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Pritt, Bobbi S.

https://orcid.org/0000-0003-0261-1326

Mayo Clinic

Mayo Clinic

Citations 143

Extraintestinal Microsporidiosis
Ramanan, Poornima , Pritt, Bobbi S. , Ramanan, Poornima , Pritt, Bobbi S

Journal of Clinical Microbiology | May 15, 2014 | Volume: 52 | Issue: 11 | Pages: 3839-3844

10.1128/jcm.00971-14 Get It

ABSTRACT Microsporidia are highly specialized obligate intracellular organisms that are closely related to fungi. Although traditionally associated with diarrheal illness in patients with AIDS, extraintestinal infections involving various organs have been reported with increasing frequency in the past decade, particularly in immunocompromised hosts. Diagnosis is usually accomplished by light microscopic identification of spores in body fluids and tissues, using a variety of stains. Transmission electron microscopy, immunofluorescence assays, or molecular methods are necessary for identification to the genus and species level. Early diagnosis is essential for preventing the significant associated morbidity and mortality of extraintestinal microsporidiosis.
Inhibition Controls for Qualitative Real-Time PCR Assays: Are They Necessary for All Specimen Matrices?
Buckwalter, Seanne P., Sloan, Lynne M., Cunningham, Scott A. , Espy, Mark J., Uhl, J. R., Jones, Mary F. , Vetter, Emily A., Mandrekar, Jayawant N. , Cockerill, Franklin R., Pritt, Bobbi S. , Patel, Robin , Wengenack, Nancy L. , Patel, Robin , Pritt, Bobbi S , Cunningham, Scott A

Journal of Clinical Microbiology | April 16, 2014 | Volume: 52 | Issue: 6 | Pages: 2139-2143

10.1128/jcm.03389-13 Get It

ABSTRACT A retrospective analysis of 386,706 specimens representing a variety of matrix types used in qualitative real-time PCR assays determined the overall inhibition rate to be 0.87% when the inhibition control was added preextraction to 5,613 specimens and 0.01% when the inhibition control was added postextraction but preamplification in 381,093 specimens. Inhibition rates of ≤1% were found for all specimen matrix types except urine and formalin-fixed, paraffin-embedded tissue.
Cutaneous Manifestations of a Zoonotic Onchocerca Species in an Adult Male, Acquired in Nova Scotia, Canada
Lai, Jonathan, Walsh, Noreen M. , Pritt, Bobbi S. , Sloan, Lynne M., Gibson, Lawrence E. , Desormeau, Leon, Haldane, David, Pritt, Bobbi S

Journal of Clinical Microbiology | February 6, 2014 | Volume: 52 | Issue: 5 | Pages: 1768-1770

10.1128/jcm.03358-13 Get It

ABSTRACT A 65-year-old male with known hypertension and hypercholesterolemia sought medical attention because of a 3-month history of skin swelling on his upper back. Histopathology and molecular techniques were employed and identified an organism in the Onchocerca genus. This represents a very uncommon example of cutaneous infection by a zoonotic Onchocerca species.
Laboratory Identification of Arthropod Ectoparasites
Mathison, Blaine A. , Pritt, Bobbi S. , Pritt, Bobbi S , Mathison, Blaine A

Clinical Microbiology Reviews | January 6, 2014 | Volume: 27 | Issue: 1 | Pages: 48-67

10.1128/cmr.00008-13 Get It

SUMMARYThe collection, handling, identification, and reporting of ectoparasitic arthropods in clinical and reference diagnostic laboratories are discussed in this review. Included are data on ticks, mites, lice, fleas, myiasis-causing flies, and bed bugs. The public health importance of these organisms is briefly discussed. The focus is on the morphological identification and proper handling and reporting of cases involving arthropod ectoparasites, particularly those encountered in the United States. Other arthropods and other organisms not of public health concern, but routinely submitted to laboratories for identification, are also briefly discussed.
Characterization of a Novel Melt Curve by Use of the Roche LightCycler HSV 1/2 Analyte-Specific Reagent Real-Time PCR Assay: Frequencies of This Novel (Low) Melt Curve and Commonly Encountered (Intermediate) Melt Curves
Boyanton, Bobby L. , Almradi, Amro, Espy, Mark J., Prada, Anne E., Pritt, Bobbi S. , Gibson, John P. , Pritt, Bobbi S

Journal of Clinical Microbiology | December 19, 2013 | Volume: 52 | Issue: 3 | Pages: 957-959

10.1128/jcm.03062-13 Get It

ABSTRACT We characterize a novel probe binding-site polymorphism detectable solely by melt curve analysis using the Roche LightCycler HSV 1/2 analyte-specific reagent real-time PCR assay. The frequencies of this novel (47°C) and previously described intermediate (60 to 62°C) melt curves were 0.016% and 4.9%, respectively.
Sparganosis Presenting as a Mammographic Abnormality
Graham, Rondell P. , Pritt, Bobbi S. , Glazebrook, Katrina N. , Shah, Sejal , Graham, Rondell P D, Graham, Rondell P , Pritt, Bobbi S

The Breast Journal | November 18, 2013 | Volume: 20 | Issue: 1 | Pages: 92-94

10.1111/tbj.12211 Get It

Iodamoeba butschlii in an anal pap test confirmed by iodine stain
Pritt, Bobbi S. , Schreiner, Andrew M., Schuetz, Audrey N. , Pritt, Bobbi S

Diagnostic Cytopathology | October 25, 2013 | Volume: 42 | Issue: 9 | Pages: 775-777

