Chemokine-Releasing Microparticles Improve Bacterial Clearance and Survival of Anthrax Spore-Challenged Mice

• Published in: PloS one 2016-09, Vol.11 (9), p.e0163163-e0163163
• Main Authors: Popova, Taissia G, Teunis, Allison, Espina, Virginia, Liotta, Lance A, Popov, Serguei G
• Format: Article
• Language: English
• Subjects: Analysis; Animal experimentation; Animals; Anthrax; Bacillus anthracis; Bacillus anthracis - physiology; Bacteria; Bacterial infections; Biology; Biology and Life Sciences; CCL3 protein; Chemokine CCL3 - administration & dosage; Chemokines; Cytokines; Drug Carriers; Female; Formulations; Granulocytes; Health aspects; Hydrogels; Infections; Infectious diseases; Inflammation; Inflammatory response; Inoculation; Interleukin-8 - administration & dosage; Leukocyte migration; Leukocytes (neutrophilic); Listeria; Listeria monocytogenes; Lymph nodes; Medicine and Health Sciences; Mice; Mice, Inbred DBA; Microparticles; Neutrophils; Political aspects; Polyacrylamide; Proteomics; Releasing; Research and Analysis Methods; Spores; Spores, Bacterial; Survival; Toxoplasma gondii
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0163163

In this study the hydrogel microparticles (MPs) were used to enhance migration of neutrophils in order to improve outcome of anthrax infection in a mouse model. Two MP formulations were tested. In the first one the polyacrylamide gel MPs were chemically coupled with Cibacron Blue (CB) affinity bait. In the second one the bait molecules within the MPs were additionally loaded with neutrophil-attracting chemokines (CKs), human CXCL8 and mouse CCL3. A non-covalent interaction of the bait with the CKs provided their gradual release after administration of the MPs to the host. Mice were challenged into footpads with Bacillus anthracis Sterne spores and given a dose of MPs a few hours before and/or after the spores. Pre-treatment with a single dose of CK-releasing MPs without any additional intervention was able to induce influx of neutrophils to the site of spore inoculation and regional lymph nodes correlating with reduced bacterial burden and decreased inflammatory response in footpads. On average, in two independent experiments, up to 53% of mice survived over 13 days. All control spore-challenged but MP-untreated mice died. The CB-coupled particles were also found to improve survival likely due to the capacity to stimulate release of endogenous CKs, but were less potent at decreasing the inflammatory host response than the CK-releasing MPs. The CK post-treatment did not improve survival compared to the untreated mice which died within 4 to 6 days with a strong inflammation of footpads, indicating quick dissemination of spores though the lymphatics after challenge. This is the first report on the enhanced innate host resistance to anthrax in response to CKs delivered and/or endogenously induced by the MPs.