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Dive into the research topics where Megin Nichols is active.

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Featured researches published by Megin Nichols.


Pediatrics | 2015

Epidemiology of Infant Meningococcal Disease in the United States, 2006-2012

Jessica R. MacNeil; Nancy M. Bennett; Monica M. Farley; Lee H. Harrison; Ruth Lynfield; Megin Nichols; Sue Petit; Arthur Reingold; William Schaffner; Ann Thomas; Tracy Pondo; Leonard W. Mayer; Thomas A. Clark; Amanda C. Cohn

BACKGROUND: The incidence of meningococcal disease is currently at historic lows in the United States; however, incidence remains highest among infants aged <1 year. With routine use of Haemophilus influenzae type b and pneumococcal vaccines in infants and children in the United States, Neisseria meningitidis remains an important cause of bacterial meningitis in young children. METHODS: Data were collected from active, population- and laboratory-based surveillance for N meningitidis conducted through Active Bacterial Core surveillance during 2006 through 2012. Expanded data collection forms were completed for infant cases identified in the surveillance area during 2006 through 2010. RESULTS: An estimated 113 cases of culture-confirmed meningococcal disease occurred annually among infants aged <1 year in the United States from 2006 through 2012, for an overall incidence of 2.74 per 100 000 infants. Among these cases, an estimated 6 deaths occurred. Serogroup B was responsible for 64%, serogroup C for 12%, and serogroup Y for 16% of infant cases. Based on the expanded data collection forms, a high proportion of infant cases (36/58, 62%) had a smoker in the household and the socioeconomic status of the census tracts where infant meningococcal cases resided was lower compared with the other Active Bacterial Core surveillance areas and the United States as a whole. CONCLUSIONS: The burden of meningococcal disease remains highest in young infants and serogroup B predominates. Vaccines that provide long-term protection early in life have the potential to reduce the burden of meningococcal disease, especially if they provide protection against serogroup B meningococcal disease.


Mbio | 2014

vanG Element Insertions within a Conserved Chromosomal Site Conferring Vancomycin Resistance to Streptococcus agalactiae and Streptococcus anginosus

Velusamy Srinivasan; Benjamin J. Metcalf; Kristen Knipe; Mahamoudou Ouattara; Lesley McGee; Patricia Lynn Shewmaker; Anita Glennen; Megin Nichols; Carol Harris; Mary Brimmage; Belinda Ostrowsky; Connie Park; Stephanie J. Schrag; Michael Frace; Scott Sammons; Bernard Beall

ABSTRACT Three vancomycin-resistant streptococcal strains carrying vanG elements (two invasive Streptococcus agalactiae isolates [GBS-NY and GBS-NM, both serotype II and multilocus sequence type 22] and one Streptococcus anginosus [Sa]) were examined. The 45,585-bp elements found within Sa and GBS-NY were nearly identical (together designated vanG-1) and shared near-identity over an ~15-kb overlap with a previously described vanG element from Enterococcus faecalis. Unexpectedly, vanG-1 shared much less homology with the 49,321-bp vanG-2 element from GBS-NM, with widely different levels (50% to 99%) of sequence identity shared among 44 related open reading frames. Immediately adjacent to both vanG-1 and vanG-2 were 44,670-bp and 44,680-bp integrative conjugative element (ICE)-like sequences, designated ICE-r, that were nearly identical in the two group B streptococcal (GBS) strains. The dual vanG and ICE-r elements from both GBS strains were inserted at the same position, between bases 1328 and 1329, within the identical RNA methyltransferase (rumA) genes. A GenBank search revealed that although most GBS strains contained insertions within this specific site, only sequence type 22 (ST22) GBS strains contained highly related ICE-r derivatives. The vanG-1 element in Sa was also inserted within this position corresponding to its rumA homolog adjacent to an ICE-r derivative. vanG-1 insertions were previously reported within the same relative position in the E. faecalis rumA homolog. An ICE-r sequence perfectly conserved with respect to its counterpart in GBS-NY was apparent within the same site of the rumA homolog of a Streptococcus dysgalactiae subsp. equisimilis strain. Additionally, homologous vanG-like elements within the conserved rumA target site were evident in Roseburia intestinalis. IMPORTANCE These three streptococcal strains represent the first known vancomycin-resistant strains of their species. The collective observations made from these strains reveal a specific hot spot for insertional elements that is conserved between streptococci and different Gram-positive species. The two GBS strains potentially represent a GBS lineage that is predisposed to insertion of vanG elements. These three streptococcal strains represent the first known vancomycin-resistant strains of their species. The collective observations made from these strains reveal a specific hot spot for insertional elements that is conserved between streptococci and different Gram-positive species. The two GBS strains potentially represent a GBS lineage that is predisposed to insertion of vanG elements.


