PLoS OnePLoS ONEplosplosonePLoS ONE1932-6203Public Library of ScienceSan Francisco, USA226622323360608PONE-D-11-2513910.1371/journal.pone.0037825Research ArticleBiologyAnatomy and PhysiologyNeurological SystemCentral Nervous SystemNeuroscienceNeurophysiologyCentral Nervous SystemPopulation BiologyEpidemiologyInfectious Disease EpidemiologyMedicineAnatomy and PhysiologyNeurological SystemCentral Nervous SystemEpidemiologyInfectious Disease EpidemiologyInfectious DiseasesBacterial DiseasesMeningitisNeglected Tropical DiseasesJapanese EncephalitisInfectious Diseases of the Nervous SystemNeurologyInfectious Diseases of the Nervous SystemAetiologies of Central Nervous System Infection in Viet Nam: A Prospective Provincial Hospital-Based Descriptive Surveillance StudyAetiologies of CNS Infection in Viet NamHo Dang TrungNghia123*Le Thi PhuongTu2WolbersMarcel212Nguyen Van MinhHoang2Nguyen ThanhVinh2VanMinh Pham2ThieuNga Tran Vu2Le VanTan2SongDiep To3Le ThiPhuong4Thi PhuongThao Nguyen5VanCong Bui6TangVu7Ngoc AnhTuan Hoang8NguyenDong9TrungTien Phan10Thi NamLien Nguyen10KiemHao Tran10Thi ThanhTam Nguyen11CampbellJames212CawsMaxine212DayJeremy212de JongMenno D.21214Van VinhChau Nguyen3Van DoornH. Rogier212TinhHien Tran2FarrarJeremy212SchultszConstance21213the VIZIONS CNS Infection NetworkPham Ngoc Thach University of Medicine, Ho Chi Minh City, Viet NamCentre for Tropical Medicine, Oxford University Clinical Research Unit, Ho Chi Minh City, Viet NamHospital for Tropical Diseases, Ho Chi Minh City, Viet NamDong Thap Provincial Hospital, Dong Thap Province, Viet NamAn Giang Provincial Hospital, An Giang Province, Viet NamKien Giang Provincial Hospital, Kien Giang Province, Viet NamSoc Trang Provincial Hospital, Soc Trang Province, Viet NamDakLak Provincial Hospital, DakLak Province, Viet NamKhanh Hoa Provincial Hospital, Khanh Hoa Province, Viet NamHue Central Hospital, Thua Thien – Hue Province, Viet NamCan Tho Central Hospital, Can Tho City, Viet NamCentre for Tropical Medicine, Oxford University, Oxford, United KingdomDepartment of Global Health, Academic Medical Center, University of Amsterdam, Amsterdam, The NetherlandsDepartment of Medical Microbiology, Academic Medical Center, University of Amsterdam, Amsterdam, The NetherlandsKhudyakovYury E.EditorCenters for Disease Control and Prevention, United States of America* E-mail: nghiahdt@oucru.org

Conceived and designed the experiments: NHDT JF CS HTT MDDJ. Performed the experiments: NHDT TLTP HNVM VNT MPV NTVT TLV DTS PLT TNTP CBV VT THNA DN TPT LNTN HTK TNTT JC CNVV. Analyzed the data: NHDT MW CS JF. Wrote the paper: NHDT JF CS JD HRVD MDDJ MC HTT.

¶ Membership of the VIZIONS CNS Infection Network is provided in the Acknowledgments.

2012255201275e37825151220112442012Ho Dang Trung et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.2012Background

Infectious diseases of the central nervous system (CNS) remain common and life-threatening, especially in developing countries. Knowledge of the aetiological agents responsible for these infections is essential to guide empiric therapy and develop a rational public health policy. To date most data has come from patients admitted to tertiary referral hospitals in Asia and there is limited aetiological data at the provincial hospital level where most patients are seen.

Methods

We conducted a prospective Provincial Hospital-based descriptive surveillance study in adults and children at thirteen hospitals in central and southern Viet Nam between August 2007– April 2010. The pathogens of CNS infection were confirmed in CSF and blood samples by using classical microbiology, molecular diagnostics and serology.

Results

We recruited 1241 patients with clinically suspected infection of the CNS. An aetiological agent was identified in 640/1241 (52%) of the patients. The most common pathogens were Streptococcus suis serotype 2 in patients older than 14 years of age (147/617, 24%) and Japanese encephalitis virus in patients less than 14 years old (142/624, 23%). Mycobacterium tuberculosis was confirmed in 34/617 (6%) adult patients and 11/624 (2%) paediatric patients. The acute case fatality rate (CFR) during hospital admission was 73/617 (12%) in adults and to 42/624 (7%) in children.

Conclusions

Zoonotic bacterial and viral pathogens are the most common causes of CNS infection in adults and children in Viet Nam.

Introduction

Despite advances in antibiotic treatment and resuscitation, infectious diseases of the central nervous system (CNS) remain life-threatening, especially in developing countries. According to the World Health Organization (WHO), there were approximately 700,000 episodes of meningitis in 2004 and 70% of these patients lived in Africa and South-East Asia [1]. Every year, Japanese encephalitis virus, an important cause of encephalitis in Asia, causes 50,000 encephalitis cases and 15,000 deaths and leaves many survivors with severe neurological and psychiatric sequelae, whilst the case fatality rate in treated patients with tuberculous meningitis (TBM) is 65% in HIV-infected patients and 25% in HIV uninfected patients in Viet Nam [2], [3]. To reduce the morbidity and mortality of CNS infections, studies are needed to establish the aetiology in order to design rational policies for prevention and empiric and specific treatment. The cause of CNS infection may vary over time, by geographic region, with age, co-morbidities, vaccination programs and the routes by which the pathogens are acquired [4][6]. However, the epidemiological data related to the aetiology of CNS infections in Viet Nam are limited and come from tertiary referral hospitals in major cities. The identification of the causes of CNS infections in Viet Nam is difficult for many reasons, including limited bacteriological culture facilities, lack of PCR and viral culture and the widespread use of antibiotics prior to presentation to any hospital. Hence, we conducted a prospective provincial hospital-based surveillance study to identify the causes of CNS infections in central and southern Viet Nam.

Materials and MethodsEthical Approval

This study was approved by the Scientific and Ethics Committee of each study site (provincial hospitals), the Hospital for Tropical Diseases and the University of Oxford Tropical Research Ethics Committee (OXTREC 01–08). Informed consent was obtained or proxy consent from a relative was obtained for a patient with GCS score <15 or a patient under 15 year-old on admission. Patients were excluded if they did not provide written informed consent.

Study Design and Setting

A prospective hospital-based descriptive surveillance study was conducted at thirteen hospitals in central and southern Viet Nam, including one district hospital (Sa Dec, Dong Thap), seven provincial hospitals (Dong Thap, An Giang, Kien Giang, Ca Mau, Bac Lieu, Soc Trang, Tra Vinh) and one central referral hospital (Can Tho) in the Mekong River Delta; one provincial hospital (Binh Phuoc) in the South East; one provincial hospital (Dak Lak) in the Central Highlands; and one provincial hospital (Khanh Hoa) and one central referral hospital (Thua Thien-Hue) in central Viet Nam (Figure 1). The study was conducted between August 2007 and April 2010.

