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Host-Pathogen Interaction & Immunity Solution — From tRNA Modification and tRF/tiRNA Responses to Infection Biology

tRNA modifications and tRNA-derived small RNAs are emerging regulators of host-pathogen interactions and immunity. tRNA modification and codon usage control regulate effector secretion in plant pathogens, and engineered tRNAs can inhibit viral replication. Arraystar's solution profiles these layers by tRNA-seq, tRF&tiRNA-seq, and modification sequencing.

Infection-responsive tRNA biology · immune cell profiling · pathogen studies

Overview

tRNA biology at the host-pathogen interface

Unconventional secretion of Magnaporthe oryzae effectors in rice cells is regulated by tRNA modification and codon usage control [1]. Phytophthora capsici infection causes dynamic alterations in tRNA modifications and their associated gene candidates in black pepper [2]. Elp3-mediated codon-dependent translation promotes mTORC2 activation and regulates macrophage polarization [3].

Anticodon engineered transfer RNA (tRNA(SUAG)) inhibits hepatitis B virus replication by promoting the degradation of core protein [4]. Arraystar's host-pathogen solution combines tRNA-seq, tRF&tiRNA-seq, and tRNA modification analysis (LC-MS, Modification Seq, tRNA Charging Seq) to profile these infection- and immunity-associated tRNA dynamics.

What is the host-pathogen interaction & immunity solution?

This solution profiles tRNA expression, tRNA modifications, and tRF/tiRNA populations in infection and immunity research, using tRNA-seq, tRF&tiRNA-seq, LC-MS, and modification sequencing, to study host-pathogen interactions and immune regulation.

Service at a Glance

Infection and immunity services — expression, modification, and fragment profiling

Service NameProfiling LayerPrice
tRF&tiRNA SequencingtRF/tiRNA expression in infection and immunity
tRNA SequencingComprehensive tRNA expression profiling
tRNA Charging SeqtRNA expression, modification & charging
LC-MS Based tRNA Modification Analysis55 nucleoside modifications (global profile)

Benefits

Why choose Arraystar for infection and immunity research

🦠

Pathogen-Relevant tRNA Biology

Profile tRNA changes in plant and human pathogens, including effector secretion regulation.

🧬

tRNA Multi-Omics

tRNA Charging Seq profiles expression, modification, and charging in one assay.

⚖️

Codon-Dependent Translation

Elp3-mediated codon-dependent translation and immune cell regulation.

📊

Global Modification Quantification

LC-MS quantifies 55 nucleoside modifications in infected versus control samples.

🧪

Antiviral Research

Engineered tRNA studies supported by tRNA expression and modification profiling.

🔬

Integrated Portfolio

Sequencing, LC-MS, and arrays combine for comprehensive host-pathogen studies.

Background

tRNA and tRF/tiRNA in host-pathogen interactions

tRNAs and their modifications are emerging regulators of host-pathogen interactions. Unconventional secretion of Magnaporthe oryzae effectors in rice cells is regulated by tRNA modification and codon usage control [1]; Phytophthora capsici infection causes dynamic alterations in tRNA modifications and their associated gene candidates in black pepper [2].

In immunity, Elp3-mediated codon-dependent translation promotes mTORC2 activation and regulates macrophage polarization [3]; loss of tRNA-modifying enzyme Elp3 activates a p53-dependent antitumor checkpoint in hematopoiesis [5].

tRFs and tiRNAs perform many biological functions as small noncoding RNAs in infection contexts; engineered transfer RNA (tRNA(SUAG)) inhibits hepatitis B virus replication by promoting the degradation of core protein [4].

Figure 1. tRF&tiRNA functions and association with diseases.
Figure 1. tRF&tiRNA functions and association with diseases.

