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Biology subjects

Monteiro, M.

Publications and source records attributed to Monteiro, M..

6 recordsLinked to original sources

Metabolism-Informed Bioreactor Model for Transferring Knowledge from Fed-batch to Continuous Biomanufacturing

Chinese hamster ovary (CHO) cells remain the dominant platform for monoclonal antibody (mAb) manufacturing, and rising demand is pushing the industry from fed-batch toward continuous operation. Continuous cultures promise sustained high cell densities and volumetric productivities, but their operation depends on reliable real-time monitoring, prediction and control. Limited intracellular observability and sparse extracellular measurements hinder this, leaving a persistent gap between mechanistic understanding and predictive deployment. Here we describe a metabolism-informed model for mAb production that embeds reactor- and intracellular-level mass balances directly within a learning architecture, while deliberately avoiding predefined kinetic rate laws and explicit steady-state assumptions. Because conservation relationships remain invariant across operating modes, this formulation provides a principled structural prior for cross-regime generalisation, positioning the model as a soft sensor for continuous bioprocesses: inferring unmeasured intracellular fluxes and one-step ahead forecasting extracellular concentrations to support process monitoring and control. Benchmarking two metabolic network sizes and three metabolic optimisation strategies, concentration predictions are indistinguishable across network sizes. Exchange flux fidelity is agnostic to solver choice, with network size mattering only for intracellular interpretability. Transferring the developed model from fed-batch to continuous operation with fine-tuning outperforming other transfer learning variants. This is consistent with the metabolic structure being invariant to mode of operation. Predicted fluxes reveal growth rate in fed-batch, rather than operating mode, as the dominant axis of metabolic variation, and identify potential regime-shift signals to guide experimental design for continuous culture characterisation. These results chart a route towards digital models sufficiently grounded in first-principles knowledge, yet adaptive for deployment under regime shifts.

systems biology↗

A next generation space antimicrobial: assessing microbial activity and reduction across the ISS

Microbial contamination in spacecraft poses a threat to crew health and operational integrity. Currently, microbial reduction aboard the International Space Station (ISS) relies on rigorous cleaning, which is time-consuming for astronauts. This study analyzes the ISS microbiome and applies a novel quaternized antimicrobial polymer coating to assess its effectiveness in mitigating microbial contamination and its durability over prolonged periods of interaction. The polymer was coated onto five material types representing common objects interacted with by the crew. Each material had six coupons placed on six placards in various ISS locations, while three placards remained on Earth to accumulate microbes from passive and direct transfer. The trial lasted six months, utilizing microbiological cell cultures and genomic analysis to assess bacterial communities and identify species. Among the six placards on the ISS, only one had sufficient viable bacteria to assess the polymers efficacy. On this placard, the polymer coating was shown to decrease culturable bacterial surface loads by 1.39 log10 (equal to a 95.9% reduction) compared with uncoated surfaces. Coated surfaces exhibited less genetic material and lower microbial species richness. Additionally, the polymer coating proved durable, persisting on ISS surfaces throughout the six-month period. This study demonstrates that the antimicrobial polymer coating can actively reduce microbial loads and remains on surfaces in zero gravity environments. Its application is likely beneficial when applied alongside other mitigation activities for viral and bacterial contamination, with potential uses in long-duration spaceflight to enhance crew health and maintain spacecraft integrity. We also generated data showing the lack of microbial presence on the ISS.

microbiology↗

Inferring the Metabolic Objectives of Mammalian Cells via Inverse Modeling of Fluxomics and Metabolomics

Metabolism reflects evolutionary priorities that govern how cells allocate resources. In mammalian cells, metabolic objectives are layered and context-dependent, making it difficult to pinpoint the priorities that underlie observed phenotypes. Here, we introduce ObjFind-M, an inverse optimization framework that infers reaction-level metabolic objectives in mammalian cells directly from fluxomic and metabolomic data. Using Chinese hamster ovary (CHO) cells as a data-rich mammalian cell system, ObjFind-M consistently identifies mitochondrial ATP synthase as the central metabolic driver, supported by key TCA cycle and electron transport chain nodes. Priorities adjust with cellular state, favoring glycolysis-TCA coupling in the growth phase and shifting toward oxidative phosphorylation and redox balance when proliferative activity slows. High recombinant protein producing CHO cells emphasize citrate shuttling and beta-oxidation, linking energy supply with biosynthetic capacity for protein secretion. Benchmarking against conventional objectives demonstrates that maximizing ATP production most accurately reproduces experimental fluxes. By quantifying metabolic objectives directly from data rather than assuming them a priori, ObjFind-M provides a framework for identifying reaction-level strategies that shape cellular decision making. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=76 SRC="FIGDIR/small/677837v1_ufig1.gif" ALT="Figure 1"> View larger version (18K): org.highwire.dtl.DTLVardef@5c507aorg.highwire.dtl.DTLVardef@a7b544org.highwire.dtl.DTLVardef@6db0d4org.highwire.dtl.DTLVardef@17464e2_HPS_FORMAT_FIGEXP M_FIG C_FIG HighlightsO_LIObjFind-M, an inverse FBA framework, infers reaction-level metabolic objectives from fluxomic and metabolomic data. C_LIO_LIATP synthase (Complex V) emerges as the top reaction, supported by NADH-generating TCA reactions such as the -ketoglutarate dehydrogenase complex. C_LIO_LICHO cells suppress formation of toxic or wasteful byproducts while emphasizing energy-efficient flux routing. C_LIO_LIGrowth vs. non-growth phases reveal shifts between biosynthesis and oxidative phosphorylation. C_LIO_LIHigh recombinant protein producers emphasize citrate shuttling and beta-oxidation, linking energy with secretory capacity. C_LIO_LIATP demand maximization provides the most accurate generalizable FBA objective C_LI

