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Multicenter Evaluation of the BioFire FilmArray Gastrointestinal Panel for Etiologic Diagnosis of Infectious Gastroenteritis
Open accessAbstract
The appropriate treatment and control of infectious gastroenteritis depend on the ability to rapidly detect the wide range of etiologic agents associated with the disease. Clinical laboratories currently utilize an array of different methodologies to test for bacterial, parasitic, and viral causes of gastroenteritis, a strategy that suffers from poor sensitivity, potentially long turnaround times, and complicated ordering practices and workflows. Additionally, there are limited or no testing methods routinely available for most diarrheagenic Escherichia coli strains, astroviruses, and sapoviruses. This study assessed the performance of the FilmArray Gastrointestinal (GI) Panel for the simultaneous detection of 22 different enteric pathogens directly from stool specimens: Campylobacter spp., Clostridium difficile (toxin A/B), Plesiomonas shigelloides , Salmonella spp., Vibrio spp., Vibrio cholerae , Yersinia enterocolitica , enteroaggregative E. coli , enteropathogenic E. coli , enterotoxigenic E. coli , Shiga-like toxin-producing E. coli ( stx 1 and stx 2 ) (including specific detection of E. coli O157), Shigella spp./enteroinvasive E. coli , Cryptosporidium spp., Cyclospora cayetanensis , Entamoeba histolytica , Giardia lamblia , adenovirus F 40/41, astrovirus, norovirus GI/GII, rotavirus A, and sapovirus. Prospectively collected stool specimens ( n = 1,556) were evaluated using the BioFire FilmArray GI Panel and tested with conventional stool culture and molecular methods for comparison. The FilmArray GI Panel sensitivity was 100% for 12/22 targets and ≥94.5% for an additional 7/22 targets. For the remaining three targets, sensitivity could not be calculated due to the low prevalences in this study. The FilmArray GI Panel specificity was ≥97.1% for all panel targets. The FilmArray GI Panel provides a comprehensive, rapid, and streamlined alternative to conventional methods for the etiologic diagnosis of infectious gastroenteritis in the laboratory setting. The potential advantages include improved performance parameters, a more extensive menu of pathogens, and a turnaround time of as short as 1 h.
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“The low percentage of failures (6/1,577 [0.38%]) is consistent with other published data on different FilmArray panels and indicates there was not a significant amount of inhibition of PCR in the samples (15).”
From Multicenter Evaluation of BioFire FilmArray Meningitis/Encephalitis Panel for Detection of Bacteria, Viruses, and Yeast in Cerebrospinal Fluid Specimens (2016) · cites this paper as [15]
In the citing paper
“The low percentage of failures (6/1,577 [0.38%]) is consistent with other published data on different FilmArray panels and indicates there was not a significant amount of inhibition of PCR in the samples (15).”
From Multicenter Evaluation of BioFire FilmArray Meningitis/Encephalitis Panel for Detection of Bacteria, Viruses, and Yeast in Cerebrospinal Fluid Specimens (2016) · cites this paper as [15]
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Items 101–200 of 471
Clinical impact of a gastrointestinal PCR panel in children with infectious diarrhoea
Truong, J., Cointe, A., Roux, É. L., Bidet, P., Michel, M., Boize, J., Mariani‐Kurkdjian, P., Caséris, M., Hobson, C. A., Desmarest, M., et al. (2021) · Archives of Disease in Childhood · doi:10.1136/archdischild-2021-322465 · Cited by 20
Diagnostic tools for tackling febrile illness and enhancing patient management
Mitsakakis, K., D’Acremont, V., Hin, S., von Stetten, F., & Zengerle, R. (2018) · Microelectronic Engineering · doi:10.1016/j.mee.2018.10.001 · Cited by 32
“6) from bioMérieux [83] is a benchtop diagnostic instrument that has three FDA-cleared panels: the Respiratory Panel [84], the Blood Culture Identification Panel [85], and the Gastrointestinal Panel [86,87].”
MethodGut colonization with vancomycin-resistant Enterococcus and risk for subsequent enteric infection
Axelrad, J. E., Lebwohl, B., Cuaresma, E., Cadwell, K., Green, P. H. R., & Freedberg, D. E. (2018) · Gut Pathogens · doi:10.1186/s13099-018-0259-4 · Cited by 26
Direct Detection of Shigella in Stool Specimens by Use of a Metagenomic Approach
Liu, J., Almeida, M., Kabir, F., Shakoor, S., Qureshi, S., Zaidi, A. K. M., Li, S., Tamboura, B., Sow, S. O., Mandomando, I., et al. (2017) · Journal of Clinical Microbiology · doi:10.1128/jcm.01374-17 · Cited by 33
Chisenga, C., Bosomprah, S., Laban, N., Kazimbaya, K., Mwaba, J., Simuy, M., & Chilengi, R. (2018) · doi:10.21767/2573-0282.100064 · Cited by 26
“as seen in our study may be due to the high sensitivity of the molecular based diagnosis method we used in this study, other reports such as Liu and colleagues [22] and many other studies [25-29] have noted that Shigella spp.”