The New England Journal of Medicine | 2014

Two cases of invasive vancomycin-resistant group B streptococcus infection.

Connie Park; Megin Nichols; Stephanie J. Schrag

Two cases of group B streptococcus infection with resistance to vancomycin, which has been a reliable agent for treating this infection, are described.


Emerging Infectious Diseases | 2015

Twenty Years of Active Bacterial Core Surveillance.

Gayle Langley; William Schaffner; Monica M. Farley; Ruth Lynfield; Nancy M. Bennett; Arthur Reingold; Ann Thomas; Lee H. Harrison; Megin Nichols; Susan Petit; Lisa Miller; Matthew R. Moore; Stephanie J. Schrag; Fernanda C. Lessa; Tami H. Skoff; Jessica R. MacNeil; Elizabeth Briere; Emily J. Weston; Chris Van Beneden

This program has directly affected public health policies and practices.


Open Forum Infectious Diseases | 2014

Invasive Haemophilus influenzae Disease in Adults ≥65 Years, United States, 2011

Amy Blain; Jessica R. MacNeil; Xin Wang; Nancy M. Bennett; Monica M. Farley; Lee H. Harrison; Catherine Lexau; Lisa Miller; Megin Nichols; Susan Petit; Arthur Reingold; William Schaffner; Ann Thomas; Thomas A. Clark; Amanda C. Cohn; Elizabeth Briere

In this older age group burden of disease and CFR both increase significantly as age increases. Several underlying conditions increased risk of disease severity and patients with severe disease were more likely to die.


Infection Control and Hospital Epidemiology | 2014

On-Site Availability of Legionella Testing in Acute Care Hospitals, United States

Laurel E. Garrison; Kristin M. Shaw; Jeffrey T. McCollum; Carol Dexter; Paula Snippes Vagnone; Jamie Thompson; Gregory Giambrone; Benjamin White; Stepy Thomas; L. Rand Carpenter; Megin Nichols; Erin Parker; Susan Petit; Lauri A. Hicks; Gayle Langley

We surveyed 399 US acute care hospitals regarding availability of on-site Legionella testing; 300 (75.2%) did not offer Legionella testing on site. Availability varied according to hospital size and geographic location. On-site access to testing may improve detection of Legionnaires disease and inform patient management and prevention efforts.


Open Forum Infectious Diseases | 2016

Meningococcal Disease in Patients With Human Immunodeficiency Virus Infection: A Review of Cases Reported Through Active Surveillance in the United States, 2000–2008

Christine M. Harris; Henry M. Wu; Jianmin Li; H. Irene Hall; Adria Lee; Elizabeth R. Zell; Lee H. Harrison; Susan Petit; Monica M. Farley; Ruth Lynfield; Lisa Miller; Megin Nichols; Arthur Reingold; William Schaffner; Ann Thomas; Jessica R. MacNeil; Thomas A. Clark; Amanda C. Cohn

Background. Although human immunodeficiency virus (HIV) infection is an established risk factor for several bacterial infections, the association between HIV infection and meningococcal disease remains unclear. Methods. Expanded chart reviews were completed on persons with meningococcal disease and HIV infection reported from 2000 through 2008 from 9 US sites participating in an active population-based surveillance system for meningococcal disease. The incidence of meningococcal disease among patients meeting Centers for Disease Control and Prevention acquired immune deficiency syndrome (AIDS) surveillance criteria was estimated using data from the National HIV Surveillance System for the participating sites. Results. Thirty-three cases of meningococcal disease in individuals with HIV infection were reported from participating sites, representing 2.0% of all reported meningococcal disease cases. Most (75.8%) persons with HIV infection were adult males aged 25 to 64 years old. Among all meningococcal disease cases aged 25 to 64 years old, case fatality ratios were similar among HIV-infected and HIV-uninfected persons (13.3% vs 10.6%; P = .6). The cumulative, mean incidence of meningococcal disease among patients aged 25 to 64 years old with HIV infection ever classified as AIDS was 3.5 cases per 100000 person years (95% confidence interval [CI], 2.1–5.6), compared with 0.3 cases per 100000 person years (95% CI, 0.3–0.3) for persons of the same age group not reported to have AIDS (relative risk = 12.9; 95% CI, 7.9–20.9). Conclusions. Individuals with HIV infection meeting the AIDS surveillance case definition have a higher incidence of meningococcal disease compared with the general adult population.


