Volume 21, Number 1—January 2015
Pneumonic Plague Outbreak, Northern Madagascar, 2011
Yersinia pestis is the causative agent of plague, a severe and life-threatening zoonotic disease. During 3 pandemics, different genotypes of this bacterium spread to various countries and caused millions of deaths (1–6).Y. pestis genotype 1.ORI3 of the biovar Orientalis was introduced to Madagascar in 1898 during the third pandemic and has persisted there endemically ever since (6,7). Worldwide, an average of 4,000 human plague cases is reported each year. Madagascar is one of the most active plague foci and has an annual average of 1,500 confirmed cases (8,9). The pathogen emerges in multiannual cycles; a peak of pathogen prevalence was observed in Madagascar in 1997 and caused ≈3000 cases, 20 times more than in 1994 (126 cases) (9).
Bubonic plague, the most common form of plague, results from the bite of an infected flea. The infection may spread hematogenously and cause secondary pneumonic plague. If the pathogen is transmitted as an aerosol by droplets or by contaminated dust, primary pneumonic plague may result. After a latency period of 1–5 days, pneumonic plague progresses to the stage of hemoptysis. At this lethal stage of the disease, which lasts ≤3 days, patients are highly infectious (10,11). Plague can be treated with antimicrobial drugs if diagnosed early and if caused by a drug-sensitive strain (9).
Worldwide, only a few pneumonic plague outbreaks have been reported (12–15). However, to understand the epidemic potential of Y. pestis, extensive outbreak analyses are essential. In 1997, a pneumonic plague outbreak occurred in Madagascar near the capital of Antananarivo (13). Health authorities responded immediately, and strain cultivation was successful. Three other pneumonic plague outbreaks have been reported, 1 in Uganda (2004) and 2 in the Democratic Republic of Congo with 87 cases (2005) and 117 cases (2006), respectively (14,15). During the 1920s–1930s, valuable descriptions of 2 plague epidemics in Manchuria, China (≈10,000 cases) were reported (10,12).
In this report, we describe an outbreak and highly progressive spread of pneumonic plague in northern Madagascar, a remote region that was supposedly free of Y. pestis, in 2011. We investigated whether Y. pestis might cause larger outbreaks or epidemics with high case-fatality rate within a short period.
The outbreak investigation protocol was approved by the Ethical Committee, Ministry of Health of Madagascar. The outbreak area contained 7 villages along a field path in the communes of Ambarakaraka and Anaborano, Ambilobe District, in northern Madagascar at an altitude <500 m. In January 2011, two brothers (boys) were working in a copper mine in Beramanja, Madagascar. On January 6, the boys returned home to Ankatakata (distance 50 km) (Figure 1). During the journey, fever, headache, and chills developed in 1 of the boys (age 13 years). Subsequently, he experienced severe chest pain, a deep cough, and hemoptysis, which are the clinical signs of pneumonic plague. He died at home on January 14 (Figure 2). It can be assumed retrospectively that this boy (index case-patient 1) had been infected with Y. pestis in Beramanja or during the journey home (Figures 1,2). On January 21, his mother, who had provided him with treatment until he died, also died (case-patient 2 in household A). Her husband (case-patient 3), daughter (case-patient 4), and granddaughter (case-patient 5) died on January 22. Symptoms of pneumonic plague had developed in these 3 persons (Figure 2; Table 1). These 3 persons were provided treatment by neighbors in household B (Figure 2).
On January 26, a second wave of human pneumonic plague cases was observed in 12 other persons (Figure 2;Table 1). During this second wave, household A (case-patients 6, 7, 12, 13, and 16) and household B (case-patients 8, 10, 11, 14, and 17) in Ankatakata were affected. Case-patient 9 was probably infected while visiting her sister-in-law (case-patient 2) in Ankatakata and transmitted the pathogen to her home (household C) in Antsakoabe (Figures 1,2). Case-patients 15 and 18 were also present in Ankatakata and transmitted the infection to Tsaratanana (household D) and Ankiganyo (household E). Case-patient 18 was responsible for a third small wave of pneumonic plague that started on January 31 and spread to Ambarakaraka (Figure 2; Table 2). This case-patient infected her brother (case-patient 19), who had carried his sister to a traditional healer (case-patient 20). Symptoms of pneumonic plague developed in all 3 persons; all 3 died (Figure 2; Table 1).
