About the Authors:
Xiang Y. Han
Roles Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Project administration, Writing – original draft, Writing – review & editing
* E-mail: [email protected]
Affiliation: Department of Laboratory Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, United States of America
ORCID logo https://orcid.org/0000-0001-8472-0870
Introduction
Legionellosis is a pulmonary infection caused by the aquatic and soil bacteria Legionella pneumophila and other Legionella spp. [1, 2]. The infection occurs after inhalation of bacteria-bearing aerosols or soil dust, with an incubation period of several days to 2 weeks [3–5]. Legionellosis impacts public health because it occurs in outbreaks as well as sporadically. While outbreaks can be traced to a single source of exposure, such as aerosols emitted from cooling towers or whirlpool spas [4, 6, 7], the exposure sources for the sporadic cases that account for 75–90% of all legionellosis cases are rarely identified [2, 8–10]. In recent years, the United States has experienced a rapid rise in legionellosis incidence [10], begging an explanation beyond diagnosis, surveillance, and reporting that have changed little in the past 30 years.
Most of the infections occur in warm months [10, 11], reflecting the optimal growth temperature of 25 to 42°C for Legionella spp. [2, 12]. Studies have noted the effects of temperature, rainfall, and river systems on legionellosis incidences at various locations [13–16]. We recently showed solar and climate effects on incidence across the United States [11]. The lower incidence rates in the western states corresponded to low precipitation, under an annual threshold of 750 mm, while the higher rates in the eastern states corresponded to more precipitation. Within the eastern states, incidence varied regionally, being promoted by warming temperature but inhibited simultaneously by intensifying solar ultraviolet radiation and longer sunshine hours. These mixed and dynamic effects could be demonstrated in multiple regressions. All these studies together affirm a major role of temperature and rainfall in dictating the abundance of Legionella spp. in the environment and shaping legionellosis incidence in concert with human factors.
Viable Legionella spp. have been isolated from rainwater puddles on road surfaces, implying potential generation of bacteria-bearing aerosols by motor vehicle traffic and exposure to drivers and passengers [17, 18]. This likelihood is supported by an elevated legionellosis incidence among professional drivers [19–21]. The revelation of inhibitive solar effect, which in converse means lack of inhibition in the absence or attenuation of sunlight, further highlights the significance of road exposure to soil bacteria in the United States, unappreciated previously, in view of daily driving for most Americans [11].
With global warming, the United States has recorded consecutive years of above-norm (1901–2000) annual mean temperatures since 1997 and precipitation surplus since 2008 [22]. In this context, we analyzed the legionellosis incidence rates in the US from 1999 to 2018 for correlation with concurrent temperature, precipitation, solar ultraviolet B (UVB) radiation, and vehicle mileage data in search of an explanation for the rapid rise in incidence. Trend analysis and regression models were applied.
Materials and methods
This was a correlative study on the surveillance of legionellosis using publicly accessible archived data. We analyzed data for the United States as a whole and for five individual states representing varied climates and legionellosis incidences (California, Florida, New Jersey, Ohio, and Wisconsin).
Data sources
The legionellosis case data from 1999 to 2018 were from the annual summary of notifiable diseases from the Centers for Disease Control and Prevention (CDC) [23]. The diagnosis required a specific test for Legionella spp., such as cultivation, urine antigen test, or strong serologic titer(s), for distinction from diverse etiologic agents of pulmonary infection. These tests had been developed and used since early 1980s, along with reporting to CDC, and from 1980 to 1998, the legionellosis incidence hardly changed in the US [2].
The population data were from the US Census projections [24] using projections 1995 to 2050 for the 1999 population with correction from the 2000 census, projections 2008 and 2009 (averaged) for 2000 to 2011, projection 2012 for 2012 and 2013, projection 2014 for 2014 and 2015, and projection 2017 for 2016 to 2018. Annual incidence rates (all 50 states) in cases per 100,000 population were calculated according to age groups of 0–39 years, 40–64 years, ≥65 years, and all ages. Age-adjusted incidence rates were also used, based on the year 2000 census age brackets, to correct the bias from the aging population.
The temperature and precipitation data for the contiguous United States (since 1895) were from the National Centers for Environmental Information [25]. Annual values of mean temperature and total precipitation as well as seasonal data from May to October were used. Long-term means from 1901 to 2000 were set as benchmark norms to derive yearly or seasonal anomalies during 1999 to 2018; these data were extracted directly from the source. Yearly anomaly values, when summed, yielded cumulative anomalies.
The UVB radiation data were from the UVB Monitoring and Research Program at Colorado State University [26, 27]. UVB data measured wavelengths of 280 to 320 nm, the main germicidal part of sunlight, across the continental United States from coordinates of 24.544°N to 49.344°N in latitude and 66°W to 125.9°W in longitude at a resolution of 0.1°. The average US UVB annual sum, in kilojoules per square meter (kJ/m2), represented the mean value from 149,400 coordinates. For the analysis of UVB mean values in five states, the following coordinates were used: 39.244°N to 41.144°N and 74.1°W to 75.2°W for New Jersey; 39.144°N to 41.444°N and 80.5°W to 84.8°W for Ohio; 42.544°N to 46.144°N and 87.6°W to 91.8°W for Wisconsin; 29.844°N to 30.744°N and 82.8°W to 87.5°W for northern Florida and 24.544°N to 30.744°N and 80.4°W to 82.7°W for southern Florida (then combined); and 34.544°N to 41.944°N and 120.4°W to 124.2°W for northern California and 32.744°N to 34.544°N and 114.5°W to 120.4°W for southern California (then combined).
