Sarah V Harding

Dr. Sarah V Harding


Research Focus & Metrics

Academic Career Length

20Years (2007-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
1 March 2007 in Vaccine
Verified
Journal Article
Closed access
SHSarah V Harding
Sarah V Harding
MSMitali Sarkar-Tyson
Mitali Sarkar-Tyson
SSSophie J. Smither
Sophie J. Smither
TATimothy P. Atkins
Timothy P. Atkins
POPetra C.F. Oyston
Petra C.F. Oyston
RTRichard W. Titball
Richard W. Titball

3 March 2023 in Antibiotics
Verified
Journal Article
Open access
PDF file
MNMichelle Nelson
Michelle Nelson
KBKay Barnes
Kay Barnes
CDCarwyn H. Davies
Carwyn H. Davies
CCChristopher K. Cote
Christopher K. Cote
JMJ. Matthew Meinig
J. Matthew Meinig
SHSarah V Harding
Sarah V Harding
Burkholderia pseudomallei, the causative agent of the disease melioidosis, has been isolated from the environment in 45 countries. The treatment of melioidosis is complex, requiring lengthy antibiotic regimens, which can result in the relapse of the disease following treatment cessation. It is important that novel therapies to treat infections with B. pseudomallei be assessed in appropriate animal models, and discussions regarding the different protocols used between laboratories are critical. A ‘deep dive’ was held in October 2020 focusing on the use of the BALB/c mouse model and the inhalational route of infection to evaluate new antibiotic therapies.

6 February 2017 in Frontiers in Microbiology
Verified
Journal Article
Open access
KHKarleigh Hamblin
Karleigh Hamblin
SAStuart Jon Armstrong
Stuart Jon Armstrong
KBKay Barnes
Kay Barnes
CDCarwyn Davies
Carwyn Davies
TLThomas Laws
Thomas Laws
HAHelen S. Atkins
Helen S. Atkins
Inhalation of Yersinia pestis can lead to pneumonic plague, which without treatment is inevitably fatal. Two novel formulations of liposome-encapsulated ciprofloxacin, ‘ciprofloxacin for inhalation’ (CFI, Lipoquin®) and ‘dual release ciprofloxacin for inhalation’ (DRCFI, Pulmaquin®) containing CFI and ciprofloxacin solution, are in development. These were evaluated as potential therapies for infection with Y. pestis. In a murine model of pneumonic plague, human-like doses of aerosolized CFI, aerosolized DRCFI or intraperitoneal (i.p.) ciprofloxacin were administered at 24 hours (representing prophylaxis) or 42 hours (representing treatment) post-challenge. All three therapies provided a high level of protection when administered 24 hours post-challenge. A single dose of CFI, but not DRCFI, significantly improved survival compared to a single dose of ciprofloxacin. Furthermore, single doses of CFI and DRCFI reduced bacterial burden in lungs and spleens to below the detectable limit at 60 hours post-challenge. When therapy was delayed until 42 hours post-challenge, a single dose of CFI or DRCFI offered minimal protection. However, single doses of CFI or DRCFI were able to significantly reduce the bacterial burden in the spleen compared to empty liposomes. A three-day treatment regimen of ciprofloxacin, CFI, or DRCFI resulted in high levels of protection (90% -100% survival). This study suggests that CFI and DRCFI may be useful therapies for Y. pestis infection, both as prophylaxis and for the treatment of plague.

18 May 2021 in Antimicrobial Agents and Chemotherapy
Verified
Journal Article
Open access
PDF file
KBKay B. Barnes
Kay B. Barnes
MRMark I. Richards
Mark I. Richards
TLThomas R. Laws
Thomas R. Laws
ANAlejandro Núñez
Alejandro Núñez
JTJoanne E. Thwaite
Joanne E. Thwaite
SHSarah V Harding
Sarah V Harding
Infection with aerosolized Francisella tularensis or Yersinia pestis can lead to lethal disease in humans if treatment is not initiated promptly. Finafloxacin is a novel fluoroquinolone which has demonstrated broad-spectrum activity against a range of bacterial species in vitro, in vivo , and in humans, activity which is superior in acidic, infection-relevant conditions.

1 December 2019 in Antimicrobial Agents and Chemotherapy
Verified
Journal Article
Open access
PDF file
KBKay B. Barnes
Kay B. Barnes
SZSteven D. Zumbrun
Steven D. Zumbrun
SHStephanie A. Halasohoris
Stephanie A. Halasohoris
PDPurvi D. Desai
Purvi D. Desai
LMLynda L. Miller
Lynda L. Miller
SHSarah V Harding
Sarah V Harding
This study investigated the in vitro activity of finafloxacin against bacterial strain panels of the biodefense pathogens. Broth microdilution assays were performed at neutral and acidic pH to determine the effectiveness of the antibiotics under conditions typical of an intracellular environment. In all instances, finafloxacin demonstrated superior activity at low pH.

12 March 2024 in Infection and Immunity
Verified
Journal Article
Open access
KBKay Barnes
Kay Barnes
PBPaul Brett
Paul Brett
MBMary Burtnick
Mary Burtnick
AVAndreas Vente
Andreas Vente
CBChristine Bentley
Christine Bentley
SHSarah V Harding
Sarah V Harding
Melioidosis is a disease that is difficult to treat due to the causative organism, Burkholderia pseudomallei being inherently antibiotic resistant and it having the ability to invade, survive, and replicate in an intracellular environment. Combination therapy approaches are routinely being evaluated in animal models with the aim of improving the level of protection and clearance of colonizing bacteria detected. In this study, a subunit vaccine layered with the antibiotic finafloxacin was evaluated in vivo against an inhalational infection with B. pseudomallei in Balb/c mice. Groups of mice vaccinated, infected, and euthanized at antibiotic initiation had a reduced bacterial load compared to those that had not been immunized. In addition, the subunit vaccine provided a synergistic effect when it was delivered with a CpG ODN and finafloxacin was initiated at 48 h post-challenge. Vaccination was also shown to improve the outcome, in a composite measure of survival and clearance. In summary, layering a subunit vaccine with the antibiotic finafloxacin is a promising therapeutic alternative for use in the treatment of B. pseudomallei infections.