Effects of a Swimming Training Session on Pulmonary Functions in Young Adult Beginners

Introduction: It is well documented that any sort of exercisedone regularly, is beneficial for health. Swimming is noexception and considered to be a very good exercise formaintaining proper health and also has a profound effect on thelung functions. Regular swimming practice gives a positiveeffect on the lungs by increasing the pulmonary capacity andthus improves the lung functions. The proposed study wascarried out with the above background, among swimmingbeginners undergoing a swimming training session to see howa course of swimming affect the lung function parameters.Material and Methods: The study was carried out on 32males and 12 females’ healthy young adults of either sex ofage group of 18-35 yrs. At the beginning of the swimmingsession recording of pulmonary functions tests was done foreach selected candidate (control group). Again procedureswere repeated at the end of three months and at the end of sixmonths for same candidates (case group).Results: In the present study, it is observed that there issignificant increase (p value <0.05) in FVC, FEV1, PEFR andMVV after three months and after six months of swimmingboth males and females separately.Conclusion: From the present study we concluded that evenafter short course of swimming training session there issignificant benefit in some parameters of lung function. Theimprove lungs function is thought to be duo to increase inrespiratory muscle mass. More elaborate and multi-centredstudies are needed to corroborate our findings

Duplex nested-PCR for detection of small ruminant lentiviruses

Abstract Small ruminant lentiviruses (SRLV) have high genetic variability which results in different viral strains around the world. This create a challenge to design sensible primers for molecular diagnosis in different regions. This work proposes a protocol of duplex nested-PCR for the precise diagnosis of SRLV. The technique was designed and tested with the control strains CAEV Co and MVV 1514. Then, field strains were submitted to the same protocol of duplex nested-PCR. Blood samples of sheep and goats were tested with AGID and nested PCR with specific primers for pol, gag and LTR. The AGID results showed low detection capacity of positive animals, while the nested PCR demonstrated a greater capacity of virus detection. Results demonstrated that LTR-PCR was more efficient in detecting positive sheep samples, whereas gag-PCR allowed a good detection of samples of positive goats and positive sheep. In addition, pol-PCR was more efficient with goat samples than for sheep. Duplex nested PCR performed with standard virus samples and field strains demonstrated that the technique is more efficient for the detection of multiple pro-viral DNA sequences. This study demonstrated a successful duplex nested PCR assay allowing a more accurate diagnosis of SRLV.

Duplex nested-PCR for detection of small ruminant lentiviruses

Abstract Small ruminant lentiviruses (SRLV) have high genetic variability which results in different viral strains around the world. This create a challenge to design sensible primers for molecular diagnosis in different regions. This work proposes a protocol of duplex nested-PCR for the precise diagnosis of SRLV. The technique was designed and tested with the control strains CAEV Co and MVV 1514. Then, field strains were submitted to the same protocol of duplex nested-PCR. Blood samples of sheep and goats were tested with AGID and nested PCR with specific primers for pol, gag and LTR. The AGID results showed low detection capacity of positive animals, while the nested PCR demonstrated a greater capacity of virus detection. Results demonstrated that LTR-PCR was more efficient in detecting positive sheep samples, whereas gag-PCR allowed a good detection of samples of positive goats and positive sheep. In addition, pol-PCR was more efficient with goat samples than for sheep. Duplex nested PCR performed with standard virus samples and field strains demonstrated that the technique is more efficient for the detection of multiple pro-viral DNA sequences. This study demonstrated a successful duplex nested PCR assay allowing a more accurate diagnosis of SRLV.