ResultClinical Impact of a Diagnostic Gastrointestinal Panel in Children
Cotter, J. M., Thomas, J. F., Birkholz, M. C., Ambroggio, L., Holstein, J. A., & Dominguez, S. R. (2021) · PEDIATRICS · doi:10.1542/peds.2020-036954 · Cited by 23
Rader, T. S., Stevens, M., & Bearman, G. M. (2021) · Current Infectious Disease Reports · doi:10.1007/s11908-021-00748-z · Cited by 28
Epidemiology of Enterotoxigenic Escherichia coli infection in Minnesota, 2016–2017
Buuck, S., Smith, K., Fowler, R., Cebelinski, E., Lappi, V., Boxrud, D., & Medus, C. (2020) · Epidemiology and Infection · doi:10.1017/s0950268820001934 · Cited by 25
“Similarly, clinical laboratories in other parts of the USA have previously reported that 78–84% of ETEC-positive specimens were also positive for at least one other pathogen [12, 14].”
BackgroundGay‐Andrieu, F., Magassouba, N., Picot, V., Phillips, C. L., Peyrefitte, C. N., Dacosta, B., Doré, A., Kourouma, F., Ligeon, V., Gauby, C., et al. (2017) · Journal of Clinical Virology · doi:10.1016/j.jcv.2017.04.015 · Cited by 30
Martín, A., Pérez-Ayala, A., Chaves, F., Lora, D., & Orellana, M. A. (2018) · Journal of Microbiological Methods · doi:10.1016/j.mimet.2017.10.016 · Cited by 25
Rogers, W. S., Westblade, L., Soave, R., Jenkins, S., van Besien, K., Singh, H., Walsh, T., Small, C., Shore, T., Crawford, C. V., et al. (2020) · Clinical Infectious Diseases · doi:10.1093/cid/ciz1068 · Cited by 24
Levenson, E. A., Martens, C., Kanakabandi, K., Turner, C. V., Virtaneva, K. I., Paneru, M., Ricklefs, S., Sosnovtsev, S. V., Johnson, J. A., Porcella, S. F., et al. (2018) · The Journal of Immunology · doi:10.4049/jimmunol.1700384 · Cited by 23
Kociolek, L., Patel, S. J., Zheng, X.-T., Todd, K., Shulman, S., & Gerding, D. (2015) · The Pediatric Infectious Disease Journal · doi:10.1097/inf.0000000000000954 · Cited by 24
“Viral pathogen identified 14 (21) 2 (14) 3 (17) 1‡ 9 (26) 0.”
InfluentialEvaluation of the BioFire Gastrointestinal Panel to Detect Diarrheal Pathogens in Pediatric Patients
Jo, S. J., Kang, H. M., Kim, J., Cho, H., Heo, W., Yoo, I. Y., & Park, Y.-J. (2021) · Diagnostics · doi:10.3390/diagnostics12010034 · Cited by 26
“than that of culturing has been reported [18].”
BackgroundYoo, I. H., Kang, H. M., Suh, W., Cho, H., Yoo, I. Y., Jo, S. J., Park, Y. J., & Jeong, D. C. (2021) · Diagnostics · doi:10.3390/diagnostics11071175 · Cited by 18
“r t ti l t l t i , t ioFire GI Panel rapidly and accurately t t i r f ir , t ri arasites that can cause AGE [19, 2,23].”
BackgroundResultValledor, S., Valledor, I., Gil-Rodríguez, M., Seral, C., & Castillo, J. (2020) · Scientific Reports · doi:10.1038/s41598-020-61202-z · Cited by 23
Appropriate Use and Future Directions of Molecular Diagnostic Testing
Graf, E. H., & Pancholi, P. (2020) · Current Infectious Disease Reports · doi:10.1007/s11908-020-0714-5 · Cited by 29
Zhu, Q., Dupont, C. L., Jones, M. B., Pham, K. M., Jiang, Z., DuPont, H. L., & Highlander, S. K. (2018) · Microbiome · doi:10.1186/s40168-018-0579-0 · Cited by 30
“Modern tools, such as the BioFire FilmArray Gastrointestinal Panel [11], are now utilized for pathogen identification.”
MethodSelf-citationSimner, P. J., Oethinger, M., Stellrecht, K., Pillai, D., Yogev, R., Leblond, H., & Mortensen, J. (2017) · Journal of Clinical Microbiology · doi:10.1128/jcm.00911-17 · Cited by 23
“These results are similar to those reported by the multicenter clinical trial for the FilmArray gastrointestinal panel (13).”
