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Featured researches published by Nora Chea.


Bulletin of The World Health Organization | 2014

Influenza seasonality and vaccination timing in tropical and subtropical areas of southern and south-eastern Asia

Siddhartha Saha; Mandeep S. Chadha; Abdullah Al Mamun; Mahmudur Rahman; Katharine Sturm-Ramirez; Malinee Chittaganpitch; Sirima Pattamadilok; Sonja J. Olsen; Ondri Dwi Sampurno; Vivi Setiawaty; Krisna Nur Andriana Pangesti; Gina Samaan; Sibounhom Archkhawongs; Phengta Vongphrachanh; Darouny Phonekeo; Andrew Corwin; Sok Touch; Philippe Buchy; Nora Chea; Paul Kitsutani; Le Quynh Mai; Vu Dinh Thiem; Raymond T. P. Lin; Constance Low; Chong Chee Kheong; Norizah Ismail; Mohd Apandi Yusof; Amado Tandoc; Vito G. Roque; Akhilesh C. Mishra

OBJECTIVE To characterize influenza seasonality and identify the best time of the year for vaccination against influenza in tropical and subtropical countries of southern and south-eastern Asia that lie north of the equator. METHODS Weekly influenza surveillance data for 2006 to 2011 were obtained from Bangladesh, Cambodia, India, Indonesia, the Lao Peoples Democratic Republic, Malaysia, the Philippines, Singapore, Thailand and Viet Nam. Weekly rates of influenza activity were based on the percentage of all nasopharyngeal samples collected during the year that tested positive for influenza virus or viral nucleic acid on any given week. Monthly positivity rates were then calculated to define annual peaks of influenza activity in each country and across countries. FINDINGS Influenza activity peaked between June/July and October in seven countries, three of which showed a second peak in December to February. Countries closer to the equator had year-round circulation without discrete peaks. Viral types and subtypes varied from year to year but not across countries in a given year. The cumulative proportion of specimens that tested positive from June to November was > 60% in Bangladesh, Cambodia, India, the Lao Peoples Democratic Republic, the Philippines, Thailand and Viet Nam. Thus, these tropical and subtropical countries exhibited earlier influenza activity peaks than temperate climate countries north of the equator. CONCLUSION Most southern and south-eastern Asian countries lying north of the equator should consider vaccinating against influenza from April to June; countries near the equator without a distinct peak in influenza activity can base vaccination timing on local factors.


Clinical Infectious Diseases | 2014

Clinical and Laboratory Findings of the First Imported Case of Middle East Respiratory Syndrome Coronavirus to the United States

Minal Kapoor; Kimberly Pringle; Alan Kumar; Stephanie Dearth; Lixia Liu; Judith Lovchik; Omar Perez; Pam Pontones; Shawn Richards; Jaime Yeadon-Fagbohun; Lucy Breakwell; Nora Chea; Nicole J. Cohen; Eileen Schneider; Dean D. Erdman; Lia M. Haynes; Mark A. Pallansch; Ying Tao; Suxiang Tong; Susan I. Gerber; David L. Swerdlow; Daniel R. Feikin

The first US case of Middle East respiratory syndrome coronavirus was confirmed in May 2014 in a 65-year-old physician who worked in Saudi Arabia and presented to an Indiana hospital on illness day 11. He had bilateral pneumonia and recovered fully.


Emerging Infectious Diseases | 2015

Improved Phenotype-Based Definition for Identifying Carbapenemase Producers among Carbapenem-Resistant Enterobacteriaceae

Nora Chea; Sandra N. Bulens; Thiphasone Kongphet-Tran; Ruth Lynfield; Kristin M. Shaw; Paula Snippes Vagnone; Marion Kainer; Daniel Muleta; Lucy E. Wilson; Elisabeth Vaeth; Ghinwa Dumyati; Cathleen Concannon; Erin C. Phipps; Karissa Culbreath; Sarah J. Janelle; Wendy Bamberg; Alice Guh; Brandi Limbago

A new, less restrictive definition increases detection of Klebsiella pneumoniae carbapenemase producers.