During our epidemiologic investigation, 41 contact persons were identified. These persons had interacted with the patients but did not show specific symptoms of pneumonic plague. All provided a serum sample for diagnostic testing (Table 2). Sixteen family contacts (c1–c16) were defined as persons who lived in the same household as an infected person during the outbreak (Figure 2; Table 2). Twenty-five other contacts (c17–c41) had spent some time with a patient or approached a patient who died during the outbreak (Figure 2; Table 2).
In Ankatakata, we found 5 family contacts (c1–c5) in households A and B who had received chemoprophylaxis on January 28. In Antsakoabe, case-patient 9 died in her home on January 26. Her husband and 3 children (c6–c9) lived in the same house. They received chemoprophylaxis on February 6 and provided serum samples on February 15. In Tsaratanana, the wife (c10) of case-patient 15 refused chemoprophylaxis. In Ankiganyo, 4 family contacts (c11–c14) of deceased case-patients 18 and 19 received chemoprophylaxis on February 6. Contact c14 was seropositive for pneumonic plague. In Ambarakaraka, 2 family contacts (c15 and c16) of case-patient 20 received chemoprophylaxis on February 9 (Figure 2; Table 2).
The status of nonfamily contacts was as follows. Case-patient 10 moved to Mandrivary, which is 8 km from Ankatakata, and died there of suspected pneumonic plague. We identified 9 contact persons (c17–c25) in Mandrivary. All except 1 (c25) had received chemoprophylaxis on January 28 and showed seronegative results. Contact 25 was a 21 year-old man who had carried case-patient 3 in Ankatakata. He had a cough and was seropositive (Table 2;Figure 2). Case-patient 11 died in Antafiabe. He had contact with 6 other persons (c26–c31). These 6 persons received chemoprophylaxis on January 28. Although 1 contact (c26) shared her bed with case-patient 11 until his death on January 27, these 2 persons did not show clinical signs or symptoms or seroconversion. We found 10 additional contacts (c32–c41), who had attended funerals for case-patients in different villages. Three of these contacts had mild pulmonary infection, but had not consulted a physician and were seronegative (Figure 2; Table 2).
Diagnosis and Case Assessment
Two weeks after the death of the index case-patient on January 28, health personnel arrived in Ankatakata. Treatment with antimicrobial drugs was provided to 5 patients (case-patients 12, 13, 15, 16, and 17), and chemoprophylaxis was provided to contact persons and health personnel according to recommendations of the World Health Organization (WHO) (9) (Figure 2; Tables 1, 2). Because we did not know that the outbreak was ongoing in Ankiganyo (30 km from Ankatakata), treatment was not provided to case-patients 18, 19, and 20 (Figures 1, 2). It was only after these 3 case-patients died that contacts of these patients received chemoprophylaxis (Figure 2; Table 2).
Because persons who died were not sampled postmortem, only a limited number of clinical samples were collected (Table 1). Of collected sputum samples, 2 (from case-patients 12 and 13) were positive for Y. pestis–specific F1 antigen by immunochromatographic rapid dipstick test (Table 1) (16). All samples were subsequently transported (>900 km) to the WHO Collaborating Center for Plague at the Institut Pasteur de Madagascar in Antananarivo. Sputum samples were incubated in bacterial culture media and inoculated into laboratory mice. However, isolation of Y. pestis was not successful (Tables 1,3). Collected serum samples were analyzed by using a Y. pestis–specific F1 antigen IgG ELISA as described (17). Positive samples were quantified by using serial dilutions. Three of 5 paired serum samples (from case-patients 12, 13, and 17) had 4-fold increases in titer in the second serum (Table 1). Of samples from contact persons, 2 of 41 single serum samples showed a positive result (Table 2).
Subsequent case assignment was conducted according to WHO recommendations for plague-endemic countries (18). Three types of cases were identified: suspected cases (specific clinical symptoms), presumptive cases (positive serologic result for antibody against F1 antigen), confirmed cases (4-fold increase in titer of antibody against F1 antigen in paired serum samples or a positive culture result) (18). When we applied these recommendations to the outbreak, we identified 17 suspected cases (in case-patients 1–11, 14–16, and 18–20), 2 presumptive cases (in c14 and c25), and 3 confirmed cases (in case-patients 12, 13, and 17) (Tables 1,2).