BackgroundResultMolecular methods for detecting and typing of Clostridium difficile
Collins, D., Elliott, B., & Riley, T. (2015) · Pathology (Sydney) · doi:10.1097/pat.0000000000000238 · Cited by 23
“9%), respectively.(113) While the use of multiplexed assays has many attractions, there are likely to be impediments to their implementation such as cost and the issue of how to deal with the increased numbers of positive tests that will arise when diarrhoeal stools are ‘screened’ for multiple pathogens simultaneously…”
BackgroundMoon, R. C., Bleak, T. C., Rosenthal, N. A., Couturier, B. A., Hemmert, R. B., Timbrook, T. T., Brown, H., & Fang, F. C. (2023) · The American Journal of Gastroenterology · doi:10.14309/ajg.0000000000002186 · Cited by 25
“A female predominance (62% among individuals aged 22 years or older) was observed in a multicenter evaluation of US outpatients with stool cultures ordered by providers (22).”
BackgroundResultde Oliveira-Tozetto, S., Santiso-Bellón, C., Ferrer-Chirivella, J. M., Navarro-Lleó, N., Vila-Vicent, S., Rodríguez-Díaz, J., & Buesa, J. (2021) · Viruses · doi:10.3390/v13020184 · Cited by 22
“The implementation of diagnostic molecular assays in clinical laboratories has contributed to an increased detection of sapovirus infections in recent years [2,3].”
BackgroundResultReproducibility of positive results for rare pathogens on the FilmArray GI Panel
Hitchcock, M. M., Hogan, C. A., Budvytiene, I., & Banaei, N. (2019) · Diagnostic Microbiology and Infectious Disease · doi:10.1016/j.diagmicrobio.2019.03.013 · Cited by 28
“Discussion While multiplex PCR assays such as the FAGP have undoubtedly improved clinicians’ ability to make a rapid, specific diagnosis for patients with acute gastroenteritis and have improved laboratory workflow efficiency, the reproducibility of low-prevalence pathogens in clinical practice remains unknown (Buss e…”
BackgroundParčina, M., Reiter‐Owona, I., Mockenhaupt, F. P., Vojvoda, V., Gahutu, J. B., Hoerauf, A. M., & Ignatius, R. (2017) · Parasitology Research · doi:10.1007/s00436-017-5720-7 · Cited by 21
“Some of these assays detect parasites among bacterial and viral pathogens (Buss et al. 2015; Khare et al. 2014; McAuliffe et al. 2013; Navidad et al. 2013; Wessels et al. 2014), and might be beneficial for the microbiological diagnosis of traveler’s diarrhea (Zboromyrska et al.”
BackgroundBeal, S. G., Assarzadegan, N., & Rand, K. H. (2015) · Expert Review of Molecular Diagnostics · doi:10.1586/14737159.2016.1134325 · Cited by 28
“[66,70] The second limitation is that conventional bacterial cultures may still be required to determine susceptibility to antibiotics and for epidemiological tracking of possible outbreaks [71] (e.”
BackgroundMethodInfluentialOsman, M., Kassem, I. I., Dabboussi, F., Cummings, K. J., & Hamzé, M. (2023) · PLoS ONE · doi:10.1371/journal.pone.0282844 · Cited by 25
“duodenalis, Cyclospora cayetanensis, and Entamoeba histolytica] [40, 41].”
Loderstädt, U., Hagen, R. M., Hahn, A., & Frickmann, H. (2021) · Tropical Medicine and Infectious Disease · doi:10.3390/tropicalmed6020096 · Cited by 25
Meyer, J., Röös, E., Combescure, C., Buchs, N. C., Frossard, J., Ris, F., Toso, C., & Schrenzel, J. (2020) · Scandinavian Journal of Gastroenterology · doi:10.1080/00365521.2020.1839128 · Cited by 17
Zhan, Z., Guo, J.-Y., Xiao, Y., He, Z., Xia, X., Huang, Z., Guan, H.-X., Ling, X., Li, J., Diao, B.-W., et al. (2020) · International Journal of Infectious Diseases · doi:10.1016/j.ijid.2020.08.020 · Cited by 21
Accurate laboratory diagnosis of human intestinal and extra-intestinal amoebiasis
Hooshyar, H., & Rostamkhani, P. (2022) · Gastroenterology and hepatology from bed to bench · doi:10.22037/ghfbb.v15i4.2496 · Cited by 21
“histolytica using fully automated PCR systems (61-66).”