Journal of Virology | 2014

Identification of Molecular Markers Associated with Alteration of Receptor-Binding Specificity in a Novel Genotype of Highly Pathogenic Avian Influenza A(H5N1) Viruses Detected in Cambodia in 2013

Sareth Rith; C. Todd Davis; Veasna Duong; Borann Sar; Srey Viseth Horm; Savuth Chin; Sovann Ly; Denis Laurent; Beat Richner; Ikwo K. Oboho; Yunho Jang; William C. Davis; Sharmi Thor; Amanda Balish; A. Danielle Iuliano; San Sorn; Davun Holl; Touch Sok; Heng Seng Seng; Arnaud Tarantola; Reiko Tsuyuoka; Amy Parry; Nora Chea; Lotfi Allal; Paul Kitsutani; Dora Warren; Michael Prouty; Paul F. Horwood; Marc-Alain Widdowson; Stephen Lindstrom

ABSTRACT Human infections with influenza A(H5N1) virus in Cambodia increased sharply during 2013. Molecular characterization of viruses detected in clinical specimens from human cases revealed the presence of mutations associated with the alteration of receptor-binding specificity (K189R, Q222L) and respiratory droplet transmission in ferrets (N220K with Q222L). Discovery of quasispecies at position 222 (Q/L), in addition to the absence of the mutations in poultry/environmental samples, suggested that the mutations occurred during human infection and did not transmit further.


Infection, Genetics and Evolution | 2013

Dynamic of H5N1 virus in Cambodia and emergence of a novel endemic sub-clade

San Sorn; Touch Sok; Sovann Ly; Sareth Rith; Nguyen Tung; Alain Viari; Laurent Gavotte; Davun Holl; Heng Seng; Nima Asgari; Beat Richner; Denis Laurent; Nora Chea; Veasna Duong; Tetsuya Toyoda; Chadwick Y. Yasuda; Paul Kitsutani; Paul Zhou; Sun Bing; Vincent Deubel; Ruben O. Donis; Roger Frutos; Philippe Buchy

In Cambodia, the first detection of HPAI H5N1 virus in birds occurred in January 2004 and since then there have been 33 outbreaks in poultry while 21 human cases were reported. The origin and dynamics of these epizootics in Cambodia remain unclear. In this work we used a range of bioinformatics methods to analyze the Cambodian virus sequences together with those from neighboring countries. Six HA lineages belonging to clades 1 and 1.1 were identified since 2004. Lineage 1 shares an ancestor with viruses from Thailand and disappeared after 2005, to be replaced by lineage 2 originating from Vietnam and then by lineage 3. The highly adapted lineage 4 was seen only in Cambodia. Lineage 5 is circulating both in Vietnam and Cambodia since 2008 and was probably introduced in Cambodia through unregistered transboundary poultry trade. Lineage 6 is endemic to Cambodia since 2010 and could be classified as a new clade according to WHO/OIE/FAO criteria for H5N1 virus nomenclature. We propose to name it clade 1.1A. There is a direct filiation of lineages 2 to 6 with a temporal evolution and geographic differentiation for lineages 4 and 6. By the end of 2011, two lineages, i.e. lineages 5 and 6, with different transmission paths cocirculate in Cambodia. The presence of lineage 6 only in Cambodia suggests the existence of a transmission specific to this country whereas the presence of lineage 5 in both Cambodia and Vietnam indicates a distinct way of circulation of infected poultry.


Emerging Infectious Diseases | 2015

Lack of transmission among close contacts of patient with case of middle east respiratory syndrome imported into the United States, 2014

Lucy Breakwell; Kimberly Pringle; Nora Chea; Donna Allen; Steve Allen; Shawn Richards; Pam Pantones; Michelle Sandoval; Lixia Liu; Michael O. Vernon; Craig Conover; Rashmi Chugh; Alfred DeMaria; Rachel Burns; Sandra Smole; Susan I. Gerber; Nicole J. Cohen; David T. Kuhar; Lia M. Haynes; Eileen Schneider; Alan Kumar; Minal Kapoor; Marlene Madrigal; David L. Swerdlow; Daniel R. Feikin

Despite 61 contacts with unprotected exposure, no secondary cases occurred.