The vehicle mileage data were from the Bureau of Transportation Statistics, including urban, rural, and total vehicle miles [28].
Statistical analyses
Data handling and analyses used Excel version 2013 [29], including plots for trend, fitting models, and correlations, and linear regressions between various parameters (explanatory variables) and incidence rates (outcome variables). Simple linear regressions were applied to each of the climate and vehicle mileage parameters first, followed by multiple linear regressions with two to all parameters to assess the promotive and/or inhibitive role of each parameter. Cautions were taken during multiple regressions to recognize and avoid spurious results due to data comparability or inherent relatedness, known as multicollinearity [30]. P values of 0.05 or less were deemed to be statistically significant.
It was noted that the incidence rates, in cases/100,000 with decimal points, were unsuitable for Poisson regression analysis that requires integers. Instead, they were taken as a normal approximation to Poisson distribution for linear regression analysis, a practice in epidemiology for large scale studies [31], such as the current one. Log transformation of the incidence rates was used at times for optimal fitting. The validities of analysis and assumptions were verified in a statistics package (IBM SPSS version 24) through such tests as Kolmogorov-Smirnov, residual analyses and P-P plots. Although each variable represented a time series from 1999 to 2018, potential cumulative effects and/or interactions of the explanatory variables made the datasets beyond simple time series. Thus, proper interpretation of significant correlations between the incidence rates and explanatory variables and model identification/fitting required biological relevance for support. The primary purpose of model construction was examination of the importance of explanatory variables, which placed focus on multiple regressions for their potential interactions and relative contributions. Autocorrelations were assessed with Durbin-Watson values.
Results
Age specific and adjusted incidence trends
The age-specific, all-age, and age-adjusted legionellosis incidence rates are shown in Fig 1 (Table 1). They remained at base line from 1999 to 2001 and then increased remarkably to reach the peak in 2018, with some year-to-year fluctuations. For the age group of 0–39 years who are least vulnerable to the infection, the rate rose 4.8-fold, from 0.10/100,000 in 1999 to 0.46/100,000 in 2018; for the age group of 40–64 years, the rise was 7.7-fold, from 0.61/100,000 to 4.71/100,000; for the age group of ≥65 years, being most vulnerable, the rise was 6.5-fold, from 1.26/100,000 to 8.1/100,000; and for all ages, the rise was 7.7-fold, from 0.40/100,000 to 3.03/100,000. The age-adjusted rate rose 6.8-fold, from 0.40/100,000 in 1999 (with 1108 cases) to 2.69/100,000 in 2018 (with 9933 cases). Consistent with the aging population, the all-age rates were slightly higher than the age-adjusted ones, in recent years in particular. For example, the age group of ≥65 years constituted 16.0% of the population in 2018, in comparison to 12.4% in 2000.
[Figure omitted. See PDF.]
Fig 1. Age-specific, all ages, and age-adjusted legionellosis incidence rates in the United States, 1999–2018, with exponentially fitted dot lines and R2 values.
https://doi.org/10.1371/journal.pone.0250364.g001
[Figure omitted. See PDF.]
Table 1. Age-specific and age-adjusted legionellosis incidence rates in cases per 100,000 population in the United States, 1999–2018, and data fitting analyses.
https://doi.org/10.1371/journal.pone.0250364.t001
The rate rises were linear from 1999 to 2016, but accelerated in 2017 and 2018, making the 1999–2018 curves fit better exponentially than linearly (Fig 1). From the exponentially fitted coefficients, an annual incidence increase of ~110% was derived (Table 1). These results suggest cumulative effects from strong underlying causes, prompting searches for environmental and human exposure factors.
Potential roles or bias from diagnosis, reporting, and/or surveillance were also assessed. While a direct assessment was difficult, an indirect approach was used via a comparison with the incidence trend of another infection, i.e., invasive pneumococcal infection. This bacterial infection is similar to legionellosis in clinical manifestations (mainly pneumonia), specific diagnostic approaches (mainly cultivation of causative bacteria and urine antigen test), and predilection for the aged (65 years and older), but different in exposure source and route (close contact with an infected person or carrier). These data were available form CDC during 2010 to 2018. As shown in S1 Fig, the incidence rates of invasive pneumococcal infection changed little during the 9 years, suggesting stability in the diagnosis and reporting of pulmonary infections. Therefore, together with the stable legionellosis incidence during 1980–1998 [2], it was unlikely that the diagnosis, surveillance, and/or reporting contributed significantly to the current rapid rise of the incidence.
Effects of climate changes
Changes in temperature, precipitation, and UVB radiation were seen during the 20-year period studied (Fig 2, S1 Table). From 1999 to 2018, the US average annual mean temperatures ranged from 11.27°C to 12.93°C, consistently above the 1901–2000 norm of 11.12°C by 0.15°C to 1.81°C, averaging 0.83°C or 7.5% (Fig 2A). In fact, the anomaly streak started with 11.22°C in 1997 and 12.35°C in 1998 and has continued to 11.49°C in 2019, for a total of 23 years thus far. Cumulative anomalies rose remarkably, from 1.03°C in 1999 to 17.05°C in 2018 (Fig 2A).
[Figure omitted. See PDF.]