Viral Acute Gastroenteritis in Special Populations
Meier, J. L. (2021) · Gastroenterology Clinics of North America · doi:10.1016/j.gtc.2021.02.003 · Cited by 33
Zimmermann, S., Horner, S., Altwegg, M., & Dalpke, A. H. (2020) · European Journal of Clinical Microbiology & Infectious Diseases · doi:10.1007/s10096-020-03837-4 · Cited by 26
Diagnóstico molecular de parasitosis intestinales
Dacal, E., Köster, P. C., & Carmena, D. (2020) · Enfermedades Infecciosas y Microbiología Clínica · doi:10.1016/j.eimc.2020.02.005 · Cited by 25
Gastroenteritis in Men Who Have Sex With Men in Seattle, Washington, 2017–2018
Newman, K. L., Newman, G. S., Cybulski, R. J., & Fang, F. C. (2019) · Clinical Infectious Diseases · doi:10.1093/cid/ciz783 · Cited by 37
“Such studies have focused largely on proctitis and proctocolitis [3, 13–15] and have mostly been conducted in sexually transmitted disease (STD) clinics with populations enriched for patients who present with classic sexually transmitted infections (eg, Chlamydia, gonorrhea, syphilis) using traditional diagnostic meth…”
MethodUtility of multiplex polymerase chain reaction (PCR) in diarrhea—An Indian perspective
Ramakrishnan, B., Gopalakrishnan, R., Nambi, P. S., Durairajan, S., Madhumitha, R., Tarigopula, A., Chandran, C., & Ramasubramanian, V. (2018) · Indian Journal of Gastroenterology · doi:10.1007/s12664-018-0889-y · Cited by 20
Slinger, R., Lau, K., Slinger, M., Moldovan, I., & Chan, F. (2017) · Annals of Clinical Microbiology and Antimicrobials · doi:10.1186/s12941-017-0188-y · Cited by 20
“Of note, work to clarify the pathogenicity of a-EPEC has become more crucial in recent years since EPEC are now detected by a commercially available molecular diarrheal panel, the Biofire FilmArray gastrointestinal panel (Biomerieux, Durham, NC) [2, 3].”
BackgroundStokes, W., Simner, P. J., Mortensen, J., Oethinger, M., Stellrecht, K., Lockamy, E., Lay, T., Bouchy, P., & Pillai, D. (2019) · Journal of Clinical Microbiology · doi:10.1128/jcm.00306-19 · Cited by 19
“Other BD Max gastrointestinal panels had similar noncompliance rates (5, 6), which are comparable to those for other gastrointestinal multiplex PCR panels (1).”
BackgroundMethodResultInfluentialAmplification chemistries in clinical virology
Dunbar, S., & Das, S. (2019) · Journal of Clinical Virology · doi:10.1016/j.jcv.2019.03.015 · Cited by 19
“These assays have demonstrated 94-100% sensitivity and > 94% specificity for the viral targets in the various clinical trial studies.”
BackgroundNew Developments in Rapid Diagnostic Testing for Children
Gonzalez, M. D., & McElvania, E. (2017) · Infectious Disease Clinics of North America · doi:10.1016/j.idc.2017.11.006 · Cited by 21
“[24] [25] [26] [27] [28] [29] [30] [31] In fact, these multiplex panels result in increased and unexpected detections that would not be identified by the ordering preference of the clinician.”
BackgroundFang, F. C., & Patel, R. (2017) · Clinical Infectious Diseases · doi:10.1093/cid/cix730 · Cited by 20
Duarte-Guevara, C., Swaminathan, V., Reddy, B., Huang, J.-C., Liu, Y.-S., & Bashir, R. (2016) · doi:10.1039/c6ra19685c · Cited by 19
Ashbaugh, H. R., Early, J. M., Johnson, M. E., Simons, M. P., Graf, P. C. F., Riddle, M. S., Swierczewski, B. E., & for the GTD Study Team (2020) · American Journal of Tropical Medicine and Hygiene · doi:10.4269/ajtmh.20-0053 · Cited by 30
Detecting Cryptosporidium in Stool Samples Submitted to a Reference Laboratory.
Mergen, K., Espina, N., Teal, A. E., & Madison-Antenucci, S. (2020) · American Journal of Tropical Medicine and Hygiene · doi:10.4269/ajtmh.19-0792 · Cited by 18
“testinal pathogens, including Cryptosporidium, have become available, and these are nowwidely used.(14,15) The commercial assays are easy to perform but can be costly.”
BackgroundWestblade, L., Satlin, M., Albakry, S., Botticelli, B., Robertson, A. E., Alston, T., Magruder, M., Zhang, L. T., Edusei, E., Chan, K., et al. (2019) · Transplant Infectious Disease · doi:10.1111/tid.13167 · Cited by 18
Stempak, L. M., Vogel, S. A., Richter, S. S., Wyllie, R., & Procop, G. W. (2018) · Archives of Pathology & Laboratory Medicine · doi:10.5858/arpa.2017-0299-oa · Cited by 23
“Unfortunately, molecular assays are usually more expensive than traditional methods, and some of the multiplex assays contain microbial targets that are not actionable with current therapeutic regimens.(5,6) Additionally, there is commonly a misconception that molecularly derived test results are superior to those fro…”
BackgroundMultiplex Nucleic Acid Amplification Testing to Diagnose Gut Infections
Anderson, N. W., & Tarr, P. I. (2018) · Gastroenterology Clinics of North America · doi:10.1016/j.gtc.2018.07.006 · Cited by 23
DiarrheagenicEscherichia coliAssociated with Acute Gastroenteritis in Children from Soriano, Uruguay
Peirano, V., Bianco, M. N., Navarro, A., Schelotto, F., & Varela, G. (2018) · Canadian Journal of Infectious Diseases and Medical Microbiology · doi:10.1155/2018/8387218 · Cited by 19
Shelygin, Y. A., Алешкин, В. А., Sukhina, M. A., Mironov, A. Y., Briko, N. I., Kozlov, R. S., Zverev, V. V., Иванович, А. С., Kovalishena, O. V., Петровна, С. Е., et al. (2018) · Koloproktologia · doi:10.33878/2073-7556-2018-0-3-7-23 · Cited by 22
Liu, X., Guan, Y.-Y., Cheng, S.-L., Huang, Y.-D., Yan, Q., Zhang, J., Huang, G.-J., Zheng, J., & Liu, T. (2016) · Journal of Microbiological Methods · doi:10.1016/j.mimet.2016.10.007 · Cited by 18
Ruzante, J. M., Olin, K., Muñoz, B., Nawrocki, J., Selvarangan, R., & Meyers, L. (2021) · PLoS ONE · doi:10.1371/journal.pone.0250767 · Cited by 18
“One example of an FDA-cleared molecular based CIDT, is the BioFire(1) FilmArray(1) Gastrointestinal (GI) Panel [12].”
