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Gajigan, A. P.

Publications and source records attributed to Gajigan, A. P..

4 recordsLinked to original sources

A high-resolution diel survey of surface ocean metagenomes, metatranscriptomes, and transfer RNA transcripts

The roles of marine microbes in ecosystem processes are inherently linked to their ability to sense, respond, and ultimately adapt to environmental change. Capturing the nuances of this perpetual dialogue and its long-term implications requires insight into the subtle drivers of microbial responses to environmental change that are most accessible at the shortest scales of time. Here, we present a multi-omics dataset comprising surface ocean metagenomes, metatranscriptomes, tRNA transcripts, and biogeochemical measurements, collected every 1.5 hours for 48 hours at two stations within coastal and adjacent offshore waters of the tropical Pacific Ocean. We expect that this integrated dataset of multiple sequence types and environmental parameters will facilitate novel insights into microbial ecology, microbial physiology, and ocean biogeochemistry and help investigate the different mechanisms of adaptation that drive microbial responses to environmental change.

microbiology↗

A dinoflagellate-infecting giant virus with a micron-length tail

Viral infection is a ubiquitous source of marine plankton mortality, but relatively few viruses that infect phytoplankton have been characterized. Here we describe a virus, PelV-1, with unusual morphological and genomic features that infects a dinoflagellate, Pelagodinium sp. Both host and virus were isolated from the epipelagic zone in the North Pacific Subtropical Gyre. PelV-1 has a [~]200 nm capsid size, and the virion variably exhibits two appendages, the presence and length of which may reflect different stages of virion maturity or artifacts of sample preparation. The appendages are a thinner 30 nm-wide tail-like structure that can extend to 2.3 {micro}m -- the longest virus appendage described to date-- and a shorter, thicker (>40-70 nm) protrusion, which appears to emerge from a star-shaped capsid opening directly opposite the attachment point of the long, thin tail. Sequencing and assembly of material in a purified lysate generated a high-coverage (> 4,000x) genome of 459 kb (33.8% GC). A second, distinct genome of 504 kb (25.8% GC) was also assembled, but had low read coverage (< 24x), suggesting the presence of a low-abundance, co-cultured virus (co-PelV). Phylogenetic analysis indicates that both PelV-1 and co-PelV are members of Mesomimiviridae. They contain various genes for the metabolism of amino acids (e.g., asparagine synthase), carbohydrates (e.g., epimerase, glycosyl hydrolase, aconitate hydratase, succinate dehydrogenase of the TCA cycle), and lipids (e.g., phospholipases), as well as other noteworthy genes (e.g., light-harvesting complex, rhodopsin, ion channel, sugar transporters, aquaporin). PelV-1 also has ORFs most similar to tail fiber genes of Synechococcus phage and other tail domain-containing protein homologs. The ecological advantages that might be conferred by the extraordinarily long tail and metabolic genes of PelV-1 is unknown, but this isolate expands the scope of morphological and metabolic diversity of viruses and suggests many more unusual marine viruses await discovery. Author summaryGiant viruses challenged our traditional views of virology due to their large size and the presence of hundreds of auxiliary metabolic genes. But despite the immense giant virus diversity discovered through sequencing, few isolates were described, and those were primarily viruses that infect amoeba host and rarely from phytoplankton. This hampers our understanding of marine host-virus interaction and thus the impact of viruses on the ocean ecosystem. Here we provide genomic and morphological characterization of a novel dinoflagellate giant virus (PelV-1) and a second co-occurring, albeit low abundance, virus (co-PelV). Dinoflagellates are vital in marine symbiosis and algal blooms but only two giant virus isolates have been described with no available genomic resources to date. Thus, this is a significant contribution to the literature on dinoflagellate viruses. Among the notable features of PelV-1 are its unique micron-length tail appendage, phagocytosis-like entry mechanism and its varied auxiliary metabolic genes including photosynthesis and energy generating genes.

microbiology↗

Phytoplankton and giant virus dynamics during different monsoon seasons, a fish kill, and a toxic bloom in a eutrophic mariculture area

Harmful algal blooms (HABs) pose a significant public health concern and can cause severe economic losses. In Bolinao, Philippines, intensive mariculture has led to diatom- or dinoflagellate-dominated HABs since the 2000s, raising risks of paralytic shellfish poisonings and fish kills. In the context of ongoing HAB monitoring and mitigation efforts, we investigated the phytoplankton and associated giant viruses during two seasons (Nov-Dec 2021 and Apr-May 2022). Our sampling encompassed a saxitoxin episode lasting 2.5 months (April-June 2022), and a fish kill (May 15-16, 2022). We used a low-cost flow-through camera (PlanktoScope) and 18S rRNA gene amplicon sequencing to identify the dominant phytoplankton. We detected the presence of Alexandrium sp., a known saxitoxin-producing alga, coincident with a toxin alert that resulted in a shellfish ban, even though it was not the dominant taxon. Using electron microscopy, we observed diverse morphologies of virus-like particles (VLPs), including "giant" icosahedral VLPs (~200 nm capsids). We assembled giant virus genomes from metagenomic data collected at different bloom phases. Phylogenetic and functional analyses suggest that the recovered genomes are primarily from viruses in the orders Imitervirales and Algavirales, encoding diverse auxiliary metabolic genes involved in nutrient transport and carbohydrate metabolism. The diversity and spatiotemporal dynamics of plankton and their viruses described in this study contributed to our understanding of the broader microbial context of HABs. ImportanceHABs are widespread phenomena that can be detrimental to livelihoods and health in coastal communities. Understanding what drives their formation, maintenance, and crash could aid in predicting, and potentially alleviating these events. Here, we report on the diversity and temporal dynamics of phytoplankton and giant viruses during a HAB event. Our findings revealed a diverse array of giant viruses belonging to thirteen families in a eutrophic coastal environment. We found evidence of associations between several phytoplankton-giant virus pairs and found a temporal/seasonal influence on phytoplankton-giant virus community structure. While future research is needed to establish definitive links between the giant viruses and HABs species succession, this study lays the groundwork for future mechanistic studies.

microbiology↗

Ultrastructural and transcriptional changes during a giant virus infection of a green alga

The complete genome sequence of the Oceanusvirus kaneohense strain (Tetraselmis virus 1; TetV-1) was previously reported, but little is known about the virus infection cycle. Using a permissive Tetraselmis isolate (UHM1315), we estimated the eclipse period (4-8 hours), latent period (16 hrs), and burst size (800-1000) of the virus and documented ultrastructural and transcriptional changes in the host during infection. Putative viral factories and electron-dense inclusion bodies appeared in the cytoplasm of infected cells by 8 and 16 h post-infection, respectively. The nucleus and chloroplasts appeared to remain intact but reduced in size after 8 h. Transcriptome sequencing suggests that the viral genome codes for 830 transcripts. Those expressed early in infection (eclipse period at 0.25 and 4 hr) were related to the initiation of transcription, DNA synthesis, translation, and host immune repression. During the later, post-eclipse period (8, 12, 16 hr), virus structural genes were expressed. For the algal host, transcripts related to lipid metabolism and endocytosis were upregulated during the early phase, while those for protein modification/ turnover/ transport were downregulated. In the later period, host transcripts associated with basic cellular processes were upregulated, while genes related to morphogenesis/development were downregulated. Many of the most highly expressed virus and host genes were of unknown function, highlighting a need for additional functional studies.

microbiology↗