Some mat-forming cyanobacteria produce harmful cyanotoxins, yet benthic species remain understudied compared to planktonic counterparts. This study assesses the diversity, distribution and toxin production of mat-forming cyanobacteria across lentic and lotic systems in Nova Scotia, Canada. We documented greater cyanobacterial species richness in lentic environments, with six dominant species distributed into two major Microcoleus clades, five of which represent putative novel taxa. Two Microcoleus species with the genetic repertoire to produce anatoxins were prevalent. One has been previously reported in Canada, while the second represents a novel species found exclusively in an environment impacted by discharge from a water treatment plant. We observed variability in the gene clusters responsible for the biosynthesis of anatoxin-a and associated analogues (ATXs), including the discovery of a novel anaG variant with a ~ 1.7 kb insertion in a Microcoleus strain dominating homoanatoxin-producing mats. This extended anaG, encoding a polyketide synthase with an additional methyltransferase domain, coexists with shorter variants, leading to the production of a mixture of ATXs. These findings highlight the genetic diversity of benthic cyanobacteria in freshwater environments, with Microcoleus as the primary contributor to the production of ATXs in both lentic and lotic systems, underscoring their potential to produce harmful toxins.
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http://dx.doi.org/10.1111/1462-2920.70067 | DOI Listing |
Trans R Soc Trop Med Hyg
March 2025
Molecular Epidemiology department, ICMR-National Institute of Malaria Research, Sector 8, Dwarka, 110077 New Delhi, India.
Background: Rapid diagnostic tests (RDTs) are vital for malaria diagnosis, especially in resource-limited areas. RDTs targeting histidine-rich protein 2 (PfHRP2) and its structural homologue PfHRP3 are commonly used for detecting Plasmodium falciparum. However, genetic deletions in these proteins can affect test accuracy.
View Article and Find Full Text PDFBackground: This study conducted genetic analysis on fetuses indicated to be at high risk by non-invasive prenatal testing (NIPT) to explore the etiology.
Methods: Karyotype analysis and single nucleotide polymorphism array (SNP-array) were performed to detect copy number variations in fetal amniotic fluid and parental peripheral blood.
Results: Fetal karyotype showed 46, X?, del (4) (q28q31.
Front Immunol
March 2025
Division of Haematology, Respiratory Medicine and Oncology, Department of Internal Medicine, Faculty of Medicine, Saga University, Saga, Japan.
High tumour mutational burden (TMB-high), identified through comprehensive genomic profiling (CGP), is a biomarker that predicts the efficacy of immune checkpoint inhibitors. CGP testing is recommended for rare cancers with limited effective treatment options. Here, we provide the first report of a malignant phyllodes tumour of the breast demonstrating TMB-high status and effective treatment with pembrolizumab.
View Article and Find Full Text PDFFront Immunol
March 2025
Department of Otorhinolaryngology Head and Neck Surgery, The First Affiliated Hospital of Naval Medical University (Changhai Hospital of Shanghai), Shanghai, China.
Immunotherapy has brought better survival benefits in the treatment of recurrent or metastatic head and neck squamous cell carcinoma (R/M HNSCC). However, owing to the lack of relevant biomarkers that could predict the efficacy of this treatment, it often has to be maintained. Here we report on a patient with stage IVA squamous cell carcinoma of the tongue who developed an unresectable lesion in the neck after surgery and radical chemoradiotherapy.
View Article and Find Full Text PDFMalariaworld J
February 2025
Department of Pharmaceutical Microbiology and Biotechnology, Nnamdi Azikiwe University, Awka Nigeria.
Introduction: The genetic diversity of correlates with its pathogenicity, therefore design of evidence-based intervention strategies to eradicate malaria requires genetic diversity surveillance. This study characterised the allelic frequencies and genetic diversity of parasites isolated from Awka, Nigeria.
Materials And Methods: Genomic DNA was extracted from 177 isolates and the polymorphic regions of the and genes were genotyped by nested polymerase chain reaction (PCR).
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