Journal of Clinical Immunology Research

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Opinion Article - Journal of Clinical Immunology Research (2022) Volume 5, Issue 6

The utilization of phytotherapy in place of traditional antibiotics to treat antimicrobial properties.

Michelle Cogo *

Department of Pharmacology, State University of Campinas, Sao Paulo, Brazil

*Corresponding Author:
Michelle Cogo
Department of Pharmacology
State University of Campinas
Sao Paulo, Brazil

Received: 06-Dec-2022, Manuscript No. AACIR-22-84433; Editor assigned: 08-Dec-2022, Pre QC No. AACIR-22-84433 (PQ); Reviewed:21-Dec-2022, QC No. AACIR-22-84433; Revised:24-Dec-2022, Manuscript No. AACIR-22-84433 (R); Published: 30-Dec-2022, DOI: 10.35841/aacir-5.6.130

Citation: Cogo M. The utilization of phytotherapy in place of traditional antibiotics to treat antimicrobial properties. J Clin Immunol. 2022;5(6):130

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The invasion of tissues by pathogens, their growth, and the host tissues' response to the infectious agent and the toxins they release are all considered infections. A sickness brought on by an infection is referred to as an infectious disease, often known as a transmissible disease or communicable disease.


Antibiotics, Antivirals, Antifungals, Antiprotozoals.


There are many different pathogens that can cause infections, but bacteria and viruses are the most common ones. Hosts' immune systems can help them combat infections. Mammalian hosts respond to infections by first going through an innate response, which frequently involves inflammation, and then going through an adaptive response. Specifically, antibiotics, antivirals, antifungals, antiprotozoals, and antihelminthics are used to treat infections. 9.2 million people died from infectious diseases in 2013, or 17% of all deaths. Infectious disease refers to the area of medicine that focuses on infections [1].

Infections generally follow a sequence of actions known as the chain of infection. Infectious agent, reservoir, entry into a susceptible host, exit, and transmission to new hosts are some of the steps in the chain of events. An infection can only spread if all of the linkages are present in the correct order. Healthcare professionals can target the infection and avoid it altogether by being aware of these methods [2]

When an organism effectively enters the body, develops, and reproduces, infection occurs. This process is known as colonisation. Most people are resistant to infection. People who have impaired or weakened immune systems are more vulnerable to long-lasting illnesses. Opportunistic infections are particularly dangerous for people with weakened immune systems. The mucosa in orifices including the mouth cavity, nose, eyes, genitalia, and anus allows the microbe to enter the host at the host-pathogen interface. The microbe can also enter through open wounds. A small number of germs can grow at the point of entrance, but the majority spread and infects the body's various organs systemically. Some pathogens (intracellular) develop within the host cells, whereas others develop unrestrainedly in physiological fluids while infected wounds have reproducing organisms and damaged tissue; wound colonisation refers to non-replicating microbes inside the wound. Extrinsic organisms invade all multicellular organisms to some extent, and the great majority of these organisms either have a mutualistic or commensal relationship with the host. The mammalian colon is colonised by anaerobic bacteria species as an example of the former, whereas the diverse staphylococcus species found on human skin are examples of the latter. These colonisations are neither infections nor parasites [3].

In many cases, the distinction between an infection and a colonisation is merely a matter of context. Even the most virulent organism needs appropriate conditions to result in a compromising infection, and non-pathogenic organisms can develop into pathogenic ones under certain circumstances. Some colonising bacteria, such Corynebacteria sp. and viridans streptococci, stop dangerous bacteria from adhering to the host and colonising it, preventing infection and hastening the healing of wounds. [4]

Gas chromatography-mass spectrometry, 16S ribosomal RNA analysis, omics, and other cutting-edge technologies have recently made it more clear to humans that microbial colonisation occurs often even in situations that they perceive to be almost sterile. It is challenging to determine which chronic wounds can be categorised as infected and how much risk of advancement there is because bacterial colonisation is common. Even if there are a lot of wounds encountered in clinical practise, the quality of the data used to evaluate symptoms and signs are poor. The significance of increased pain as a sign of infection was evaluated in a study [5]


Since the beginning of this century, opiates and infectious diseases have been linked, but as we enter the next century, many unanswered issues about the mechanical connection between opiates and infection persist. Opioids alter immune function and affect susceptibility to infection, according to a substantial body of evidence from studies conducted both In vivo and In vitro.

PCR-based process

Polymerase chain reaction (PCR) based measure catalyst connected immuno-sorbent examine (ELISA) and instruments depend on broad advancement (up to 24 h) to create an adequate number of cells for discovery. Following improvement, the measure requires DNA intensification and identification. The whole cycle from advancement through discovery might require a few hours to days [5]. On account of test readiness processes and auxiliary lab hardware (shakers, hatcheries, microplate perusers) such identification framework may not be pragmatic as PONT gadgets. One more usually used innovation depends on one or the other norm or ongoing PCR (qPCR) contingent upon the instrument and takes up to 3.5 h for recognition. The framework is restricted to utilizing PCR technique in this manner incapable to play out different biomarkers location.


  1. Risdahl JM, Khanna KV, Peterson PK, et al Opiates and infection. J Neuroimmunol. 1998;83(1-2):4-18.
  2. Indexed at, Google Scholar, Cross Ref

  3. Gavazzi G, Krause KH. Ageing and infection. The Lancet Infect Dis. 2002;2(11):659-66.
  4. Google Scholar, Cross Ref

  5. Vasta GR Roles of galectins in infection. Nat Rev Microbiol. 2009;7(6):424-38.
  6. Google ScholarCross Ref

  7. Miller CHInfection control. Dental Clin of North Am. 1996;40(2):437-56.
  8. Google Scholar, Cross Ref

  9. Weinberg ED. iron and infection. Microbiol Rev. 1978;42(1):45-66.
  10. Google Scholar

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