Heather Hendrickson | |
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Born | |
Academic background | |
Alma mater | University of Pittsburgh |
Thesis |
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Doctoral advisor | Professor Jeffrey G. Lawrence |
Academic work | |
Institutions | University of Canterbury,Massey University |
Website | hendricksonlab |
Heather Hendrickson is an American microbiologist based in New Zealand. She is an Associate Professor in the School of Biological Sciences at the University of Canterbury in Christchurch,New Zealand. She previously worked at Massey University,Auckland,New Zealand. Her research is focussed on the evolution of bacterial cell shape,and the discovery of bacteriophages that can attack antibiotic-resistant bacteria and the bee disease American foulbrood.
Hendrickson was born in Salt Lake City,Utah,and moved to California as a young child;she describes herself as "obsessed with birds and bugs from a really young age." [1] Her family members were conservative Church of Jesus Christ of Latter-Day Saints (Mormons) who did not believe in evolution;in her household there were rules such as "no drinking alcohol,coffee or tea,no popular music and no one smokes. Girls had to wear skirts to church and we were trained as a kid to be a homemaker." [1] However,by the time she went to graduate school in Pittsburgh,she had become an atheist. [1]
Hendrickson graduated from the University of Utah in 2000 with a Bachelor of Science,then completed a PhD in Molecular,Cellular and Developmental Biology at the University of Pittsburgh in 2008. She spent three years as a postdoctoral researcher at the Biochemistry Department of the University of Oxford,as an HFSP Long-Term Fellow,researching variability of DNA replication in Escherichia coli . [2] [3] Hendrickson moved to the Albany campus of Massey University as a lecturer in evolutionary genetics,rising to Senior Lecturer in Molecular Bioscience in 2015. [4] [5] She moved from Massey University to become a Senior Lecturer at the University of Canterbury in 2022. She is currently the president of the New Zealand Microbiological Society. [6]
Hendrickson studies microbial evolution,specifically bacteriophages and genomics of bacteria. Her research has two main components:transitions in bacterial evolution,including the evolution of cell shape, [7] and the discovery of new bacteriophages,especially ones which could counter antibiotic-resistant bacteria. [8] She uses a combination of experimental evolution,cell biology,and bacterial genomics. [6]
Analysis of the evolutionary tree of bacteria suggests the ancestral bacterium was rod-shaped. Hendrickson studies the way bacteria like Deinococcus , Staphylococcus ,and Streptococcus bacteria evolved a spherical shape. [9] All three of these genera lack the gene for the protein MreB (the equivalent of actin in eukaryotes) which controls the width of rod-shaped bacteria. Normally deleting this gene kills the bacterium,but Hendrickson's lab has evolved a rod-like bacterial strain that can withstand the deletion of the MreB gene,enabling them to study how a spherical shape has evolved. [9]
To study the process of endosymbiosis,where one single-celled organism captures and incorporates another into its body,Hendrickson and her collaborators ran 10,000-generation experiments with mixtures of amoebae and their bacterial prey,to monitor possible collaborative partnerships that formed and sequence their genomes. [10]
Hendrickson's lab works on discovering and understanding the biology of bacteriophages that attack the bacteria Pseudomonas , Lactocococus , Mycobacterium ,and Paenibacillus . [9] In collaboration with the American Foulbrood Management Agency,they are currently investigating phages that kill the bacterium Paenibacillus larvae ,which causes American foulbrood (AFB) disease in honey bees. [9] In New Zealand,antibiotics may not be used to control AFB because they leave residues in the honey,so hives are usually destroyed instead. The Hendrickson lab screens soil samples collected by beekeepers from beneath healthy hives,looking for bacteriophages that could be used to prevent AFB infection. [11]
Hendrickson and her colleagues also work on discovering new bacteriophages that might be effective against antibiotic-resistant bacteria. [12] [13] Six of her students discovered bacteriophages that could kill Mycobacterium smegmatis ,a relative of the tuberculosis bacterium M. tuberculosis ,which can infect the lungs of vulnerable people such as cystic fibrosis sufferers. [14]
A bacteriophage, also known informally as a phage, is a virus that infects and replicates within bacteria and archaea. The term is derived from Ancient Greek φαγεῖν (phagein) 'to devour' and bacteria. Bacteriophages are composed of proteins that encapsulate a DNA or RNA genome, and may have structures that are either simple or elaborate. Their genomes may encode as few as four genes and as many as hundreds of genes. Phages replicate within the bacterium following the injection of their genome into its cytoplasm.