Transmission of caprine arthritis encephalitis virus between sheep / Transmissão do vírus da artrite encefalite caprina entre ovinos

ABSTRACT: This study was conducted to evaluate caprine arthritis encephalitis virus (CAEV) transmission among sheep using 15 lambs that were distributed in 2 experimental groups. The exposed group consisted of 10 lambs that remained with their mothers, who were experimentally infected with CAEV. The non-exposed group was characterized as the control group and was comprised of 5 lambs that remained with their CAEV-negative mothers. Blood samples were collected monthly from birth until 1 year of life. To evaluate the transmission, an agar gel immunodiffusion test (AGID), enzyme immunoassay (ELISA), immunoblotting (IB), and nested polymerase chain reaction (nPCR) techniques were used. The non-exposed group was negative in all of the tests throughout the whole experiment. In the exposed group, 2 individuals had positive nPCR results. Positive nPCR samples were sequenced for comparison with the original goat strains and were shown to be similar to the CAEV-Cork strain. Seroconversion was not detected, and clinical manifestations were not observed. Thus, after 1 year of observation, it was verified that CAEV transmission among sheep is possible; however, with discreet frequency. This was an initial study, and other experiments are needed to analyze the adaptive capacity of the CAEV to remain in an infected sheep flock and cause the disease.

RESUMO: O estudo foi conduzido para avaliar a transmissão do vírus da artrite encefalite caprina (CAEV) entre ovinos, utilizando 15 cordeiros, distribuídos em dois grupos experimentais. O grupo exposto foi constituído por 10 cordeiros, mantidos com suas mães, que foram infectadas, experimentalmente, com CAEV. O grupo não exposto caracterizou-se como grupo controle e foi formado por cinco cordeiros, mantidos com suas matrizes, negativas para CAEV. Foram colhidas amostras de sangue mensalmente, do periodo que compreende o nascimento até um ano de vida. Para avaliar a transmissão, foram utilizadas as técnicas de imunodifusão em gel de agarose (IDGA), ensaio imunoenzimático (ELISA), immunoblotting (IB) e reação em cadeia da polimerase do tipo nested (nPCR). O grupo não exposto se manteve negativo aos testes durante todo o experimento. Já no grupo exposto, dois indivíduos apresentaram resultados positivos na nPCR. As amostras positivas na nPCR foram sequenciadas para serem comparadas com as cepas originais de caprinos, comprovando se tratar de lentivírus semelhante à cepa CAEV-Cork. A soroconversão não foi detectada e a manifestação clínica não foi observada. Sendo assim, após um ano de observação, verificou-se que a transmissão do CAEV entre ovinos é possível, entretanto, com discreta frequência. Este foi um estudo inicial, e outros experimentos são necessários para analisar a capacidade adaptativa do CAEV de permanecer em rebanho ovino infectado e, com isso, causar doença.

Goat umbilical cord cells are permissive to small ruminant lentivirus infection in vitro

Abstract Small ruminant lentiviruses isolated from peripheral blood leukocytes and target organs can be propagated in vitro in fibroblasts derived from goat synovial membrane cells. These cells are obtained from tissues collected from embryos or fetuses and are necessary for the establishment of the fibroblast primary culture. A new alternative type of host cells, derived from goat umbilical cord, was isolated and characterized phenotypically with its main purpose being to obtain cell monolayers that could be used for the diagnosis and isolation of small ruminant lentiviruses in cell culture. To accomplish this goal, cells were isolated from umbilical cords; characterized phenotypically by flow cytometry analysis; differentiate into osteogenic, chondrogenic and adipogenic lineage; and submitted to viral challenge. The proliferation of goat umbilical cord cells was fast and cell monolayers formed after 15 days. These cells exhibited morphology, immunophenotype, growth characteristics, and lineage differentiation potential similar to mesenchymal stem cells of other origins. The goat umbilical cord derived cells stained positive for vimentin and CD90, but negative for cytokeratin, CD34 and CD105 markers. Syncytia and cell lysis were observed in cell monolayers infected by CAEV-Cork and MVV-K1514, showing that the cells are permissive to small ruminant lentivirus infection in vitro. These data demonstrate the proliferative competence of cells derived from goat umbilical cords and provide a sound basis for future research to standardize this cell lineage.