10.1371/journal.pone.0037825.g001Locations of study sites.

Map of southern Vietnam indicating participating hospitals and population density in the catchment area of each site.

Participants and Recruitment

Patients who presented at the infectious diseases ward, intensive care unit or paediatric ward of participating hospitals, were eligible if they met all of the following inclusion criteria; at least one month of age; fever ≥ 38°C (axillary); at least one of the following symptoms or signs: headache, neck stiffness, altered consciousness and focal neurological signs; and a cerebrospinal fluid (CSF) sample taken. Patients were excluded if they or their relatives did not provide written informed consent. The attending physician examined the patients and completed a standardized clinical data form. Data collected included demographics, history and examination findings, past medical history, laboratory findings, treatment and outcome. Four milliliters of CSF were taken from each adult patient and 2 mls from children 5 years of age or older and 1 ml from children under five. Cerebrospinal fluid was sent to the hospital laboratory for cell count, biochemistry measurements and microbiology investigations according to the local standard of care. A half to one milliliter was stored at –20°C and later transferred to the Hospital for Tropical Diseases in Ho Chi Minh City (HTD) on dry ice for further investigations, including 200 µl for diagnostic PCR (bacteria and virus) and 100 µl for JE and Dengue serology. All bacterial isolates from CSF and blood cultures had identification confirmed at HTD and antimicrobial susceptibility assessment.

DefinitionsAdults and children

Patients were assigned as adults if they were older than or equal to 15 years of age on the day of admission according to Vietnamese law. If they were less than 15 years of age, they were assigned as children.

Case definitions of clinical syndromes

Clinical syndromes were defined in accordance with WHO case definitions of bacterial meningitis (BM) and viral encephalitis (VE), and using a consensus case definition of TBM [7], [8]. If CSF lactate was available, it was included in the case definition of BM and viral encephalitis/meningitis (VE/M) (see Table 1). A patient was considered to not have a CNS infection if they had normal CSF parameters with no pathogen identified, and if the clinical diagnosis at discharge was non-infectious such as stroke, epilepsy, psychiatric disorder, drug or alcohol toxicity, hepatic encephalopathy, sepsis, or benign febrile convulsion.

10.1371/journal.pone.0037825.t001Case definitions of clinical syndromes.
Bacterial meningitis (modified from case definition of BM of WHO [7])
Laboratory-confirmed (at least one of the following criteria)Probable
-Positive culture, Gram stain or real-time PCR of CSF sample-Sudden onset of fever (>38°C) (less than 7 days)
-Positive bacterial blood culture and clinical syndrome consistent with BM (see probable criteria)-AND at least one of the following signs:
oMeningeal signs (neck stiffness, Kernig sign and Brudzinski sign)
OAltered consciousness
-AND CSF examination showing at least one of the following:
oLeukocytosis (≥10 cells/µl) AND at least 2 of the following criteria1:
•an elevated protein (>1 g/l)
•decreased glucose (<2.2 mmol/l or less than 50% of blood glucose)
•lactate ≥4 mmol/l
OTurbid appearance (when WC is missing or WC <10/µl)
-AND no aetiologic agent was identified
Viral encephalitis/meningitis (modified from case definition of acute encephalitis syndrome of WHO [7])
Laboratory-confirmedProbable
-Laboratory confirmation by real-time PCR (enterovirus and Herpes simplex) or MAC ELISA (Japanese Encephalitis virus) on CSF-Acute onset of fever (less than 7 days)
-A case was classified as probable Japanese encephalitis (JE) if a patient had the following criteria:-AND at least one of the following:
oFulfilled the case definition of probable VE/MOMeningeal signs (neck stiffness, Kernig sign, and Brudzinski sign)
oJEV specific IgM titre in CSF was in the range from 8–12 UoChange in mental status (confusion, disorientation, coma or inability to talk)
oNo other pathogen detected.oNew onset of seizures (excluding simple febrile seizures)
-A case was classified as Dengue encephalitis/meningitis, if Dengue virus specific IgM titre in CSF was higher than 12 U-AND CSF examination showing at least one of the following:
-A case was classified as possible Dengue encephalitis/meningitis if patient had the following criteria:OLeukocytosis (≥10 cells/µl) AND at least 2 of these criteria2:
oFulfilled case definition of probable VE/M•protein ≤1 g/l
oDengue virus specific IgM titre in CSF was in the range from 8–12 U•normal glucose (≥2.2 mmol/l or ≥50% of blood glucose)
oNo other pathogen detected.•lactate <4 mmol/l
OClear appearance (when WC is missing or WC <10/µl)
-AND no aetiologic agent was identified
Tuberculous meningitis [8]
Laboratory-confirmedProbable
Positive smear (acid-fast bacilli, AFB) or real-time PCR of CSF-Total diagnostic score ≥10 (when cerebral imaging is not available) or ≥12 (when cerebral imaging is available)
-At least 2 points should either come from CSF or cerebral imaging criteria.
Possible
-Total diagnostic score of 6–9 points (when cerebral imaging is not available) or 6–11 points (when cerebral imaging is available)
-Possible tuberculosis cannot be diagnosed or excluded without doing a lumbar puncture or cerebral imaging.
Cryptococcal meningitis
An India ink stain of CSF positive showing encapsulated yeasts, orCryptococcus neoformans cultured from CSF.
Eosinophilic meningitis
ConfirmedProbable
Meningitis and a percentage of eosinophils in CSF greater than 10% [63]-Percentage of eosinophilic cells in blood >10%
-AND meningitis manifestations
-AND no pathogen confirmed in CSF by culture, PCR or ELISA method

If lactate concentration was not available, a patient was diagnosed as BM when having at least one of the remaining criteria.

If lactate concentration was not available, a patient was diagnosed as VE/M when having the two remaining criteria.

Microbiological InvestigationsBlood and CSF culture

Blood and CSF cultures were performed in the microbiology laboratory of the hospitals using standard culture methods. Blood culture was performed using a BD BACTEC® 9050 blood culture system (BD Microbiology, USA) in Dong Thap and Kien Giang hospitals, and by the BacT/Alert blood culture system (bioMérieux, France) in Hue Central hospital. Manual blood culture using commercially available blood culture media purchased in Vietnam (Nam Khoa Biotek, Ho Chi Minh city, Viet Nam) were used in the remaining hospitals. CSF cultures were incubated overnight in candle jars, except in Hue Central hospital where a CO2 incubator was available. Laboratories used the locally available tools for identification of isolates from positive cultures. In addition, all bacterial isolates were sent to HTD for bacterial identification and antimicrobial susceptibility testing.

Molecular methods

Internally controlled real-time PCR was used for the detection of Streptococcus pneumoniae, Haemophilus influenzae type b, Neisseria meningitidis, Streptococcus suis serotype 2, Herpes simplex virus 1 and 2, enteroviruses (generic) and Mycobacterium tuberculosis in CSF samples using methods published previously [9][12]. The RealAccurate™ Mycobacterium tuberculosis PCR kit (Patho Finder, Maastricht, The Netherlands), targeting the IS6110 sequence, was used to confirm the clinical diagnosis of TBM. This PCR kit is validated for use on respiratory samples. Its sensitivity, specificity, positive predictive value and negative predictive value were evaluated at the HTD laboratory using an appropriate set of CSF samples, including 24 TBM CSF samples confirmed by CSF smear (AFB) or mycobacterial growth indicator tube (MGIT) culture method, 16 BM CSF samples confirmed by culture and 2 Herpes simplex encephalitis CSF samples confirmed by PCR and were 67%, 94%, 94% and 68%, respectively (unpublished data).