BackgroundMethodResultInfluentialEsona, M., Ward, M., Wikswo, M. E., Rustempasic, S. M., Gautam, R., Perkins, C., Selvarangan, R., Harrison, C., Boom, J., Englund, J., et al. (2021) · Journal of Infectious Diseases · doi:10.1093/infdis/jiab177 · Cited by 17
“Other genotypes include G12P[4], G3P[4], G2P[8], G12P[6], G6P[8], G9P[4], G2P[6], G3P[6], and G4P[8].”
BackgroundInfluentialSobczyk, J., Jain, S., Sun, X.-Y., Karris, M., Wooten, D., Stagnaro, J., & Reed, S. (2020) · Open Forum Infectious Diseases · doi:10.1093/ofid/ofz547 · Cited by 17
“An outbreak of Cyclospora was detected by the FilmArray GPP one week before detection by conventional testing [14].”
MethodResultBiswas, J. S., Lentaigne, J., Hill, N. E., Harrison, J. J., Mackenzie, H., Akorli, E., Burns, D. S., Hutley, E. J., Connor, P., & Woods, D. R. (2018) · Travel Medicine and Infectious Disease · doi:10.1016/j.tmaid.2018.12.004 · Cited by 18
McAuliffe, G. N., Bissessor, L., Williamson, D. A., Moore, S., Wilson, J., Dufour, M., Taylor, S., & Upton, A. (2017) · Pathology · doi:10.1016/j.pathol.2017.02.003 · Cited by 18
New molecular diagnostic tools in traveller's diarrhea.
Vila, J. (2017) · Journal of Travel Medicine · doi:10.1093/jtm/taw071 · Cited by 17
“In a large study including 1556 stool specimens, Buss et al.25 compared the FilmArray GI panel with conventional stool cultures and molecular methods.”
BackgroundRamanan, P., Espy, M., Khare, R., & Binnicker, M. (2017) · Diagnostic microbiology and infectious disease · doi:10.1016/j.diagmicrobio.2017.01.009 · Cited by 17
Simons, C. C., & Capraro, G. A. (2024) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dkae279 · Cited by 16
“These technologies have contributed to meaningful improvements to both patient care 5–7 and laboratory workflow, 8–10 begging the question: why have not more laboratories adopted them?”
BackgroundFreedman, S. B., Xie, J., Lee, B. E., Ali, S., Pang, X.-L., Chui, L., Zhuo, R., Vanderkooi, O. G., Tellier, R., Funk, A. L., et al. (2021) · Clinical Infectious Diseases · doi:10.1093/cid/ciab451 · Cited by 19
Marcelin, J. R., Brewer, C., Beachy, M. W., Lyden, E. R., Winterboer, T., Murphy, C. N., Fey, P. D., Hood, L., & Schooneveld, T. C. V. (2019) · Infection Control and Hospital Epidemiology · doi:10.1017/ice.2019.78 · Cited by 16
Self-citationAxelrad, J. E., Joelson, A. M., Nobel, Y. R., Whittier, S., Lawlor, G. O., Riddle, M. S., Green, P. H. R., & Lebwohl, B. (2018) · Digestive Diseases and Sciences · doi:10.1007/s10620-018-5087-3 · Cited by 14
Robinson, M. L., & Manabe, Y. C. (2017) · American Journal of Tropical Medicine and Hygiene · doi:10.4269/ajtmh.16-0667 · Cited by 18
“pathogens within a syndrome, ranging from diarrhea to meningoencephalitis.(80,81) Using an isothermal technique named nicking endonuclease amplification reaction, Alere”
MethodMelting curve analysis reveals false-positive norovirus detection in a molecular syndromic panel
Matic, N., Lawson, T., Young, M., Jang, W., Bilawka, J., Gowland, L., Ritchie, G., Leung, V., Payne, M., Stefanovic, A., et al. (2024) · medRxiv · doi:10.1101/2024.02.23.24303102 · Cited by 15
Toriro, R., Pallett, S., Woolley, S., Bennett, C., Hale, I., Heylings, J., Wilkins, D., Connelly, T., Muia, K., Avery, P., et al. (2024) · Open Forum Infectious Diseases · doi:10.1093/ofid/ofae001 · Cited by 15
“On site, fresh fecal samples were analyzed for 22 pathogen targets (Supplementary Table 1) using the multiplex PCR BioFire FilmArray gastrointestinal (GI) panel, in accordance with the manufacturer's guidelines (bioMérieux, Marcy-l'Étoile, France) [6, 20].”