All 20 patients with pneumonic plague had sudden onset of fever, cough, hemoptysis, and chest pain. The latency period was 4–6 days, and the infectious period was 48–72 hours (Figure 2). When given antimicrobial drugs, 5 patients (case-patients 12, 13, 15, 16, and 17) survived (Table 1). In contrast, the 15 case-patients who were not treated died of pneumonic plague. Of the 36 persons living in affected households A–F, 20 showed specific symptoms and 15 died. The overall attack rate was 55%, and the case-fatality rate was 75% (Figure 2).
Because of poor accessibility to the remote area of the outbreak and thunderstorms, a field investigation on the plague focus was not started until April 1, which was 2 months after the outbreak (Table 3). No dead rats were observed before, during, and after the outbreak, which is an unusual finding for a plague epidemic in Madagascar.
The sampling sites were chosen in the 2 villages (Ambakirano and Ankatakata) and surrounding woodlands of Antsisoboko and Antanabe (Figure 1). A total of 36 traps were set during 30 nights. Sixty-four rodents were trapped: 51 black rats (Rattus rattus), 3 house mice (Mus musculus), 6 greater hedgehogs (Setifer setosus), 3 short-tailed shrews (Microgale brevicaudata), and 1 Asian house shrew (Suncus murinus). Serum or spleen samples were obtained from these 64 rodents and from 5 dogs (Table 3). Pathogens were not isolated from these animals. Fleas were not detected in flea-specific traps.
Bacteriologic culture, serologic analysis, and molecular testing were conducted as described for human samples. Bacteriological culture results was negative, but 1 S. setosus hedgehog and 2 dogs were seropositive for IgG against F1 by ELISA (Table 3).
Molecular diagnostics of Y. pestis DNA was performed by using a PCR specific for the Y. pestis plasminogen activator and capsule antigen fraction 1 genes as reported (19,20). Samples from case-patients 12 and 13 showed positive results for Y. pestis DNA (Table 3). For comparison, samples from person with confirmed human plague were also analyzed: 1 each from Mandritsara (2010) and Bealanana (2011) (400 km from Ambilobe) and 1 from Ankazobe (2010) (800 km from Ambilobe) (Table 4). Of animal spleen samples collected, 5 samples from R. rattus rats were positive for Y. pestis DNA (Table 3).
We analyzed 14 canonical single-nucleotide polymorphisms (SNPs) to determine the SNP genotype (phylogenetic position) of 10 Y. pestis–positive samples within the 1.ORI3 group (s232, s1362, s1375, s190, s197, s1367, s1004, s1025, s1377, s1089, s1363, s206, s1373, and s152) according to a hierarchical molecular typing approach (1). All 10 samples showed an identical 1.ORI3-k SNP pattern; we also found 1 derived SNP (s232) and 13 ancestral SNPs (Table 4).
In a second typing approach, Y. pestis–specific clustered regularly interspaced short palindromic repeats (CRISPRs) were identified (21–23). Sequences obtained were compared with sequences reported (21–23) and those in the CRISPR database (http://crispr.u-psud.fr/). All 10 Y. pestis–positive samples had an identical Ypa locus (a1-a2-a3-a4-a5-a6-a7-a8). For the Ypb locus, 1 spacer reduction (b5) was detected in a sample from case-patient 13. The other 9 samples showed an identical Ypb locus (b1-b2-b3-b4-b5). Seven samples had an identical Ypc locus (c1-c2-c3). However, within this locus, a new, and to our knowledge, Madagascar-specific spacer c12 was detected in R. rattus rodent sample R16 from Ambarakaraka and in a Bealanana-013 sample from 2010 (Table 4). The newly found spacer sequence originated from a phage: c12: 5′-ATCGAGGCGGGCCGGAAGAATGTCACGGCGGTT-3′ (by BLAST analysis; http://blast.ncbi.nlm.nih.gov/Blast.cgi). The presence of spacer c12 shows a correlation with a 1-nt reduction in the precedent spacer (c3>c3′) in both samples (Table 4). Despite performing several PCRs, we could not amplify the Ypc locus from R. rattus rodent sample R05 from Antanabe (Table 4).