10.1371/journal.pone.0037825.g002Study profile.

(*) Other diagnosis included sinusitis (5 cases), brain tumours (9 cases), cerebral malaria (8 cases), mental disorders (7 cases), headache (7 cases), typhoid fever (5 cases), fever unknown origin (3 cases), autoimmune diseases (12 cases), diarrhoea (6 cases), lumbar disc herniation (2 cases), congenital heart diseases (2 cases), hydrocephalus (1 case), tetanus (1 case), severe anaemia (1 case) and chronic colitis (1 case).

Serological methods (CSF samples)

To confirm infection with JE virus or Dengue virus, a JEV/DENV IgM ELISA assay (Venture Technologies Sdn Bhd Malaysia), was used. This assay uses antigens from JEV and DENV1-DENV4 to demonstrate and distinguish recent infection by these two flaviviruses [13].

10.1371/journal.pone.0037825.t002Demographic data, clinical diagnosis and outcome of patients with CNS infection enrolled in the study.
CharacteristicsAdults (n = 617)Children (n = 624)p value3
Median age, years (IQR)38 (24; 52)4 (1.29; 9)_
Male, n (%)431 (70)385 (62)0.002
Rural, n (%)502 (81)527 (85)0.1
Regions, n (%)<0.001
-Mekong river delta353 (57)309 (49)
-Central Viet Nam211 (34)204 (33)
-Central highlands38 (6)104 (17)
-South East10 (2)6 (1)
-Others15 (1)1 (0)
Ethnicity, n (%)<0.001
-Kinh528 (86)478 (77)
-Khmer64 (10)68 (11)
-E de10 (1.5)27 (4)
-Raglai3 (0.5)14 (2)
-Others212 (2)37 (6)
HIV status, n (%)
-Positive10 (2)0 (0)-
-Negative488 (79)50 (8)-
-Unknown119 (19)574 (92)-
Diagnosis, n (%)<0.001
-Bacterial meningitis302 (49)150 (24)
oConfirmed cases198 (32)91 (15)
oProbable cases104 (17)59 (9)
-Viral encephalitis/meningitis209 (34)432 (69)
oConfirmed cases76 (12)206 (33)
oProbable cases133 (22)226 (36)
-Tuberculous meningitis87 (14)31 (5)
oConfirmed cases34 (5)11 (1.7)
oProbable cases10 (2)2 (0.3)
oPossible cases43 (7)18 (3)
-Eosinophilic meningitis4 (0.6)1 (0.1)
-Cryptococcal meningitis2 (0.3)0 (0)
-Cerebral toxoplasmosis1 (0.1)0 (0)
-Dual infection12 (2)10 (2)
Outcomes, n (%)<0.001
-Alive429 (70)493 (79)
-Died73 (12)42 (7)
-Transferred to other hospitals88 (14)71 (11)
-Unknown outcome27 (4)18 (3)

Cambodia, Laos.

Cham, Co Tu, Dao, H’Mong, Jarai, M’Nong, Mong, Nung, Pa Ko, STieng, Ta Oi, Tay, Thai, Xo Dang, Van Kieu, Chinese and Laotian.

Chi-squared test or Fisher’s exact test (when one or more of the expected count is less than 5).

Analysis

All variables were summarized by group (adult or children). Patients were assigned to confirmed or probable BM, VE/M or TBM according to the pre-specified case definitions of clinical syndromes (Table 1). Epidemiological characteristics of patients were analyzed for all patients with confirmed or probable CNS infections. Categorical variables were summarized as numbers and percentages (%). Continuous variables were summarized as median and interquartile range (IQR). Categorical baseline variables were compared between adults and children using chi-squared test or Fisher’s exact test (when one or more of the expected cell counts was less than 5). Time trends and seasonality of overall admission numbers of children and adults with CNS infections as well as seasonality of the number of S. suis meningitis cases was assessed using Poisson regression models, which modelled the monthly admission counts depending on a hospital effect, a global linear time trend and a sinusoidal shape for the seasonality effect (modelled with a sine- and a cosine-term, i.e. a cosinor model) [14]. The log-number of days per month was used as an offset in the model to correct for unequal lengths of the month. For testing seasonality we tested whether the sine- and the cosine-term could jointly be omitted from the model using a likelihood ratio test. All analyses were performed with Stata version 10.1 (StataCorp, College Station, Texas, USA) and R version 2.11.1 (R Foundation for Statistical Computing, Vienna, Austria) software.

10.1371/journal.pone.0037825.g003Time distribution of adult CNS infection admissions per study site.

Number of cases: absolute number of adult patients with CNS infection enrolled in the study per month.

10.1371/journal.pone.0037825.g004Time distribution of paediatric CNS infection admission per study site.

Number of cases: absolute number of children with CNS infection enrolled in the study per month.

10.1371/journal.pone.0037825.g005Time distribution of adult CNS infection admissions by all major pathogens at Hue Central hospital.

Number of cases: number of adult patients with CNS infection enrolled in the study at Hue Central hospital per month for 8 pathogens (results of PCR, serology and bacterial culture combined).

Results

Between August 2007 and April 2010, 1740 patients fulfilling the inclusion criteria were admitted to 2 central, 10 provincial and 1 district hospitals. None refused to provide consent. Clinical data were not available for 95 patients, including 52 adults and 43 children. In these 95 patients, pathogens were confirmed in 12/52 adults (eight S. suis serotype 2, one S. pneumoniae, one JE virus, one enterovirus and one co-infection with S. suis and enterovirus) and in 13/43 children (four enteroviruses, two JE viruses, two dengue viruses, two H. influenzae, one N. meningitidis and two co-infections with S. pneumoniae and JE virus). After reviewing the clinical presentation and hospital tests of 1645 patients that had complete clinical data and a CSF sample taken, we excluded 247 paediatric and 157 adult patients in the final analysis of the causative aetiology (Figure 2). These patients all had normal CSF data and a clinical history consistent with a non-infectious cause. Thus 1241 patients (617 adults, 624 children) were included in the final analysis.

