Subject(s)
Chilblains/virology , Clinical Laboratory Techniques/methods , Coronavirus Infections/diagnosis , Pneumonia, Viral/diagnosis , Skin Diseases/virology , Spike Glycoprotein, Coronavirus/isolation & purification , Adult , Betacoronavirus/isolation & purification , Biopsy , COVID-19 , COVID-19 Testing , Chilblains/diagnosis , Chilblains/pathology , Coronavirus Infections/complications , Coronavirus Infections/pathology , Coronavirus Infections/virology , Endothelium, Vascular/pathology , Endothelium, Vascular/virology , Female , Foot , Humans , Immunohistochemistry , Pandemics , Pneumonia, Viral/complications , Pneumonia, Viral/pathology , Pneumonia, Viral/virology , RNA, Viral/isolation & purification , Reverse Transcriptase Polymerase Chain Reaction , SARS-CoV-2 , Skin/blood supply , Skin/pathology , Skin/virology , Skin Diseases/diagnosis , Skin Diseases/pathology , Sweat Glands/pathology , Sweat Glands/virologyABSTRACT
We report an 8-year-old girl who developed generalized anhidrosis following presumptive H1N1 infection. Pure autonomic dysfunction is an unusual complication following H1N1 infection and specially generalized anhidrosis without other autonomic dysfunction have not been reported before.
Subject(s)
Hypohidrosis/diagnosis , Hypohidrosis/virology , Influenza A Virus, H1N1 Subtype/pathogenicity , Influenza, Human/complications , Child , Chronic Disease , Female , Humans , Influenza, Human/diagnosis , Influenza, Human/virology , Sweat Glands/innervation , Sweat Glands/physiopathology , Sweat Glands/virology , Sympathetic Nervous System/physiopathology , Sympathetic Nervous System/virologyABSTRACT
OBJECTIVE: To explore the distribution of severe acute respiratory syndrome (SARS)-associated coronavirus (SARS-CoV) in SARS autopsy tissues at the molecular level. METHODS: In situ hybridization was used to detect the expression and location of SARS-CoV RNA polymerase gene in autopsy tissues from SARS-Cov-infected subjects, including the lung, spleen, lymph nodes, pituitary, pancreas, parathyroid, adrenal glands, gastrointestinal tract, skin, brain, liver, kidney, blood vessels, striated muscles of the limbs, bone marrow, heart, ovary, uterus and testicles. RESULT: SARS-CoV RNA was detected in the cytoplasm of the alveolar epithelia, infiltrating mononuclear phagocytes in the lungs, serous gland epithelium of the trachea/bronchus, monocytes in the spleen and lymph nodes, acinar cells in the pancreas, acidophilic cells in the parathyroid and pituitary, adrenal cortical cells, epithelia of the alimentary tracts, gastric parietal cells, sweat gland cells, brain neurons, hepatocytes near the central vein, epithelia of the distal renal tubules, bone marrow promyelocytes, and endothelia of the small veins. CONCLUSIONS: SARS-CoV invades various organs of the body and distributes in a similar fashion to CD13, the receptor of human coronavirus 229E. The detection of SARS-CoV in the sweat glands, alimentary tracts and epithelia of the distal convoluted tubules of the kidney may help identify the transmission routes of SARS-CoV.
Subject(s)
In Situ Hybridization/methods , RNA, Viral/analysis , Severe acute respiratory syndrome-related coronavirus/isolation & purification , Autopsy , Humans , Kidney Tubules, Distal/virology , Severe acute respiratory syndrome-related coronavirus/genetics , Severe Acute Respiratory Syndrome/diagnosis , Severe Acute Respiratory Syndrome/transmission , Sweat Glands/virologyABSTRACT
Hepatitis C virus (HCV) replicates in salivary glands of chronic hepatitis C patients and is released into the saliva, suggesting that HCV may replicate in other exocrine glands. The presence of positive and negative HCV RNA strands was demonstrated by in situ hybridization, and of HCV core protein by immunohistochemistry, in sweat glands and keratinocytes in healthy skin biopsies from 15 patients with chronic hepatitis C and 10 anti-HCV negative patients with chronic liver disease. Positive and negative HCV RNA strands were detected in 9.6 +/- 5.2% and 4.2 +/- 3.8%, respectively, of the epithelial cells of eccrine sweat glands. Core protein was detected in 6.0 +/- 3.93% of these cells. HCV RNA resistant to RNase digestion (encapsidated HCV RNA) was detected in 10/10 sweat samples from HCV-infected patients. Positive and negative HCV RNA strands were detected in 6.7 +/- 2.97% and 3.0 +/- 3.08% of the keratinocytes, respectively. HCV core protein was found in 4.5 +/- 2.76% of these cells. No HCV RNA or HCV core protein was detected in the skin biopsies from the 10 anti-HCV negative patients. In conclusion, HCV replicates in eccrine sweat glands cells and keratinocytes in healthy skin and is released into the sweat.