10.1002/dc.23042 Get It

We report the finding of Iodamoeba butschlii amebic cysts on a liquid‐based anal Pap smear from an HIV‐positive male. Iodine staining of the smear confirmed the diagnosis. It is important to distinguish I. butschlii from pathogenic ameobae and other organisms seen on anal Pap smears. Diagn. Cytopathol 2014;42:775–777. © 2013 Wiley Periodicals, Inc.
Detection and Identification of Yeasts from Formalin-Fixed, Paraffin-Embedded Tissue by Use of PCR-Electrospray Ionization Mass Spectrometry
Simner, Patricia J. , Buckwalter, Seanne P., Uhl, James R., Wengenack, Nancy L. , Pritt, Bobbi S. , Pritt, Bobbi S

Journal of Clinical Microbiology | August 29, 2013 | Volume: 51 | Issue: 11 | Pages: 3731-3734

10.1128/jcm.01967-13 Get It

ABSTRACT Diagnosis of yeast infection is typically accomplished by fungal smear and culture, histopathologic examination, and/or serologic studies. Newer assays based on mass spectrometry may be useful for yeast identification when histologic examination is inconclusive, fungal cultures are not ordered, or cultures fail to yield a causative agent. The purpose of this study was to evaluate the ability of the PLEX-ID broad fungal assay to accurately detect and identify yeasts in formalin-fixed paraffin-embedded (FFPE) tissues. Tissue samples from 78 FFPE specimens with both histopathology and corresponding culture results for a variety of yeasts were tested using the PLEX-ID broad fungal assay. A 40-μm FFPE tissue section from each specimen was digested with proteinase K followed by nucleic acid extraction and PCR using broad-range fungal primers. Yeast DNA in amplified products was identified using electrospray ionization mass spectrometry. Discordant results were resolved by D2 rRNA gene sequencing. PLEX-ID analysis detected yeast DNA in 78.2% (61/78) of the cases, of which 91.8% (56/61) were concordant with culture results. Of the 5 discordant positive results, 4 PLEX-ID results were considered to result from environmental contaminants, while 1 clinically important discrepancy was observed ( Blastomyces dermatitidis by culture and Cryptococcus neoformans by PLEX-ID). Sequencing of the discordant sample was unsuccessful. The majority of histopathology results (89.7% [70/78]) correlated with culture results. The PLEX-ID broad fungal assay identifies fungi directly from FFPE tissues and can be a useful adjunct to traditional culture and histopathology tests.
Disseminated microsporidiosis in a renal transplant recipient: case report and review of the literature
Nagpal, Avish , Pritt, Bobbi S. , Lorenz, Elizabeth C. , Amer, Hatem , Nasr, Samih H. , Cornell, Lynn D. , Iqbal, Seher, Wilhelm, Mark , Amer, Hatem , Pritt, Bobbi S , Cornell, Lynn

Transplant Infectious Disease | August 16, 2013 | Volume: 15 | Issue: 5 | Pages: 526-532

10.1111/tid.12119 Get It

AbstractMicrosporidia are opportunistic pathogens that usually cause a limited disease in the gastrointestinal tract. Occasionally, they can cause disseminated disease. In solid organ transplant recipients, disseminated disease has been reported only rarely. We describe a 68‐year‐old woman who presented with fever, cough, and acute kidney injury 6 months after kidney transplantation. Dissemination was confirmed by identification of microsporidial spores in urine and bronchoalveolar lavage fluid. Polymerase chain reaction analysis identified the species as Encephalitozoon cuniculi.
Executive Summary: A Guide to Utilization of the Microbiology Laboratory for Diagnosis of Infectious Diseases: 2013 Recommendations by the Infectious Diseases Society of America (IDSA) and the American Society for Microbiology (ASM)a
Baron, Ellen Jo , Weinstein, Melvin P., Richter, Sandra S. , Gilligan, Peter H., Thomson, Richard B., Bourbeau, Paul, Kehl, Sue C., Robinson-Dunn, Barbara, Schwartzman, Joseph D., Chapin, Kimberle, Snyder, James W. , Forbes, Betty A., Patel, Robin , Rosenblatt, Jon E., Pritt, Bobbi S. , Miller, J. Michael , Carroll, Karen C. , Dunne, William Michael , Patel, Robin , Pritt, Bobbi S

Clinical Infectious Diseases | July 23, 2013 | Volume: 57 | Issue: 4 | Pages: 485-488

10.1093/cid/cit441 Get It

Abstract The critical role of the microbiology laboratory in infectious disease diagnosis calls for a close, positive working relationship between the physician and the microbiologists who provide enormous value to the health care team. This document, developed by both laboratory and clinical experts, provides information on which tests are valuable and in which contexts, and on tests that add little or no value for diagnostic decisions. Sections are divided into anatomic systems, including Bloodstream Infections and Infections of the Cardiovascular System, Central Nervous System Infections, Ocular Infections, Soft Tissue Infections of the Head and Neck, Upper Respiratory Infections, Lower Respiratory Tract infections, Infections of the Gastrointestinal Tract, Intraabdominal Infections, Bone and Joint Infections, Urinary Tract Infections, Genital Infections, and Skin and Soft Tissue Infections; or into etiologic agent groups, including Tickborne Infections, Viral Syndromes, and Blood and Tissue Parasite Infections. Each section contains introductory concepts, a summary of key points, and detailed tables that list suspected agents; the most reliable tests to order; the samples (and volumes) to collect in order of preference; specimen transport devices, procedures, times, and temperatures; and detailed notes on specific issues regarding the test methods, such as when tests are likely to require a specialized laboratory or have prolonged turnaround times. There is redundancy among the tables and sections, as many agents and assay choices overlap. The document is intended to serve as a reference to guide physicians in choosing tests that will aid them to diagnose infectious diseases in their patients.