Wharton's jelly cells from sheep umbilical cord maintained with different culture media are permissive to in vitro infection by Small Ruminant Lentiviruses / Células da geleia de Wharton do cordão umbilical ovino mantidas em diferentes meios de cultivo são permissivas à infecção in vitro por lentivírus de pequenos ruminantes

This study aimed to isolate cells from the Wharton's jelly of umbilical cord (WJUC) of sheep collected during natural parturition using different culture media, in addition to reporting for the first time the permissiveness of these cells to in vitro infection by small ruminant lentiviruses. Ten umbilical cords were collected from healthy sheep. Each cord explants were grown in different media consisting of MEM, low glucose DMEM, M199, and RPMI-1640. The permissiveness of infection of sheep cells from WJUC was tested with CAEV-Cork and MVV-K1514 strains, inoculating 0.1 MOI of each viral strain. Four supernatants from each strain were obtained from WJUC sheep cell cultures infected in different media. The results demonstrated the presence of cytopathic effect after the in vitro infection by CAEV-Cork and MVV-K1514 with all of the tested culture media. Nested-PCR detected proviral DNA in all supernatants. Supernatants containing CAEV-Cork viruses had TCID 50/ml titres of 10 5.5 in MEM, 10 4.0 in low glucose DMEM, 105.0 in M199, and 10 5.7 in RPMI-1640. Supernatants containing the MVV-K1514 virus had TCID 50/ml titres of 10 4.3 in MEM, 10 3.5 in low-glucose DMEM, 10 4.7 in M199, and 10 3.5 in RPMI-1640. Sheep cells from WJUC are permissive to in vitro infection by small ruminant lentivirus.(AU)

O objetivo deste estudo foi isolar células da geleia de Wharton do cordão umbilical (GWCU) ovino coletado por ocasião do parto natural, utilizando-se diferentes meios de cultivo, além de relatar, pela primeira vez, sua permissividade à infecção in vitro por lentivírus de pequenos ruminantes (LVPRs). Dez cordões umbilicais foram coletados de ovelhas hígidas e soronegativas para LVPRs pelo teste de imunodifusão em gel de agarose (IDGA). De cada cordão, explantes foram cultivados em quatro meios distintos que consistiram em MEM, DMEM baixa glicose, meio 199 e RPMI-1640, todos acrescidos de 10% de soro fetal bovino em estufa com atmosfera úmida e 5% de CO2 a 37ºC. A permissividade de infecção das células GWCU ovino foi testada frente às cepas CAEV-Cork e MVV-K1514, inoculando-se 0,1 MOI de cada cepa viral e corando as monocamadas com May Grunwald Giemsa para visualização do efeito citopático. Foram obtidos quatro sobrenadantes CAEV-Cork e quatro MVV-K1514, provenientes do cultivo de células GWCU ovino infectadas por 21 dias em meios distintos, dos quais foram realizadas titulação em membrana sinovial caprina e extração do DNA pró-viral para realização de nested-PCR e eletroforese em gel de agarose a 2%. Os resultados demonstraram a presença de efeito citopático na infecção in vitro tanto por CAEV-Cork como por MVV-K1514 em todos os meios de cultivo, sendo visualizados sincícios e lise celular em microscópio invertido. A nested-PCR detectou o DNA pró-viral tanto do CAEV-Cork como do MVV-K1514 em todos os sobrenadantes. Os sobrenadantes contendo o vírus CAEV-Cork apresentaram títulos em TCID50/mL de 10 5,5 em MEM, 10 4,0 em DMEM baixa glicose, 10 5,0 em meio 199 e 10 5,7 em RPMI-1640. Os sobrenadantes contendo o vírus MVV-K1514 apresentaram título em TCID 50/mL de 10 4,3 em MEM, 10 3,5 em DMEM baixa glicose, 10 4,7 em meio 199 e 10 3,5 em RPMI-1640. Células GWCU ovino são permissivas à infecção in vitro pelos lentivírus de pequenos ruminantes CAEV-Cork e MVV-K1514.(AU)

Effect of Yoga on pulmonary function tests.

Background: Yoga is considered to be a very good exercise for maintaining proper health. The present work was planned to find effects of 10 weeks Yoga practice on some pulmonary function tests. Methods: The present study was conducted on 40 subjects, (30 males and 10 females) who came voluntarily as subjects for the project with written and informed consent. It was a prospective study on healthy volunteers from both sex of age between 20 to 65 years. Various Pulmonary Function Tests (PFTs) were measured. Results: Respiratory rate was decreased while Breath Holding Time (BHT) and Maximum Ventilatory Volume (MVV) were found to be increased in both male and female subjects. Conclusions: From this study we conclude that yoga practice can be advocated to improve respiratory efficiency for healthy individuals as well as an alternative therapy or as adjunct to conventional therapy in respiratory diseases.

