| Literature DB >> 35719840 |
Takashi Onodera1,2, Akikazu Sakudo3, Yoshifumi Iwamaru4, Takashi Yokoyama1, Makoto Haritani1, Katsuaki Sugiura1, Hidekatsu Shimakura5, Takeshi Haga5, Rumiko Onishi6, Koichi Furusaki7.
Abstract
Calcium bicarbonate does not act as a disinfectant at neutral pH; however, it exerts strong antimicrobial activity after it is placed in a high-voltage electric field, whereby it assumes an alkaline pH (12.4). Moreover, the microbicidal activity of the resulting solution (named CAC-717) is not influenced by the presence of organic material or resistance of the agent to inactivation. When sprayed on the skin surface, the pH of CAC-717 decreases rapidly to 8.84. CAC-717 comprises fine particles of 50-500 nm. When these mesoscopic crystals are dissolved in water, they destroy the genomes of bacteria or viruses and neutralize the infectious properties of abnormal prion proteins produced in ScN2a cells. The severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2) pandemic has resulted in unprecedented international demand for disinfectants. A small titer of SARS-CoV-2 remains infectious even after 30 sec in growth medium at pH 12.4. CAC-717 has exhibited a strong virucidal effect (3.6 to 4.4 log10 decrease) against all examined SARS-CoV-2 isolates, including mutant forms. Similarly, human noroviruses also remain intact at pH 12.4; however, CAC-717 has been shown to cause a 3.25 log10 reduction in norovirus genomic RNA compared to untreated samples. Existing evidence suggests that an unidentified mechanism controls the virucidal activity of CAC-717. Copyright: © Onodera et al.Entities:
Keywords: SARS-CoV-2; Xanthomonas campestris pv. campestris; calcium carbonate; human norovirus; mesoscopic structure; prions
Year: 2022 PMID: 35719840 PMCID: PMC9198988 DOI: 10.3892/br.2022.1540
Source DB: PubMed Journal: Biomed Rep ISSN: 2049-9434
Figure 1Scanning electron microscopy images of mesoscopic CAC-717 particles generated after high-voltage treatment of a calcium bicarbonate aqueous solution. The images were obtained using a Hitachi S-4800 electron microscope at 15 kV with a (A) magnification of x20,000 and scale bar, 2000 nm and (B) magnification of x100,000 and scale bar 500 nm.
Figure 2CAC-717 stones. A scale ruler is shown below (each small division is 1 mm).
Antimicrobial, antiviral, and prion-inhibiting effects of CAC-717.
| Pathogen titer | ||||
|---|---|---|---|---|
| Pathogen | Duration of treatment (min) | Untreated | CAC-717 | (Refs.) |
| 0.5 | 8.22 log10 CFU/ml | 5.63 log10 CFU/ml | ( | |
|
| 2 | 1.52x109±0.35x109 CFU/ml | 7.50x106±2.50x106 CFU/ml | ( |
|
| 2 | 2.14x107±0.12x107 CFU/ml | Undetectable | ( |
|
| 1 | 5.98 log10 TCID50/ml | Undetectable | ( |
|
| 2 | 7.26x105±2.70x105 TCID50/ml | <10 TCID50/ml | ( |
|
| 15 | 6.58 log10 TCID50/ml | <1.50 log10 TCID50/ml | ( |
|
| 60 | 9.95 log10 PMCA50/ml | 5.20 log10 PMCA50/ml | ( |
Detailed materials and methods are reported in each reference. CFU, colony-forming unit; PMCA, protein misfolding cyclic amplification; TCID50, tissue culture infectious dose.
Figure 3CAC-717 treatment of cabbage seeds contaminated with Xcc. Seeds were treated with distilled water or CAC-717 at 25˚C for 30 min. (A) Viable cell counts (expressed as colony-forming units) of Xcc recovered from seeds and incubated at 25˚C on yeast extract dextrose CaCO3 medium for 3 days. (B) Incidence of disease in CAC-717-treated or untreated seeds. Data are derived from triplicate samples and are representative of the mean ± standard error of the mean from two experiments. *P<0.05 (Mann-Whitney U test). Cited from Sakudo et al (14) under the terms of the Created Commons Attribution 4.0 International license. Xcc, Xanthomonas campestris pv. campestris.
Figure 4PrPSc inactivation evaluated by PMCA. Brain homogenate of CD-1 mice was used as PrPSc source to infect N2a cells, and PMCA buffer was used to dilute samples (dilution series are indicated above the blots). PMCA products from R9 of amplification were analyzed by western blotting after proteinase K digestion (2). (A) Control samples treated with PBS. (B) CAC-717-treated samples. Except for the NS, amplification was performed in quadruplicate. Molecular mass markers are indicated on the right-hand side. Cited from Sakudo et al (2) under the Created Commons Attribution 4.0 International license. PrPSc, scrapie prion; PMCA, protein misfolding cyclic amplification; R9, round 9; NS, non-seeded control.
Virucidal efficacy of CAC-717 against SARS-CoV-2.
| Viral titer (TCID50/ml) | |||
|---|---|---|---|
| Strain | Variant type | Distilled water | CAC-717 |
| SARS-CoV-2/WK-521 | Original | 4.9 | ≤0.6 |
| SARS-CoV-2/KH-1/2021 | Original | 5.0 | ≤0.6 |
| hCoV-19/Japan/QK002/2020 | α | 4.2 | ≤0.6 |
| hCoV-19/Japan/TY8-612/2021 | β | 4.8 | ≤0.6 |
| hCoV-19/Japan/TY7-501/2021 | γ | 4.4 | ≤0.7 |
| SARS-CoV-2/KH-25/2021 | δ | 4.9 | ≤0.6 |
Aliquots of virus were mixed with 49 volumes of CAC-717, incubated for 5 min, and SARS-CoV-2 titers were measured (22). TCID50, tissue culture infectious dose.