Fig 2. Climate changes in the United States, 1999–2018.
Top (A): Annual mean temperature (°C); Middle (B): annual precipitation (mm); Bottom (C): annual sum of solar ultraviolet B radiation (kJ/m2).
https://doi.org/10.1371/journal.pone.0250364.g002
The precipitation anomalies were more recent (Fig 2B). During 1999–2007, the annual precipitations fluctuated around the 1901–2000 norm of 760.5 mm. Starting in 2008, 10 of the 11 years showed above-norm precipitation, averaging 802.2 mm. The only exception was 2012, a very dry year (699.3 mm), in which the record (since 1895) high annual mean temperature (12.93°C) also occurred. The anomalies were most pronounced in 2015 (878.6 mm) and in 2018 (880.1 mm), which exceeded the norm by 118.1 mm (15.5%) and 119.6 mm (15.7%), respectively. An upward trending from 1999 to 2018 was significant (R2 = 0.3692, P = 0.004, Fig 2B). Cumulative anomalies also rose markedly from 2008 to 2018. The anomalous streak continued in 2019 with 883.4 mm, a record (since 1974) level of 16.2% over the norm.
In contrast to the rising temperature and precipitation during the 20 years studied, the UVB radiation trended downward significantly despite considerable fluctuations (R2 = 0.3157, P = 0.010, Fig 2C). The lowest was in 2011 (7334 kJ/m2). The trend continued in 2019 with a level of 8707 kJ/m2, below the 1999–2018 mean of 10406 kJ/m2.
The climate parameters were analyzed in linear regressions with the age-adjusted legionellosis incidence rates (Table 2). In simple regressions, the annual mean temperature did not correlate with incidence rates, but precipitation showed a positive correlation, suggesting a promotive effect, and UVB radiation showed an inverse correlation, suggesting an inhibitive effect. In multiple regressions, better correlations were obtained, particularly for temperature when combined with precipitation, suggesting a synergistic effect. Because of the seasonality of legionellosis in the summer and fall, the analyses were repeated using the temperature and precipitation data from May to October. The results showed significant correlations with temperature in simple regression (P = 0.023) and multiple regressions (P = 0.0008) along with precipitation (Table 2).
[Figure omitted. See PDF.]
Table 2. Linear regressions between age-adjusted legionellosis incidence rates and concurrent temperature, precipitation, and UVB radiation in the United States, 1999–2018.
https://doi.org/10.1371/journal.pone.0250364.t002
More significantly, the rising cumulative anomalies of temperature and precipitation paralleled the rising legionellosis incidence with robust regressions (Table 2, Fig 3), which explained the cumulative effects and implied possible changes in the ecology of Legionella bacteria. The correlation with temperature anomaly also fitted better exponentially than linearly (R2 = 0.9421 versus R2 = 0.9145, Fig 3). In addition, from 1999 to 2008, prior to the rising trend of precipitation surplus, only temperature anomaly correlated significantly with the rise in incidence, in a separate multiple regression analysis (adjusted R2 = 0.8807, P = 0.0003) (Table 2 footnote). This result explained the first significant incidence increase in 2003, seven years after the start of anomalous run.
[Figure omitted. See PDF.]
Fig 3.
Correlations between age-adjusted legionellosis incidence rates and cumulative anomalies of temperature (up) and precipitation (low) in the United States, 1999–2018, with fitted dot lines, R2 values, and equations.
https://doi.org/10.1371/journal.pone.0250364.g003
Together, the climate analyses suggest that rising temperature and precipitation and decreasing UBV radiation have contributed to the rising legionellosis incidence. The 2018 incidence peak could be attributed to the cumulative effects, record high precipitation (880.1 mm), near record low UVB radiation (7488 kJ/m2), and continued above-norm temperature (11.96°C) (S1 Table). Examples of yearly fluctuations included the 2011 incidence peak (1.26/100,000), corresponding to the record low UVB level (7334 kJ/m2), and the 2012 incidence valley (1.08/100,000), corresponding to record drought and a high UVB level (12001 kJ/m2) (S1 Table).
Correlation with vehicle miles driven
From 1999 to 2018, the vehicle mileage driven in the United States changed gradually with decrease of rural miles and increase of urban miles, resulting in a net increase of total miles (S2 Table). As shown in Fig 4, the urban vehicle miles rose 1.4-fold from 1628 billion miles in 1999 to 2262 billion miles in 2018, and correlated exponentially with the rising legionellosis incidence rates (R2 = 0.9417, P = 1.5E-12). The total vehicle miles rose 1.2-fold from 2690 billion miles in 1999 to 3240 billion miles in 2018, and also correlated with incidence (R2 = 0.8424, P = 1.2E-08). The declining rural miles correlated inversely with incidence (R2 = 0.7499, P = 8.1E-07).
[Figure omitted. See PDF.]
Fig 4. Correlations between age-adjusted legionellosis incidence rates and vehicle miles driven in the United States, 1999–2018, with fitted dot lines, R2 values, and equations.
https://doi.org/10.1371/journal.pone.0250364.g004
Therefore, the vast total vehicle miles, 9882 miles (15904 km) per capita in 2018, and correlations verified the significance of road exposure to soil bacteria and its contribution to the rise in incidence. In addition, an interactive parameter of total vehicle miles and annual precipitation, in the form of multiplication, was found to promote legionellosis in robust multiple regressions along with cumulative temperature anomalies (Table 2). This result substantiated more road exposure when driving on wet roads during or following precipitation, a biologically sound process that was raised previously [11, 17, 18].
