Literature DB >> 33498380

Beyond the IFA: Revisiting the ELISA as a More Sensitive, Objective, and Quantitative Evaluation of Spotted Fever Group Rickettsia Exposure.

Navatha Alugubelly1, John V Stokes1, Claire E Cross1, Anne-Marie L Ross1, Anna E Crawford1, Gabrielle F Fiihr1, Andrea S Varela-Stokes1.   

Abstract

Based on limited serological studies, at least 10% of the US population has been exposed to spotted fever group Rickettsia (SFGR) species. The immunofluorescence antibody assay (IFA) has been the gold standard for the serodiagnosis of rickettsial infections such as spotted fever rickettsiosis (SFR). However, the IFA is semi-quantitative and subjective, requiring a high level of expertise to interpret it correctly. Here, we developed an enzyme-linked immunosorbent assay (ELISA) for the serodiagnosis of Rickettsia parkeri infection in the guinea pig. Our ELISA is an objective, quantitative, and high-throughput assay that shows greater sensitivity and resolution in observed titers than the IFA. We methodically optimized relevant parameters in sequence for optimal signal-to-noise ratio and low coefficient of variation% values. We used a guinea pig model as it is a part of our overall research efforts to understand the immunological and clinical response to SFGR species after tick transmission. Guinea pigs are a useful model to study SFR and show clinical signs of SFR, such as fever and eschars. We anticipate that this assay will be easily adapted to other hosts, including humans and other SFGR species.

Entities:  

Keywords:  Amblyomma; Rickettsia amblyommatis; Rickettsia parkeri; guinea pig; rickettsial diseases; serology; tick-borne diseases

Year:  2021        PMID: 33498380      PMCID: PMC7909427          DOI: 10.3390/pathogens10020088

Source DB:  PubMed          Journal:  Pathogens        ISSN: 2076-0817


  23 in total

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Journal:  J Clin Microbiol       Date:  1997-04       Impact factor: 5.948

4.  Comparison of Commercial Enzyme-Linked Immunosorbent Assay and Immunofluorescence Assay for Diagnosis of Acute Rickettsia typhi Infections.

Authors:  Dewi Lokida; Pratiwi Sudarmono; Herman Kosasih; Deni Pepy Butar-Butar; Gustiani Salim; Ungke Antonjaya; Rizky Amalia Sari; Abu Tholib Aman; Ida Parwati; Mansyur Arif; Chuen-Yen Lau; Muhammad Karyana
Journal:  Vector Borne Zoonotic Dis       Date:  2019-08-26       Impact factor: 2.133

5.  Expanding Recognition of Rickettsia parkeri Rickettsiosis in Southern Arizona, 2016-2017.

Authors:  Hayley D Yaglom; Mariana Casal; Sharon Carson; Catherine L O'Grady; Victor Dominguez; Joseph Singleton; Ida Chung; Heidi Lodge; Christopher D Paddock
Journal:  Vector Borne Zoonotic Dis       Date:  2019-10-22       Impact factor: 2.133

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Journal:  J Infect Dis       Date:  1983-11       Impact factor: 5.226

7.  Antibodies reactive to Rickettsia rickettsii among children living in the southeast and south central regions of the United States.

Authors:  Gary S Marshall; Gordon G Stout; Richard F Jacobs; Gordon E Schutze; Helene Paxton; Steven C Buckingham; John P DeVincenzo; Mary Anne Jackson; Venusto H San Joaquin; Steven M Standaert; Charles R Woods
Journal:  Arch Pediatr Adolesc Med       Date:  2003-05

8.  Human Infections by Multiple Spotted Fever Group Rickettsiae in Tennessee.

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Journal:  Am J Trop Med Hyg       Date:  2016-03-28       Impact factor: 2.345

9.  Rickettsia 364D: a newly recognized cause of eschar-associated illness in California.

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Journal:  Clin Infect Dis       Date:  2010-02-15       Impact factor: 9.079

10.  Establishment, maintenance and description of cell lines from the tick Ixodes scapularis.

Authors:  U G Munderloh; Y Liu; M Wang; C Chen; T J Kurtti
Journal:  J Parasitol       Date:  1994-08       Impact factor: 1.276

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