10.1371/journal.pone.0037825.t003Laboratory confirmed aetiology for adults with CNS infection enrolled in the study.
Pathogen, n (%)Adults (n = 617)
PCR or serology resultsBacterial culture resultsCombined results of PCR, serology and culture
Bacteria
Streptococcus suis serotype 2147 (24)99 (16)147 (24)
Streptococcus pneumoniae35 (6)15 (2)35 (6)
Haemophilus influenzae type b0 (0)0 (0)0 (0)
Neisseria meningitidis3 (0.5)1 (0.1)4 (0.6)
Streptococcus spp2 (0.3)2 (0.3)
Staphylococcus spp1 (0.1)1 (0.1)
Escherichia coli2 (0.3)2 (0.3)
Acinetobacter spp1 (0.1)1 (0.1)
Klebsiella pneumoniae5 (0.8)5 (0.8)
Enterococcus spp1 (0.1)1 (0.1)
Virus
Japanese Encephalitis (JE) virus11 (2)11 (2)
Dengue virus23 (4)23 (4)
Enteroviruses20 (3)20 (3)
Herpes simplex22 (4)22 (4)
Tuberculosis
Mycobacterium tuberculosis34 (5)34 (5)
Fungi
Cryptococcus neoformans2 (0.3)2 (0.3)
Dual infection
Dengue virus + S. suis serotype 22 (0.3)1 (0.1)2 (0.3)
Dengue virus + S. pneumoniae1 (0.1)0 (0)1 (0.1)
Dengue virus + N. meningitidis1 (0.1)0 (0)1 (0.1)
Dengue virus + M. tuberculosis2 (0.3)2 (0.3)
Dengue virus + Eosinophilic meningitis12 (0.3)2 (0.3)
JE virus + S. pneumoniae1 (0.1)0 (0)1 (0.1)
Enteroviruses + M. tuberculosis1 (0.1)1 (0.1)
K. pneumoniae + M. tuberculosis1 (0.1)1 (0.1)
K. pneumoniae + Herpes simplex1 (0.1)1 (0.1)
Unknown aetiology2310 (50)487 (79)295 (48)

Number of eosinophils in CSF sample was 352/880 (40%) in one case and 330/1320 (25%) in another case.

“Unknown aetiology” corresponds to the probable cases.

10.1371/journal.pone.0037825.t004Laboratory confirmed aetiology for children with CNS infection enrolled in the study.
Pathogen, n (%)Children (n = 624)
PCR or serology resultsBacterial culture resultsCombined results of PCR, serology and culture
Bacteria
Streptococcus suis serotype 20 (0)0 (0)0 (0)
Streptococcus pneumoniae36 (6)16 (3)37 (6)
Haemophilus influenzae type b39 (6)9 (1)39 (6)
Neisseria meningitidis6 (1)2 (0.3)6 (1)
Staphylococcus spp3 (0.5)3 (0.5)
Escherichia coli2 (0.3)2 (0.3)
Acinetobacter spp1 (0.1)1 (0.1)
Klebsiella pneumoniae1 (0.1)1 (0.1)
Salmonella spp2 (0.3)2 (0.3)
Virus
Japanese Encephalitis (JE) virus142 (23)142 (23)
Dengue virus14 (2)14 (2)
Enteroviruses36 (6)36 (6)
Herpes simplex14 (2)14 (2)
Tuberculosis
Mycobacterium tuberculosis11 (2)11 (2)
Dual infection
Dengue virus + H. influenzae type b3 (0.5)1 (0.1)3 (0.5)
JE virus + N.meningitidis1 (0.1)0 (0)1 (0.1)
JE virus + H. influenzae type b3 (0.5)0 (0)3 (0.5)
JE virus + Salmonella spp1 (0.1)1 (0.1)
JE virus + Staphylococcus spp1 (0.1)1 (0.1)
Enteroviruses + H. influenzae type b1 (0.1)0 (0)1 (0.1)
Unknown aetiology1318 (51)585 (94)306 (49)

“Unknown aetiology” corresponds to the probable cases.

Epidemiological Characteristics of CNS Infection

Over 80% of CNS infection patients lived in rural areas and belonged to the Kinh ethnic group. The proportion of ethnic minorities amongst children was higher than that in adults (23% versus 14%, p<0.001) (Table 2). The ratio of males to females was 1.92/1.00. The aetiology of CNS infection in children was different to that in adults. VE/M were responsible for 432/624 (70%) of paediatric CNS infections, compared to 209/617 (34%) of adult infections. Acute BM and TBM were more common in the adults (Table 2). The overall case fatality rate (CFR) at provincial hospitals was 73/617 (12%) in adults compared to 42/624 (7%) in children (Table 2). Of patients with TBM, 24/87 (28%) adult patients and 12/31 (39%) paediatric patients died before receiving anti-tuberculosis drugs.

The number of patients admitted to each of the participating hospitals and their distribution in time is depicted in Figure 3 and 4. Analysis of admission patterns of adult patients with CNS infections by Poisson regression revealed on overall linear decline in the incidence by −13% per year (95%CI [−23%; −1%]) and a significant seasonality effect (p<0.01) indicating peak incidence in June and a difference between the peak vs. the average incidence of +21% (95%CI [+8%; 36%]). However, the linear trend failed to reach conventional significance after adjustment for overdispersion (p = 0.06). Moreover, the seasonal pattern was driven by Hue Central hospital alone - the test for seasonality was significant there (p<0.001) but did not reach significance in all other hospitals combined (p = 0.36) (Figure 3). The seasonality at Hue Central hospital was driven by S. suis infection (Figure 5).

10.1371/journal.pone.0037825.t005Laboratory confirmed aetiology for adult patients meeting the case definition of bacterial meningitis enrolled in the study (excluding dual infections).
Pathogen, n (%)Adults (n = 302)
PCR resultsCulture resultsCombined results of PCR and culture
Streptococcus suis serotype 2147 (49)99 (33)147 (49)
Streptococcus pneumoniae35 (12)15 (5)35 (12)
Haemophilus influenzae type b0 (0)0 (0)0 (0)
Neisseria meningitidis3 (1)1 (0.1)4 (1)
Streptococcus spp2 (0.6)2 (0.6)
Staphylococcus spp1 (0.3)1 (0.3)
Escherichia coli2 (0.6)2 (0.6)
Acinetobacter spp1 (0.3)1 (0.3)
Klebsiella pneumoniae5 (2)5 (2)
Enterococcus spp1 (0.3)1 (0.3)
Unknown aetiology1117 (38)175 (58)104 (34)

“Unknown aetiology” corresponds to the probable cases.

10.1371/journal.pone.0037825.t006Laboratory confirmed aetiology for paediatric patients meeting the case definition of bacterial meningitis enrolled in the study (excluding dual infections).
Pathogen, n (%)Children (n = 150)
PCR resultsCulture resultsCombined results of PCR and culture
Streptococcus suis serotype 20 (0)0 (0)0 (0)
Streptococcus pneumoniae36 (24)16 (11)37 (25)
Haemophilus influenzae type b39 (26)9 (6)39 (26)
Neisseria meningitidis6 (4)2 (1)6 (4)
Staphylococcus spp3 (2)3 (2)
Escherichia coli2 (1)2 (1)
Acinetobacter spp1 (1)1 (1)
Klebsiella pneumoniae1 (1)1 (1)
Salmonella spp2 (1)2 (1)
Unknown aetiology169 (46)114 (76)59 (39)

“Unknown aetiology” corresponds to the probable cases.

10.1371/journal.pone.0037825.g006Pathogens of bacterial meningitis by age group (excluding dual infection cases).

Laboratory confirmed aetiology per agegroup (bars) for patients meeting the case definition of bacterial meningitis. “Unknown aetiology” corresponds to patients with a diagnosis of probable bacterial meningitis.

A seasonal pattern of paediatric CNS infection admissions was also noted. Analysis of admission patterns by Poisson regression showed a significant seasonality effect (p<0.001). The admissions to hospitals peaked in June with an amplitude of difference (peak month vs. average) of +51% (95%CI [+34%; +69%]) and a linear time trend of −24% per year (95% CI [−33%; −14%], p<0.001) (Figure 4).