Analysis of five representative states
In view of the diversity of geography and climate across the United States, five representative states were analyzed: California (Pacific coast), Florida (southeast Atlantic coast), Wisconsin (central north), New Jersey (mid-Atlantic coast), and Ohio (Great Lakes region). As shown in Fig 5, these states differed remarkably in legionellosis incidence rates; in 2018, for example, Ohio had the highest all-age incidence (930 cases, 7.96/100,000), Wisconsin (5.69/100,000) and New Jersey (4.14/100,000) were above the US average (3.03/100,000), and California (1.15/100,000) and Florida (2.33/100,000) were below the US average. These states also showed considerable fluctuations in the course of incidence rise during the 20 years.
[Figure omitted. See PDF.]
Fig 5. Legionellosis incidence rates (all ages) in California, Florida, New Jersey, Ohio, and Wisconsin, 1999–2018, with exponentially fitted dot lines and R2 values.
https://doi.org/10.1371/journal.pone.0250364.g005
The regression results for the five states are shown in Table 3 (S3 Table for detailed data). For all states, rising vehicle miles and decreasing UVB radiation levels were significantly correlated to the rising incidence rates. All states showed above-norm temperatures, for all 20 years in California and New Jersey and for 17 to 19 years in the others. An upward rising trend was statistically significant for the warm states of California and Florida but not for the cooler states (S3 Table footnote). The precipitation varied during the 20-year period: dry California experienced an increasing deficit compared with the state norm (average of 7.4% deficit), wet Florida was close to the state norm (average of 1.3% deficit), and the moderate states showed a significant surplus (average of 7.3% to 8.9% surplus).
[Figure omitted. See PDF.]
Table 3. Regression analyses between the legionellosis incidence rates and total vehicle miles and climate parameters in selected states, 1999–2018.
https://doi.org/10.1371/journal.pone.0250364.t003
Due to incidence fluctuations, annual mean temperature and precipitation correlated sub-optimally or poorly in these states, with lower R2 values (Table 3). However, cumulative anomalies correlated well, particularly for cooler Wisconsin, Ohio, and New Jersey. The correlations for Ohio also fitted exponentially, suggesting consistent cumulative effects. In multiple regression analyses, the promotive synergism between precipitation and vehicle miles was also noted for the wet states of Wisconsin, Ohio, New Jersey, and Florida, but not for dry California. Conversely, for California, worsening cumulative precipitation deficit correlated inversely with incidence (Table 3), implying an inhibitive effect that opposes the promotive effect of temperature rise. These effects corresponded to the incidence decreases in 2017 and 2018 (Fig 5), unlike the other four states. The record drought in 2013 (since 1895) with a precipitation of 201.4 mm (deficit by 64.6%) also coincided with the incidence drop that year.
The incidence fluctuations in New Jersey and Wisconsin were significant and thus examined further. New Jersey showed fluctuations from 2009 to 2017, averaging 2.36/100,000, before rising again to the peak in 2018 (Fig 5). These variations paralleled precipitation levels, such as those in 2009 (1350.5 mm, surplus by 18.3%), 2011 (1624.3 mm, surplus by 42.2%, a record since 1895), 2016 (1005.6 mm, deficit by 11.9%), and 2018 (1644.9 mm, surplus by 44.0%, a new record) (S3 Table). The correlation accorded with the strong synergy between precipitation and vehicle miles (P = 5.3E-06) (Table 3), most notable in New Jersey.
For cold Wisconsin (S3 Table), the incidence rates decreased slightly from 1999 to 2003, rose from 2004 to a peak in 2013 (2.76/100,000), fluctuated in 2014–2016 (averaging 1.89/100,000), and rose again sharply in 2017 to the peak in 2018 (a 3-fold rise in 3 years) (Fig 5). The nadir in 2003 (0.33/100,000) corresponded to the peak UVB radiation activity (15830 kJ/m2) and drought, whereas the higher incidence rates in 2013–2018 coincided with a 6-year streak of precipitation surplus (averaging 957.5 mm, surplus by 20.5%). The 2018 peak paralleled record high precipitation (1009.4 mm, surplus by 27.0%), a near record low UVB radiation level (6745 kJ/m2), and continued above-norm temperature (6.22°C). More effects of annual temperature variations were also seen. For examples, the 2013 incidence peak followed record (since 1895) heat in 2012 (8.56°C, 48.1% above norm), while the 2014 incidence drop (1.65/100,000) corresponded to the record (since 1973) low temperature that year (4.56°C, 21.1% below norm). The average temperature rise during 1999–2018 was 0.99°C or 17.1% above the state norm of 5.78°C, the highest percentage among the five states. Along with this, the legionellosis incidence also rose most steeply, 17-fold from nadir in 2003 to peak in 2018. Thus, the effect of warming temperature was most pronounced in cold Wisconsin. The dramatic effect undermined regression fitting, in view of the least R2 values among the five states (Table 3).
