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1.
Int J Sports Physiol Perform ; 19(3): 315-321, 2024 Mar 01.
Article in English | MEDLINE | ID: mdl-38134892

ABSTRACT

INTRODUCTION: This case study aimed to describe potential changes in neuromuscular activation and synergies after an 8-day cross-country mountain-bike stage race. METHODS: A peak power output test was performed 5 days before the race. Two days before the start and after 7 days of racing, the athlete performed a power-based Lamberts Submaximal Cycling Test, including surface electromyography, and completed a Daily Analysis of Life Demands of Athletes questionnaire. Neuromuscular activation, in terms of root mean square, timing (onset-offset) of muscle activation, and synergies, was obtained from electromyography recordings. RESULTS: The athlete reported an increase in symptoms of experienced stress after the stage race on the Daily Analysis of Life Demands of Athletes questionnaire. Both biceps femoris and tibialis anterior muscles showed a reduction in normalized amplitude after the stage race. In addition, the number of synergies that was necessary to describe neuromuscular activation increased from 2 to 3. CONCLUSIONS: In this case study, the increase in synergies suggests that, after the stage race, the athlete showed a more complex muscle-recruitment pattern. This may indicate that muscle coordination can change when muscle fatigue occurs; however, further research is needed to confirm these results in a larger sample.


Subject(s)
Bicycling , Hamstring Muscles , Humans , Bicycling/physiology , Muscle, Skeletal/physiology , Muscle Fatigue/physiology , Electromyography
2.
J Parasitol ; 99(6): 1133-6, 2013 Dec.
Article in English | MEDLINE | ID: mdl-23641900

ABSTRACT

Avian hemosporidian parasites are a genetically diverse group of parasites with a near cosmopolitan distribution. Over the past 2 decades, several PCR protocols have been designed to detect these parasites. The majority of these protocols amplify part of or the entire mitochondrial cytochrome b gene. However, many of these protocols co-amplify 2 genera (Haemoproteus and Plasmodium), making it impossible to determine which genus is amplified without post-PCR analysis. A uniform database (MalAvi), containing sequences amplified with the primers HAEMF and HAEMR2, has been developed to increase comparability across studies. We analyzed sequences from the MalAvi database and new sequences and found that digestion with EcoRV could be used to distinguish Haemoproteus from the majority of Plasmodium sequences. In addition, we tested 220 wild birds from Costa Rica and the United States for avian hemosporidians and assessed the ability of EcoRV to distinguish these 2 genera. Thirty-six positive samples were sequenced to confirm the restriction profiles, and we also analyzed 63 new hemosporidian sequences from ongoing studies in the United States for the restriction site. Among these new samples, all of the 85 Haemoproteus (subgenus Parahaemoproteus) and 14 Plasmodium were distinguishable. Overall, 887 of 898 (98.8%) sequences from our studies and the MalAvi database were assigned to the correct genus. Of these samples, all Haemoproteus samples were correctly identified and all but 11 Plasmodium samples were correctly identified by the EcoRV assay. Overall, this restriction enzyme protocol is able to quickly and efficiently classify these 2 genera of avian malarial parasites and would be useful for researchers interested in identifying parasites to genus-level, studies focused on sequence analysis of only a single genus, or for detecting co-infections that would need cloning prior to sequence analysis.


Subject(s)
Bird Diseases/diagnosis , Genome, Mitochondrial , Haemosporida/isolation & purification , Plasmodium/isolation & purification , Protozoan Infections, Animal/diagnosis , Restriction Mapping/standards , Animals , Anseriformes/parasitology , Bird Diseases/parasitology , Birds , Costa Rica , Cytochromes c/genetics , Cytochromes c/metabolism , Databases, Nucleic Acid , Deoxyribonucleases, Type II Site-Specific , Diagnosis, Differential , Haemosporida/genetics , Malaria, Avian/diagnosis , Malaria, Avian/parasitology , Passeriformes/parasitology , Plasmodium/genetics , Polymerase Chain Reaction , Polymorphism, Restriction Fragment Length , Protozoan Infections, Animal/parasitology , United States
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