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Volume 13, Number 4—April 2007

Letter

Pneumonic Plague, Northern India, 2002

Suggested citation for this article

To the Editor: A small outbreak of primary pneumonic plague took place in the Shimla District of Himachal Pradesh State in northern India during February 2002. Sixteen cases of plague were reported with a case-fatality rate of 25% (4/16). The infection was confirmed to the molecular level with PCR and gene sequencing (1). A previous outbreak in this region during 1983 was suggestive of pneumonic plague (22 cases, 17 deaths) but was not confirmed. In India, the last laboratory-confirmed case of plague was reported in 1966 from Karnataka State (2).

The index patient for the 2002 outbreak lived in a hamlet in the Himalayas. He went hunting on January 28, 2002, in a nearby forest at a height of ≈500–600 m from his house. There, he killed a sick wild cat and skinned it. He returned home on February 2 and sought treatment for fever, chills, and headache. On February 4, breathlessness, chest pain, and hemoptysis developed; radiologic findings were suggestive of lobar pneumonia, and treatment with augmentin was begun. He died the next day. Subsequently, 13 of his relatives exhibited a similar illness, although 2 additional patients acquired infection in the hospital. The incubation period for those patients was 1–4 days, which is consistent with that of pneumonic plague.

A team of microbiologists, epidemiologists, and entomologists visited the village after 7 more cases were reported until February 12, 2002, followed by a team from the National Institute of Communicable Diseases (NICD), New Delhi. The following case-patient definition was used: a person who sought treatment for fever of rapid onset, chills, chest pain, breathlessness, headache, prostration, and hemoptysis. A total of 16 cases were reported from 3 hospitals in the area: a local civil hospital, the state medical college, and a regional tertiary care hospital. Clinical material collected from the case-patients and their contacts was initially processed in the laboratories of these hospitals. Wayson staining provided immediate presumptive diagnosis, and confirmatory tests were performed at NICD. Diagnosis of plague was confirmed for 10 (63%) of 16 patients (1).

NICD conducted the following laboratory tests on 2 suspected culture isolates, 2 sputum specimens, 1 lung autopsy material specimen, and 1 lung lavage sample (Table): 1) direct fluorescent antibody test for Yersinia pestis; 2) culture and bacteriophage lysis test; and 3) PCR and gene sequencing to detect Y. pestis–specific genes (pla and F1). All these tests confirmed that isolates were Y. pestis and met all the World Health Organization’s recommended criteria (3).

Antibodies against F1 antigen of Y. pestis were detected by passive hemagglutination testing of paired serum samples. Although 5 patients showed a >4-fold rise, 1 patient showed a >4-fold fall in antibody titer. In contrast, samples from 6 patients were negative for Y. pestis, and no change was found in the titers from 1 patient. No serum sample was collected from the index patient; for the 2 other patients who died, 1 of the single serum samples became contaminated, and the other was positive for Y. pestis (4). Paired serum samples from the case-patients were collected on a single day 4 weeks apart during the visit of the NICD team, regardless of the duration of symptoms.

Antimicrobial drug sensitivity testing was carried out by the Kirby-Bauer disk diffusion method. All isolates were sensitive to doxycycline, tetracycline, chloramphenicol, streptomycin, ciprofloxacin, gentamicin, and amikacin but were resistant to penicillin.

No fleas or other ectoparasites were found on the 6 cats, 8 dogs, 6 cows, 4 calves or 2 trapped rodents in the village. One serum sample, with pooled blood from 3 dogs was negative for antibodies against F1 antigen. Before these infections occurred, a heavy snowfall in the region had reduced the activity of rodents and was unfavorable for the survival and multiplication of rat fleas. The snow also helped restrict the spread of the infection because of reduced movement of the local population (1).

Primary pneumonic plague is acquired by inhaling infective droplets from persons or animals and rarely by accidental aerosol exposure. Y. pestis is a category A agent of bioterrorism (5). It is not truly airborne; person-to-person transmission requires face-to-face exposure within 2 m of a coughing patient (2). During 1977–1998, in the western United States, 23 cases of cat-associated human plague were reported. Bites, scratches, or other contact with infectious material while handling infected cats resulted in 17 cases of bubonic plague, 1 case of primary septicemic plague, and 5 cases of primary pneumonic plague (6).