MethodBrendish, N., Beard, K. R., Malachira, A. K., Tanner, A., Sanga-Nyirongo, L., Gwiggner, M., Cummings, J. R. F., Moyses, H., & Clark, T. (2023) · Lancet. Infectious Diseases (Print) · doi:10.1016/s1473-3099(23)00066-x · Cited by 15
Hong, S., Zaki, T., Main, M. L., Hine, A. M., Chang, S., Hudesman, D., & Axelrad, J. (2021) · Inflammatory Bowel Diseases · doi:10.1093/ibd/izaa336 · Cited by 15
Ali, I., & Roy, S. (2020) · Journal of Clinical Microbiology · doi:10.1128/jcm.01986-20 · Cited by 15
Dong, T.-H., Ma, X.-P., Sheng, N., Qi, X.-M., Chu, Y., Song, Q.-X., Zou, B., & Zhou, G.-H. (2020) · Sensors and actuators. B, Chemical · doi:10.1016/j.snb.2020.128919 · Cited by 15
Brenton, L., Waters, M. J., Stanford, T., & Giglio, S. (2020) · Journal of Microbiological Methods · doi:10.1016/j.mimet.2020.106047 · Cited by 19
“Discrepant resolution is commonplace in clinical microbiology, however inherently biased approaches investigating only samples that disagree are often used (Buss et al., 2015; Faron et al., 2016b; Faron et al., 2015; Harrington et al., 2015; Kost et al., 2017; Mashock et al., 2017).”
BackgroundGyawali, P., Croucher, D., & Hewitt, J. (2018) · Environmental science and pollution research international · doi:10.1007/s11356-018-2869-2 · Cited by 15
Jameel, S. K., Shafek, M., Abdulmohsen, A., Mohamed, N. S., Naji, S., & Mohammed, T. T. (2016) · doi:10.4236/aim.2016.69069 · Cited by 15
“cholera; numerous diagnostic laboratory tests are applied [25] [26] including stool culture, biochemical test, specialized microscopy, serological test and these include polyvalent, Ogawa, Inaba antisera testing, and singleplex PCR, conventional coupled PCR or real-time PCR with fluorescence; for detecting different g…”
MethodAbbott, A. N., & Fang, F. C. (2017) · Clinical Microbiology Newsletter · doi:10.1016/j.clinmicnews.2017.08.004 · Cited by 13
Tansarli, G. S., Allen, D. R., & Fang, F. C. (2025) · Open Forum Infectious Diseases · doi:10.1093/ofid/ofaf445 · Cited by 15
“[21, 24, 40–42].”
Carmon, D., Rohana, H., Azrad, M., & Peretz, A. (2023) · Diagnostics · doi:10.3390/diagnostics13061094 · Cited by 14
“%) and Sapovirus (5/17, 29.4%); and only one parasite (1/61, 1.6”
BackgroundInfluentialKanwar, N., Jackson, J., Bardsley, T., Pavia, A., Bourzac, K., Holmberg, K., & Selvarangan, R. (2023) · Journal of Clinical Microbiology · doi:10.1128/jcm.01652-22 · Cited by 14
Self-citationHigh Seropositivity Rate of Neutralizing Antibodies to Astrovirus VA1 in Human Populations
Janowski, A. B., Owen, M. C., Dudley, H. M., López, T., Espinosa, R., Elvin-Lewis, M. P. F., Colichón, A., Arias, C. F., Burbelo, P. D., & Wang, D. (2021) · mSphere · doi:10.1128/msphere.00484-21 · Cited by 17
Decuir, M., Fowler, R., Cebelinski, E., Smith, K. E., Boxrud, D., & Medus, C. (2021) · Open Forum Infectious Diseases · doi:10.1093/ofid/ofab247 · Cited by 14
Castany-Feixas, M., Simó, S., Garcia-Garcia, S., de Sevilla, M. F., Launes, C., Kalkgruber, M., Gené, A., Muñoz-Almagro, C., & Brotons, P. (2021) · European Journal of Clinical Microbiology and Infectious Diseases · doi:10.1007/s10096-021-04266-7 · Cited by 14
Clinical interpretation of enteric molecular diagnostic tests.