Aetiology of CNS Infection

An aetiological agent was identified in 640/1241 (52%) of patients (Table 3 and 4). The most common pathogens were Streptococcus suis serotype 2 in adults (147/617, 24%) and JE virus in children (142/624, 23%). Mycobacterium tuberculosis was confirmed by PCR in 34/617 (6%) of adults and 11/624 (2%) of children. Dual infection was demonstrated in 22 cases (12 adults, 10 children). Dual infection was most commonly due to dengue virus accompanying a bacterial pathogen (9/22 cases) or JE virus and a bacterial pathogen (7/22 cases).

10.1371/journal.pone.0037825.t007Laboratory confirmed aetiology for patients meeting the case definition of viral encephalitis/meningitis enrolled in the study (excluding dual infections).
Pathogen, n (%)Adults (n = 209)Children (n = 432)p value1
JE virus11 (5)142 (33)<0.001
Dengue virus23 (11)14 (3)<0.001
Enteroviruses20 (10)36 (8)0.603
Herpes simplex22 (11)14 (3)<0.001
Unknown aetiology2133 (64)226 (52)0.007

Chi-squared test or Fisher’s exact test (when one or more of the expected count is less than 5).

“Unknown aetiology” corresponds to the probable cases.

10.1371/journal.pone.0037825.g007Pathogens of viral encephalitis/meningitis by age group (excluding dual infection cases).

Laboratory confirmed aetiology per agegroup (bars) for patients meeting the case definition of viral meningitis/encephalitis (excluding dual infection cases). “Unknown aetiology” corresponds to patients with a diagnosis of probable viral encephalitis/meningitis.

Aetiology of Bacterial Meningitis

Bacterial pathogens were identified in 198/302 (66%) of adult patients who fulfilled the clinical criteria of BM, by culture or real-time PCR method. S. suis serotype 2 caused meningitis in 147/302 (49%) of the adult BM group, which was four times higher than meningitis cases caused by S. pneumoniae in this population. S. suis was not isolated from paediatric patients. In children, H. influenzae type b (39/150, 26%) and S. pneumoniae (37/150, 25%) were the main pathogens causing BM (Table 5 and 6). The aetiology of BM varied by age. H. influenzae type b was the most common pathogen in children less than 1 year of age, causing 27/66 (41%) of cases. Over 90% (36/39) of H. influenzae type b cases were reported in the first five years of life. In adults, S. suis serotype 2 caused less than 6/70 (9%) of cases of BM in younger patients (<30 years of age), but was responsible for 141/232 (61%) of BM cases in patients over 30 years old. Twenty five percent of BM cases in children and young adults (56/220) were caused by S. pneumoniae but it was identified in less than 10% (16/232) of patients with BM older than 30 years (Figure 6).

Aetiology of Viral Encephalitis/Meningitis

JE virus was the most common pathogen identified in patients with clinical encephalitis and was responsible for 142/432 (33%) of paediatric VE/M cases. Dengue virus, enteroviruses and Herpes simplex virus were the most common identified viral pathogens in adults, each pathogen accounting for 10% of infections (23/209, 20/209 and 22/209, respectively). A viral pathogen was not identified in 56% (359/641) of patients (Table 7). JE virus was responsible for nearly 40% of encephalitis/meningitis cases in the age group 1–14, but was less common in patients younger than 1 year or older than 15 years (Figure 7).

Tuberculous Meningitis

TBM was responsible for 122/1241 (10%) of cases, including 87/617 (14%) of adult patients and 31/624 (5%) of pediatric patients. Forty nine cases (40%) were confirmed by commercial real-time PCR. Twelve of 122 (10%) patients were classified as probable TBM cases and 61/122 (50%) patients as possible TBM cases using the case definition (see Tables 1, 2 and 3 and 4).

Discussion

This is the first prospective provincial hospital-based surveillance study on CNS infection in Viet Nam. The participating hospitals function as primary care hospitals for CNS infection patients in their catchment area and therefore the data reflect the burden of disease and associated pathogens within the population. S. suis serotype 2 was the predominant microorganism found in adult patients and was four times as common in adult patients as S. pneumoniae (49% vs. 12%), the most common cause of BM in Europe and the United States [15], [16]. The results of this study strengthen the results from earlier studies carried out in tertiary referral hospitals in Viet Nam, and in some other intensive pig rearing countries in Asia, in which S. suis is the most important pathogen of BM in adult patients [17][21]. JE virus, the most common identified cause of paediatric CNS infection, was responsible for 23% (142/624) of paediatric cases. These findings clearly point at the important role of zoonotic infections in Vietnam, given that pigs, the main source of meat in Vietnam, function as the main reservoir for both pathogens.

The culture method was less sensitive than the PCR method in detection of the main pathogens of bacterial meningitis (Table 3, 4, 5 and 6). This may be related to the fact that nearly half of BM patients (236/452) had received antibiotic drugs prior to admission. Hence, the prevalence of other bacterial infections, which were not tested by PCR method, could be possibly underestimated.

We observed seasonality of CNS infections in both adults and children. In the adult population seasonality was driven by S. suis serotype 2 infections observed at Hue Central hospital. Hue is located in central Vietnam, where there is a larger fluctuation of air ambient temperature during the year, in comparison with the more stable air temperature of the southern provinces. We have previously shown that ingestion of high risk food items is an important risk factor for S. suis infection in Vietnam, in addition to occupational or direct contact due to skin lesions [22]. Bacterial load in contaminated food items is likely to be higher when food is kept at higher ambient temperatures, and this may explain the seasonal pattern observed in Hue. In China and Thailand, more S. suis patients are also admitted during the rainy season, between June and September [19], [23]. In the case of JE, epidemiological studies have shown that after the monsoon rains Culex mosquitoes, the main vector of JE, breed prolifically with consequent increased disease transmission. In addition, temperature may be an important factor as larval developmental time and extrinsic incubation period of JEV are shorter at higher temperatures [2].

Similar to other studies on CNS infections in Vietnam, the observed ratio between males and females was greater than 1 [3], [24], [25]. In S. suis meningitis, male sex is a risk factor related to exposure to pork and pigs, and the ratio of male to female is about 4/1 [22]. For other etiologies we do not have a good explanation for the male dominance.

H. influenzae type b (Hib) conjugate vaccine has just been introduced to the Vietnamese National Expanded Program on Immunization (NEPI) since June 2010. Consequently, this pathogen was still the most common cause of BM in children, causing a similar proportion of disease as found in other studies from around the world before the Hib conjugate vaccine era [26][30]. The incidence rate of Hib meningitis in Vietnamese children is likely to decrease sharply in the next few years, especially in the age group of children less than 5 years of age. In contrast, conjugate multi-valent S. pneumoniae vaccines are not included in the NEPI and JE vaccine is only introduced into NEPI for children 1–5 years of age in the high-risk districts, which are mostly in northern provinces [31].