Effect of yoga practices on respiratory parameters in healthy young adults.

Background & Objectives: Besides spiritual achievements, the practice of yoga is accompanied by a number of beneficial physiological effects in the body. The regular practice of yoga integrates the mind and the body.It produces many systemic psycho-physical effects in the body, besides its specific effects on the respiratory functions.The aim of the present study was to assess the beneficial effects of yoga in the improvements in the pulmonary functions of young healthy adults. Methods: The study group consisted of 30 young adults (19 males and 11 females) who were students of first year M.B.B.S.,medical college Baroda.They were motivated to participate in yoga workshop for one hour daily for four weeks. The first phase of the recording of the pulmonary parameters (M.V.V,FVC,FEV1,PEFR) was done at the beginning of their course. The second phase of the recording was done after 4 weeks of the regular yoga practice. The data were analyzed using student’s Paired T – test. Results: Participants had a mean±SD age of 17.81 ± 0.48 years, height of 164.21±5.09 cm and weight of 54.34±5.63kg. The MVV(L/MIN) - before yoga practice showed a value of 97.4±24.4 and after , it showed a value of 119±28. The FVC(ml) - before yoga practice showed a value of 2575 ±631and after , it showed a value of 2768 ±618. The FEV1(ml)- before yoga practice showed a value of 2270± 636 and after , it showed a value of 2476 ±570. The PEFR(L/MIN) - before yoga practice showed a value of 479±103 and after , it showed a value of 585±120. For all the parameters, a P value of <0.01 was considered as statistically significant. Conclusion: There was a statistically significant increase in all the above lung parameters in the regular yoga practitioners.This study proposes that regular practice of yoga can improve health related aspects of physical fitness and general wellbeing.

A comparative study of pulmonary functions in different age groups.

Background and objectives: The respiratory system changes with age and understanding these changes helps detect and prevent respiratory dysfunctions in the elderly. Pulmonary function, as measured by spirometry is an important predictor of morbidity and mortality of elderly persons. The aim of the present study was to see the effects of aging on pulmonary functions. Methods : The study included 150 subjects of different ages from 20 years and above. Subjects were divided in six groups depending on their age. (1) 20-29 yrs (2) 30-39 yrs (3) 40-49 yrs (4) 50-59 yrs (5) 60-69 yrs (6) 70 yrs and above. 25 subjects were included in each group. FVC , FEV1, FEV1 /FVC%, PEFR, FEF25%-75%, MVV were measured. Results: Comparing 20-29 yrs with 70 yrs and above show mean FVC (4.33 vs 1.68 litre, p<0.001) ,FEV1(3.91 vs 1.19 litre p<0.001), FEV1 /FVC%(90.30 vs 70.0 p<0.001), PEFR(9.81 vs 3.31 lit/sec p<0.001), FEF25%-75%(6.65 vs 1.89 lit/sec p<0.001), MVV(93.94 vs 55.96 lit/min p<0.001). Conclusion: Our study concluded that FVC, FEV1, FEV1/FVC, PEFR, FEF25- 75% and MVV decrease with age. It is probably a result of decreased strength of expiratory muscles, decreased chest wall compliance and increased tendency of airways to close during forced expiratory effort causing air trapping in the lungs.

Assessment of Respiratory Muscle Endurance in Type 1 & 2 Diabetes Mellitus.

Maximum Voluntary Ventilation (MVV) test is an objective dynamic method of measuring the working capacity of respiratory muscles. Therefore, we designed the present study to determine the effect imposed by diabetes mellitus (Type 2) on respiratory muscle endurance in Jammu diabetic patients. In the present study, 100 diabetic patients of 50 Type I and 50 Type 2 and 50 healthy control. MVV showed significant decrease in male diabetic patients on oral medication. The findings suggest that there is significant decrease of respiratory muscle endurance in male diabetics on oral medication.