The Hospital for Tropical Diseases, Wellcome Trust Major Overseas Programme, Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam
Cristina de Cozar
GSK Global Health, Tres Cantos, Madrid, Spain
David R Willé
GSK R&D, Stevenage, United Kingdom
Beatriz Urones
GSK Global Health, Tres Cantos, Madrid, Spain
Alvaro Cortés
GSK Global Health, Tres Cantos, Madrid, Spain
Alan Price
GSK Global Health, Tres Cantos, Madrid, Spain
Nhu Tran Do Hoang
The Hospital for Tropical Diseases, Wellcome Trust Major Overseas Programme, Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam
Tuyen Ha Thanh
The Hospital for Tropical Diseases, Wellcome Trust Major Overseas Programme, Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam
Molly McCloskey
Division of Allergy and Infectious Disease, Center for Emerging and Re-emerging Infectious Diseases University of Washington School of Medicine, Seattle, United States
Shareef Shaheen
Division of Allergy and Infectious Disease, Center for Emerging and Re-emerging Infectious Diseases University of Washington School of Medicine, Seattle, United States
Denise Dayao
Department of Infectious Disease and Global Health, Tufts University Cummings School of Veterinary Medicine, North Grafton, United States
Amanda Martinot
Department of Infectious Disease and Global Health, Tufts University Cummings School of Veterinary Medicine, North Grafton, United States
Jaime de Mercado
GSK Global Health, Tres Cantos, Madrid, Spain
Pablo Castañeda
GSK Global Health, Tres Cantos, Madrid, Spain
Adolfo García-Perez
GSK Global Health, Tres Cantos, Madrid, Spain
Benson Singa
Kenya Medical Research Institute, Nairobi, Kenya
Patricia Pavlinac
Department of Global Health, University of Washington, Seattle, United States
Judd Walson
Division of Allergy and Infectious Disease, Center for Emerging and Re-emerging Infectious Diseases University of Washington School of Medicine, Seattle, United States
Maria Santos Martínez-Martínez
GSK Global Health, Tres Cantos, Madrid, Spain
Samuel LM Arnold
Division of Allergy and Infectious Disease, Center for Emerging and Re-emerging Infectious Diseases University of Washington School of Medicine, Seattle, United States
Saul Tzipori
Department of Infectious Disease and Global Health, Tufts University Cummings School of Veterinary Medicine, North Grafton, United States
University of Cambridge School of Clinical Medicine, Cambridge Biomedical Campus, Cambridge, United Kingdom; Department of Medicine, University of Cambridge School of Clinical Medicine, Cambridge Biomedical Campus, Cambridge, United Kingdom
Background: Diarrhoea remains one of the leading causes of childhood mortality globally. Recent epidemiological studies conducted in low-middle income countries (LMICs) identified Shigella spp. as the first and second most predominant agent of dysentery and moderate diarrhoea, respectively. Antimicrobial therapy is often necessary for Shigella infections; however, we are reaching a crisis point with efficacious antimicrobials. The rapid emergence of resistance against existing antimicrobials in Shigella spp. poses a serious global health problem. Methods: Aiming to identify alternative antimicrobial chemicals with activity against antimicrobial resistant Shigella, we initiated a collaborative academia-industry drug discovery project, applying high-throughput phenotypic screening across broad chemical diversity and followed a lead compound through in vitro and in vivo characterisation. Results: We identified several known antimicrobial compound classes with antibacterial activity against Shigella. These compounds included the oral carbapenem Tebipenem, which was found to be highly potent against broadly susceptible Shigella and contemporary MDR variants for which we perform detailed pre-clinical testing. Additional in vitro screening demonstrated that Tebipenem had activity against a wide range of other non-Shigella enteric bacteria. Cognisant of the risk for the development of resistance against monotherapy, we identified synergistic behaviour of two different drug combinations incorporating Tebipenem. We found the orally bioavailable prodrug (Tebipenem pivoxil) had ideal pharmacokinetic properties for treating enteric pathogens and was effective in clearing the gut of infecting organisms when administered to Shigella-infected mice and gnotobiotic piglets. Conclusions: Our data highlight the emerging antimicrobial resistance crisis and shows that Tebipenem pivoxil (licenced for paediatric respiratory tract infections in Japan) should be accelerated into human trials and could be repurposed as an effective treatment for severe diarrhoea caused by MDR Shigella and other enteric pathogens in LMICs. Funding: Tres Cantos Open Lab Foundation (projects TC239 and TC246), the Bill and Melinda Gates Foundation (grant OPP1172483) and Wellcome (215515/Z/19/Z).