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      The Dog Mite, Demodex canis: Prevalence, Fungal Co-Infection, Reactions to Light, and Hair Follicle Apoptosis

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          Abstract

          Infection rate, reaction to light, and hair follicle apoptosis are examined in the dogmite, Demodex canis Leydig (Prostigmata: Demodicidae), in dogs from the northern area of Taiwan. An analysis of relevant samples revealed 7.2% (73/1013) prevalence of D. canis infection. Infection during the investigation peaked each winter, with an average prevalence of 12.5% (32/255). The infection rates significantly varied in accordance with month, sex, age, and breed (p < 0.05). Most of the lesions were discovered on the backs of the infected animals, where the infection rate was 52.1% (38/73) (P < 0.05). The epidemiologic analysis of infection based on landscape area factor, found that employing a map-overlapping method showed a higher infection rate in the eastern distribution of Taiwan's northern area than other areas. Isolation tests for Microsporum canis Bodin (Onygenales: Arthrodermataceae) and Trichophyton mentagrophyte Robin (Blanchard) on the D. canis infected dogs revealed prevalence rates of 4.4% (2/45) and 2.2% (1/45), respectively. Observations demonstrated that D. canis slowly moved from a light area to a dark area. Skin samples were examined for cellular apoptosis by activated caspase3 immunohistochemical staining. Cells that surrounded the infected hair follicles were activated caspase3-positive, revealing cell apoptosis in infected follicles via the activation of caspase3.

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          Most cited references33

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          Caveolin-1 expression negatively regulates cell cycle progression by inducing G(0)/G(1) arrest via a p53/p21(WAF1/Cip1)-dependent mechanism.

          Caveolin-1 is a principal component of caveolae membranes in vivo. Caveolin-1 mRNA and protein expression are lost or reduced during cell transformation by activated oncogenes. Interestingly, the human caveolin-1 gene is localized to a suspected tumor suppressor locus (7q31.1). However, it remains unknown whether caveolin-1 plays any role in regulating cell cycle progression. Here, we directly demonstrate that caveolin-1 expression arrests cells in the G(0)/G(1) phase of the cell cycle. We show that serum starvation induces up-regulation of endogenous caveolin-1 and arrests cells in the G(0)/G(1) phase of the cell cycle. Moreover, targeted down-regulation of caveolin-1 induces cells to exit the G(0)/G(1) phase. Next, we constructed a green fluorescent protein-tagged caveolin-1 (Cav-1-GFP) to examine the effect of caveolin-1 expression on cell cycle regulation. We directly demonstrate that recombinant expression of Cav-1-GFP induces arrest in the G(0)/G(1) phase of the cell cycle. To examine whether caveolin-1 expression is important for modulating cell cycle progression in vivo, we expressed wild-type caveolin-1 as a transgene in mice. Analysis of primary cultures of mouse embryonic fibroblasts from caveolin-1 transgenic mice reveals that caveolin-1 induces 1) cells to exit the S phase of the cell cycle with a concomitant increase in the G(0)/G(1) population, 2) a reduction in cellular proliferation, and 3) a reduction in the DNA replication rate. Finally, we demonstrate that caveolin-1-mediated cell cycle arrest occurs through a p53/p21-dependent pathway. Taken together, our results provide the first evidence that caveolin-1 expression plays a critical role in the modulation of cell cycle progression in vivo.
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            Cell-specific targeting of caveolin-1 to caveolae, secretory vesicles, cytoplasm or mitochondria.

            In commonly used tissue culture cells, caveolin-1 is embedded in caveolae membranes. It appears to reach this location after being cotranslationally inserted into ER membranes, processed in the Golgi and shipped to the cell surface. We now report that caveolae are not the preferred location for caveolin-1 in all cell types. Skeletal muscle cells and keratinocytes target caveolin-1 to the cytosol while in exocrine and endocrine cells it accumulates in the secretory pathway. We also found that airway epithelial cells accumulate caveolin-1 in modified mitochondria. The cytosolic and the secreted forms appear to be incorporated into a soluble, lipid complex. We conclude that caveolin-1 can be targeted to a variety of intracellular destinations, which suggests a novel mechanism for the intracellular traffic of this protein.
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              High rate of Microsporum canis feline and canine dermatophytoses in Northeast Brazil: epidemiological and diagnostic features.

              Over a one year period (November 2000-December 2001), clinical specimens from 189 dogs and 38 cats, from the city of Fortaleza, Ceará, Brazil, were examined at the Specialized Medical Mycology Center at the Federal University of Ceará to detect animals with dermatophytoses. The mycological analyses were conducted by direct microscopy and by fungal culture on Sabouraud agar, Sabouraud chloramphenicol agar and Mycosel agar. Dermatophytes were isolated from 27 of the 189 (14.3%) canine specimens and 14 of the 38 (36.8%) feline specimens. The identified dermatophytes were Microsporum canis (95%), M. gypseum (2.5%) and Trichophyton mentagrophytes var. mentagrophytes (2.5%). Microsporum canis was the most common species isolated (92.6% and 100%, for dogs and cats respectively). The percentage of positive direct microscopic examinations of clinical specimens and positive cultures was 61%. There was a high proportion of positive cultures from cats less than 1 year of age, but in dogs no significant differences were detected. There were no significant differences between the sexes. Dermatophytes were more frequently isolated in March, April and May, but no significant differences were detected in the seasonal distribution of canine and feline dermatophytoses.
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                Author and article information

                Journal
                J Insect Sci
                J. Insect Sci
                insc
                Journal of Insect Science
                University of Wisconsin Library
                1536-2442
                2011
                29 June 2011
                : 11
                : 76
                Affiliations
                [ 1 ]Taipei City Animal Protection Office, No. 109, Ln. 600, Wu-Xin Street, Taipei 11048, Taiwan
                [ 2 ]Department of Parasitology, Taipei Medical University, No. 250, Wu-Xin Street,Taipei 11042, Taiwan
                [ 3 ]Graduate Institute of Biomedical Sciences, Chang Gung University, College of Medicine, 259 Wen-Hwa 1st Road, Kwei-Shan Tao-Yuan 33302, Taiwan
                [ 4 ]Department of Animal Science and Technology, National Taiwan University, No. 1, Sec. 4, Roosevelt Road, Taipei 10617, Taiwan
                [ 5 ]Department of Public Health, Taipei Medical University, No. 250, Wu-Xin Street, Taipei 11042, Taiwan
                [ 6 ]Land Environmental Information Consulting Association, 20F-1, No.6 Bau Ching St. Hsing-dian, Taipei 23143, Taiwan
                [ 7 ]School of Veterinary Medicine National Taiwan University, No. 1, Sec. 4, Roosevelt Road, Taipei 10617, Taiwan
                Author notes
                [*] [ * ]Corresponding author

                Editor: T.X. Liu was editor of this paper

                Article
                10.1673/031.011.7601
                3281427
                21867442
                bc72ec74-7d7c-493f-9bce-7496dedb0e7d
                © 2011

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 19 May 2010
                : 10 October 2010
                Page count
                Pages: 13
                Categories
                Article

                Entomology
                taiwan,fungi,map overlay
                Entomology
                taiwan, fungi, map overlay

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