IMI) can improve animal health and welfare in dairy herds. The implementation of sensors and automatic milking systems (AMS) in dairy production inherently increases the amount of available data and hence also the potential for new approaches to mastitis management. To utilize the full potential of data from AMS and auxiliary sensors, a better understanding of physiological and pathological changes in milking traits associated with different udder pathogens may be imperative. This observational study aimed to investigate pathogen-specific patterns in milking traits recorded in AMS. The milking traits included; online somatic cell count (OCC), electrical conductivity (EC), milk yield (MY), and average milk flow rate (AMF). Data were collected for a study period of 2 years and included 101 492 milkings from 237 lactations in 169 cows from one farm. Measurements of OCC were recorded at cow-level and data on EC, MY, and AMF were obtained at quarter-level. In addition to the data obtained from the AMS, altogether 5756 quarter milk samples (QMS) were collected. Milk samples were obtained monthly for bacteriological culturing. We included findings of 13 known mastitis pathogens to study pathogen-specific patterns in milking traits. These patterns were compared with those in a baseline group consisting of cows that did not have any positive milk culture results throughout the lactation period. Patterns of the milking traits are described for all positive samples both across 305 d in milk (DIM), and in the 15-d period before a positive bacteriological sample. The association between a positive sample and the milking traits (ln(OCC), EC-IQR; the ratio between the quarter with the highest and the quarter with the lowest level of EC, and MY) for the 15 d before the detection of a pathogen was assessed using mixed effects linear regression models. All pathogens were associated with alterations in the level and variability of ln(OCC) relative to lactations with no positive bacteriological samples. A positive sample for Staph. aureus was associated with increased values for MY during the 15 d before a positive diagnosis. It is biologically plausible to interpret changes in OCC and EC-IQR as consequences of an intramammary infection (IMI), while higher MY in bacteriologically-positive cows is most likely linked to the increased risk of infection in high-yielding cows. In this study, the most notable changes in the traits (OCC and EC-IQR) were observed for Staph. aureus and Strep. dysgalactiae, followed by Strep. simulans, Strep. uberis, and Lactococcus lactis. Even if we did not detect significant associations between positive bacteriology and EC-IQR, visual assessment and descriptive statistics indicated that there might be differences suggesting that it could be an informative trait for detecting infection when combined with OCC and possibly other relevant traits using machine learning algorithms.

The current study aimed to investigate new udder health traits based on data from automatic milking systems (AMS) for use in routine genetic evaluations. Data were from 77 commercial herds; out of these, 24 had equipment for measuring online cell count (OCC), whereas all had data on electrical conductivity (EC). A total of 4,714 Norwegian Red dairy cows and 2,363,928 milkings were included in the genetic analyses. Electrical conductivity was available on quarter level for each milking, whereas OCC was measured per milking. The AMS traits analyzed were log-transformed online cell count (lnOCC), maximum conductivity (ECmax), mean conductivity (ECmean), elevated mastitis risk (EMR), and log-transformed EMR (lnEMR). In addition, lactation mean somatic cell score (LSCS) was collected from the Norwegian dairy herd recording system. Elevated mastitis risk expresses the probability of a cow having mastitis and was calculated from smoothed lnOCC values according to individual trend and level of the OCC curve. The udder health traits from AMS were analyzed as repeated milkings from 30 to 320 DIM, and LSCS as repeated parities. In addition, both ECmax and lnOCC were analyzed as multiple traits by splitting the lactation into 5 periods. (Co)variance components were estimated from bivariate mixed linear animal models, and investigated traits showed genetic variation. Estimated heritabilities of ECmean, ECmax, and lnEMR were 0.35, 0.23, and 0.12, respectively, whereas EMR and lnOCC both showed heritabilities of 0.09. Heritability varied between periods of lactation, from 0.04 to 0.13 for lnOCC and from 0.12 to 0.27 for ECmax, although standard errors of certain periods were large. Genetic correlations among the AMS traits ranged from 0 to 0.99. The genetic correlations between EC-based traits and OCC-based traits in AMS were 0. Genetic correlations with LSCS were favorable, ranging from 0.37 to 0.80 (±0.11-0.22). The strongest correlation (0.80 ± 0.13) was found between LSCS and lnEMR. Results question the value of ECmax and ECmean as indicators of udder health in genetic evaluations and suggest OCC to be more valuable in this manner. This study demonstrates a potential of using AMS data as additional information on udder health for genetic evaluations, although further investigation is recommended before these traits can be implemented.

