Unbiased Metagenomic Sequencing for Pediatric Meningitis in Bangladesh Reveals Neuroinvasive Chikungunya Virus Outbreak and Other Unrealized Pathogens

Globally, there are an estimated 10.6 million cases of meningitis and 288,000 deaths every year, with the vast majority occurring in low- and middle-income countries. In addition, many survivors suffer from long-term neurological sequelae. Most laboratories assay only for common bacterial etiologies using culture and directed PCR, and the majority of meningitis cases lack microbiological diagnoses, impeding institution of evidence-based treatment and prevention strategies. We report here the results of a validation and application study of using unbiased metagenomic sequencing to determine etiologies of idiopathic (of unknown cause) cases. This included CSF from patients with known neurologic infections, with idiopathic meningitis, and without infection admitted in the largest children’s hospital of Bangladesh and environmental samples. Using mNGS and machine learning, we identified and confirmed an etiology (viral or bacterial) in 40% of idiopathic cases. We detected three instances of Chikungunya virus (CHIKV) that were >99% identical to each other and to a strain previously recognized to cause systemic illness only in 2017. CHIKV qPCR of all remaining stored 472 CSF samples from children who presented with idiopathic meningitis in 2017 at the same hospital uncovered an unrecognized CHIKV meningitis outbreak. CSF mNGS can complement conventional diagnostic methods to identify etiologies of meningitis, and the improved patient- and population-level data can inform better policy decisions. ABSTRACT The burden of meningitis in low-and-middle-income countries remains significant, but the infectious causes remain largely unknown, impeding institution of evidence-based treatment and prevention decisions. We conducted a validation and application study of unbiased metagenomic next-generation sequencing (mNGS) to elucidate etiologies of meningitis in Bangladesh. This RNA mNGS study was performed on cerebrospinal fluid (CSF) specimens from patients admitted in the largest pediatric hospital, a World Health Organization sentinel site, with known neurologic infections (n = 36), with idiopathic meningitis (n = 25), and with no infection (n = 30), and six environmental samples, collected between 2012 and 2018. We used the IDseq bioinformatics pipeline and machine learning to identify potentially pathogenic microbes, which we then confirmed orthogonally and followed up through phone/home visits. In samples with known etiology and without infections, there was 83% concordance between mNGS and conventional testing. In idiopathic cases, mNGS identified a potential bacterial or viral etiology in 40%. There were three instances of neuroinvasive Chikungunya virus (CHIKV), whose genomes were >99% identical to each other and to a Bangladeshi strain only previously recognized to cause febrile illness in 2017. CHIKV-specific qPCR of all remaining stored CSF samples from children who presented with idiopathic meningitis in 2017 (n = 472) revealed 17 additional CHIKV meningitis cases, exposing an unrecognized meningitis outbreak. Orthogonal molecular confirmation, case-based clinical data, and patient follow-up substantiated the findings. Case-control CSF mNGS surveys can complement conventional diagnostic methods to identify etiologies of meningitis, conduct surveillance, and predict outbreaks. The improved patient- and population-level data can inform evidence-based policy decisions. IMPORTANCE Globally, there are an estimated 10.6 million cases of meningitis and 288,000 deaths every year, with the vast majority occurring in low- and middle-income countries. In addition, many survivors suffer from long-term neurological sequelae. Most laboratories assay only for common bacterial etiologies using culture and directed PCR, and the majority of meningitis cases lack microbiological diagnoses, impeding institution of evidence-based treatment and prevention strategies. We report here the results of a validation and application study of using unbiased metagenomic sequencing to determine etiologies of idiopathic (of unknown cause) cases. This included CSF from patients with known neurologic infections, with idiopathic meningitis, and without infection admitted in the largest children’s hospital of Bangladesh and environmental samples. Using mNGS and machine learning, we identified and confirmed an etiology (viral or bacterial) in 40% of idiopathic cases. We detected three instances of Chikungunya virus (CHIKV) that were >99% identical to each other and to a strain previously recognized to cause systemic illness only in 2017. CHIKV qPCR of all remaining stored 472 CSF samples from children who presented with idiopathic meningitis in 2017 at the same hospital uncovered an unrecognized CHIKV meningitis outbreak. CSF mNGS can complement conventional diagnostic methods to identify etiologies of meningitis, and the improved patient- and population-level data can inform better policy decisions.

[1]  O. Levine,et al.  Sequelae due to bacterial meningitis among African children: a systematic literature review , 2009, BMC medicine.

[2]  C. Ross,et al.  Meningitis and Encephalitis Associated with Mumps Infection , 1972, Archives of disease in childhood.

[3]  Haniye Sadat Sajadi,et al.  Global, regional, and national incidence, prevalence, and years lived with disability for 354 diseases and injuries for 195 countries and territories, 1990–2017: a systematic analysis for the Global Burden of Disease Study 2017 , 2018, The Lancet.

[4]  Madeline Y Mayday,et al.  Pulmonary Metagenomic Sequencing Suggests Missed Infections in Immunocompromised Children , 2018, bioRxiv.

[5]  T. Cherian,et al.  Global Invasive Bacterial Vaccine-Preventable Diseases Surveillance — 2008–2014 , 2014, MMWR. Morbidity and mortality weekly report.

[6]  Katherine S. Pollard,et al.  Integrating host response and unbiased microbe detection for lower respiratory tract infection diagnosis in critically ill adults , 2018, Proceedings of the National Academy of Sciences.