Infection Control and Hospital Epidemiology | 2014

Brucella abortus Exposure during an Orthopedic Surgical Procedure in New Mexico, 2010

Megin Nichols; Deborah Thompson; Joshua T. Carothers; Judy Klauber; Robyn A. Stoddard; Marta A. Guerra; Tina J. Benoit; Rita M. Traxler

Brucellosis, a zoonotic disease transmitted through inhalation of infectious aerosolized particles, is endemic in many areas, including Mexico.(1, 2, 3, 4) Manifestations of disease can range from subclinical illness to osteoarticular disease and chronic sequelae.(4) It is a potential occupational hazard among laboratory workers.(3) Although Brucella infection is not usually a risk to medical staff, prosthetic joint infections have been encountered during surgery.(5–9) We report a case of periprosthetic Brucella infection and the subsequent investigation into possible transmission to operating room and laboratory staff. Objectives of the investigation included infection prevention, case-finding and examination into potential routes of Brucella spp. transmission.


Open Forum Infectious Diseases | 2016

Penicillin Use in Meningococcal Disease Management: Active Bacterial Core Surveillance Sites, 2009

Amy Blain; Sema Mandal; Henry Wu; Jessica R. MacNeil; Lee H. Harrison; Monica M. Farley; Ruth Lynfield; Lisa Miller; Megin Nichols; Sue Petit; Arthur Reingold; William Schaffner; Ann Thomas; Shelley M. Zansky; Raydel D. Anderson; Brian H. Harcourt; Leonard W. Mayer; Thomas A. Clark; Amanda C. Cohn

In 2009, in the Active Bacterial Core surveillance sites, penicillin was not commonly used to treat meningococcal disease. This is likely because of inconsistent availability of antimicrobial susceptibility testing and ease of use of third-generation cephalosporins. Consideration of current practices may inform future meningococcal disease management guidelines.


Open Forum Infectious Diseases | 2018

Obesity, Diabetes, and the Risk of Invasive Group B Streptococcal Disease in Nonpregnant Adults in the United States

Samantha Pitts; Nisa M. Maruthur; Gayle Langley; Tracy Pondo; Kathleen A. Shutt; Rosemary Hollick; Stephanie J. Schrag; Ann Thomas; Megin Nichols; Monica M. Farley; James Watt; Lisa Miller; William Schaffner; Corinne Holtzman; Lee H. Harrison

Abstract Background Rates of invasive group B Streptococcus (GBS) disease, obesity, and diabetes have increased in US adults. We hypothesized that obesity would be independently associated with an increased risk of invasive GBS disease. Methods We identified adults with invasive GBS disease within Active Bacterial Core surveillance during 2010–2012 and used population estimates from the Behavioral Risk Factor Surveillance System to calculate invasive GBS incidence rates. We estimated relative risks (RRs) of invasive GBS using Poisson analysis with offset denominators, with obesity categorized as class I/II (body mass index [BMI] = 30–39.9 kg/m2) and class III (BMI ≥ 40.0 kg/m2). Results In multivariable analysis of 4281 cases, the adjusted RRs of invasive GBS disease were increased for obesity (class I/II: RR, 1.52; 95% confidence interval [CI], 1.14–2.02; and class III: RR, 4.87; 95% CI, 3.50–6.77; reference overweight) and diabetes (RR, 6.04; 95% CI, 4.77–7.65). The adjusted RR associated with class III obesity was 3-fold among persons with diabetes (95% CI, 1.38–6.61) and nearly 9-fold among persons without diabetes (95% CI, 6.41–12.46), compared with overweight. The adjusted RRs associated with diabetes varied by age and BMI, with the highest RR in young populations without obesity. Population attributable risks of invasive GBS disease were 27.2% for obesity and 40.1% for diabetes. Conclusions Obesity and diabetes were associated with substantially increased risk of infection from invasive GBS. Given the population attributable risks of obesity and diabetes, interventions that reduce the prevalence of these conditions would likely reduce the burden of invasive GBS infection.

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Ann Thomas

Brigham and Women's Hospital

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Lisa Miller

Colorado Department of Public Health and Environment

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Susan Petit

Connecticut Agricultural Experiment Station

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Ruth Lynfield

Centers for Disease Control and Prevention

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Gayle Langley

Centers for Disease Control and Prevention

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Jessica R. MacNeil

National Center for Immunization and Respiratory Diseases

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