Management of udder health is particularly focused on preventing new infections. Data from the DeLaval Online Cell Counter (DeLaval, Tumba, Sweden) may be used in forecasting to improve decision support for improved udder health management. It provides online cell counts (OCC) as a proxy for somatic cell counts from every milking at the cow level. However, these values are typically too insensitive and nonspecific to indicate subclinical intramammary infection (IMI). Our aim was to describe and evaluate use of dynamic transmission models to forecast subclinical IMI episodes using milk cultures or changes in OCC patterns over time. The latter was expressed by an elevated mastitis risk variable. Data were obtained from the dairy herd of the Norwegian University of Life Sciences (Oslo, Norway). In total, 173 cows were sampled monthly for bacteriological milk culture during a 17-mo study period and 5,330 quarter milk samples were cultured. Mastitis pathogens identified were assigned to 1 of 2 groups, Pat 1 or Pat 2. Pathogens from which a high cell count would be expected during a subclinical IMI episode were assigned to the Pat 1 group. Pathogens not in the Pat 1 group were assigned to the Pat 2 group. Staphylococcus epidermidis, Staphylococcus aureus, and Streptococcus dysgalactiae were the most common Pat 1 pathogens. Corynebacterium bovis, Staphylococcus chromogenes, and Staphylococcus haemolyticus were the most common Pat 2 pathogens. The OCC were successfully recorded from 82,182 of 96,542 milkings. The current study included 324 subclinical IMI episodes. None of the mastitis pathogens demonstrated a basic reproduction number (R0) >1. Patterns of OCC change related to an episode of Pat 1 subclinical IMI at specificity levels of 80, 90, and 95% at sensitivity levels of 69, 59, and 48% respectively, demonstrated an R0 >1. An existing infection was significant for transmission for several Pat 2 pathogens, but only for Staphylococcus aureus and Staphylococcus epidermidis among Pat 1 pathogens. Dynamic transmission models showed that patterns of OCC change related to an episode of Pat 1 subclinical IMI were significantly related to the same pattern occurring in susceptible cows at specificity levels of 80, 90, and 99% at sensitivity levels of 69, 48, and 8%, respectively. We conclude that changes in herd prevalence of subclinical IMI can be predicted using dynamic transmission models based on patterns of OCC change. Choice of specificity level depends on management goals and tolerance for false-positive alerts.

Timely and accurate identification of cows with intramammary infections is essential for optimal udder health management. Various sensor systems have been developed to provide udder health information that can be used as a decision support tool for the farmer. Among these sensors, the DeLaval Online Cell Counter (DeLaval, Tumba, Sweden) provides somatic cell counts from every milking at cow level. Our aim was to describe and evaluate diagnostic sensor properties of these online cell counts (OCC) for detecting an intramammary infection, defined as an episode of subclinical mastitis or a new case of clinical mastitis. The predictive abilities of a single OCC value, rolling averages of OCC values, and an elevated mastitis risk (EMR) variable were compared for their accuracy in identifying cows with episodes of subclinical mastitis or new cases of clinical mastitis. Detection of subclinical mastitis episodes by OCC was performed in 2 separate groups of different mastitis pathogens, Pat 1 and Pat 2, categorized by their known ability to increase somatic cell count. The data for this study were obtained in a field trial conducted in the dairy herd of the Norwegian University of Life Sciences. Altogether, 173 cows were sampled at least once during a 17-mo study period. The total number of quarter milk cultures was 5,330. The most common Pat 1 pathogens were Staphylococcus epidermidis, Staphylococcus aureus, and Streptococcus dysgalactiae. The most common Pat 2 pathogens were Corynebacterium bovis, Staphylococcus chromogenes, and Staphylococcus haemolyticus. The OCC were successfully recorded from 82,182 of 96,542 milkings during the study period. For episodes of subclinical mastitis the rolling 7-d average OCC and the EMR approach performed better than a single OCC value for detection of Pat 1 subclinical mastitis episodes. The EMR approach outperformed the OCC approaches for detection of Pat 2 subclinical mastitis episodes. For the 2 pathogen groups, the sensitivity of detection of subclinical mastitis episodes was 69% (Pat 1) and 31% (Pat 2), respectively, at a predefined specificity of 80% (EMR). All 3 approaches were equally good at detecting new cases of clinical mastitis, with an optimum sensitivity of 80% and specificity of 90% (single OCC value).