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Featured researches published by Jana M. Ritter.


The Lancet | 2016

Pathology of congenital Zika syndrome in Brazil: a case series

Roosecelis Brasil Martines; Julu Bhatnagar; Ana Maria de Oliveira Ramos; Helaine Pompeia Freire Davi; Silvia D’Andretta Iglezias; Cristina Takami Kanamura; M. Kelly Keating; Gillian Hale; Luciana Silva-Flannery; Atis Muehlenbachs; Jana M. Ritter; Joy Gary; Dominique Rollin; Cynthia S. Goldsmith; Sarah Reagan-Steiner; Yokabed Ermias; Tadaki Suzuki; Kleber Giovanni Luz; Wanderson Kleber de Oliveira; Robert S. Lanciotti; Amy J. Lambert; Wun-Ju Shieh; Sherif R. Zaki

BACKGROUND Zika virus is an arthropod-borne virus that is a member of the family Flaviviridae transmitted mainly by mosquitoes of the genus Aedes. Although usually asymptomatic, infection can result in a mild and self-limiting illness characterised by fever, rash, arthralgia, and conjunctivitis. An increase in the number of children born with microcephaly was noted in 2015 in regions of Brazil with high transmission of Zika virus. More recently, evidence has been accumulating supporting a link between Zika virus and microcephaly. Here, we describe findings from three fatal cases and two spontaneous abortions associated with Zika virus infection. METHODS In this case series, formalin-fixed paraffin-embedded tissue samples from five cases, including two newborn babies with microcephaly and severe arthrogryposis who died shortly after birth, one 2-month-old baby, and two placentas from spontaneous abortions, from Brazil were submitted to the Infectious Diseases Pathology Branch at the US Centers for Disease Control and Prevention (Atlanta, GA, USA) between December, 2015, and March, 2016. Specimens were assessed by histopathological examination, immunohistochemical assays using a mouse anti-Zika virus antibody, and RT-PCR assays targeting the NS5 and envelope genes. Amplicons of RT-PCR positive cases were sequenced for characterisation of strains. FINDINGS Viral antigens were localised to glial cells and neurons and associated with microcalcifications in all three fatal cases with microcephaly. Antigens were also seen in chorionic villi of one of the first trimester placentas. Tissues from all five cases were positive for Zika virus RNA by RT-PCR, and sequence analyses showed highest identities with Zika virus strains isolated from Brazil during 2015. INTERPRETATION These findings provide strong evidence of a link between Zika virus infection and different congenital central nervous system malformations, including microcephaly as well as arthrogryposis and spontaneous abortions. FUNDING None.


Emerging Infectious Diseases | 2017

Zika Virus RNA Replication and Persistence in Brain and Placental Tissue.

Julu Bhatnagar; Demi Rabeneck; Roosecelis Brasil Martines; Sarah Reagan-Steiner; Yokabed Ermias; Lindsey B.C. Estetter; Tadaki Suzuki; Jana M. Ritter; M. Kelly Keating; Gillian Hale; Joy Gary; Atis Muehlenbachs; Amy J. Lambert; Robert S. Lanciotti; Titilope Oduyebo; Dana Meaney-Delman; Fernando Bolaños; Edgar Alberto Parra Saad; Wun-Ju Shieh; Sherif R. Zaki

Zika virus is causally linked with congenital microcephaly and may be associated with pregnancy loss. However, the mechanisms of Zika virus intrauterine transmission and replication and its tropism and persistence in tissues are poorly understood. We tested tissues from 52 case-patients: 8 infants with microcephaly who died and 44 women suspected of being infected with Zika virus during pregnancy. By reverse transcription PCR, tissues from 32 (62%) case-patients (brains from 8 infants with microcephaly and placental/fetal tissues from 24 women) were positive for Zika virus. In situ hybridization localized replicative Zika virus RNA in brains of 7 infants and in placentas of 9 women who had pregnancy losses during the first or second trimester. These findings demonstrate that Zika virus replicates and persists in fetal brains and placentas, providing direct evidence of its association with microcephaly. Tissue-based reverse transcription PCR extends the time frame of Zika virus detection in congenital and pregnancy-associated infections.