Tarr, G., Tarr, P., & Freedman, S. (2019) · Clinical Microbiology and Infection · doi:10.1016/j.cmi.2019.08.018 · Cited by 14
Wagner, K., Springer, B., Pires, V. P., & Keller, P. M. (2019) · Diagnostic microbiology and infectious disease · doi:10.1016/j.diagmicrobio.2018.11.006 · Cited by 14
“Recently, many syndromic point-of-care tests were launched that enable the detection of a panel of viral, bacterial, and fungal pathogens (Buss et al., 2015; Leber et al., 2016; Popowitch et al., 2013).”
BackgroundValenzuela, C., Legarraga, P., Peña, A., Arenas, Á., Berkowitz, L., Ramírez, G., Wozniak, A., García, P., & Álvarez-Lobos, M. (2018) · PLoS ONE · doi:10.1371/journal.pone.0207850 · Cited by 20
Rauw, K. D., Detemmerman, L., Breynaert, J., & Piérard, D. (2016) · European Journal of Clinical Microbiology and Infectious Diseases · doi:10.1007/s10096-016-2688-7 · Cited by 14
“EPEC and EAEC, two DEC types that are not routinely searched for in our laboratory, were frequently detected in our patients, and this was also seen in other studies conducted with the FA-GI Panel in the United States and Europe [1, 20, 21].”
BackgroundResultInfluentialSever, A., Ben-Zvi, H., Melamed, S., Sachs, N., Krause, I., & Bilavsky, E. (2022) · Acta paediatrica · doi:10.1111/apa.16610 · Cited by 13
Verma, A., Hine, A. M., Joelson, A., Mei, R.-N., Pitts, R., Lebwohl, B., & Axelrad, J. (2022) · Therapeutic Advances in Gastroenterology · doi:10.1177/17562848221092593 · Cited by 13
Aetiology of traveller's diarrhea: A nested case-control study.
Schaumburg, F., Correa-Martínez, C., Niemann, S., Köck, R., & Becker, K. (2020) · Travel Medicine and Infectious Disease · doi:10.1016/j.tmaid.2020.101696 · Cited by 13
Zhang, J.-Y., Guan, H.-X., Zhao, W.-S., Zhang, H., Wang, W., Ling, X., Xiao, Y., Guo, J.-Y., Huang, Z., Xu, Y., et al. (2019) · Foodborne pathogens and disease · doi:10.1089/fpd.2019.2642 · Cited by 13
“The correlation between pathogens and coinfections varied in different studies and may be affected by the sampling area and study population (Buss et al. , 2015; Alejo-Cancho et al. , 2017; Piralla et al. , 2017).”
Infection and propagation of astrovirus VA1 in cell culture
Janowski, A. B., & Wang, D. (2018) · Current Protocols in Microbiology · doi:10.1002/cpmc.73 · Cited by 13
Multiplex PCR for Detection and Identification of Microbial Pathogens
Poritz, M. A., & Lingenfelter, B. (2018) · Advanced Techniques in Diagnostic Microbiology · doi:10.1007/978-3-319-95111-9_19 · Cited by 13
“Studies using the FilmArray GI Panel identified a pathogen in 40–50% of stool samples [41, 45, 46].”
MethodCiesielczuk, H., Wilks, M., Castelain, S., Choquet, M., Morotti, M., Pluquet, E., Sambri, V., Tassinari, M., Zannoli, S., Cavalié, L., et al. (2018) · European Journal of Clinical Microbiology and Infectious Diseases · doi:10.1007/s10096-018-3345-0 · Cited by 13
Detection of Gastrointestinal Pathogens in Oncology Patients by Highly Multiplexed Molecular Panels
Otto, C. C., Chen, L.-H., He, T.-J., Tang, Y.-W., & Babady, N. (2017) · European Journal of Clinical Microbiology and Infectious Diseases · doi:10.1007/s10096-017-2981-0 · Cited by 13
“coli and their recovery in mixed infections is consistent with previous reports and unlikely to represent false-positive results or contamination, although these possibilities were not investigated further in our study [7, 9].”
ResultMeltzer, A. C., Newton, S., Lange, J. J., Hall, N. C., Vargas, N. M., Huang, Y., Moran, S., & Ma, Y. (2022) · Journal of the American College of Emergency Physicians Open · doi:10.1002/emp2.12616 · Cited by 14
Beckman, A. K., & Ferrieri, P. (2019) · Laboratory Medicine · doi:10.1093/labmed/lmz022 · Cited by 9
Case Report: Diagnosis of Cryptosporidiosis in Renal Transplantation in a Low-Prevalence Setting.
Zheng, S., Ko, K. K. K., Chan, K. S., & Venkatachalam, I. (2019) · American Journal of Tropical Medicine and Hygiene · doi:10.4269/ajtmh.18-0651 · Cited by 12
“In this study, the comparator assay was real-time polymerase chain reaction (PCR).(7) Our case demonstrates host susceptibility, with infection in a renal transplant recipient presenting with a gastroenteritis syndrome.”