[7]  Joseph L. DeRisi,et al.  Pulmonary Metagenomic Sequencing Suggests Missed Infections in Immunocompromised Children , 2018, medRxiv.

[8]  J. Andrews,et al.  Towards sustainable public health surveillance for enteric fever. , 2015, Vaccine.

[9]  G. Pugliese,et al.  Severe Streptococcus pyogenes Infections, United Kingdom, 2003–2004 , 2008, Emerging infectious diseases.

[10]  J. McCullers,et al.  Bacillus cereus bacteremia and meningitis in immunocompromised children. , 2001, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

[11]  J. Scott,et al.  Enhanced diagnosis of pneumococcal meningitis with use of the Binax NOW immunochromatographic test of Streptococcus pneumoniae antigen: a multisite study. , 2009, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

[12]  A. Naheed,et al.  Surveillance for invasive Streptococcus pneumoniae disease among hospitalized children in Bangladesh: antimicrobial susceptibility and serotype distribution. , 2009, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

[13]  Marc Lecuit,et al.  Chikungunya virus–associated encephalitis: A cohort study on La Réunion Island, 2005–2009 , 2016, Neurology.

[14]  Sergey I. Nikolenko,et al.  SPAdes: A New Genome Assembly Algorithm and Its Applications to Single-Cell Sequencing , 2012, J. Comput. Biol..

[15]  Raydel D. Mair,et al.  Laboratory methods for the diagnosis of meningitis caused by neisseria meningitidis, streptococcus pneumoniae, and haemophilus influenza; WHO manual. 2nd ed. , 2011 .

[16]  N. Loman,et al.  A culture-independent sequence-based metagenomics approach to the investigation of an outbreak of Shiga-toxigenic Escherichia coli O104:H4. , 2013, JAMA.

[17]  M. Renouil,et al.  Chikungunya virus–associated encephalitis , 2016, Neurology.

[18]  N. Neff,et al.  FLASH: a next-generation CRISPR diagnostic for multiplexed detection of antimicrobial resistance sequences , 2018, bioRxiv.

[19]  J. Brooke Stenotrophomonas maltophilia: an Emerging Global Opportunistic Pathogen , 2012, Clinical Microbiology Reviews.

[20]  Maureen H Diaz,et al.  Causes and incidence of community-acquired serious infections among young children in south Asia (ANISA): an observational cohort study , 2018, The Lancet.

[21]  U. Misra,et al.  Molecular Epidemiological Study of Enteroviruses Associated with Encephalitis in Children from India , 2012, Journal of Clinical Microbiology.

[22]  Doug Stryke,et al.  Laboratory validation of a clinical metagenomic sequencing assay for pathogen detection in cerebrospinal fluid. , 2019, Genome research.

[23]  M. Antonio,et al.  Using pneumococcal and rotavirus surveillance in vaccine decision-making: A series of case studies in Bangladesh, Armenia and the Gambia. , 2018, Vaccine.

[24]  Ari J. Green,et al.  Chronic Meningitis Investigated via Metagenomic Next-Generation Sequencing , 2018, JAMA neurology.

[25]  Shane S. Sturrock,et al.  Geneious Basic: An integrated and extendable desktop software platform for the organization and analysis of sequence data , 2012, Bioinform..

[26]  Madeline Y Mayday,et al.  Miniaturization and optimization of 384-well compatible RNA sequencing library preparation , 2019, PloS one.

[27]  T. Solomon,et al.  The neurological complications of chikungunya virus: A systematic review , 2018, Reviews in medical virology.

[28]  B. Long,et al.  Mumps: An Emergency Medicine-Focused Update. , 2017, The Journal of emergency medicine.

[29]  Mohammad Hossein Khosravi,et al.  Global, regional, and national age-sex-specific mortality for 282 causes of death in 195 countries and territories, 1980–2017: a systematic analysis for the Global Burden of Disease Study 2017 , 2018, Lancet.

[30]  N. Crowcroft,et al.  The epidemiology of acute encephalitis , 2007, Neuropsychological rehabilitation.

[31]  T. Popović,et al.  Laboratory methods for the diagnosis of meningitis caused by Neisseria meningitidis, Streptococcus pneumoniae, and Haemophilus influenzae , 1998 .

[32]  Judith Breuer,et al.  Encephalitis diagnosis using metagenomics: application of next generation sequencing for undiagnosed cases , 2018, Journal of Infection.

[33]  Y. Morikawa,et al.  Clinical manifestations of Bacillus cereus meningitis in newborn infants , 1999, Journal of paediatrics and child health.

[34]  N. Crowcroft,et al.  Challenge of the unknown , 2010, Neurology.

[35]  M. Alvesson Talking in Organizations: Managing Identity and Impressions in an Advertising Agency , 1994 .

[36]  K. Dooley,et al.  Tuberculous meningitis , 2017, Nature Reviews Neurology.

[37]  Bagher Forghani,et al.  In search of encephalitis etiologies: diagnostic challenges in the California Encephalitis Project, 1998-2000. , 2003, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

[38]  R. Lanciotti,et al.  Chikungunya Virus in US Travelers Returning from India, 2006 , 2007, Emerging infectious diseases.

[39]  D. Hamer,et al.  Rapid Diagnosis of Pneumococcal Meningitis: Implications for Treatment and Measuring Disease Burden , 2005, The Pediatric infectious disease journal.

[40]  E. Crawford,et al.  Depletion of Abundant Sequences by Hybridization (DASH): using Cas9 to remove unwanted high-abundance species in sequencing libraries and molecular counting applications , 2015, bioRxiv.