JAMA | 2013

Raccoon Rabies Virus Variant Transmission Through Solid Organ Transplantation

Neil M. Vora; Sridhar V. Basavaraju; Katherine A. Feldman; Christopher D. Paddock; Lillian A. Orciari; Steven Gitterman; Stephanie Griese; Ryan M. Wallace; Maria A. Said; Dianna M. Blau; Gennaro Selvaggi; Andres Velasco-Villa; Jana M. Ritter; Pamela A. Yager; Agnes Kresch; Mike Niezgoda; Jesse D. Blanton; Valentina Stosor; Edward M. Falta; G. Marshall Lyon; Teresa R. Zembower; Natalia Kuzmina; Prashant K. Rohatgi; Sergio Recuenco; Sherif R. Zaki; Inger K. Damon; Richard Franka; Matthew J. Kuehnert

IMPORTANCE The rabies virus causes a fatal encephalitis and can be transmitted through tissue or organ transplantation. In February 2013, a kidney recipient with no reported exposures to potentially rabid animals died from rabies 18 months after transplantation. OBJECTIVES To investigate whether organ transplantation was the source of rabies virus exposure in the kidney recipient, and to evaluate for and prevent rabies in other transplant recipients from the same donor. DESIGN Organ donor and all transplant recipient medical records were reviewed. Laboratory tests to detect rabies virus-specific binding antibodies, rabies virus neutralizing antibodies, and rabies virus antigens were conducted on available specimens, including serum, cerebrospinal fluid, and tissues from the donor and the recipients. Viral ribonucleic acid was extracted from tissues and amplified for nucleoprotein gene sequencing for phylogenetic comparisons. MAIN OUTCOMES AND MEASURES Determination of whether the donor died from undiagnosed rabies and whether other organ recipients developed rabies. RESULTS In retrospect, the donors clinical presentation (which began with vomiting and upper extremity paresthesias and progressed to fever, seizures, dysphagia, autonomic dysfunction, and brain death) was consistent with rabies. Rabies virus antigen was detected in archived autopsy brain tissue collected from the donor. The rabies viruses infecting the donor and the deceased kidney recipient were consistent with the raccoon rabies virus variant and were more than 99.9% identical across the entire N gene (1349/1350 nucleotides), thus confirming organ transplantation as the route of transmission. The 3 other organ recipients remained asymptomatic, with rabies virus neutralizing antibodies detected in their serum after completion of postexposure prophylaxis (range, 0.3-40.8 IU/mL). CONCLUSIONS AND RELEVANCE Unlike the 2 previous clusters of rabies virus transmission through solid organ transplantation, there was a long incubation period in the recipient who developed rabies, and survival of 3 other recipients without pretransplant rabies vaccination. Rabies should be considered in patients with acute progressive encephalitis of unexplained etiology, especially for potential organ donors. A standard evaluation of potential donors who meet screening criteria for infectious encephalitis should be considered, and risks and benefits for recipients of organs from these donors should be evaluated.


Cell Reports | 2017

Frequent Zika Virus Sexual Transmission and Prolonged Viral RNA Shedding in an Immunodeficient Mouse Model

Nisha K. Duggal; Jana M. Ritter; Samuel E. Pestorius; Sherif R. Zaki; Brent S. Davis; Gwong-Jen J. Chang; Richard A. Bowen; Aaron C. Brault

SUMMARY Circulation of Zika virus (ZIKV) was first identified in the Western hemisphere in late 2014. Primarily transmitted through mosquito bite, ZIKV can also be transmitted through sex and from mother to fetus, and maternal ZIKV infection has been associated with fetal malformations. We assessed immunodeficient AG129 mice for their capacity to shed ZIKV in semen and to infect female mice via sexual transmission. Infectious virus was detected in semen between 7 and 21 days post-inoculation, and ZIKV RNA was detected in semen through 58 days post-inoculation. During mating, 73% of infected males transmitted ZIKV to uninfected females, and 50% of females became infected, with evidence of fetal infection in resulting pregnancies. Semen from vasectomized mice contained significantly lower levels of infectious virus, though sexual transmission still occurred. This model provides a platform for studying the kinetics of ZIKV sexual transmission and prolonged RNA shedding also observed in human semen.