A prophage is a bacteriophage genome that is integrated into the circular bacterial chromosome or exists as an extrachromosomal plasmid within the bacterial cell. Integration of prophages into the bacterial host is the characteristic step of the lysogenic cycle of temperate phages. Prophages remain latent in the genome through multiple cell divisions until activation by an external factor, such as UV light, leading to production of new phage particles that will lyse the cell and spread. As ubiquitous mobile genetic elements, prophages play important roles in bacterial genetics and evolution, such as in the acquisition of virulence factors.
Phage therapy, viral phage therapy, or phagotherapy is the therapeutic use of bacteriophages for the treatment of pathogenic bacterial infections. This therapeutic approach emerged at the beginning of the 20th century but was progressively replaced by the use of antibiotics in most parts of the world after the Second World War. Bacteriophages, known as phages, are a form of virus that attach to bacterial cells and inject their genome into the cell. The bacteria's production of the viral genome interferes with its ability to function, halting the bacterial infection. The bacterial cell causing the infection is unable to reproduce and instead produces additional phages. Phages are very selective in the strains of bacteria they are effective against.
Transduction is the process by which foreign DNA is introduced into a cell by a virus or viral vector. An example is the viral transfer of DNA from one bacterium to another and hence an example of horizontal gene transfer. Transduction does not require physical contact between the cell donating the DNA and the cell receiving the DNA, and it is DNase resistant. Transduction is a common tool used by molecular biologists to stably introduce a foreign gene into a host cell's genome.
Escherichia virus T4 is a species of bacteriophages that infect Escherichia coli bacteria. It is a double-stranded DNA virus in the subfamily Tevenvirinae of the family Straboviridae. T4 is capable of undergoing only a lytic life cycle and not the lysogenic life cycle. The species was formerly named T-even bacteriophage, a name which also encompasses, among other strains, Enterobacteria phage T2, Enterobacteria phage T4 and Enterobacteria phage T6.
Filamentous bacteriophages are a family of viruses (Inoviridae) that infect bacteria, or bacteriophages. They are named for their filamentous shape, a worm-like chain, about 6 nm in diameter and about 1000-2000 nm long. This distinctive shape reflects their method of replication: the coat of the virion comprises five types of viral protein, which are located in the inner membrane of the host bacterium during phage assembly, and these proteins are added to the nascent virion's DNA as it is extruded through the membrane. The simplicity of filamentous phages makes them an appealing model organism for research in molecular biology, and they have also shown promise as tools in nanotechnology and immunology.
Lacticaseibacillus casei is an organism that belongs to the largest genus in the family Lactobacillaceae, a lactic acid bacteria (LAB), that was previously classified as Lactobacillus casei. This bacteria has been identified as facultatively anaerobic or microaerophilic, acid-tolerant, non-spore-forming bacteria.
Lysogeny, or the lysogenic cycle, is one of two cycles of viral reproduction. Lysogeny is characterized by integration of the bacteriophage nucleic acid into the host bacterium's genome or formation of a circular replicon in the bacterial cytoplasm. In this condition the bacterium continues to live and reproduce normally, while the bacteriophage lies in a dormant state in the host cell. The genetic material of the bacteriophage, called a prophage, can be transmitted to daughter cells at each subsequent cell division, and later events can release it, causing proliferation of new phages via the lytic cycle.
Bacteriophages (phages), potentially the most numerous "organisms" on Earth, are the viruses of bacteria. Phage ecology is the study of the interaction of bacteriophages with their environments.
Allan McCulloch Campbell was an American microbiologist and geneticist and the Barbara Kimball Browning Professor Emeritus in the Department of Biology at Stanford University. His pioneering work on Lambda phage helped to advance molecular biology in the late 20th century. An important collaborator and member of his laboratory at Stanford University was biochemist Alice del Campillo Campbell, his wife.