The incidence rates in Ohio were consistently above the national average rates: by 1.9-fold in 1999 (0.75/100,000 vs. 0.40/100,000), 2.1-fold in 2009 (2.45/100,000 vs. 1.15/100,000), 2.6-fold in 2015 (4.93/100,000 vs. 1.89/100,000), and 2.6-fold in 2018 (7.96 vs. 3.03/100,000) (Fig 5). They have been the highest in the United States since 2015, surpassing New York and Pennsylvania that had an incidence rate of 4.39/100,000 and 2.97/100,000 in 2015 respectively. The rates also rose relatively steadily with some year-to-year fluctuations in relation to precipitation surplus or deficit (S3 Table); the curve fitted exponentially with an R2 of 0.9095 and a coefficient of e0.0966 (Fig 5), the latter equaling an annual increase of 110.1%, identical to the national data. The 2018 peak could be attributed to the cumulative effects, high precipitation (1293.6 mm, surplus by 33.0%), low UVB radiation (6970 kJ/m2), and continued temperature anomaly (11.22°C, 9.8% above norm) (S3 Table).
Therefore, in spite of variations, climate changes contributed to the overall rises in legionellosis incidence in the five states with diverse climates. When these states were combined, the incidence rates rose more steadily with little fluctuation, peaking at 2.96/100,000 in 2018 and fitting well exponentially with an R2 of 0.9699 and a coefficient of e0.1017 (S2 Fig), similar to the all-age incidence curve for the United States. The sharp rises in cooler Wisconsin, Ohio, and New Jersey in 2017 and 2018 suggested an elevation of the density of Legionella spp. in the environment as a result of warmer temperature and precipitation surplus.
Discussion
In this study we have shown that climate changes contributed remarkably to the rapidly rising legionellosis incidence rates in the United States from 1999 to 2018. The incidence rose exponentially at an annual rate of ~110%, higher in recent years, which correlated well with cumulative effects of the above-norm temperature since 1997 and precipitation surplus since 2008. During the 20-year study period, levels of solar UVB radiation, which is germicidal, have been decreasing, correlating inversely with the rise in incidence.
Our data support the notion that the climate anomalies have likely elevated the density of Legionella bacteria in the environment, particularly in cooler states. The continued anomalies noted in 2019, a record precipitation of 883.4 mm in particular, forecast a high legionellosis incidence rate (to be available in late 2020). For instance, from January to July (31 weeks), there have been 4522 cases, well above the 2018 number of 4210 cases during the same period (107%) [32]. Our further study on the monthly incidence changes during the 20 years in the U.S. also added filling details on how monthly temperatures, precipitation levels, and sunlight intensity influenced the rise and fall of legionellosis in seasons, to support and complement the above annual data and conclusions [Han XY, unpublished, 2020]. The study showed four main findings: a large seasonal incidence plateau has evolved in recent years from the usually small seasonal incidence hill in the summer and fall 20 years earlier; carryover effect from warm months to cold months was evident; much warmer winters have raised baseline status in incidence and bacterial density in the environment; and strong sunlight in the summer was suppressive whereas weakened sunlight in the fall was permissive.
Climate change affects ecosystems. In a recent experimental study on a soil ecosystem, warming temperature and increased precipitation were found to increase soil temperature and promote the growth of soil microorganisms [33]. Another study showed that warming temperature increased soil microbial activity across a temperature gradient and that the impact of warming was greater in regions with lower temperature [34]. These findings lend support to our epidemiologic evidence of more Legionella bacteria in the environment and the result of greater warming effect on legionellosis in cold Wisconsin. The ubiquitous nature of Legionella bacteria in soil has been appreciated via microbiological studies [18, 35–37], as well as investigation of soil dust-related outbreaks [5, 38, 39]. Similarly, warming temperature also affects microbes in aquatic environments, such as seasonal variation of Legionella spp. in rivers and lakes [40, 41]. Environmental Legionella spp. tend to be diverse, but L. pneumophila serogroup 1 and sequence types are still more common than other species [17, 18, 42]. Among clinical isolates, L. pneumophila serogroup 1 predominates [43], reflecting higher pathogenicity of this species.
With more Legionella bacteria in the environment, more exposures, in dosage and/or frequency, may arise from human activities. The present study has substantiated the role of road exposure to soil bacteria by showing the vast vehicle miles driven in the United States, 3240 billion total miles or 9882 miles (15904 km) per capita in 2018, and the concordant rise with legionellosis incidence during the 20 years studied. Thus, road exposure could be the long-sought hidden source for most sporadic cases, with such exposure conceivably occurring more at night, on days with rain, clouds, fog, or high humidity, driving with open windows or riding a motorcycle, and in northern states with low sunlight intensity. Consecutive rainy days in the summer likely foster the highest levels of road bacteria. Heavy traffic in urban areas, such as during morning and evening rush hours, also aggravates aerosol formation and exposure. This aspect is evidenced by the better correlation between incidence and urban vehicle miles (Fig 4).
Future studies to monitor Legionella spp. on roads and in soil are needed to corroborate and further evaluate road exposure risk. In this regard, the current COVID-19 pandemic unfortunately provided an unprecedented opportunity. From the start of lockdowns in mid-March to August 29, 2020, it has drastically reduced the number of legionellosis cases to 40% of otherwise predicted cases following much less driving, which vindicated preliminarily the high significance of road exposure [Han XY, unpublished, 2021].