Clinical Infectious Diseases | 2015

The First Association of a Primary Amebic Meningoencephalitis Death With Culturable Naegleria fowleri in Tap Water From a US Treated Public Drinking Water System

Jennifer R. Cope; Raoult Ratard; Vincent R. Hill; Theresa Sokol; Jonathan Jake Causey; Jonathan S. Yoder; Gayatri Mirani; Bonnie Mull; Kimberly Mukerjee; Jothikumar Narayanan; Meggie E. Doucet; Yvonne Qvarnstrom; Charla N. Poole; Olugbenga Akingbola; Jana M. Ritter; Zhenggang Xiong; Alexandre J. da Silva; Dawn M. Roellig; Russell B. Van Dyke; Harlan Stern; Lihua Xiao; Michael J. Beach

BACKGROUND Naegleria fowleri is a climate-sensitive, thermophilic ameba found in warm, freshwater lakes and rivers. Primary amebic meningoencephalitis (PAM), which is almost universally fatal, occurs when N. fowleri-containing water enters the nose, typically during swimming, and migrates to the brain via the olfactory nerve. In August 2013, a 4-year-old boy died of meningoencephalitis of unknown etiology in a Louisiana hospital. METHODS Clinical and environmental testing and a case investigation were initiated to determine the cause of death and to identify potential exposures. RESULTS Based on testing of cerebrospinal fluid and brain specimens, the child was diagnosed with PAM. His only reported water exposure was tap water; in particular, tap water that was used to supply water to a lawn water slide on which the child had played extensively prior to becoming ill. Water samples were collected from both the home and the water distribution system that supplied the home and tested; N. fowleri was identified in water samples from both the home and the water distribution system. CONCLUSIONS This case is the first reported PAM death associated with culturable N. fowleri in tap water from a US treated drinking water system. This case occurred in the context of an expanding geographic range for PAM beyond southern states, with recent case reports from Minnesota, Kansas, and Indiana. This case also highlights the role of adequate disinfection throughout drinking water distribution systems and the importance of maintaining vigilance when operating drinking water systems using source waters with elevated temperatures.


American Journal of Pathology | 2013

Exserohilum Infections Associated with Contaminated Steroid Injections: A Clinicopathologic Review of 40 Cases

Jana M. Ritter; Atis Muehlenbachs; Dianna M. Blau; Christopher D. Paddock; Wun-Ju Shieh; Clifton P. Drew; Brigid Batten; Jeanine Bartlett; Maureen G. Metcalfe; Cau D. Pham; Shawn R. Lockhart; Mitesh Patel; Lindy Liu; Tara L. Jones; Patricia W. Greer; Jeltley L. Montague; Elizabeth H. White; Dominique Rollin; Cynthia Seales; Donna Stewart; Mark V. Deming; Mary E. Brandt; Sherif R. Zaki

September 2012 marked the beginning of the largest reported outbreak of infections associated with epidural and intra-articular injections. Contamination of methylprednisolone acetate with the black mold, Exserohilum rostratum, was the primary cause of the outbreak, with >13,000 persons exposed to the potentially contaminated drug, 741 confirmed drug-related infections, and 55 deaths. Fatal meningitis and localized epidural, paraspinal, and peripheral joint infections occurred. Tissues from 40 laboratory-confirmed cases representing these various clinical entities were evaluated by histopathological analysis, special stains, and IHC to characterize the pathological features and investigate the pathogenesis of infection, and to evaluate methods for detection of Exserohilum in formalin-fixed, paraffin-embedded (FFPE) tissues. Fatal cases had necrosuppurative to granulomatous meningitis and vasculitis, with thrombi and abundant angioinvasive fungi, with extensive involvement of the basilar arterial circulation of the brain. IHC was a highly sensitive method for detection of fungus in FFPE tissues, demonstrating both hyphal forms and granular fungal antigens, and PCR identified Exserohilum in FFPE and fresh tissues. Our findings suggest a pathogenesis for meningitis involving fungal penetration into the cerebrospinal fluid at the injection site, with transport through cerebrospinal fluid to the basal cisterns and subsequent invasion of the basilar arteries. Further studies are needed to characterize Exserohilum and investigate the potential effects of underlying host factors and steroid administration on the pathogenesis of infection.