systems biology↗

High throughput isolation of male gametophyte cells of Solanum lycopersicum var. Micro-Tom by fluorescence-activated cell sorting.

Efficient isolation of male gametes has enabled unprecedented advances in omics research, crucial for elucidating the molecular mechanisms governing male gametogenesis and fertilization. In this study, we developed a method for isolating generative and sperm cells from the economically important crop Solanum lycopersicum. A double fluorescent marker line was generated in the tomato variety Micro-Tom, employing mTurquoise and mScarlet-I fluorescent proteins under the control of promoters exhibiting preferential activity in generative and sperm cells, respectively. Then we developed a protocol that combines male gamete release from pollen of this line and SYTOX Red live/dead cell stain to obtain viable cells by Fluorescence-activated cell sorting. This allows the isolation of generative cells from mature pollen grains, and of sperm cells from pollen tubes after semi-in vivo growth, both in high quantity and purity. Additionally, an unexpected mScarlet-I signal in the vegetative nucleus, that persists until the sperm cells are formed, allows the sorting of vegetative nuclei. We anticipate that our novel double-marker line will accelerate research into tomato male gametogenesis, thereby enhancing efforts to improve the resilience of fertilization processes to climate change.

plant biology↗

First description of a herpesvirus infection in genus Lepus

During the necropsies of Iberian hares obtained in 2018/2019, along with signs of the nodular form of myxomatosis, other unexpected external lesions were also observed. Histopathology revealed nuclear inclusion bodies in stromal cells suggesting the additional presence of a nuclear replicating virus. Transmission electron microscopy further demonstrated the presence of herpesvirus particles in the tissues of affected hares. We confirmed the presence of herpesvirus in 13 MYXV-positive hares by PCR and sequencing analysis. Herpesvirus-DNA was also detected in seven healthy hares, suggesting its asymptomatic circulation. Phylogenetic analysis based on DNA polymerase gene, grouped this virus within the gammaherpesviruses, close to herpesviruses from bats and rodents. We propose to name this new virus Leporid gammaherpesvirus 5 (LeHV-5), according to the International Committee on Taxonomy of Viruses standards. The impact of herpesvirus infection on the reproduction and mortality of the Iberian hare is yet unknown but may aggravate the decline of wild populations caused by the recently emerged natural recombinant myxoma virus.

microbiology↗

Soft drug-resistant ovarian cancer cells invade via two distinct mechanisms utilizing myosin IIB

The failure of chemotherapeutic drugs in treatment of various cancers is attributed to the acquisition of drug resistance. However, the invasion mechanisms of drug-resistant cancer cells remains incompletely understood. Here we address this question from a biophysical perspective by mapping the phenotypic alterations in ovarian cancer cells (OCCs) resistant to cisplatin and paclitaxel. We show that cisplatin-resistant (CisR), paclitaxel-resistant (PacR) and dual drug-resistant (i.e., resistant to both drugs) OCCs are softer and more contractile than drug-sensitive cells. Protease inhibition suppresses invasion of CisR cells but not of PacR and dual cells, suggesting protease-dependent mode of invasion in CisR cells and protease-independent mode in PacR and dual cells. Despite these differences, actomyosin contractility, mediated by the RhoA-ROCK2-Myosin IIB signaling pathway regulates both modes of invasion. Myosin IIB modulates matrix metalloproteinase-9 (MMP-9) secretion in CisR cells and nuclear squeezing in PacR and dual cells, thereby highlighting its importance as a potential therapeutic target for treatment of drug-resistant ovarian cancer cells.\n\nFinancial SupportAuthors acknowledge financial support from IIT Bombay Healthcare Initiative, CSIR andDepartment of Biotechnology (Govt. of India) (Grant # BT/PR14658/MED/31/107/2010).AK and BTwere supported by fellowships from UGC and CSIR respectively (Govt. of India).\n\nAuthors declare no competing financial interests\n\nAuthor contributions: AK, PR and SS designed the experiments. AK performed most of the experiments and analyzed the data.BT and SG developed drug resistant cell lines and did RT-PCR. MM performed western blot. AD performed AFM experiments. SD performed gelatin zymography. ABB, PM, AM and AD helped with live cell imaging experiments. AK and SS wrote the manuscript. All authors read and approved the final manuscript.\n\nSummary statement: This study identifies drug-specific differences in the modes of invasion utilized by ovarian cancer cells, and demonstrates the role of myosin IIB in regulating both modes of invasion.

biophysics↗