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Introduction

Bacteriophages are viruses that can infect and destruct bacteriums. This belongings of the bacteriophages was exploited and used against bacteriums that were anti-biotic resistant. The major restraint with antibiotics was that bacterium developed opposition against these antibiotics, enabling them to last despite the application of the specific antibiotic drugs ( Berkowitz 1995 ) . This proved to be a terrible job in destructing the bacterium and forestalling the slaughter brought about by them. This proved the platform for the coming of bacteriophage therapeutics. The usage of bacteriophages as curative agents was made possible, since they had more specificity than the usual drugs and the phages were successful in perforating the biofilm covered by the polyose bed ( Aguita 2009 ) , which was found to be an obstruction for the common drugs in making the bacterium and killing them. Bacteriophage therapy finds its Markss in a broad scope of medical Fieldss such as Human medical specialty, Veterinary Science, Dentistry and even Agriculture.

Bacteriophages are any viruses that can assail and kill bacteriums. Bacteriophages have an outer protein mirid bug that holds the familial stuff interior ( Mc Grath et Al 2007 ) . The organic structure can be divided into a caput, neckband and tail part. The caput holds the familial stuff and the tail has fibres that enable the retention of the bacteriophages onto the bacterial walls and finally ensuing in passing of the familial stuff into the bacterium to enable the reproduction of phages and devastation of the bacterium. The bacteriophage lifecycle can be of two ways.

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Lytic Cycle

The lytic rhythm consequences in the decease of the bacterial host ( JG Black 2002 ) . The rhythm is of five phases, ( seen in Fig 1. )

Attachment – the bacteriophage attaches to the surface of the bacteriums by the aid of its tail fibres.

Penetration – the phage releases enzymes to weaken the cell wall of the bacteriums and so injects its familial stuff into the bacterium.

Biosynthesis – the phage DNA is integrated with the host Deoxyribonucleic acid and this makes the host to synthesise the phage DNA and other related constituents.

Assembly – the phage DNA and constituents that were synthesized are put together to organize new phage atoms.

Maturation & A ; Lysis – after the assembly is complete, the phage particles green goodss and enzyme that breaks the bacterial cell wall and doing the lysis of the bacteriums and let go ofing the phages from interior.

Lysogenic Cycle

This rhythm is complementary to the lytic rhythm of the bacteriophage ( Bertani 1953 ) . The following are the stairss of lysogenic rhythms, ( seen in Fig 1. )

Entry – the familial stuff of the bacteriophage enters the host bacterial cell

Integration – the viral DNA integrates with the host Deoxyribonucleic acid

Replication – the host cell DNA copies the viral chromosomes

Cell division – the host cell divides and along with the host familial stuff, the viral familial stuff is transmitted into the girl bacterial cells.

Lytic rhythm – after the cell division, the hibernating viral DNA enters lytic rhythm and it follows similar stairss from the lytic rhythm ensuing in the generation of the phage atoms and their release.

The lysogenic rhythm of bacteriophages, the lysogenicity does n’t ensue in the lysis of the host cells and therefore the phages that exhibit lysogenicities are non ideal in developing the phage therapy.

Fig. 1 – Shows the complementarity between the lytic and lysogenic rhythms of Bacteriophage generation ( beginning: Modified from Lytic & A ; Lysogenic rhythm, Wikipedia )

Mechanism of onslaught on Host cells

The expected terminal consequence in phage therapy is the lysis of the bacterial host cells infected by the phages. There are many different schemes employed by the phages to lyse the septic bacterium. The phages with dual isolated Deoxyribonucleic acid ; the lysis of the bacterial hosts is catalyzed by the proteins Holin and Endolysin ( Loessner et al 1998 ) . Holin works as a transporter, it helps the motion of the endolysin enzyme to the bacterial peptidoglycan bed. Endolysin with the aid of its catalytic belongingss enables the debasement of the peptidoglycan bed. Unlike the two-base hit stranded DNA possessing phages, the smaller Deoxyribonucleic acid or RNA phages have proteins that interfere with the peptidoglycan bring forthing enzymes in the host cells and this finally helps the phages to do lysis of the host cells.

Bacterial Host Specificity

The common antibiotics that are used have a broad scope of host specificity, this makes them lose the significance for “ specificity ” and therefore they do non be given to be really efficient with their marks. However, the host scope of phages is much narrower in comparing ( Nunes et al 1978 ) . Furthermore, the phages are found to be less harmful to the organic structure flora unlike the commonly used antibiotics. There are a big assortment of host specific phage strains that have been developed to aim the specific pathogens.