Archives of Pathology & Laboratory Medicine | 2017

Zika Virus: Pathology From the Pandemic.

Jana M. Ritter; Roosecelis Brasil Martines; Sherif R. Zaki

CONTEXT -As the number of Zika virus (ZIKV) infections continues to grow, so, too, does the spectrum of recognized clinical disease, in both adult and congenital infections. Defining the tissue pathology associated with the various disease manifestations provides insight into pathogenesis and diagnosis, and potentially future prevention and treatment, of ZIKV infections. OBJECTIVE -To summarize the syndromes and pathology associated with ZIKV infection, the implications of pathologic findings in the pathogenesis of ZIKV disease, and the use of pathology specimens for diagnosis of ZIKV infection. DATA SOURCES -The major sources of information for this review were published articles obtained from PubMed and pathologic findings from cases submitted to the Infectious Diseases Pathology Branch at the Centers for Disease Control and Prevention. CONCLUSIONS -Pathologic findings associated with ZIKV infection are characteristic but not specific. In congenital Zika syndrome, tissue pathology is due to direct viral infection of neural structures, whereas in Guillain-Barré syndrome, pathology is likely due to a postviral, aberrant host-directed immune response. Both fetal and placental pathology specimens are useful for ZIKV diagnosis by molecular and immunohistochemical assays; however, the implications of ZIKV detection in placentas from second- and third-trimester normal live births are unclear, as the potential postnatal effects of late gestational exposure remain to be seen.


Clinical Infectious Diseases | 2016

Clinical and Pathological Evaluation of Mycobacterium marinum Group Skin Infections Associated With Fish Markets in New York City

Tiffany Y. Sia; Sarah Taimur; Dianna M. Blau; Jennifer Lambe; Joel Ackelsberg; Kari Yacisin; Julu Bhatnagar; Jana M. Ritter; Wun-Ju Shieh; Atis Muehlenbachs; Kenneth Shulman; Danny Fong; Elaine Kung; Sherif R. Zaki

BACKGROUND From December 2013 through May 2014, physicians, dermatopathologists, and public health authorities collaborated to characterize an outbreak of Mycobacterium marinum and other nontuberculous mycobacterial skin and soft tissue infections (SSTIs) associated with handling fish in New York Citys Chinatown. Clinicopathologic and laboratory investigations were performed on a series of patients. METHODS Medical records were reviewed for 29 patients. Culture results were available for 27 patients and 24 biopsy specimens were evaluated by histopathology, immunohistochemistry (IHC) staining for acid-fast bacilli (AFB), and mycobacterial polymerase chain reaction (PCR) assays. RESULTS All patients received antibiotics. The most commonly prescribed antibiotic regimen was clarithromycin and ethambutol. Of the 29 patients in this case series, 16 (55%) received surgical treatment involving incision and drainage, mass excision, and synovectomy. Of these, 7 (44%) had deep tissue involvement. All patients showed improvement. For those with culture results, 11 of 27 (41%) were positive for M. marinum; the remainder showed no growth. Poorly formed granulomas (96%), neutrophils (75%), and necrosis (79%) were found in 24 biopsies. Of 15 cases that were culture-negative and analyzed by other methods, 9 were PCR positive for M. marinum group species, 8 were IHC positive, and 3 were positive by AFB stains. CONCLUSIONS A multidisciplinary approach was used to identify cases in an outbreak of M. marinum infections. The use of histopathology, culture, and IHC plus PCR from full thickness skin biopsy can lead to improved diagnosis of M. marinum SSTIs compared to relying solely on mycobacterial culture, the current gold standard.