Three plague pandemics and numerous plague epidemics have been caused by Y. pestis in the past 1,500 years (2,4,7,12,24). During the second medieval pandemic, which also included the Black Death period, 50% (≈50 million persons) of the human population in Europe reportedly died of plague (2,4). At the beginning of the 20th century, 10,000 persons died during 2 plague epidemics in Manchuria, China (12). Although plague is still endemic to other countries, the reported numbers of plague patients has decreased to an average of 4,000/year since 1954. Also, there has been a slight decrease regarding the highest reported case number from countries in Asia and Africa (8,9).
Since the introduction of plague to Madagascar in 1898, the Institute Pasteur in Antananarivo was assigned to control this disease. The pneumonic plague outbreak in 2011 shows that despite introduction of education programs, a plan to investigate plague outbreaks promptly, and a trained task force, plague outbreaks cannot be prevented. However, in contrast to control of historical plague, when treatment with antimicrobial drugs was not available and the disease could spread unhindered, the present outbreak was stopped quickly after 27 days because of successful treatment with antimicrobial drugs (Figure 2). The good response of the patients to these drugs suggests that the Y. pestis strain that caused this outbreak was susceptible to streptomycin. However, streptomycin-resistant Y. pestis strains were isolated in Madagascar in 1995 and also during the outbreak in 2011 (25; M. Rajerison, pers. comm.). Therefore, drug-resistant Y. pestis strains may pose a new challenge to health authorities.
During the outbreak in 2011, persons shared single-room houses, lived in extended families, and closely cared for each other. Patients were not isolated. Because of social conventions, some persons trusted a traditional healer rather than physicians. This finding led to the third wave of the outbreak, which included 3 case-patients with pneumonic plague who died (Figure 2; Table 1).
WHO lists plague as a disease for which patients should be quarantined and requires that pneumonic plague patients are isolated from healthy persons (9). However, during the latency period before hemoptysis, sputum contains hardly any infectious organisms (11,26). Simple countermeasures, such as protective facial masks, are efficient in preventing transmission by droplets. Also, turning one’s head away from or turning one’s back toward a healthy person has a major prophylactic effect (26). This finding might explain why c26, who shared the same bed with case-patient 11 until his death, was not infected (Tables 1, 2). Thus, knowledge of the pathogenesis of Y. pestis in humans is essential for persons who live in plague-endemic countries.
It has been suggested that patients with bubonic plague and patients who have died of plague are not directly infectious to other humans (9,26). This suggestion is consistent with findings in the present study because contacts (c32–c41) who only attended the funerals did not show symptoms or seroconversion (Table 2; Figure 2).
Plague is endemic to Madagascar, especially in the central highlands (7). At an altitude >800 m, large numbers of rodent species and insectivores live in the rain forest. Those animals represent the classical natural focus for Y. pestis (7). The low-elevation seaport villages of Mahajanga and Antananarivo are exceptions to this altitude factor. Because of trade and stockpiling of grain and other food products, homophilous species, such as the black rat (R. rattus) and the Norwegian rat (R. norvegicus), play a major role in the urban lifecycle of plague (6,7,27). The present outbreak occurred at an altitude <500 m in a region that does not have much commercial or economic activity. Because of this finding, there was a low prevalence of small mammals in this area, and only a low number of rodents and insectivores were trapped during the epidemiologic investigation (Table 3). This factor resulted in the plague outbreak not being immediately recognized.
Although the outbreak Y. pestis strain could not be isolated, information was obtained by molecular analyses of human and animal samples. All samples contained the Madagascar-specific 1.ORI3-k genotype of Y. pestis, as previously reported (1,6). Results of CRISPR typing identified >1 genotype, which indicated that the outbreak area was a natural plague focus before the outbreak in 2011 (Table 4). This result is supported by an unusual high prevalence (12%, 8/69) of Y. pestis–positive animal samples (Table 3) compared with prevalences in previous studies (28–30). We suggest that Y. pestis strains containing the major CRISPR profile, which was found in 6 of 10 samples, was responsible for the present outbreak (Table 4). This CRISPR genotype has also been found in samples from the central highlands. The isolate from case-patient 13 lost the b5 spacer (Table 4). This phenomenon has been reported for other CRISPR profiles, and a different genotype has been assessed (21–23). A third Y. pestis CRISPR genotype was found in the R. rattus rodent R16 sample and in the human Bealanana 013 sample from 2010; this genotype includes the new element c3′–c12 of phage origin (Table 4) (21). The loss of 1 nt at the end of the spacer, as observed in in c3>c3′, has been previously reported (22).
