{"title":"Quantitative PCR Analysis of Haemosporidian Infection Intensity in a Temperate Bird Community.","authors":"Alžbeta Šujanová, Eva Špitalská, Radovan Václav","doi":"10.1111/1749-4877.13031","DOIUrl":null,"url":null,"abstract":"<p><p>Avian haemosporidians are vector-borne parasites with complex transmission dynamics influenced by host ecology and environmental factors. Both prevalence and parasitemia are key measures in host-parasite studies. While prevalence reflects the proportion of infected individuals in a population, parasitemia provides insights into the intensity of infection within hosts, offering a different but complementary perspective. In this study, we used quantitative PCR (qPCR) to investigate seasonal and interannual variation in haemosporidian infection intensity among 266 individuals from six bird species in a temperate woodland in Slovakia over 3 years (2017-2019). We focused on the four most abundant taxonomic groups: Erithacus rubecula, Sylvia atricapilla, two parid species (Parus major, Cyanistes caeruleus), and two turdid species (Turdus merula, T. philomelos). Our results revealed distinct, taxon-specific seasonal trajectories. Turdid species showed similar unimodal summer peaks, whereas parids lacked early spring infections and exhibited a steady decline from summer to autumn. E. rubecula demonstrated a gradual increase across the season, while S. atricapilla showed a bimodal pattern with peaks in late spring and early autumn. Spring intensities were highest in 2017-2018, likely due to relapse or new infections, and lowest in 2019, coinciding with warmer and wetter conditions. These findings highlight how seasonal variation in environmental conditions, such as temperature and precipitation, interacts with host life history to shape infection intensity patterns. Our study emphasizes the importance of integrating ecological context with molecular tools to better understand haemosporidian dynamics in wild bird populations.</p>","PeriodicalId":13654,"journal":{"name":"Integrative zoology","volume":" ","pages":""},"PeriodicalIF":3.7000,"publicationDate":"2025-08-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Integrative zoology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1111/1749-4877.13031","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ZOOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Avian haemosporidians are vector-borne parasites with complex transmission dynamics influenced by host ecology and environmental factors. Both prevalence and parasitemia are key measures in host-parasite studies. While prevalence reflects the proportion of infected individuals in a population, parasitemia provides insights into the intensity of infection within hosts, offering a different but complementary perspective. In this study, we used quantitative PCR (qPCR) to investigate seasonal and interannual variation in haemosporidian infection intensity among 266 individuals from six bird species in a temperate woodland in Slovakia over 3 years (2017-2019). We focused on the four most abundant taxonomic groups: Erithacus rubecula, Sylvia atricapilla, two parid species (Parus major, Cyanistes caeruleus), and two turdid species (Turdus merula, T. philomelos). Our results revealed distinct, taxon-specific seasonal trajectories. Turdid species showed similar unimodal summer peaks, whereas parids lacked early spring infections and exhibited a steady decline from summer to autumn. E. rubecula demonstrated a gradual increase across the season, while S. atricapilla showed a bimodal pattern with peaks in late spring and early autumn. Spring intensities were highest in 2017-2018, likely due to relapse or new infections, and lowest in 2019, coinciding with warmer and wetter conditions. These findings highlight how seasonal variation in environmental conditions, such as temperature and precipitation, interacts with host life history to shape infection intensity patterns. Our study emphasizes the importance of integrating ecological context with molecular tools to better understand haemosporidian dynamics in wild bird populations.
期刊介绍:
The official journal of the International Society of Zoological Sciences focuses on zoology as an integrative discipline encompassing all aspects of animal life. It presents a broader perspective of many levels of zoological inquiry, both spatial and temporal, and encourages cooperation between zoology and other disciplines including, but not limited to, physics, computer science, social science, ethics, teaching, paleontology, molecular biology, physiology, behavior, ecology and the built environment. It also looks at the animal-human interaction through exploring animal-plant interactions, microbe/pathogen effects and global changes on the environment and human society.
Integrative topics of greatest interest to INZ include:
(1) Animals & climate change
(2) Animals & pollution
(3) Animals & infectious diseases
(4) Animals & biological invasions
(5) Animal-plant interactions
(6) Zoogeography & paleontology
(7) Neurons, genes & behavior
(8) Molecular ecology & evolution
(9) Physiological adaptations