Background References

  1. Li G, et al. Unconventional secretion of Magnaporthe oryzae effectors in rice cells is regulated by tRNA modification and codon usage control. Nature Microbiology, 2023. PMID: 37563288
  2. Usha A, et al. Phytophthora capsici infection causes dynamic alterations in tRNA modifications and their associated gene candidates in black pepper. Computational and Structural Biotechnology Journal, 2022. PMID: 36420148
  3. Chen D, et al. Elp3-mediated codon-dependent translation promotes mTORC2 activation and regulates macrophage polarization. The EMBO Journal, 2022. PMID: 35920020
  4. Yang X, et al. Anticodon Engineered Transfer RNA (tRNA(SUAG)) Inhibits Hepatitis B Virus Replication by Promoting the Degradation of Core Protein. Advanced Science, 2025. PMID: 40940305

Solution Workflow — Building Your Evidence Chain

From infected or immune samples to tRNA-level insights

1

Sample & RNA QC

RNA quality and quantity assessment before the project proceeds, with small-RNA-retaining purification.

2

tRNA & tRF/tiRNA Expression Profiling

tRNA-seq and/or tRF&tiRNA-seq profile expression changes in infected versus control samples.

3

Modification Profiling

LC-MS quantifies global modification changes; tRNA Charging Seq adds modification and charging layers.

4

Bioinformatics

Differential analyses with detailed annotations and publication-quality graphics.

5

Integrative Interpretation

Cross-reference expression, modification, and fragment data with infection and immune phenotypes.

Bioinformatics & Deliverables

Deliverables for host-pathogen projects

Each service includes detailed bioinformatics analyses to facilitate insights into tRNA biology, diseases, and biomarker applications.

Standard Deliverables

Research Applications

Host-pathogen and immunity research applications

Plant Pathogen Effectors

tRNA modification and codon usage control regulate unconventional effector secretion in Magnaporthe oryzae (Nat Microbiol, 2023).

Oomycete Infection

Phytophthora capsici infection causes dynamic alterations in tRNA modifications in black pepper (Comput Struct Biotechnol J, 2022).

Macrophage Polarization

Elp3-mediated codon-dependent translation promotes mTORC2 activation and regulates macrophage polarization (EMBO J, 2022).

Antiviral tRNA Research

Anticodon engineered transfer RNA inhibits hepatitis B virus replication by promoting core protein degradation (Adv Sci, 2025).

Hematopoiesis & Immunity

Loss of tRNA-modifying enzyme Elp3 activates a p53-dependent antitumor checkpoint in hematopoiesis (J Exp Med, 2021).

Choosing the Right Strategy for Your Study

Method selection depends on your research question

DimensiontRF&tiRNA SequencingtRNA SequencingtRNA Charging SeqLC-MS Analysis
Primary outputtRF/tiRNA expressiontRNA expressionExpression, modification & charging55 nucleoside modifications
Best forSmall RNA responses in infectiontRNA pool changesIntegrated tRNA multi-omicsGlobal modification status
ResolutionFragment-levelGene-levelSingle-nucleotide (predicted)Nucleoside-level
Recommended RNA> 1 µg> 2 µg> 5 µg10*–15 µg

Sample Requirements

Official Arraystar sample submission requirements for host-pathogen projects

RNA Amount & Quality

  • Total RNA input: > 1 µg for tRF&tiRNA-seq, > 2 µg for tRNA-seq, > 5 µg for tRNA Charging Seq, and 10*–15 µg for LC-MS (official recommended minimums, including sample QC). Supply twice the recommended minimum to avoid project delays.
  • Purification: TRIzol / RNA precipitation or an RNA isolation kit. Because tRNA and tRF/tiRNA are < 200 nt, use a kit specified to retain small RNAs (e.g. Qiagen miRNeasy).
  • Concentration: > 20 ng/µL by Nanodrop; OD260/280 ~2.0 (acceptable 1.7–2.1); OD260/230 > 1.8.
  • Integrity: sharp 18S/28S rRNA bands by gel, or RIN > 7.0 by Bioanalyzer (serum/plasma/exosome/FFPE RNA exempt).
  • DNase treatment: optional for sequencing; required for qPCR projects.