BackgroundMethodBeczkiewicz, A., Cebelinski, E., Decuir, M., Lappi, V., Wang, X., Smith, K. E., Boxrud, D., & Medus, C. (2018) · Clinical Infectious Diseases · doi:10.1093/cid/ciy890 · Cited by 12
Seid, L., Stokes, W., Bayih, A., Getie, S., Abere, A., Tesfa, H., & Pillai, D. (2018) · BMC Infectious Diseases · doi:10.1186/s12879-018-3265-8 · Cited by 12
Humphrey, J. M., Ranbhise, S. U., Ibrahim, E., Al‐Romaihi, H. E., Farag, E., Abu-Raddad, L. J., & Glesby, M. J. (2016) · American Journal of Tropical Medicine and Hygiene · doi:10.4269/ajtmh.16-0464 · Cited by 12
“This finding is consistent with prior surveillance studies utilizing multiplex PCR.(9,12,28)”
BackgroundMethodResultInfluentialUse of a Molecular Panel To Aid in Diagnosis of Culture-Negative Meningitis
Bard, J. D., Naccache, S. N., & Bender, J. M. (2016) · Journal of Clinical Microbiology · doi:10.1128/jcm.01957-16 · Cited by 13
Steyer, A., Virant, M. J., Petrovec, M., Pokorn, M., Grosek, Š., Steyer, A. F., Šoba, B., Uršič, T., Cerar, T., Kolenc, M., et al. (2016) · The Pediatric Infectious Disease Journal · doi:10.1097/inf.0000000000001208 · Cited by 12
“Recently, many new or novel methods with a syndromic approach have been presented and have shown good sensitivity; some of them have already been Food and Drug Administration– approved.(74,75) With the implementation of such methods, co-infections will be noted more often.”
BackgroundBhimani, A., Bhatt, T., Ibrahim, M., Detroja, A., Koradiya, J., Mandaliya, V. B., Maharshi, A., Sanghvi, G., & Bishoyi, A. K. (2025) · Diagnostic microbiology and infectious disease · doi:10.1016/j.diagmicrobio.2025.117125 · Cited by 11
Amoebic Liver Abscess: Potential Application of New Diagnostic Techniques for an Old Pathogen
Portunato, F., Bartalucci, C., Vena, A., Giacobbe, D., Porcile, E., Montanelli, P., Piol, N., Centanaro, M., Andorno, E., & Bassetti, M. (2024) · Infectious Disease and Therapy · doi:10.1007/s40121-024-00934-1 · Cited by 11
Varma, S., Trudeau, S. J., Li, J., & Freedberg, D. E. (2023) · Inflammatory Bowel Diseases · doi:10.1093/ibd/izad035 · Cited by 12
Metadata
- Authors
- Buss, S. N., Leber, A., Chapin, K., Fey, P. D., Bankowski, M. J., Jones, M. K., Rogatcheva, M., Kanack, K. J., & Bourzac, K. M.
- Affiliations
- University of Nebraska Medical Center (US)
- Nationwide Children's Hospital (US)
- Lifespan (US)
- University of Hawaiʻi at Mānoa (US)
- BioFire Diagnostics (United States) (US)
- Venue
- Journal of Clinical Microbiology
- Publisher
- American Society for Microbiology
- Published
- 2015-03
- Volume
- 53
- Issue
- 3
- Pages
- 915-925
- ISSN
- 0095-1137 (ISSN-L)
- 1098-660X
- PMC
- PMC4390666
- OpenAlex
- W2169792847
- Cited by
- 554
- References
- 0
- Citations by year
- 2026: 43 · 2025: 46 · 2024: 42 · 2023: 62 · 2022: 43 · 2021: 51 · 2020: 61 · 2019: 41 · 2018: 58 · 2017: 48 · 2016: 39 · 2015: 18
- FWCI
- 42.22
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Journal of Clinical Microbiology (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- BioFire Diagnostics
- National Institutes of Health
- National Institute of Allergy and Infectious Diseases (R01AI104593, R01AI089489)
- Topics
- Health Sciences › Medicine › Infectious Diseases › Viral gastroenteritis research and epidemiology
- Health Sciences › Medicine › Microbiology (medical) › Bacterial Identification and Susceptibility Testing
- Life Sciences › Agricultural and Biological Sciences › Food Science › Salmonella and Campylobacter epidemiology
- Keywords
- infectious gastroenteritis, enteric pathogens, multiplex PCR, sensitivity and specificity, diarrheagenic Escherichia coli, norovirus, rotavirus, sapovirus, Cryptosporidium, Giardia lamblia, Shiga toxin-producing Escherichia coli, rapid molecular diagnostics
- MeSH terms
- Adolescent, Adult, Aged, Aged, 80 and over, Animals, Bacteria, Child, Child, Preschool, Feces, Female, Gastroenteritis, Humans, Infant, Infant, Newborn, Male, Microbiological Techniques, Middle Aged, Parasites, Prospective Studies, Sensitivity and Specificity, Time Factors, Viruses, Molecular Diagnostic Techniques, Young Adult
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