Earlier studies have shown that higher precipitation levels occurring in warm summer months lead to more legionellosis cases, by a lag of several days to 2 weeks (approximately one incubation period) [13, 14, 44]. Increased precipitation means more water on the ground to aid bacterial proliferation in bodies of water and in soil. More relevantly, precipitation also brings soil bacteria to paved roads, attenuates sunlight to retain bacterial viability, and forms traffic-borne aerosols, all of which favor more and immediate exposure to drivers and passengers in traffic, coinciding the incubation period. This process is now backed by the data on synergistic interaction between precipitation and vehicle miles driven (Tables 2 and 3), most notable in New Jersey, a mid-Atlantic state with record precipitation surpluses in 2011 and 2018, moderate solar strength, annual mean temperature at the US average, and above-norm temperature run since 1979 as recorded [25].
While precipitation promotes road exposure mainly in sporadic cases that account for ~95% of all legionellosis cases in the US in recent decade [Han XY, unpublished, 2021], it may also aid outbreaks in certain settings. For example, in a recent outbreak investigation, heavy rainfalls were noted to precede a fountain-related community outbreak by 1 to 2 weeks to suggest a promotive role [45]. Presumably, in the context of this discussion, the rainfalls could have attenuated sunlight, produced more aerosols, and/or raised atmospheric humidity to aid the survival of aerosols and bacteria for more exposure. High humidity has been shown to promote occurrence of legionellosis in sporadic cases [13, 44]. It is likely that high humidity prolongs traffic-borne aerosols in the air, and thus more host exposure.
The promotive effect of precipitation, shown in this study at the national and state levels, could be viewed as a surrogate of both precipitated water and attenuated sunlight in terms of less ultraviolet radiation and fewer sunshine hours. While the present study analyzed the effect of UVB radiation, the effect of sunshine duration, another significant solar inhibitor of legionellosis [11], was not assessed due to the lack of accurate longitudinal data on hours of sunshine in the United States. This aspect, a limitation, may require further assessment in the future. Lack of precipitation, on the other hand, not only shrinks bodies of water and diminishes soil moisture to limit bacterial proliferation but also reduces road exposure. Accordingly, we observed the 2012 incidence valley in face of a severe drought year in the U.S. (Figs 1 and 2B) as well as the incidence decreases in California in 2017 and 2018 due to sustained drought (Fig 5 and Table 3). These effects were detailed in the seasonality study [Han XY, unpublished, 2020]. These longitudinal results complement our cross-sectional data on the correlation of low legionellosis incidence rates with low precipitation levels in the western U.S. states [11]. Thus, drought suppresses legionellosis.
The significance of road exposure further suggests that many sporadic or community-acquired cases could be prevented through road precautions, such as wearing a mask, driving with closed vehicle windows, and keeping vehicles clean and maintained. These measures are particularly important for individuals with predisposing risk factors, such as weakened immunity, respiratory diseases, diabetes, and old age [1, 6, 46]. Development of a vaccine may be considered as well.
More Legionella spp. in the environment, soil in particular due to the ubiquitous nature and lack of purification treatment, may also readily contaminate water supplies, cooling towers, and whirlpool spas, leading to more and/or larger-scale outbreaks. Recent examples include the 2019 outbreak in North Carolina that infected 136 individuals and was related to whirlpool spas [47], the 2015 outbreak in New York City that infected 138 and was related to cooling towers [6], and the 2014–2015 outbreak in Michigan that infected 86 and was related to water supply and hospital settings [48]. These outbreaks typify exposure sources and illustrate challenges to prevent them in the wake of new environmental norms of warmer temperature, precipitation surplus, and more bacteria. They raise the needs of new standards for outbreak surveillance and early detection, maintenance of water-related facilities, and regulations. In fact, the New York City outbreak has led to legislation on the use and maintenance of cooling towers in the city and state [6].
Legionella-bearing aerosols emitted from cooling towers may reach individuals on streets and in communities via atmospheric dispersion within a radius. Most reported transmission radii were up to two miles (3.2 km), such as in the New York City outbreak and in another that occurred in Wisconsin [6, 49]. The longest radii reached 11 km and 7.5 km that took place in Quebec City, Canada and in Harnes City in northern France, respectively [50, 51]. The Harnes City outbreak, having occurred in November to January for 79 days, unlike the summer time in the other three outbreaks, conforms lack of solar bactericidal and desiccating effects in the distant drift of aerosols in the winter when the solar strength and temperature in northern France are both at nadir (ultraviolet index of zero to one). The solar strengths in northern United States (New York and Wisconsin) and Canada (Quebec) are moderate in the summer, with peak ultraviolet indices of 6, 5, and 4 in July, respectively, as noted [11, 52], where airborne transmission is more likely at night and early in the morning or in cloudy/rainy days. In a recent analysis of atmospheric conditions during 13 outbreaks that occurred in Europe and were related to cooling towers, foggy weathers were noted to be present in four outbreaks, including the Harnes City outbreak [53]. The water droplets (aerosols) in a fog afloat Legionella-laden aerosols from cooling towers longer in the air for dissemination.
Indoor aerosols generated from contaminated whirlpool spas at exhibition, such as in the North Carolina outbreak [47], expose people to the aerobic bacteria readily owing to the ground-level immediately inhalable aerosols, bacterial proliferation promoted by heating and aeration through whirling and bubbling of water, and lack of solar control. A similar whirlpool spas-related outbreak that occurred in the Netherlands earlier led to 188 cases of legionellosis, the largest of its kind [7]. Traffic-borne aerosols, such as generated at night in warm months, share some of these features. These aerosols may expose roadside people, particularly in densely populated areas, in addition to drivers and passenger inside a vehicle. For instance, in New York City, professional drivers and outdoor/street workers in repair, protective services, cleaning, and construction have been noted to incur higher incidence of legionellosis than general working population [20].
