scholarly journals Studies on experimentally-induced massive hepatic cell necrosis. Organ distribution Propionibacterium acnes and effects of the cell wall fraction of Propionibacterium acnes on hepatocytotoxicity.

1989 ◽  
Vol 12 (1) ◽  
pp. 71-77
Author(s):  
Yasuhiro Mizoguchi ◽  
Hiroshi Kuboi ◽  
Kenzo Kobayashi ◽  
Seiji Morisawa ◽  
Ikuya Yano
1990 ◽  
Vol 13 (2) ◽  
pp. 136-141
Author(s):  
Yasuhiro Mizoguchi ◽  
Hiroshi Kuboi ◽  
Shuichi Seki ◽  
Kenzo Kobayashi ◽  
Sukeo Yamamoto ◽  
...  

Hepatology ◽  
1992 ◽  
Vol 16 (2) ◽  
pp. 462-468 ◽  
Author(s):  
Norifumi Kawada ◽  
Natsuo Ueda ◽  
Yasuhiro Mizoguchi ◽  
Kenzo Kobayashi ◽  
Takeyuki Monna ◽  
...  

1985 ◽  
Vol 97 (6) ◽  
pp. 1669-1678 ◽  
Author(s):  
Masato NAGAOKA ◽  
Kei-ichi KAMISANGO ◽  
Hideji FUJII ◽  
Kei-ichi UCHIKAWA ◽  
Isao SEKIKAWA ◽  
...  

2021 ◽  
Vol 99 (9) ◽  
Author(s):  
Gilberto Solano-Suárez ◽  
Luciano S Caixeta ◽  
Alexander Masic ◽  
Diego Manríquez ◽  
Luciana Hatamoto-Zervoudakis ◽  
...  

Abstract The main objective of this study was to evaluate the effect of peripartal administration of a commercially available nonspecific immune stimulant (mycobacterium cell wall fraction; MCWF [Amplimune, NovaVive Inc., Napanee, ON, Canada]) on the incidence of disease during early lactation and subsequent fertility of dairy cows. A second objective was to characterize the dynamics of circulating white blood cells (WBC) and metabolic markers following treatment administration. Cows in an United States Department of Agriculture (USDA) organic-certified dairy herd were blocked by parity and, based on sequential calving dates, randomly assigned to receive two injections (5 mL s.c.) of either a placebo (saline solution) as a control (CON; n = 71) or MCWF (n = 65) at enrollment (7 d before expected calving) and within 24 h after calving. Blood samples were collected from a subsample of the study population (MCWF = 16; CON = 18) for WBC count at enrollment, at day 2 post enrollment, and at days 1, 3, 7, and 14 after calving. Serum fatty acids, beta-hydroxybutyrate, and Ca concentrations were determined at days 1 and 7 postpartum (MCWF = 21; CON = 21). Main outcome variables included incidence risk of peripartal and early lactation health disorders and pregnancy at first artificial insemination (AI), at 100, and at 150 days in milk (DIM). In addition, the average daily milk yield up to 90 DIM and death and live culling before 305 DIM were compared. Treatment effects were assessed using multivariable logistic regression, time-to-event analyses, and repeated measures analysis of variance (ANOVA). A treatment effect on the incidence risk of some of the health disorders in the study was established. Incidence risk of metritis and clinical mastitis <28 DIM was smaller in MCWF than in CON cows (36.9% vs. 50.7% and 6.3% vs. 19.7%, respectively). On the contrary, the incidence risk of respiratory disease <28 DIM was smaller in CON (0%) than in MCWF (7.7%). Reproductive performance of multiparous cows was affected by MCWF administration: pregnancy at first AI and pregnancy at 100 and 150 DIM were greater in MCWF than in CON (35.6% vs. 19.2%; 51.1% vs. 25.0%; and 64.4% vs. 40.4%, respectively). Overall, median intervals from calving to pregnancy were 90 vs. 121 d in MCWF and CON cows, respectively. No treatment effects on the dynamics of circulating WBC or in postpartum metabolic status were established. No differences for milk yield or for the proportion of cows that survived up to 305 DIM were determined, although cows in MCWF left the herd earlier than cows in CON. In conclusion, incidence risks of metritis and mastitis in early lactation were smaller in cows receiving MCWF, whereas the incidence risk of respiratory disease was smaller in CON. Fertility significantly improved in MCWF compared with CON cows. As this study was performed in an organic-certified dairy, specific health and reproductive management practices may affect the external validity of the current findings.


mBio ◽  
2017 ◽  
Vol 8 (2) ◽  
Author(s):  
Jeff Quigley ◽  
V. Keith Hughitt ◽  
Carlos A. Velikovsky ◽  
Roy A. Mariuzza ◽  
Najib M. El-Sayed ◽  
...  

ABSTRACT The cell wall of Mycobacterium tuberculosis is composed of unique lipids that are important for pathogenesis. Indeed, the first-ever genetic screen in M. tuberculosis identified genes involved in the biosynthesis and transport of the cell wall lipid PDIM (phthiocerol dimycocerosates) as crucial for the survival of M. tuberculosis in mice. Here we show evidence for a novel molecular mechanism of the PDIM-mediated virulence in M. tuberculosis. We characterized the DNA interaction and the regulon of Rv3167c, a transcriptional repressor that is involved in virulence regulation of M. tuberculosis, and discovered that it controls the PDIM operon. A loss-of-function genetic approach showed that PDIM levels directly correlate with the capacity of M. tuberculosis to escape the phagosome and induce host cell necrosis and macroautophagy. In conclusion, our study attributes a novel role of the cell wall lipid PDIM in intracellular host cell modulation, which is important for host cell exit and dissemination of M. tuberculosis. IMPORTANCE Mycobacterium tuberculosis is a major human pathogen that has coevolved with its host for thousands of years. The complex and unique cell wall of M. tuberculosis contains the lipid PDIM (phthiocerol dimycocerosates), which is crucial for virulence of the bacterium, but its function is not well understood. Here we show that PDIM expression by M. tuberculosis is negatively regulated by a novel transcriptional repressor, Rv3167c. In addition, we discovered that the escape of M. tuberculosis from its intracellular vacuole was greatly augmented by the presence of PDIM. The increased release of M. tuberculosis into the cytosol led to increased host cell necrosis. The discovery of a link between the cell wall lipid PDIM and a major pathogenesis pathway of M. tuberculosis provides important insights into the molecular mechanisms of host cell manipulation by M. tuberculosis. IMPORTANCE Mycobacterium tuberculosis is a major human pathogen that has coevolved with its host for thousands of years. The complex and unique cell wall of M. tuberculosis contains the lipid PDIM (phthiocerol dimycocerosates), which is crucial for virulence of the bacterium, but its function is not well understood. Here we show that PDIM expression by M. tuberculosis is negatively regulated by a novel transcriptional repressor, Rv3167c. In addition, we discovered that the escape of M. tuberculosis from its intracellular vacuole was greatly augmented by the presence of PDIM. The increased release of M. tuberculosis into the cytosol led to increased host cell necrosis. The discovery of a link between the cell wall lipid PDIM and a major pathogenesis pathway of M. tuberculosis provides important insights into the molecular mechanisms of host cell manipulation by M. tuberculosis.


2019 ◽  
Vol 70 ◽  
pp. 408-416 ◽  
Author(s):  
Mohd Saqib ◽  
Rahul Khatri ◽  
Bindu Singh ◽  
Ananya Gupta ◽  
Sangeeta Bhaskar

Sign in / Sign up

Export Citation Format

Share Document