MMWR supplements | 2016

Infection Prevention and Control for Ebola in Health Care Settings — West Africa and United States

Jeffrey C. Hageman; Carmen Hazim; Katie Wilson; Paul Malpiedi; Neil Gupta; Sarah Bennett; Amy Kolwaite; Abbigail Tumpey; Kristin J. Brinsley-Rainisch; Bryan Christensen; Carolyn V. Gould; Angela Fisher; Michael A. Jhung; Douglas Hamilton; Kerri Moran; Lisa J. Delaney; Chad H. Dowell; Michael Bell; Arjun Srinivasan; Melissa K. Schaefer; Ryan Fagan; Nedghie Adrien; Nora Chea; Benjamin J. Park

The 2014-2016 Ebola virus disease (Ebola) epidemic in West Africa underscores the need for health care infection prevention and control (IPC) practices to be implemented properly and consistently to interrupt transmission of pathogens in health care settings to patients and health care workers. Training and assessing IPC practices in general health care facilities not designated as Ebola treatment units or centers became a priority for CDC as the number of Ebola virus transmissions among health care workers in West Africa began to affect the West African health care system and increasingly more persons became infected. CDC and partners developed policies, procedures, and training materials tailored to the affected countries. Safety training courses were also provided to U.S. health care workers intending to work with Ebola patients in West Africa. As the Ebola epidemic continued in West Africa, the possibility that patients with Ebola could be identified and treated in the United States became more realistic. In response, CDC, other federal components (e.g., Office of the Assistant Secretary for Preparedness and Response) and public health partners focused on health care worker training and preparedness for U.S. health care facilities. CDC used the input from these partners to develop guidelines on IPC for hospitalized patients with known or suspected Ebola, which was updated based on feedback from partners who provided care for Ebola patients in the United States. Strengthening and sustaining IPC helps health care systems be better prepared to prevent and respond to current and future infectious disease threats.The activities summarized in this report would not have been possible without collaboration with many U.S. and international partners (http://www.cdc.gov/vhf/ebola/outbreaks/2014-west-africa/partners.html).


PLOS ONE | 2014

Epidemiological and Virological Characteristics of Influenza Viruses Circulating in Cambodia from 2009 to 2011

Srey Viseth Horm; Sek Mardy; Sareth Rith; Sovann Ly; Seng Heng; Sirenda Vong; Paul Kitsutani; Vannra Ieng; Arnaud Tarantola; Sowath Ly; Borann Sar; Nora Chea; Buth Sokhal; Ian G. Barr; Anne Kelso; Paul F. Horwood; Ans Timmermans; Aeron C. Hurt; Chanthap Lon; David Saunders; Sam An Ung; Nima Asgari; Maria Concepcion Roces; Sok Touch; Naomi Komadina; Philippe Buchy

Background The Cambodian National Influenza Center (NIC) monitored and characterized circulating influenza strains from 2009 to 2011. Methodology/Principal Findings Sentinel and study sites collected nasopharyngeal specimens for diagnostic detection, virus isolation, antigenic characterization, sequencing and antiviral susceptibility analysis from patients who fulfilled case definitions for influenza-like illness, acute lower respiratory infections and event-based surveillance. Each year in Cambodia, influenza viruses were detected mainly from June to November, during the rainy season. Antigenic analysis show that A/H1N1pdm09 isolates belonged to the A/California/7/2009-like group. Circulating A/H3N2 strains were A/Brisbane/10/2007-like in 2009 before drifting to A/Perth/16/2009-like in 2010 and 2011. The Cambodian influenza B isolates from 2009 to 2011 all belonged to the B/Victoria lineage represented by the vaccine strains B/Brisbane/60/2008 and B/Malaysia/2506/2004. Sequences of the M2 gene obtained from representative 2009–2011 A/H3N2 and A/H1N1pdm09 strains all contained the S31N mutation associated with adamantanes resistance except for one A/H1N1pdm09 strain isolated in 2011 that lacked this mutation. No reduction in the susceptibility to neuraminidase inhibitors was observed among the influenza viruses circulating from 2009 to 2011. Phylogenetic analysis revealed that A/H3N2 strains clustered each year to a distinct group while most A/H1N1pdm09 isolates belonged to the S203T clade. Conclusions/Significance In Cambodia, from 2009 to 2011, influenza activity occurred throughout the year with peak seasonality during the rainy season from June to November. Seasonal influenza epidemics were due to multiple genetically distinct viruses, even though all of the isolates were antigenically similar to the reference vaccine strains. The drug susceptibility profile of Cambodian influenza strains revealed that neuraminidase inhibitors would be the drug of choice for influenza treatment and chemoprophylaxis in Cambodia, as adamantanes are no longer expected to be effective.