Ohio has led the United States in legionellosis incidence for several years, with reasons suggested recently [11]. The present study has further shown contribution from climate changes. The number of 930 cases in a state with 11.7 million residents in 2018 is alarming. The state has the third lowest sunshine hours in the United States, following Alaska and Washington, averaging 2245 hours annually [11], and increased precipitation in 2017 and 2018 further weakened solar inhibition on the incidence. By contrast, California, Florida, New Jersey, and Wisconsin all have longer annual sunshine duration, i.e., 3055, 2927, 2517, and 2468 hours, respectively [11]. These hours correspond inversely to their respective legionellosis incidence.
In conclusion, climate changes and road exposure explain the rapidly rising legionellosis incidence rates in the United States from 1999 to 2018. The incidence is predicted to rise further. Further investigation and preventive actions are urgently needed.
Supporting information
S1 Fig. Age-specific, all ages, and age-adjusted incidence of invasive pneumococcal infection in the United States, 2010–2018.
https://doi.org/10.1371/journal.pone.0250364.s001
(DOCX)
S2 Fig. All age legionellosis incidence rates in the United States and in combined 5 states of California, Florida, New Jersey, Ohio, and Wisconsin, 1999–2018, with exponentially fitted dot lines, R2 values, and equations.
https://doi.org/10.1371/journal.pone.0250364.s002
(DOCX)
S1 Table. Temperature, precipitation, and solar ultraviolet B radiation data for the United States, 1999–2018.
https://doi.org/10.1371/journal.pone.0250364.s003
(DOCX)
S2 Table. Vehicle miles driven in the United States, 1999–2018.
https://doi.org/10.1371/journal.pone.0250364.s004
(DOCX)
S3 Table. All-age incidence (cases/100,000), total vehicle miles, temperature, precipitation, and solar ultraviolet B radiation data in selected states, 1999–2018.
https://doi.org/10.1371/journal.pone.0250364.s005
(DOCX)
Acknowledgments
The author thanks Sunita Patterson of Scientific Publications, Research Medical Library, MD Anderson Cancer Center, for editorial review and comments.
Citation: Han XY (2021) Effects of climate changes and road exposure on the rapidly rising legionellosis incidence rates in the United States. PLoS ONE 16(4): e0250364. https://doi.org/10.1371/journal.pone.0250364
1. Edelstein PH, Roy CR. 2015. Legionnaires’ disease and Pontiac fever, p 2933–2944. In Bennett JE, Dolin R, Blaser MJ (ed), Mandell, Douglas, and Bennett’s Principles and Practice of Infectious Diseases, 8th ed, Philadelphia, PA. Saunders.
2. Fields B, Benson R, Besser R. 2002. Legionella and Legionnaires’ disease: 25 years of investigation. Clin Microbiol Rev. 15:506–526. pmid:12097254
3. McDade JE, Shepard CC, Fraser DW, Tsai TR, Redus MA, Dowdle WR. 1977. Legionnaires’ disease: isolation of a bacterium and demonstration of its role in other respiratory disease. N Engl J Med. 297:1197–1203. pmid:335245
4. Band JD, LaVenture M, Davis JP, Mallison GF, Skaliy P, Hayes PS, et al. 1981. Epidemic Legionnaires’ disease. Airborne transmission down a chimney. JAMA 245:2404–2407. pmid:7230470
5. Redd SC, Lin FY, Fields BS, Biscoe J, Plikaytis BB, Powers P, et al. 1990. A rural outbreak of Legionnaires’ disease linked to visiting a retail store. Am J Public Health 80:431–434. pmid:2316763
6. Weiss D, Boyd C, Rakeman JL, et al. 2017. A large community outbreak of Legionnaires disease associated with a cooling tower in New York City, 2015. Public Health Rep. 132:241–250. pmid:28141970
7. Den Boer JW, Yzerman EP, Schellekens J, Lettinga KD, Boshuizen HC, Van Steenbergen JE, et al. 2002. A large outbreak of Legionnaires’ disease at a flower show, the Netherlands, 1999. Emerg Infect Dis 8:37–43. pmid:11749746
8. Beauté J. 2017. The European Legionnaires’ Disease Surveillance Network. Legionnaires’ disease in Europe, 2011–2015. Euro Surveill 22. pmid:28703097
9. Den Boer JW, Euser SM, Brandsema P, Reijnen L. Bruin JP. 2015. Results from the National Legionella outbreak detection program, the Netherlands, 2002–2012. Emerg Infect Dis. 21:1167–1173. pmid:26079594
10. Centers for Disease Control and Prevention. 2019. Legionnaires’ disease surveillance summary report, United States, 2014–2015. https://www.cdc.gov/Legionella/health-depts/surv-reporting/2014-15-surv-report-508.pdf. Accessed February 18, 2020.