VE/M offers a considerable diagnostic challenge to physicians. Previous aetiological studies have reported that at least 60% of patients hospitalized with encephalitis had no cause identified despite extensive laboratory testing [25], [32][35]. Though our study focused on the common viral pathogens of encephalitis/meningitis in Viet Nam, the proportion of patients with suspected VE/M with no pathogen identified was also approximately 60% of all cases [36][38]. JE virus is the most important identified cause of encephalitis in the South-East Asia, being responsible for 24% of VE/M cases with over 90% of cases reported in children aged <15 years in this study. JE rarely occurs in adults who live in endemic regions presumably because of exposure to virus during childhood and subsequent immunity [6]. JE may be more common in the north of Viet Nam than in the central and south of Viet Nam. It caused 217/421 (50%) of acute encephalitis syndrome cases in five northern provinces [31]. Another important arboviral infection in humans, dengue, has become the most important epidemic disease in this country. Neurological manifestations of dengue infection were reported in 0.5–6% of hospitalized dengue hemorrhagic fever patients [37], [39], [40]. In this study, dengue virus, detected by the presence of specific IgM in CSF, was the only pathogen in 39/641 suspected VE/M cases (6.1%), including 25 adults and 14 children. Our result are similar to other studies in the dengue endemic region, where the proportion of dengue virus ranged from 4.2% to 47% of patients with encephalitis [25], [37], [41][43]. Dengue should be considered in patients who present with the clinical features of encephalitis, whether or not classical manifestations of dengue are present [37], [44].

In Europe and North America, enteroviruses are among the most common causes of viral meningitis in children [45], [46]. In this study, enteroviruses were the second most common viral pathogen in both adults and children. However, 15/20 adult patients, compared to 6/36 paediatric patients, lived in Thua Thien – Hue province and 14 of these adults, compared to none of the children, were admitted to Hue Central hospital in the period from June to September 2009 (Figure 5). The adult cases observed in our study may therefore be related to an outbreak in Thua Thien – Hue province in the summer of 2009.

Rapid and early diagnosis of CNS infections is fundamental to patient outcome. Physicians face numerous difficulties in establishing a TBM diagnosis, including the often non-specific manifestations, low sensitivity of Ziehl-Neelsen staining and nucleic acid amplification and delays in classical culture methods [47]. To diagnose TBM in this study, we applied the consensus case definition of TBM, which included clinical, CSF, and cerebral imaging information and could be used regardless of patient’s age and HIV status [8]. A commercial real-time PCR test was used to help confirm TBM. Ranking after S. suis serotype 2 meningitis and JE, TBM, which was confirmed in 49 (40%) of suspected TBM cases, was the third most common cause of CNS infection in our study. This is the first report of TBM in a context of CNS infection in Vietnamese provincial hospitals. While TBM was the cause of 143/357 (40%) adult suspected CNS infections admitted to HTD [48], the overall TBM proportion and its proportion stratified for adults and children were 10% (122/1241), 15% (91/617) and 5% (31/624), respectively in this study. The proportion of TBM at HTD may be higher because HTD receives patients who fail to respond to treatment with antimicrobial agents for the treatment of BM from provincial hospitals, and these patients are often diagnosed with TBM. In addition, the HIV prevalence may be higher in Ho Chi Minh City and surrounding areas resulting in a higher incidence of TBM. The protective role of BCG vaccination against TBM in children may explain why TBM accounted for a lower proportion of cases in children than in adults [49], [50].

Dual infections in CNS infection, such as among members of herpesviruses or between a member of this group and a bacterium, have previously been reported in both immunocompetent and immunocompromised patients diagnosed using PCR methods and/or intrathecal antibody determinations [51][56]. In this study, we found 20 dual infection cases in 1241 suspected CNS infection patients. Most cases (18/20 cases) were infected with an endemic virus (JE virus, dengue virus or enteroviruses) and a bacterium. DENV and JEV are both endemic in south Vietnam and infection is often asymptomatic. Dual infection of JEV and enteroviruses or H. influenzae type b and enteroviruses was also reported in other studies in South-East Asia [25], [57]. Our findings emphasize the role of these viruses as a co-infection pathogen in an endemic region and suggest that testing for other pathogens should still be considered when a single pathogen has been identified in the CSF. While the clinical relevance of these co-infections remain unclear, it is tempting to speculate about the interplay between viral and bacterial CNS infections, for example by facilitating entry of one or the other into the CNS compartment [25].

Cryptococcus neoformans is one of the most important HIV-related opportunistic infections in South-East Asia, where one third of CNS infection in HIV/AIDS patients are due to this pathogen [58][61]. It also causes meningitis in HIV uninfected patients in Viet Nam [62]. Only two cases were reported in our study. This may be explained by the limitation of microbiological culture facilities at the provincial hospitals or by the fact that lumbar punctures were not performed in HIV infected patients at these hospitals. In Viet Nam, attending physicians rarely do lumbar puncture on HIV patients at remote provincial hospitals because of their poor prognosis or relative’s refusal.

CNS infections have a high morbidity and mortality. The case fatality rate (CFR) in this study was 12% in adults and 7% in children, but varied widely according to underlying pathogen, ranging from 5–10% in acute BM and VE/M to 30–40% in TBM. This CFR was likely related to deaths prior to prescription of anti-tuberculous drugs because most TBM patients in Vietnam are admitted first to an infectious diseases unit or a neurology unit in a general hospital before being transferred to a specialist tuberculosis unit or hospital where TBM specific treatment is started. This highlights the critical importance of considering TBM in the differential diagnosis of CNS infection throughout Viet Nam and the need for early diagnosis and treatment.

In conclusion, we identified a cause in 640/1241 (52%) suspected CNS infection cases using molecular diagnostic, serological and culture methods. The three most common pathogens in children were JE virus, H. influenzae type b and S. pneumoniae. Meanwhile, S. suis serotype 2 meningitis, an emerging zoonosis in intensive pig rearing countries, caused one fourth (147/617) of adult suspected CNS infection or a half (147/302) of adult purulent BM in Viet Nam. We also found that case fatality rate of TBM exceeded 30% at the provincial hospitals before TBM diagnosis was established. As patient outcome is directly related to early diagnosis and treatment, physicians should always think of TBM in the context of CNS infection in developing countries.

We thank all the patients participated in the research and all of the doctors and nurses, who cared for the patients, from 13 provincial hospitals in the VIZIONS CNS Infection Network.

The VIZIONS CNS Infection Network

Dong Thap Provincial Hospital (Tran Quoc Loi, Nguyen Truong Son, Phan Van Be Bay, Nguyen Thi Hong Tham and Le Thi Phuong).

Sa Dec District Hospital (Le Trung Tri and Nguyen Thi Nguyet Binh).

An Giang Provincial Hospital (Doan Cong Du, Nguyen Thi Phuong Thao, Truong Thi My Tien and Tran Thi Phi La).

Kien Giang Provincial Hospital (Bui Van Cong, Pham Ngoc Diep, Duong Phuoc Dong, Tran Thi Mong Lanh and Pham Van Dom).

Ca Mau Provincial Hospital (Tran Quang Dung, Phan Nhut Tri, Tang Thi Ho and Nguyen Anh Tai).

Bac Lieu Provincial Hospital (Quach Van Luc and Dinh Xuan Phuoc).

Soc Trang Provincial Hospital (Tang Vu, Huynh Thi Thu Thuy, Tran Thi Nguyet Hong, Au Huu Duc, Manh Anh Mai and Nguyen Huu Thu).