American Journal of Transplantation | 2014

First confirmed cases of Middle East respiratory syndrome coronavirus (MERS-CoV) infection in the United States, updated information on the epidemiology of MERS-CoV infection, and guidance for the public, clinicians, and public health authorities - May 2014

Stephanie R. Bialek; Donna Allen; Francisco Alvarado-Ramy; Ray R. Arthur; Arunmozhi Balajee; David M. Bell; Susan Best; Carina Blackmore; Lucy Breakwell; Andrew Cannons; Clive Brown; Martin S. Cetron; Nora Chea; Christina Chommanard; Nicole J. Cohen; Craig Conover; Antonio Crespo; Jeanean Creviston; Aaron T. Curns; Rebecca M. Dahl; Stephanie Dearth; Alfred DeMaria; Fred Echols; Dean D. Erdman; Daniel R. Feikin; Mabel Frias; Susan I. Gerber; Reena Gulati; Christa Hale; Lia M. Haynes

Since mid-March 2014, the frequency with which cases of Middle East respiratory syndrome coronavirus (MERS-CoV) infection have been reported has increased, with the majority of recent cases reported from Saudi Arabia and United Arab Emirates (UAE). In addition, the frequency with which travel-associated MERS cases have been reported and the number of countries that have reported them to the World Health Organization (WHO) have also increased. The first case of MERS in the United States, identified in a traveler recently returned from Saudi Arabia, was reported to CDC by the Indiana State Department of Health on May 1, 2014, and confirmed by CDC on May 2. A second imported case of MERS in the United States, identified in a traveler from Saudi Arabia having no connection with the first case, was reported to CDC by the Florida Department of Health on May 11, 2014. The purpose of this report is to alert clinicians, health officials, and others to increase awareness of the need to consider MERS-CoV infection in persons who have recently traveled from countries in or near the Arabian Peninsula. This report summarizes recent epidemiologic information, provides preliminary descriptions of the cases reported from Indiana and Florida, and updates CDC guidance about patient evaluation, home care and isolation, specimen collection, and travel as of May 13, 2014.


American Journal of Tropical Medicine and Hygiene | 2016

Real-Time Polymerase Chain Reaction Detection of Angiostrongylus cantonensis DNA in Cerebrospinal Fluid from Patients with Eosinophilic Meningitis

Yvonne Qvarnstrom; Maniphet Xayavong; Ana Cristina Arámburu da Silva; Sarah Y. Park; A. Christian Whelen; Precilia S. Calimlim; Rebecca Sciulli; Stacey Honda; Karen Higa; Paul Kitsutani; Nora Chea; Seng Heng; Stuart Johnson; Carlos Graeff-Teixeira; LeAnne M. Fox; Alexandre J. da Silva

Angiostrongylus cantonensis is the most common infectious cause of eosinophilic meningitis. Timely diagnosis of these infections is difficult, partly because reliable laboratory diagnostic methods are unavailable. The aim of this study was to evaluate the usefulness of a real-time polymerase chain reaction (PCR) assay for the detection of A. cantonensis DNA in human cerebrospinal fluid (CSF) specimens. A total of 49 CSF specimens from 33 patients with eosinophilic meningitis were included: A. cantonensis DNA was detected in 32 CSF specimens, from 22 patients. Four patients had intermittently positive and negative real-time PCR results on subsequent samples, indicating that the level of A. cantonensis DNA present in CSF may fluctuate during the course of the illness. Immunodiagnosis and/or supplemental PCR testing supported the real-time PCR findings for 30 patients. On the basis of these observations, this real-time PCR assay can be useful to detect A. cantonensis in the CSF from patients with eosinophilic meningitis.

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Paul Kitsutani

Centers for Disease Control and Prevention

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Daniel R. Feikin

Centers for Disease Control and Prevention

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Lia M. Haynes

National Center for Immunization and Respiratory Diseases

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Lucy Breakwell

Centers for Disease Control and Prevention

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Nicole J. Cohen

Centers for Disease Control and Prevention

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Susan I. Gerber

National Center for Immunization and Respiratory Diseases

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Alfred DeMaria

Massachusetts Department of Public Health

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Craig Conover

Illinois Department of Public Health

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Donna Allen

Oklahoma State Department of Health

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