Search Results Heading

MBRLSearchResults

mbrl.module.common.modules.added.book.to.shelf
Title added to your shelf!
View what I already have on My Shelf.
Oops! Something went wrong.
Oops! Something went wrong.
While trying to add the title to your shelf something went wrong :( Kindly try again later!
Are you sure you want to remove the book from the shelf?
Oops! Something went wrong.
Oops! Something went wrong.
While trying to remove the title from your shelf something went wrong :( Kindly try again later!
    Done
    Filters
    Reset
  • Discipline
      Discipline
      Clear All
      Discipline
  • Is Peer Reviewed
      Is Peer Reviewed
      Clear All
      Is Peer Reviewed
  • Item Type
      Item Type
      Clear All
      Item Type
  • Subject
      Subject
      Clear All
      Subject
  • Year
      Year
      Clear All
      From:
      -
      To:
  • More Filters
3 result(s) for "Haigh, Brendan J"
Sort by:
Feeding bovine milks with low or high IgA levels is associated with altered re-establishment of murine intestinal microbiota after antibiotic treatment
Antibiotics are a vital and commonly used therapeutic tool, but their use also results in profound changes in the intestinal microbiota that can, in turn, have significant health consequences. Understanding how the microbiota recovers after antibiotic treatment will help to devise strategies for mitigating the adverse effects of antibiotics. Using a mouse model, we have characterized the changes occurring in the intestinal microbiota immediately after five days exposure to ampicillin, and then at three and fourteen days thereafter. During the fourteen day period of antibiotic recovery, groups of mice were fed either water, cows’ milk containing high levels of IgA, or cows’ milk containing low levels of IgA as their sole source of liquid. Effects on microbiota of feeding milks for 14 days were also assessed in groups of mice that had no ampicillin exposure. Changes in microbiota were measured by high throughput sequencing of the V4 to V6 variable regions of the 16S ribosomal RNA gene. As expected, exposure to ampicillin led to profound changes to the types and abundance of bacteria present, along with a loss of diversity. At 14 days following antibiotic exposure, mice fed water had recovered microbiota compositions similar to that prior to antibiotics. However, feeding High-IgA milk to mice that has been exposed to antibiotics was associated with altered microbiota compositions, including increased relative abundance of Lactobacillus and Barnesiella compared to the start of the study. Mice exposed to antibiotics then fed Low-IgA milk also showed increased Barnesiella at day 14. Mice without antibiotic perturbation, showed no change in their microbiota after 14 days of milk feeding. Overall, these findings add to a knowledge platform for optimizing intestinal function after treatment with antibiotics in the human population.
Host defence related responses in bovine milk during an experimentally induced Streptococcus uberis infection
Background Milk contains a range of proteins of moderate or low abundance that contribute to host defence. Characterisation of these proteins, the extent to which their abundance is regulated by pathogenic stimuli, and the variability of their response between and within individual animals would facilitate a better understanding of the molecular basis for this important function of milk. Results We have characterised the host defence proteins in bovine milk and their responses to intra-mammary infection by a common Gram positive mastitis pathogen, Streptococcus uberis , using a combination of 2D gel electrophoresis and GeLC mass spectrometry. In total, 68 host defence-associated proteins were identified, 18 of which have a direct antimicrobial function, 23 of which have a pathogen-recognition function, and 27 of which have a role in modulating inflammatory or immune signalling. The responsiveness of seven proteins was quantified by western blotting; validating the proteomic analyses, quantifying the within- and between animal variability of the responses, and demonstrating the complexity and specificity of the responses to this pathogen. Conclusions These data provide a foundation for understanding the role of milk in host-microbe interaction. Furthermore they provide candidate biomarkers for mastitis diagnosis, and will inform efforts to develop dairy products with improved health-promoting properties.
Community Health Navigator assisted transition of care from hospital to community: A randomised control trial
Background: Internationally, the roles of Community Health Workers, also known as Community Health Navigators (CHNs), have been developed as an intervention to improve the transition of people to their homes following a hospital admission. Generally, CHNs are trusted members of the communities they serve. This trusting relationship enables them to serve as a link between health services, social services and the community to facilitate access and improve the quality and cultural competence of service delivery. Research has found that CHNs can reduce barriers to access for marginalised communities, identify emerging needs, and can make health services more responsive. The CHN’s are employed by the Sydney Local Health District and are embedded within the Planned Care team under the governance of the Aged Health Rehabilitation and Chronic Care Clinical Stream. This trial aims to evaluate the impact of CHNs who support people with chronic conditions to transition from hospital to their homes. The CHNs are employed by a Local Health District and embedded within the health service. The trial, which is currently underway, will evaluate the impact of a CHN intervention’s on 60-day unplanned hospital readmission, medication adherence, health literacy, quality of life, experience of health care and health service use, compared to usual care. Implementation of the navigator role will also be qualitatively appraised, incorporating data from patients, health professionals and the navigators themselves. Trial population: Patients aged over 40 years and living with chronic health conditions in a Local Health District in Sydney, Australia.   Engagement: This trial is underpinned and guided by a multi-stakeholder partnership of health planners, primary healthcare providers, and consumers. These stakeholders have joined in co-designing this study to evaluate the effectiveness and cost of CHN follow-up of patients after discharge as a key strategy in preventing re-hospitalisation, and to develop the CHN roles and functions. What we are doing: This parallel group, pragmatic RCT design will randomly allocate patients after hospital discharge to the CHN intervention or usual care arm. Comparison of outcomes will be made between intervention and control groups. Results: This RCT is currently underway. Interviews with 27 health staff and a co-design process with 18 participants have informed the development of the CHN roles and the implementation of the trial. Codesign participants were generally enthusiastic about the potential of the CHNs, but there were concerns about how these roles could fit within existing services and supervision arrangements, and the CHNs’ competence to fulfil their roles. A detailed CHN training program was developed with emphases on communication, rapport-building, services that can be referred to, and supervision arrangements. Three CHNs are currently employed. Lessons: This study includes an intervention embedded in a real-world healthcare setting. The co-design process enabled the CHN roles to be well-described and to have the potential to meet the needs of the study population and to be responsive to service stakeholders. The CHN are integrated into existing health service structures and processes, and are embedded in an established outreach team. Next steps: Reporting on study.