Tra Vinh Provincial Hospital (Lam Thi Kim Ngoc).

Can Tho Central Hospital (Nguyen Thi Thanh Tam, Tran Ngo Phuc My, Ngo Van Ut, Lam Tan Phuong, Le Khanh Toan and Dang Quang Tam).

Binh Phuoc Provincial Hospital (Ho Dinh Dung).

Dak Lak Provincial Hospital (Nguyen Hai, Hoang Ngoc Anh Tuan, Hoang Thi Thuy Tien and Tran Thi Ngoc Oanh).

Khanh Hoa Provincial Hospital (Nguyen Dong, Phan The Long, Nguyen Thanh Ngan, Mang Thi Phuong Mai, Pham EnGa, Luu Thi Minh Huong, Nguyen Thi Thuy Ai, Nguyen Ngoc Anh, Nguyen Van Xang and Nguyen Manh Tien).

Hue Central Hospital (Phan Trung Tien, Nguyen Thi Nam Lien, Tran Kiem Hao, Nguyen Thi Nhu Ly, Tran Duy Hoa, Bui Van Doan, Duong Thi Bich Hoa, Tran Thi Thu Anh, Nguyen Xuan Hien, Vo Kim Thanh, Duong Van Thong, Dinh Quang Tuan, Pham Thi Minh Khoa, Hoang Trong Hanh, Tran Thi Diem Lan, Nguyen Thai Thuan, Bui Manh Hung and Bui Duc Phu).

Competing Interests: The authors have declared that no competing interests exist.

Funding: This work was supported by the Wellcome Trust Major Overseas Programme. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

