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Background Objectives: India has made significant progress in combating malaria and reducing malaria-related mortality and morbidity. Yet, local transmission and malaria hotspots are important hurdles as India looks to achieve malaria elimination by 2030. Gadchiroli district is a highly malaria-endemic area in Maharashtra, India. It accounts for more than 50% of the reported malaria cases in the state. An. culicifacies and Anopheles fluviatilis are the primary malaria vector in the area. However, the status of vector sibling species is unknown in the district In this study, we aimed to identify the sibling species of Anopheles fluviatilis present in the district.
Methods: An. fluviatilis were collected from the human dwelling of the Dhanora block of the Gadchiroli district. The anopheline mosquitoes were identified morphologically and dissected for detachment of the head and thorax. Sibling species, Incrimination investigations, and analyses of blood meal sources were conducted using polymerase chain reaction (PCR).
Results: Two sibling species of An. fluviatilis S and U were present in the study area. Sibling species S was more prevalent than sibling species U. An. fluviatilis S was found to ingest human blood meal. An. fluviatilis U was feeding on cattle. Nevertheless, none of the samples were found positive for sporozoites or oocysts.
Interpretation Conclusion: The propensity for malaria transmission varies across sibling species of An. fluviatilis. An. fluviatilis sibling-species S is more prevalent in the Gadchiroli district than sibling species U. The sibling species S was reported to play a major role in malaria transmission in central India. An. fluvilitilis S feeds on humans and sibling species U was found to be more zoophilic. The resting behaviour of both the species was in human dwelling, and it can enhance interaction with the sprayed walls. Consequently, to achieve the objective of malaria elimination, it is imperative to conduct a study of vector bionomics at the sibling species level to designate the most suitable vector control tools.
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http://dx.doi.org/10.4103/jvbd.jvbd_187_24 | DOI Listing |
Proc Biol Sci
September 2025
Groningen Institute for Evolutionary Life Sciences, University of Groningen, Groningen, The Netherlands.
Siblings are an important part of an individual's early-life environment and may therefore play an important role in shaping an individual's survival. The quantification of sibling effects on survival is challenging, however, especially in long-lived species with extended parental care and overlapping generations, such as humans. Here, we use historical parish data from Switzerland to quantify how the number of older siblings and their survival status, age and sex are associated with childhood survival.
View Article and Find Full Text PDFGenes (Basel)
August 2025
Institute of Genetics, Vetsuisse Faculty, University of Bern, 3001 Bern, Switzerland.
Hereditary ataxias are a highly heterogenous group of diseases characterized by loss of coordination. In this study, we investigated a family of random-bred dogs, in which two siblings were affected by a slowly progressive ataxia. They presented with clinical signs of progressive cerebellar ataxia, hypermetria, and absent menace response.
View Article and Find Full Text PDFInt J Mol Sci
August 2025
Nankai University School of Medicine, Nankai University, Tianjin 300071, China.
Ankylosing spondylitis (AS) displays wide inter-patient variability that is not accounted for by HLA-B27 alone, suggesting that additional immune and metabolic modifiers contribute to disease severity. Using a genetically matched design, we profiled peripheral blood mononuclear cells from two brother pairs discordant for AS severity and one healthy brother pair. Strand-specific RNA-seq was analyzed with a family-blocked DESeq2 model, while untargeted metabolites were quantified using gas chromatography-mass spectrometry (GC-MS) and liquid chromatography-mass spectrometry (LC-MS).
View Article and Find Full Text PDFBiomedicines
August 2025
Department of Dermatology, Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou 310052, China.
: Bullous congenital ichthyosiform erythroderma (BCIE) is an inherited keratinization disorder caused by pathogenic variants in specific genes. Here, we report a pair of half-siblings with BCIE and tinea capitis due to () and then review the species of ichthyosis previously reported with infection. : We performed dermatological examination, fungal culture, and genetic analysis using whole-exome sequencing (WES) and blocker displacement amplification (BDA)-based Sanger sequencing.
View Article and Find Full Text PDFGen Comp Endocrinol
August 2025
Centre for Bioinnovation, University of the Sunshine Coast, Sippy Downs, Queensland 4556, Australia; School of Science, Technology and Engineering, University of the Sunshine Coast, Sippy Downs, Queensland 4556, Australia. Electronic address:
The corallivorous Crown-of-Thorns Starfish (COTS; Acanthaster cf. solaris) has become a major pest across the Indo-Pacific, primarily due to anthropogenic environmental factors that have increased populations beyond sustainable levels. These effects are costly to both the economy and ecology of coral reefs and require human intervention.
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