Shipping Instructions

  • Ship RNA in nuclease-free water (> 20 ng/µL), freeze-dried, or in ethanol; store at −80 °C or in liquid nitrogen.
  • Use nuclease-free certified, screw-cap 1.5 mL microtubes; seal caps with Parafilm; place tubes in a plastic bag.
  • Use 10 kg dry ice as refrigerant; include a signed Project Form and the sample list.
  • Ship to: Arraystar Inc., 9430 Key West Avenue #128, Rockville, MD 20850, USA. Contact us before shipping.

FAQ

Common questions about host-pathogen interaction & immunity studies

How are tRNA modifications involved in host-pathogen interactions?
tRNA modification and codon usage control regulate unconventional secretion of Magnaporthe oryzae effectors in rice cells, and Phytophthora capsici infection causes dynamic alterations in tRNA modifications in black pepper. LC-MS and modification sequencing profile these quantitative changes during infection and immunity studies.
Which services profile immune cell tRNA biology?
Elp3-mediated codon-dependent translation regulates macrophage polarization. tRNA-seq profiles tRNA expression changes, tRNA Charging Seq adds modification and charging layers, and tRF&tiRNA-seq captures tRNA-derived small RNA responses in immune cells during activation and polarization studies across experimental conditions, infection models, and immune cell types.
Can the solution support antiviral tRNA research?
Yes. Anticodon engineered transfer RNA (tRNA(SUAG)) inhibits hepatitis B virus replication by promoting core protein degradation. tRNA expression and modification profiling support studies of engineered tRNAs and their antiviral mechanisms in cellular and animal infection models with quantitative readouts in both cellular and whole-organism contexts.
What is the minimum amount of RNA required?
Recommended minimums are more than 1 µg of total RNA for tRF&tiRNA-seq, more than 2 µg for tRNA-seq, more than 5 µg for tRNA Charging Seq, and 10–15 µg for LC-MS analysis — official Arraystar recommended minimums for the entire experiment in a single attempt, including sample QC.
What bioinformatics analyses are included?
Sequencing projects include differential expression with detailed annotation, subtype analysis, and volcano plots; tRNA Charging Seq adds differential modification and charging analyses; LC-MS projects include raw and normalized peak data with chromatograms and differential modification among samples for interpretation and reporting, with documentation for straightforward use.
Can the solution be combined with other Arraystar services?
Yes. tRNA modification sequencing (m1A, m3C, m1G, m2,2G; m7G; m3C), tRNA PCR arrays, and other services can be added for integrated studies within Arraystar's tRNA research portfolio, connecting infection biology with epitranscriptomic regulation and immunity research programs in one integrated study design.

Selected Publications

Key References for Host-Pathogen Interaction & Immunity Research

  1. Li G, et al. Unconventional secretion of Magnaporthe oryzae effectors in rice cells is regulated by tRNA modification and codon usage control. Nature Microbiology, 2023. PMID: 37563288
  2. Usha A, et al. Phytophthora capsici infection causes dynamic alterations in tRNA modifications and their associated gene candidates in black pepper. Computational and Structural Biotechnology Journal, 2022. PMID: 36420148
  3. Chen D, et al. Elp3-mediated codon-dependent translation promotes mTORC2 activation and regulates macrophage polarization. The EMBO Journal, 2022. PMID: 35920020
  4. Yang X, et al. Anticodon Engineered Transfer RNA (tRNA(SUAG)) Inhibits Hepatitis B Virus Replication by Promoting the Degradation of Core Protein. Advanced Science, 2025. PMID: 40940305
  5. Rosu A, et al. Loss of tRNA-modifying enzyme Elp3 activates a p53-dependent antitumor checkpoint in hematopoiesis. Journal of Experimental Medicine, 2021. PMID: 33507234
  6. Goffena J, et al. Elongator and codon bias regulate protein levels in mammalian peripheral neurons. Nature Communications, 2018. PMID: 29497044

Ready to Profile tRNA Biology in Infection and Immunity?

Arraystar profiles tRNA expression, modifications, and tRF/tiRNA responses for host-pathogen and immunity research — get a quote and a project timeline tailored to your study.