References WHO 2008 The global burden of diseases: 2004 update. Geneva, Switzerland World Health Organization SolomonTDungNMKneenRGainsboroughMVaughnDW 2000 Japanese encephalitis. J Neurol Neurosurg Psychiatry 68 405 415 10727474 ThwaitesGENguyenDBNguyenHDHoangTQDoTT 2004 Dexamethasone for the treatment of tuberculous meningitis in adolescents and adults. N Engl J Med 351 1741 1751 15496623 LuCHHuangCRChangWNChangCJChengBC 2002 Community-acquired bacterial meningitis in adults: the epidemiology, timing of appropriate antimicrobial therapy, and prognostic factors. Clin Neurol Neurosurg 104 352 358 12140104 PeltolaH 2000 Worldwide Haemophilus influenzae type b disease at the beginning of the 21st century: global analysis of the disease burden 25 years after the use of the polysaccharide vaccine and a decade after the advent of conjugates. Clin Microbiol Rev 13 302 317 10756001 SolomonT 2004 Flavivirus encephalitis. N Engl J Med 351 370 378 15269317 WHO 2003 WHO-recomended standards for surveillance of selected vaccine-preventable diseases. Geneva, Switzerland World Health Organisation MaraisSThwaitesGSchoemanJFTorokMEMisraUK 2010 Tuberculous meningitis: a uniform case definition for use in clinical research. Lancet Infect Dis 10 803 812 20822958 CorlessCEGuiverMBorrowREdwards-JonesVFoxAJ 2001 Simultaneous detection of Neisseria meningitidis, Haemophilus influenzae, and Streptococcus pneumoniae in suspected cases of meningitis and septicemia using real-time PCR. J Clin Microbiol 39 1553 1558 11283086 JeromeKRHuangMLWaldASelkeSCoreyL 2002 Quantitative stability of DNA after extended storage of clinical specimens as determined by real-time PCR. J Clin Microbiol 40 2609 2611 12089286 BeldMMinnaarRWeelJSolCDamenM 2004 Highly sensitive assay for detection of enterovirus in clinical specimens by reverse transcription-PCR with an armored RNA internal control. J Clin Microbiol 42 3059 3064 15243060 NgaTVNghiaHDTu leTPDiepTSMaiNT 2011 Real-time PCR for detection of Streptococcus suis serotype 2 in cerebrospinal fluid of human patients with meningitis. Diagn Microbiol Infect Dis 70 461 467 21767702 CardosaMJWangSMSumMSTioPH 2002 Antibodies against prM protein distinguish between previous infection with dengue and Japanese encephalitis viruses. BMC Microbiol 2 9 12019028 BarnettAGDobsonAJ 2010 Analysing Seasonal Health Data (Statistics for Biology and Health): Springer GjiniABStuartJMLawlorDACartwrightKAChristensenH 2006 Changing epidemiology of bacterial meningitis among adults in England and Wales 1991–2002. Epidemiol Infect 134 567 569 16638165 DurandMLCalderwoodSBWeberDJMillerSISouthwickFS 1993 Acute bacterial meningitis in adults. A review of 493 episodes. N Engl J Med 328 21 28 8416268 YuHJingHChenZZhengHZhuX 2006 Human Streptococcus suis outbreak, Sichuan, China. Emerg Infect Dis 12 914 920 16707046 SuankratayCIntalapapornPNunthapisudPArunyingmongkolKWildeH 2004 Streptococcus suis meningitis in Thailand. Southeast Asian J Trop Med Public Health 35 868 876 15916083 KayRChengAFTseCY 1995 Streptococcus suis infection in Hong Kong. Qjm 88 39 47 7894987 MaiNTHoaNTNgaTVLinh leDChauTT 2008 Streptococcus suis meningitis in adults in Vietnam. Clin Infect Dis 46 659 667 19413493 WertheimHFNguyenHNTaylorWLienTTNgoHT 2009 Streptococcus suis, an important cause of adult bacterial meningitis in northern Vietnam. PLoS One 4 e5973 19543404 HoDTLeTPWolbersMCaoQTNguyenVM 2011 Risk Factors of Streptococcus suis Infection in Vietnam. A Case-Control Study. PLoS One 6 e17604 21408132 WangkaewSChaiwarithRTharavichitkulPSupparatpinyoK 2006 Streptococcus suis infection: a series of 41 cases from Chiang Mai University Hospital. J Infect 52 455 460 16690131 NguyenTHTranTHThwaitesGLyVCDinhXS 2007 Dexamethasone in Vietnamese adolescents and adults with bacterial meningitis. N Engl J Med 357 2431 2440 18077808 LeVTPhanTQDoQHNguyenBHLamQB 2010 Viral etiology of encephalitis in children in southern Vietnam: results of a one-year prospective descriptive study. PLoS Negl Trop Dis 4 e854 21049060 TranTTLeQTTranTNNguyenNTPedersenFK 1998 The etiology of bacterial pneumonia and meningitis in Vietnam. Pediatr Infect Dis J 17 S192 194 9781761 MuangchanaCChunsuttiwatSRerks-NgarmSKunasolP 2009 Bacterial meningitis incidence in Thai children estimated by a rapid assessment tool (RAT). Southeast Asian J Trop Med Public Health 40 553 562 19842443 Al-TawfiqJAAbukhamsinA 2009 Burden and etiology of community-acquired bacterial meningitis in a hospital in Eastern Saudi Arabia: 1993–2005. Med Sci Monit 15 PI10 14 19179978 ChoHKLeeHKangJHKimKNKimDS 2010 The causative organisms of bacterial meningitis in Korean children in 1996–2005. J Korean Med Sci 25 895 899 20514311 MolyneuxERiordanFAWalshA 2006 Acute bacterial meningitis in children presenting to the Royal Liverpool Children’s Hospital, Liverpool, UK and the Queen Elizabeth Central Hospital in Blantyre, Malawi: a world of difference. Ann Trop Paediatr 26 29 37 16494702 YenNTDuffyMRHongNMHienNTFischerM 2010 Surveillance for Japanese encephalitis in Vietnam, 1998–2007. Am J Trop Med Hyg 83 816 819 20889870 GlaserCAHonarmandSAndersonLJSchnurrDPForghaniB 2006 Beyond viruses: clinical profiles and etiologies associated with encephalitis. Clin Infect Dis 43 1565 1577 17109290 GranerodJAmbroseHEDaviesNWClewleyJPWalshAL 2010 Causes of encephalitis and differences in their clinical presentations in England: a multicentre, population-based prospective study. Lancet Infect Dis 10 835 844 20952256 YongYKChongHTWongKTTanCTDeviS 2008 Aetiology of viral central nervous system infection, a Malaysian study. Neurology Asia 13 65 71 HuppatzCDurrheimDNLeviCDaltonCWilliamsD 2009 Etiology of encephalitis in Australia, 1990–2007. Emerg Infect Dis 15 1359 1365 19788802 HaDHuongVLoanHThongDDeubelV 1994 Current situation of Japanese encephaltis in the South of Viet Nam, 1976–1992. Trop Med 202 214 SolomonTDungNMVaughnDWKneenRThaoLT 2000 Neurological manifestations of dengue infection. Lancet 355 1053 1059 10744091 TuPVThaoNTPereraDHuuTKTienNT 2007 Epidemiologic and virologic investigation of hand, foot, and mouth disease, southern Vietnam, 2005. Emerg Infect Dis 13 1733 1741 18217559 CamBVFonsmarkLHueNBPhuongNTPoulsenA 2001 Prospective case-control study of encephalopathy in children with dengue hemorrhagic fever. Am J Trop Med Hyg 65 848 851 11791985 HendartoSKHadinegoroSR 1992 Dengue encephalopathy. Acta Paediatr Jpn 34 350 357 1509881 JacksonSMullingsABennettFKhanCGordon-StrachanG 2008 Dengue Infection in Patients Presenting with Neurological Manifestations in a Dengue Endemic Population. West Indian Med J 57 473 476 SoaresCNCabral-CastroMJPeraltaJMde FreitasMRZalisM 2011 Review of the etiologies of viral meningitis and encephalitis in a dengue endemic region. J Neurol Sci SreyVHSadonesHOngSMamMYimC 2002 Etiology of encephalitis syndrome among hospitalized children and adults in Takeo, Cambodia, 1999–2000. Am J Trop Med Hyg 66 200 207 12135294 VaratharajA 2010 Encephalitis in the clinical spectrum of dengue infection. Neurol India 58 585 591 20739797 IhekwabaUKKudesiaGMcKendrickMW 2008 Clinical features of viral meningitis in adults: significant differences in cerebrospinal fluid findings among herpes simplex virus, varicella zoster virus, and enterovirus infections. Clin Infect Dis 47 783 789 18680414 LeeBEChawlaRLangleyJMForgieSEAl-HosniM 2006 Paediatric Investigators Collaborative Network on Infections in Canada (PICNIC) study of aseptic meningitis. BMC Infect Dis 6 68 16603090 ThwaitesGChauTTMaiNTDrobniewskiFMcAdamK 2000 Tuberculous meningitis. J Neurol Neurosurg Psychiatry 68 289 299 10675209 ThwaitesGEChauTTStepniewskaKPhuNHChuongLV 2002 Diagnosis of adult tuberculous meningitis by use of clinical and laboratory features. Lancet 360 1287 1292 12414204 KumarPKumarRSrivastavaKLKumarM 2005 Protective role of BCG vaccination against tuberculous meningitis in Indian children: a reappraisal. Natl Med J India 18 7 11 15835483 TrunzBBFinePDyeC 2006 Effect of BCG vaccination on childhood tuberculous meningitis and miliary tuberculosis worldwide: a meta-analysis and assessment of cost-effectiveness. Lancet 367 1173 1180 16616560 VianelloFBarbaroFCogoPFurlanATrevenzoliM 2008 Co-infection with Mycoplasma pneumoniae and human herpesvirus 6 (HHV-6) in an immunocompetent child with meningoencephalitis: a random association? Infection 36 174 176 17926004 CasasITenorioAde OryFLozanoAEchevarriaJM 1996 Detection of both herpes simplex and varicella-zoster viruses in cerebrospinal fluid from patients with encephalitis. J Med Virol 50 82 92 8890045 YamamotoTNakamuraY 2000 A single tube PCR assay for simultaneous amplification of HSV-1/−2, VZV, CMV, HHV-6A/−6B, and EBV DNAs in cerebrospinal fluid from patients with virus-related neurological diseases. J Neurovirol 6 410 417 11031694 TangYWEspyMJPersingDHSmithTF 1997 Molecular evidence and clinical significance of herpesvirus coinfection in the central nervous system. J Clin Microbiol 35 2869 2872 9350749 KoskiniemiMPiiparinenHMannonenLRantalaihoTVaheriA 1996 Herpes encephalitis is a disease of middle aged and elderly people: polymerase chain reaction for detection of herpes simplex virus in the CSF of 516 patients with encephalitis. The Study Group. J Neurol Neurosurg Psychiatry 60 174 178 8708648 WeinbergABlochKCLiSTangYWPalmerM 2005 Dual infections of the central nervous system with Epstein-Barr virus. J Infect Dis 191 234 237 15609233 OoiMHWongSCPodinYAkinWdel SelS 2007 Human enterovirus 71 disease in Sarawak, Malaysia: a prospective clinical, virological, and molecular epidemiological study. Clin Infect Dis 44 646 656 17278054 ParkBJWannemuehlerKAMarstonBJGovenderNPappasPG 2009 Estimation of the current global burden of cryptococcal meningitis among persons living with HIV/AIDS. Aids 23 525 530 19182676 GaniemARParwatiIWisaksanaRvan der ZandenAvan de BeekD 2009 The effect of HIV infection on adult meningitis in Indonesia: a prospective cohort study. Aids 23 2309 2316 19770694 TansuphasawadikulSAmornkulPNTanchanpongCLimpakarnjanaratKKaewkungwalJ 1999 Clinical presentation of hospitalized adult patients with HIV infection and AIDS in Bangkok, Thailand. J Acquir Immune Defic Syndr 21 326 332 10428112 LeTHong ChauTTKim CucNTSi LamPManh SieuTP 2010 AIDS-associated Cryptococcus neoformans and Penicillium marneffei coinfection: a therapeutic dilemma in resource-limited settings. Clin Infect Dis 51 e65 68 20887205 ChauTTMaiNHPhuNHNghiaHDChuongLV 2010 A prospective descriptive study of cryptococcal meningitis in HIV uninfected patients in Vietnam - high prevalence of Cryptococcus neoformans var grubii in the absence of underlying disease. BMC Infect Dis 10 199 20618932 Lo ReV3rdGluckmanSJ 2003 Eosinophilic meningitis. Am J Med 114 217 223 12637136