Deletion of Two Genes in Burkholderia pseudomallei MSHR668 That Target Essential Amino Acids Protect Acutely Infected BALB/c Mice and Promote Long Term Survival

Melioidosis is an emerging disease that is caused by the facultative intracellular pathogen . It is intrinsically resistant to many antibiotics and host risk factors play a major role in susceptibility to infection. Currently, there is no human or animal vaccine against melioidosis. In this study, m...

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Published in:Vaccines (Basel) 2019-11, Vol.7 (4), p.196
Main Authors: Amemiya, Kei, Dankmeyer, Jennifer L, Biryukov, Sergei S, Treviño, Sylvia R, Klimko, Christopher P, Mou, Sherry M, Fetterer, David P, Garnes, Preston G, Cote, Christopher K, Worsham, Patricia L, DeShazer, David
Format: Article
Language:English
Subjects:
Amino acids
Animal vaccines
Antibiotics
Antigens
Burkholderia pseudomallei
Chronic infection
Deletion
Deletion mutant
Diabetes
E coli
Immune response (cell-mediated)
Infections
Lethal dose
Melioidosis
Mortality
Pathogens
Plasmids
Pneumonia
Proteins
Risk analysis
Risk factors
Splenocytes
Survival
Vaccines
Virulence
γ-Interferon
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Summary:Melioidosis is an emerging disease that is caused by the facultative intracellular pathogen . It is intrinsically resistant to many antibiotics and host risk factors play a major role in susceptibility to infection. Currently, there is no human or animal vaccine against melioidosis. In this study, multiple MSHR668 deletion mutants were evaluated as live attenuated vaccines in the sensitive BALB/c mouse model of melioidosis. The most efficacious vaccines after an intraperitoneal challenge with 50-fold over the 50% median lethal dose (MLD ) with K96243 were 668 Δ and 668 Δ . Both vaccines completely protected mice in the acute phase of infection and showed significant protection (50% survivors) during the chronic phase of infection. The spleens of the survivors that were examined were sterile. Splenocytes from mice vaccinated with 668 Δ and 668 Δ expressed higher amounts of IFN-γ after stimulation with antigens than splenocytes from mice vaccinated with less protective candidates. Finally, we demonstrate that 668 Δ is nonlethal in immunocompromised NOD/SCID mice. Our results show that 668 Δ and 668 Δ provide protective cell-mediated immune responses in the acute phase of infection and promote long term survival in the sensitive BALB/c mouse model of melioidosis.
ISSN:2076-393X
2076-393X
DOI:10.3390/vaccines7040196