American Journal of Tropical Medicine and Hygiene | 2017

Differential Neurovirulence of African and Asian Genotype Zika Virus Isolates in Outbred Immunocompetent Mice

Brent S. Davis; Nisha K. Duggal; Gwong-Jen J. Chang; Jana M. Ritter; Erin M. McDonald; Hannah Romo; Aaron C. Brault; Farshad Guirakhoo

Abstract. Although first isolated almost 70 years ago, Zika virus (ZIKV; Flavivirus, Flaviviridae) has only recently been associated with significant outbreaks of disease in humans. Several severe ZIKV disease manifestations have also been recently documented, including fetal malformations, such as microcephaly, and Guillain–Barré syndrome in adults. Although principally transmitted by mosquitoes, sexual transmission of ZIKV has been documented. Recent publications of several interferon receptor knockout mouse models have demonstrated ZIKV-induced disease. Herein, outbred immunocompetent CD-1/ICR adult mice were assessed for susceptibility to disease by intracranial (i.c.) and intraperitoneal (i.p.) inoculation with the Ugandan prototype strain (MR766; African genotype), a low-passage Senegalese strain (DakAr41524; African genotype) and a recent ZIKV strain isolated from a traveler infected in Puerto Rico (PRVABC59; Asian genotype). Morbidity was not observed in mice inoculated by the i.p. route with either MR766 or PRVABC59 for doses up to 6 log10 PFU. In contrast, CD-1/ICR mice inoculated i.c. with the MR766 ZIKV strain exhibited an 80–100% mortality rate that was age independent. The DakAr41524 strain delivered by the i.c route caused 30% mortality, and the Puerto Rican ZIKV strain failed to elicit mortality but did induce a serum neutralizing immune response in 60% of mice. These data provide a potential animal model for assessing neurovirulence determinants of different ZIKV strains as well as a potential immunocompetent challenge model for assessing protective efficacy of vaccine candidates.


American Journal of Pathology | 2016

Cardiac Tropism of Borrelia burgdorferi: An Autopsy Study of Sudden Cardiac Death Associated with Lyme Carditis

Atis Muehlenbachs; Brigid C. Bollweg; Thadeus Schulz; Joseph D. Forrester; Marlene DeLeon Carnes; Claudia R. Molins; Gregory Ray; Peter M. Cummings; Jana M. Ritter; Dianna M. Blau; Thomas A. Andrew; Margaret Prial; Dianna L. Ng; Joseph A. Prahlow; Jeanine H. Sanders; Wun Ju Shieh; Christopher D. Paddock; Martin E. Schriefer; Paul S. Mead; Sherif R. Zaki

Fatal Lyme carditis caused by the spirochete Borrelia burgdorferi rarely is identified. Here, we describe the pathologic, immunohistochemical, and molecular findings of five case patients. These sudden cardiac deaths associated with Lyme carditis occurred from late summer to fall, ages ranged from young adult to late 40s, and four patients were men. Autopsy tissue samples were evaluated by light microscopy, Warthin-Starry stain, immunohistochemistry, and PCR for B. burgdorferi, and immunohistochemistry for complement components C4d and C9, CD3, CD79a, and decorin. Post-mortem blood was tested by serology. Interstitial lymphocytic pancarditis in a relatively characteristic road map distribution was present in all cases. Cardiomyocyte necrosis was minimal, T cells outnumbered B cells, plasma cells were prominent, and mild fibrosis was present. Spirochetes in the cardiac interstitium associated with collagen fibers and co-localized with decorin. Rare spirochetes were seen in the leptomeninges of two cases by immunohistochemistry. Spirochetes were not seen in other organs examined, and joint tissue was not available for evaluation. Although rare, sudden cardiac death caused by Lyme disease might be an under-recognized entity and is characterized by pancarditis and marked tropism of spirochetes for cardiac tissues.

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Sherif R. Zaki

Centers for Disease Control and Prevention

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Atis Muehlenbachs

Centers for Disease Control and Prevention

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Dianna M. Blau

Centers for Disease Control and Prevention

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Ellen N. Kersh

Centers for Disease Control and Prevention

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Janet M. McNicholl

Centers for Disease Control and Prevention

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Julu Bhatnagar

Centers for Disease Control and Prevention

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Wun-Ju Shieh

Centers for Disease Control and Prevention

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Dominique Rollin

Centers for Disease Control and Prevention

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Jeanine H. Sanders

Centers for Disease Control and Prevention

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Roosecelis Brasil Martines

Centers for Disease Control and Prevention

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