In our report, close and prolonged contact with the index patient while providing care (for example, wiping his face during hemoptysis, supporting him during a bout of coughing, taking him to the hospital in a vehicle) resulted in secondary cases. Because of the severe winter, poor ventilation in houses further helped the illness spread. All patients acquired infection before plague was suspected. Initially, patients were treated for community-acquired pneumonia, which delayed the proper treatment and led to deaths. A patient admitted for status epilepticus was infected by her attendant, who in turn, acquired infection from a terminally ill plague patient for whom he provided some care. The patient with epilepsy and her attendant shared a common room with the terminally ill wife of the index patient, which was small and poorly ventilated. Surprisingly, the relative of the index case-patient who had accompanied him to the forest survived the infection; whereas, the wife and sister of the index patient died. No spread to healthcare workers was noted.

When plague was suspected immediate preventive measures were taken, for example, fumigation of the index patient’s residence and any vehicles used for transporting the patients; active surveillance and education; standard work precautions; chemoprophylaxis for patient contacts and paramedics; and isolation and treatment of patients (1). The transmission rate for primary pneumonic plague is relatively low compared with that of many other communicable diseases; the average number of secondary cases per primary case is 1.3, according to a study done by Gani and Leach (7).

The key element in the control of small outbreaks of primary pneumonic plague could be the intensity of disease surveillance system (7). As a result, the state government has established a Plague Surveillance Unit in District Shimla of Himachal Pradesh in 2002 (1).

Manohar Lal Gupta* and Anuradha Sharma*Comments to Author 
Author affiliations: *Indira Gandhi Medical College, Shimla, Himachal Pradesh, India;

Acknowledgment

We thank B.D. Negi for his selfless service in collecting and processing samples from patients and their contacts in harsh field conditions. We are also thankful to NICD, New Delhi, for confirming Y. pestis in the culture isolates and serum samples.

References

  1. Outbreak of pneumonic plague in village Hatkoti, District Shimla, Himachal Pradesh, India, February 2002. New Delhi (India): Directorate General of Health Services, Ministry of Health and Family Welfare; April 30, 2002.
  2. Dennis DT, Gage KL, Gratz N, Poland JD, Tikhomirov E. Plague manual: epidemiology, distribution, surveillance and control. Geneva: World Health Organization; 1999.
  3. World Health Organization. Plague manual: epidemiology, distribution, surveillance and control (WHO/CDS/CSR/EDC/99/2); 1999. p. 50
  4. Investigation report on “acute febrile illness with haemoptysis” outbreak in Hatkoti village, Jubbal-Kotkhai block of Shimla District, Himachal Pradesh, February 2002. New Delhi (India): National Institute of Communicable Diseases; 2002 [cited 2007 Feb 28]. Available from pib.nic.in/archieve/lreleng/lyr2002/rmar2002/13032002/r1303200219.html
  5. Dennis DT, Chow CC. Plague. Pediatr Infect Dis J. 2004;23:6971.PubMed
  6. Gage KL, Dennis DT, Orloski KA, Ettestad P, Brown TL, Reynolds PJ, Cases of cat-associated human plague in the Western US, 1977–1998. Clin Infect Dis. 2000;30:893900.PubMed
  7. Gani R, Leach S. Epidemiologic determinants for modeling pneumonic plague outbreaks. Emerg Infect Dis. 2004;10:60814.PubMed

Table

Suggested citation for this article: Gupta ML, Sharma A. Pneumonic plague, northern India, 2002 [letter]. Emerg Infect Dis [serial on the Internet]. 2007 Apr [date cited]. Available from http://wwwnc.cdc.gov/eid/article/13/4/05-1105.htm

DOI: 10.3201/eid1304.051105

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Table of Contents – Volume 13, Number 4—April 2007

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Anuradha Sharma, Mohindera Apartments, Nav-Bahar, Shimla, 171002, (H.P.), India;





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