THE USE OF POLYMERASE CHAIN REACTION IN CLINICAL INFECTIOUS DISEASES

1996 ◽  
Vol 5 (3) ◽  
pp. 180-184 ◽  
Author(s):  
Carl E. Haisch
Ophthalmology ◽  
2013 ◽  
Vol 120 (9) ◽  
pp. 1761-1768 ◽  
Author(s):  
Sunao Sugita ◽  
Manabu Ogawa ◽  
Norio Shimizu ◽  
Tomohiro Morio ◽  
Nobuyuki Ohguro ◽  
...  

Author(s):  
N.A. Bezborodova ◽  
◽  
V.V. Kozhuhovskaya ◽  
M.V. Petropavlovsky ◽  
O.G. Tomskikh ◽  
...  

2017 ◽  
Vol 38 (7) ◽  
pp. 863-866 ◽  
Author(s):  
Rachel A. Foster ◽  
Kristi Kuper ◽  
Z. Kevin Lu ◽  
P. Brandon Bookstaver ◽  
Christopher M. Bland ◽  
...  

Rapid diagnostic technologies (RDTs) significantly reduce organism identification time and can augment antimicrobial stewardship program (ASP) activities. An electronic survey quantified familiarity with and utilization of RDTs by clinical pharmacists participating in ASPs. Familiarity was highest with polymerase chain reaction (PCR). Formal infectious diseases training was the only significant factor influencing RDT familiarity.Infect Control Hosp Epidemiol 2017;38:863–866


2013 ◽  
Vol 1 (1) ◽  
pp. 28-36 ◽  
Author(s):  
Kordo B.A. Saeed ◽  
Nusreen S. Ahmad

The polymerase chain reaction (PCR) has revolutionized the detection of DNA and RNA. Real-Time PCR (RT-PCR) is becoming the gold standard test for accurate, sensitive and fast diagnosis for a large range of infectious agents. Benefits of this procedure over conventional methods for measuring RNA include its sensitivity, high throughout and quantification. RT-PCR assays have advanced the diagnostic abilities of clinical laboratories particularly microbiology and infectious diseases. In this review we would like to briefly discuss RT-PCR in diagnostic microbiology laboratory, beginning with a general introduction to RT-PCR and its principles, setting up an RT-PCR, including multiplex systems and the avoidance and remediation of contamination issues. A segment of the review would be devoted to the application of RT-PCR in clinical practice concentrating on its role in the diagnosis and treatment of infectious diseases.


Author(s):  
Vladimir Anatolievich Klimov

At all times mankind strived for progressive changes, and for a long time has been looking for new ways to diagnose and treat diseases in order to prolong life. Scientists have constantly attempted to introduce the latest techniques, and if in the 20th century an understanding of the course of various processes at the cellular level was achieved, at the latest stage of development there is already a transition to the study of the molecular and even atomic composition of individual derivatives, which should contribute to the transition to a qualitatively new level of process understanding. The first to speak about nanotechnology was Richard Phillips Feynman, who back in 1959 spoke about the possibility of controlling matter precisely at the atomic level. At the present stage, nanotechnology is increasingly being introduced into medical science, in particular, in the field of laboratory diagnostics of infectious diseases. More recently, this fact has received practical confirmation on the example of organizing large-scale testing of the population for the presence of the coronavirus infection. The methods used on the basis of atomic force molecular detectors provide a unique opportunity for visualization and identification of protein markers of pathological processes and conditions with a sensitivity several orders of magnitude higher than that of standard laboratory studies. This principle was the basis for the implementation of the polymerase chain reaction method, the essence of which lies in the multiple multiplication of microscopic concentrations of pathogen DNA fragments in a patient’s biological sample under artificial conditions. As a result of a complex process called amplification, under the influence of enzymes and changes in temperature (from 50 to 95 °C), two DNA molecules are formed from one DNA molecule. In this case, there is a copying of a DNA section that is present only in that type of pathogenic microorganism that is of interest to a specialist at the moment. The cycle of formation of a new DNA molecule takes about 3 minutes, while 30-40 cycles is quite enough to obtain the proper number of molecules required for reliable visual determination of the desired agent by electrophoresis.


2021 ◽  
Vol 15 (4) ◽  
pp. 339-344
Author(s):  
Breno Kalyl Freitas Nascimento ◽  
Luciana dos Santos Medeiros ◽  
Leandro dos Santos Machado ◽  
Vânia Maria França Ribeiro

A large proportion of emerging infectious diseases (60.3%) globally are zoonotic pathogens, and of these, 71.8% originate from wild animals. Salmonellosis and psittacosis, diseases caused by Salmonella spp. and Chlamydophila psittaci, respectively, in wild animals are zoonoses with great risks to public health. Therefore, this study aimed to investigate the presence of Salmonella spp. and C. psittaci in parrots domiciled in Rio Branco, Acre. The animals in the study were raised as pets, and selection was performed based on convenience criteria. The birds were manually restrained to collect biological materials. Subsequently, conventional microbiological and biochemical tests were performed to identify Salmonella spp., and polymerase chain reaction analyses were conducted to identify C. psittaci and Salmonella spp. It was not possible to isolate Salmonella spp. and C. psittaci in the sampled birds. However, the presence of these bacteria in parrots cannot be ruled out because intermittent release and diagnostic limitations are widely described in the literature.


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