Despite performing several PCRs, we could not amplify the complete Ypc locus in the R. rattus rodent R05 sample from Antanabe (Table 4), a finding that has been previously reported (21). We suggest that 4 CRISPR genotypes of Y. pestis were present in the outbreak area, which indicates that Ambilobe was a natural plague focus even before the outbreak. Unnoticed presence of pathogens near human populations requires higher surveillance activity, as recently reported (7). In contrast, it has been reported that hereditary resistance against Y. pestis might develop in rats (7,31).
One question that also needs to be addressed is why plague caused millions of deaths during devastating pandemics in the past while today plague is restricted to some geographic locations. One possible explanation would be the presence of additional virulence factors in historical plague strains, which have been lost from current Y. pestis strains.
To answer this question, 2 ancient Y. pestis genomes were sequenced and compared with sequences of current Y. pestis isolates. The ancient genomes were from a pandemic European Y. pestis pestis biovar Antiqua isolate (genotype 1.ANT) that originated during the Black Death period (3), and from a pandemic Y. pestis pestis biovar Antiqua isolate (genotype 0.ANT), which was isolated from a patient who died during the plague of Justinian in Germany (5). Sequences of current Y. pestis genomes used for comparison were from the nonhuman pathogenic Chinese Y. pestis microtus strain (91001: 0.PE4, biovar Xilingolensis) and from the Y. pestis pestis strain (CO92: 1.ORI1, biovar Orientalis) (3,5).
Analyses showed that genomes of ancient Y. pestis strains did not contain additional virulence genes that might explain higher virulence. (3,5). Furthermore, because plague epidemics were caused by different biovars or genotypes in Asia, Europe, and Africa (3,5,6,10,12–15), we assume that various Y. pestis subtypes are similar in virulence. Thus, factors other than differences in virulence might better explain the decrease in the reported plague cases. It is more likely that the general perception and understanding of infectious agents; improved hygiene; trade management; knowledge of plague pathogenesis in humans; vector control; specific outbreak management, including selective isolation of infectious patients; and chemoprophylaxis and treatment with antimicrobial drugs, have accounted for the decrease in plague cases (9,11,15,26).
In conclusion, the 1.ORI3-k genotype of Y. pestis identified in the present study has virulence comparable with that of ancestral genotypes that caused other epidemics. The course and outcome of a human plague epidemic depend on this virulence, as well as on education, public awareness, life style, infrastructure, isolation of patients, and medical care. However, there is an unpredictable pathogenic potential in drug-resistant strains that has not been estimated and needs to be studied.
Dr Richard is a scientist in the Department of Epidemiology at the Institute Pasteur, Dakar, Senegal. His research interests are tropical diseases, public health priorities, analysis of surveillance data from sentinel network and cohort studies, and evaluation of emergent risks and antibiotic resistance testing.
We thank Abdou Salam Nasser, Ravoniarisoa Marie Georgette, Noromihaja Randriananja, and Joely Razafilalaintsoa for assistance during the epidemiologic study, and Michaela Projahn and Gabriele Echle for assistance during pathogen typing and laboratory analysis.
This study was supported by the Institut Pasteur de Madagascar, the President’s Malaria Initiative/US Agency for International Development, and the US Department of Homeland Security (project no. DHS-09-ST-108-001/MGN3EL7-01).
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Suggested citation for this article: Richard V, Riehm JM, Herindrainy P, Soanandrasana R, Ratsitoharina M, Rakotomanana F, et al. Pneumonic plague outbreak, northern Madagascar, 2011. Emerg Infect Dis [Internet]. 2015 Jan [date cited]. http://dx.doi.org/10.3201/eid2101.131828