Esther Miriam Zimmer Lederberg was an American microbiologist and a pioneer of bacterial genetics. She discovered the bacterial virus lambda phage and the bacterial fertility factor F, devised the first implementation of replica plating, and furthered the understanding of the transfer of genes between bacteria by specialized transduction.
Bacteria are ubiquitous, mostly free-living organisms often consisting of one biological cell. They constitute a large domain of prokaryotic microorganisms. Typically a few micrometres in length, bacteria were among the first life forms to appear on Earth, and are present in most of its habitats. Bacteria inhabit the air, soil, water, acidic hot springs, radioactive waste, and the deep biosphere of Earth's crust. Bacteria play a vital role in many stages of the nutrient cycle by recycling nutrients and the fixation of nitrogen from the atmosphere. The nutrient cycle includes the decomposition of dead bodies; bacteria are responsible for the putrefaction stage in this process. In the biological communities surrounding hydrothermal vents and cold seeps, extremophile bacteria provide the nutrients needed to sustain life by converting dissolved compounds, such as hydrogen sulphide and methane, to energy. Bacteria also live in mutualistic, commensal and parasitic relationships with plants and animals. Most bacteria have not been characterised and there are many species that cannot be grown in the laboratory. The study of bacteria is known as bacteriology, a branch of microbiology.
Lysins, also known as endolysins or murein hydrolases, are hydrolytic enzymes produced by bacteriophages in order to cleave the host's cell wall during the final stage of the lytic cycle. Lysins are highly evolved enzymes that are able to target one of the five bonds in peptidoglycan (murein), the main component of bacterial cell walls, which allows the release of progeny virions from the lysed cell. Cell-wall-containing Archaea are also lysed by specialized pseudomurein-cleaving lysins, while most archaeal viruses employ alternative mechanisms. Similarly, not all bacteriophages synthesize lysins: some small single-stranded DNA and RNA phages produce membrane proteins that activate the host's autolytic mechanisms such as autolysins.
Persister cells are subpopulations of cells that resist treatment, and become antimicrobial tolerant by changing to a state of dormancy or quiescence. Persister cells in their dormancy do not divide. The tolerance shown in persister cells differs from antimicrobial resistance in that the tolerance is not inherited and is reversible. When treatment has stopped the state of dormancy can be reversed and the cells can reactivate and multiply. Most persister cells are bacterial, and there are also fungal persister cells, yeast persister cells, and cancer persister cells that show tolerance for cancer drugs.
A corynebacteriophage is a DNA-containing bacteriophage specific for bacteria of genus Corynebacterium as its host. Corynebacterium diphtheriae virus strain Corynebacterium diphtheriae phage introduces toxigenicity into strains of Corynebacterium diphtheriae as it encodes diphtheria toxin, it has subtypes beta c and beta vir. According to proposed taxonomic classification, corynephages β and ω are unclassified members of the genus Lambdavirus, family Siphoviridae.
Autographiviridae is a family of viruses in the order Caudovirales. Bacteria serve as natural hosts. There are 373 species in this family, assigned to 9 subfamilies and 133 genera.
The CTXφ bacteriophage is a filamentous bacteriophage. It is a positive-strand DNA virus with single-stranded DNA (ssDNA).
Martha Rebecca Jane Clokie is a professor of microbiology at the University of Leicester. Her research investigates the identification and development of bacteriophages that kill pathogens in an effort to develop new antimicrobials.
Multidrug-resistant bacteria are bacteria that are resistant to three or more classes of antimicrobial drugs. MDR bacteria have seen an increase in prevalence in recent years and pose serious risks to public health. MDR bacteria can be broken into 3 main categories: Gram-positive, Gram-negative, and other (acid-stain). These bacteria employ various adaptations to avoid or mitigate the damage done by antimicrobials. With increased access to modern medicine there has been a sharp increase in the amount of antibiotics consumed. Given the abundant use of antibiotics there has been a considerable increase in the evolution of antimicrobial resistance factors, now outpacing the development of new antibiotics.
Integrative and conjugative elements (ICEs) are mobile genetic elements present in both gram-positive and gram-negative bacteria. In a donor cell, ICEs are located primarily on the chromosome, but have the ability to excise themselves from the genome and transfer to recipient cells via bacterial conjugation.