Advantage of Phage Therapy over Antibiotics ( Table 1 )

Table 1. Shows the advantages of Phages over Antibiotics

( Beginning: Modified from Phagetherapycenter.com )

Bacteriophages

Antibiotics

The Edge

Very Specific

Wide spectrum scope

Bacteriophages specifically lyse the mark bacterium, unlike Antibiotics which besides target the utile microbic vegetation inside the organic structure

Reproduction at the site of infection

They are processed by the metabolic maps inside the organic structure.

Bacteriophage reproduction at the site makes them available at the site of infection and thereby makes them more effectual

Minimal side effects observed

Multiple side effects

The sides effects in Bacteriophages are chiefly due to the endotoxins from the lysed bacterium, and non from the Phage atom as such

Bacteriophage immune bacteriums remain susceptible to other phages holding same scope

Anti-biotic opposition is non merely limited to the mark bacterium.

Wide spectrum of antibiotics creates many mutant strains of bacteriums that are antibiotic resistant and non merely the mark bacterium that alteration

Easier to choose phages that can aim antibiotic immune bacteriums. Usually takes merely yearss or hebdomads

Developing newer drugs to aim the antibiotic resistant bacterium is clip devouring.

Easier to place strains of phages and assail the antibiotic resistant bacteriums.

Infections targeted by Bacteriophage Therapy

In 1917, when the bacteriophage was discovered by Felix d’Herelle at the Pasteur Institute in Paris, there were many trusting to utilize bacteriophages as curative agents and in 1920s, Eliava Institute, Georgia started research in this and tried to set the same into pattern. At the clip, phage therapy was targeted towards dysentery, enteric fever, sepsis and cholera ( Carlton 1999 ) . But the rapid find of several antibiotics put the phage therapy to rest. Although it was subsequently identified that the phage therapy could turn out far more effectual compared to the antibiotics ; research showed that bacteriophages could be used as both healing and preventative agents. In the intervention of dysentery, bacteriophages non merely pull off to destruct the bugs but besides prevent the infection from distributing farther, provided the medicine was given at the initial phases of the enteric infection. Present research has paved manner for phage therapy to be used in a broad assortment of diseases and infections such as TB, cholera, typhoid etc. A new signifier of medicine evolved which used the antibiotics along with the phage therapy ensuing in improved instances of recovery. Harmonizing to Saratov ‘s Scientific Research Center, Georgia, phage therapy has been implemented and successful clinical surveies were performed against infectious-allergic rinosinusopathy, infectious-allergic bronchial asthma, post-surgical non-epidemic infections, urinary piece of land infection, cuticular infections in babes etc ( Saratov ‘s Scientific Research Centre web page ) .

Disadvantages of Bacteriophage Therapy ( Matsuzaki et al. 2005 )

Lysogeny and Harmful cistrons: the phage familial stuff that integrates with the host cell familial stuff can assist conveying antibiotic resistant between cistrons of the host. Hence phages following lysogenic rhythm are non utile in phage therapy.

Bacterial Growth Impact: the growing environment of bacteriums can change its familial stuff to accommodate to the alterations and this can impact their susceptibleness to the phages.

Bacterial Endotoxins: when the bacteriums are lysed, they release endotoxins can be harmful to the organic structure.

Pharmacokinetic informations: the deficiency sufficient pharmacokinetic informations, anticipations for the clinical efficaciousness of phages on mark bacterium is losing.

Host scope: the narrow specificity of phages prevents them from infecting bacteriums belonging to the same subgroup within the species. Hence designation of the right species of infection doing bacteriums is critical in phage therapy.

Contamination: Any bacterial taint nowadays in the phage merchandises could turn out fatal to the patients.

Decision

The find of antibiotic immune bacterium is lifting alarmingly and the find of specific antibiotics aiming these takes up batch of clip and resources. Bacteriophages on the other manus have high specificity towards their mark bacterial hosts. This belongings when decently exploited can turn out utile and do important part in contending infections caused by antibiotic immune bacteriums. The phage therapy can be used both as remedy and preventative therapy. This non merely increases the range of phage therapy but besides provides new platforms to dispute a figure of infections.

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