Cold-water immersion (CWI) after exercise is a method used by sportsmen to improve recovery. The aim of the study was to assess the effect of a 3 min CWI on the inflammatory state by measuring levels of interleukin 6 (IL-6), interleukin 10 (IL-10), tumor necrosis factor α (TNF-α), and transforming growth factor β1 (TGF-β1), and activities of α1-antitrypsin (AAT) and lysosomal enzymes, including arylsulfatase (ASA), acid phosphatase (AcP), and cathepsin D (CTS D), in the blood of healthy recreational athletes. Male volunteers (n = 22, age 25 ± 4.8 yr) performed a 30 min submaximal aerobic exercise, followed by a 20 min rest at room temperature (RT-REST) or a 20 min rest at room temperature with an initial 3 min 8 °C water bath (CWI-REST). Blood samples were taken at baseline, immediately after exercise, and after 20 min of recovery. The IL-6, IL-10, and TNF-α levels and the AAT activity increased significantly immediately after exercise. The IL-6 level was significantly higher after CWI-REST than after RT-REST. No changes in the activities of the lysosomal enzymes were observed. The effect of a 3 min CWI on the level of inflammatory markers during post-exercise recovery was limited. Thus, it might be considered as a widely available method of regeneration for recreational athletes.
Toxoplasma gondii is a worldwide distributed protozoan parasite. This apicomplexan parasite infects one-third of the population worldwide, causing toxoplasmosis, considered one of the neglected parasitic infections. In healthy humans, most infections are asymptomatic. However, in immunocompromised patients, the course of the disease can be life-threatening. Human immunodeficiency virus (HIV)-infected patients have a very high burden of Toxoplasma gondii co-infection. Thus, it is essential to use modern, sensitive, and specific methods to properly monitor the course of toxoplasmosis in immunodeficient patients.
<br><b>Introduction:</b> The observation of the epidemiology of toxoplasmosis may prevent the development of a severe form of the disease in HIV patients.</br> <br><b>Aim:</b> The aim of the study was to evaluate the seroprevalence of <i>Toxoplasma gondii</i> in the population of the Kuyavian-Pomeranian Voivodeship at high risk of contracting HIV.</br> <br><b>Material and methods:</b> Blood serum samples of 43 patients of the Consulting and Diagnostic AIDS Center were tested for the presence of anti-HIV-1/HIV-2 antibodies and p24 antigen, and for the presence of anti-toxoplasma IgM and IgG antibodies.</br> <br><b>Results:</b> Anti-toxoplasma IgG antibody prevalence of 53.5% (23/43) was found in the study population, while the examination of specific IgM antibodies was negative. A high IgG antibody avidity index was obtained in 18 (94.7%) seropositive samples. Thirty (69.77%) of the samples were female, and 13 (30.23%) were male. Among men, HIV was detected in 1 (7.69%), and IgG antibodies against <i>T. gondii</i> in 7 (53.85%) samples. IgG antibodies against <i>T. gondii</i> were found in 16 (53.33%) women. The HIV-positive individual was 24 years old. The presence of antibodies against <i>T. gondii</i> in the IgG class was found in people of different ages (in women aged 38.44 ±13.00 years old and in men aged 29.29 ±10.86 years old). The risky situation that could cause HIV infection is in most cases sexual contacts (79.07%).</br> <br><b>Conclusions:</b> High seroprevalence of <i>T. gondii</i> was found among the studied subjects at a high risk of HIV infection. Further research is required on a larger study group.</br>
Introduction: Respiratory tract infections are caused by various factors including respiratory viruses, for example influenza virus and respiratory syncytial virus (RSV). Surveillance of influenza and other respiratory viruses is carried out as part of the SENTINEL and NON SENTINEL programs in Poland.<br>Aim of study: Determination of the frequency of selected types of influenza and RSV viruses using real-time reverse transcription polymerase chain reaction method (real-time RT-PCR) in a selected population of inhabitants of the kuyavian-pomeranian voivodeship in the epidemic season 2017/2018, i.e. from 1 October 2017 to 30 April 2018.<br>Material and methods: 201 throat and nasal swabs were tested using real-time RT-PCR method for the detection of the presence of genetic material RNA of influenza virus and RSV. The study population was divided into 7 groups depending on age.<br>Results. Positive samples accounted for 48.26% of the swabs tested. The genetic material RNA of influenza virus was found in 95 (47.26) samples and RSV in 2 (1,00%) samples. Influenza B virus was most frequently isolated. The most prevalence of infections was observed in people under 25 years of age.<br>Conclusions: Surveillance of influenza in the SENTINEL and NON SENTINEL programs constitute an important role in assessing the virological and epidemiological situation prevailing in a given area. The results cover part of the population, hence the data may be underestimated. It is necessary to continue studies and observe the virological and epidemiological situation in the polish population.
Giardia intestinalis is one of the most common food-borne protozoa. The sensitivity of pathogens to physical and chemical factors is the basis for developing measures to reduce the incidence of the population. Several methods are available to detect the presence of G. intestinalis. The study determines the influence of 22 selected factors on the survival assessment and detection of G. intestinalis DNA in trophozoites axenically cultured. The influence of a given factor on the test result was observed in the case of 17 factors (77.3%) in the microscopic method, while only in the case of 3 (13.6%) substances in the real-time PCR method. Prevention of G. intestinalis infections, e.g., by ensuring food and water safety, is a crucial issue affecting public health. The experiment was conducted on trophozoites as the first approach. It is necessary to continue research and observe the epidemiological situation. In future studies, the impact of the studied factors on the survival assessment and detection of Giardia intestinalis DNA in axenically cultured cysts should be determined.
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