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Research

Research interests

My research interests lie in how bacteria, the bacteriophages that infect them and their hosts interact, and in how these interactions shape infection and antibiotic resistance.

Research theme 01

Phage therapy

Bacteriophages, or phages, are viruses that infect bacteria. Lytic phages use the host cell to make new phage particles and release them by bursting the cell, while temperate phages can integrate into the host genome and remain dormant. Because a phage usually infects a narrow range of bacterial strains, it can target a pathogen while sparing much of the surrounding microbiota.

Why it matters

Rising antibiotic resistance has renewed interest in phage therapy as a complement or alternative to antibiotics. Using phages well depends on understanding how they find, infect and propagate in their hosts, how bacteria resist infection, and how phages can be produced reliably.

My master’s thesis asked how host cell density and culture-derived molecules affect bacteriophage propagation when hosts are scarce.

Related work

Schematic of a bacteriophage attaching to a bacterial cell, showing the capsid, contractile tail and tail fibres.
Schematic of a tailed bacteriophage attaching to a bacterial host. Original illustration.

Research theme 02

Host–pathogen interactions

Infection is shaped by interactions between a pathogen and its host: how microbes attach to and enter host cells, acquire nutrients and evade defences, and how the host’s cells and immune system detect and respond to them. The same interactions determine whether an infection is cleared, persists or causes disease.

Why it matters

Translational bioscience aims to turn this mechanistic understanding into better diagnostics, therapies and preventive strategies. Host–pathogen interactions are a core research interest of my doctoral studies in Translational Biosciences at the University of Missouri.

Related work

Schematic of bacteria adhering to a host cell, with one bacterium internalised in a vacuole beside the nucleus.
Schematic of bacteria adhering to a host cell, with one bacterium internalised beside the nucleus. Original illustration.

Research theme 03

Antibiotic resistance

Bacteria become resistant to antibiotics through mutations and by acquiring resistance genes from other bacteria, often on plasmids and other mobile genetic elements. Common mechanisms include reduced drug uptake, efflux pumps that expel the drug, enzymes that inactivate it, and changes to the drug’s target.

Why it matters

Food animals and food products can carry resistant bacteria, making them potential reservoirs from which resistance can spread. My undergraduate thesis tested E. coli isolated from raw beef in Dhaka against 20 antibiotics and examined their plasmid profiles. All 17 isolates were resistant to penicillin and oxacillin, and two were resistant to 15 of the antibiotics tested.

Related work

Schematic of a bacterium showing reduced uptake, efflux pumps, enzymatic inactivation, an altered target and a resistance plasmid.
Common mechanisms of antibiotic resistance in a bacterial cell. Original illustration.

Current research

Doctoral research

I am a PhD student in the Translational Biosciences programme at the University of Missouri–Columbia, advised by Dr. Pamela Brown in the Division of Biological Sciences.

My current research in the Brown Lab examines how the plant pathogen Agrobacterium tumefaciens grows and elongates its cells, work I have presented as a research poster. Bacterial cell growth depends on building and remodelling the cell wall, a process targeted by many antibiotics.

A B M Rezwanul Kabir explaining his research poster on cell growth and elongation in Agrobacterium tumefaciens to a meeting attendee
Discussing a research poster on cell growth and elongation in Agrobacterium tumefaciens.
Three schematic habitats of extremophiles: a hot spring, a salt lake and acidic rock drainage.
Extremophile habitats relevant to bioremediation. Original illustration.

Related publication

Book chapter · De Gruyter · 2023

An Overview of Extremophiles as Microbial Armament for Bioremediation

Extremophiles are microorganisms that thrive in conditions such as high temperature, high salinity or extreme pH. This co-authored chapter gives an overview of extremophiles as tools for bioremediation, the use of microbes to break down or remove environmental pollutants.