11. Han XY. 2019. Solar and climate effects explain the wide variation in legionellosis incidence rates in the United States. Appl Environ Microbiol. 85:e1776–19. pmid:31519664
12. Sharaby Y, Rodríguez-Martínez S, Oks O, Pecellin M, Mizrahi H, Peretz A, et al. (2017) Temperature-dependent growth modeling of environmental and clinical Legionella pneumophila multilocus variable-number tandem-repeat analysis (MLVA) genotypes. Appl Environ Microbiol. 83:e03295–16. pmid:28159784
13. Fisman DN, Lim S, Wellenius GA, Johnson C, Britz P, Gaskins M, et al. 2005. It’s not the heat, it’s the humidity: wet weather increases legionellosis risk in the greater Philadelphia metropolitan area. J Infect Dis 192:2066–2073. pmid:16288369
14. Hicks LA, Rose CE Jr, Fields BS, Drees ML, Engel JP, Jenkins PR, et al. 2007. Increased rainfall is associated with increased risk for legionellosis. Epidemiol Infect 135:811–817. pmid:17121693
15. Ng V, Tang P, Jamieson F, Drews SJ, Brown S, Low DE, et al. 2008. Going with the flow: legionellosis risk in Toronto, Canada is strongly associated with local watershed hydrology. Ecohealth 5:482–490. pmid:19370300
16. Cassell K, Gacek P, Warren JL, Raymond PA, Cartter M, Weinberger DM. (2018) Association between sporadic legionellosis and river systems in Connecticut. J Infect Dis. 217:179–187. pmid:29211873
17. Sakamoto R, Ohno A, Nakahara T, Satomura K, Iwanaga S, Kouyama Y, et al. 2009. Legionella pneumophila in rainwater on roads. Emerg Infect Dis 15:1295–1297. pmid:19751596
18. van Heijnsbergen E, de Roda Husman AM, Lodder WJ, Bouwknegt M, Docters van Leeuwen AE, Bruin JP, et al. 2014. Viable Legionella pneumophila bacteria in natural soil and rainwater puddles. J Appl Microbiol 117:882–890. pmid:24888231
19. Den Boer JW, Nijhof J, Friesema I. Risk factors for sporadic community-acquired Legionnaires’ disease. A 3-year national case-control study. 2006. Public Health. 120:566–571. pmid:16707144
20. Farnham A, Alleyne L, Cimini D, Balter S. 2014. Legionnaires’ disease incidence and risk factors, New York, New York, USA, 2002–2011. Emerg Infect Dis 20:1795–1802. pmid:25513657
21. Wallensten A, Oliver I, Ricketts K, Kafatos G, Stuart JM, Joseph C. 2010. Windscreen wiper fluid without added screen wash in motor vehicles: a newly identified risk factor for Legionnaires’ disease. Eur J Epidemiol 25:661–665. pmid:20532623
22. National climate report–annual 2018. https://www.ncdc.noaa.gov/sotc/national/201813. Accessed August 13, 2020.
23. https://www.cdc.gov/mmwr/mmwr_nd/. Accessed February 18, 2020.
24. https://www.census.gov/topics/population.html. Accessed February 18, 2020.
25. https://www.ncdc.noaa.gov/cag/time-series. Accessed February 18, 2020.
26. https://uvb.nrel.colostate.edu/UVB/da_ContourDailySums.jsf. Accessed February 18, 2020.
27. Bigelow DS, Slusser JR, Beaubien AF, Gibson JH. 1998. The USDA Ultraviolet Radiation Monitoring Program. Bull Am Meteorol Soc 79(4):601–615.
28. https://www.bts.gov/content/us-vehicle-miles. Accessed February 18, 2020.
29. Multiple regression in Excel. https://www.youtube.com/watch?v=cXiZ_t2NK1k. Accessed March 18, 2020.
30. Berry WD, Feldman S. 1985. Multiple Regression in Practice. Thousand Oaks, CA. SAGE Publications, Inc., (e-publication 2011).
31. Flanders WD, Kleinbaum DG. 1995. Basic models for disease occurrence in epidemiology. Int J Epidemiol. 24:1–7. pmid:7797329
32. https://wonder.cdc.gov/nndss/nndss_weekly_tables_menu.asp. Accessed July 17, 2020.
33. Chen Q, Niu B, Hu Y, Luo T, Zhang G. (2020) Warming and increased precipitation indirectly affect the composition and turnover of labile-fraction soil organic matter by directly affecting vegetation and microorganisms. Sci Total Environ. 714:136787. pmid:31982765
34. Nottingham AT, Baath E, Reischke S, Salinas N, Meir P. (2019) Adaptation of soil microbial growth to temperature: using a tropical elevation gradient to predict future changes. Glob Chang Biol. 25(3):827–838. pmid:30372571
35. Travis TC, Brown EW, Peruski LF, Siludjai D, Jorakate P, Salika P, et al. (2012) Survey of Legionella spp. in Thai soil. Int J Microbiol. 2012:218791. pmid:22287969
36. Conza L, Pagani SC, Gaia V. (2013) Presence of Legionella and free-living amoebae in composts and bioaerosols from composting facilities. PLoS One. 8(7):e68244. pmid:23844174
37. van Heijnsbergen E, van Deursen A, Bouwknegt M, Bruin JP, de Roda Husman AM, Schalk JA. Presence and persistence of viable, clinically relevant Legionella pneumophila bacteria in garden soil in the Netherlands. (2016) Appl Environ Microbiol. 82(17):5125–31. pmid:27316958
38. Thacker SB, Bennett JV, Tsai TF, Fraser DW, McDade JE, Shepard CC, et al. (1978) An outbreak in 1965 of severe respiratory illness caused by the Legionnaires’ disease bacterium. J. Infect Dis. 138:512–619. pmid:361897
39. Cramp GJ, Harte D, Douglas NM, Graham F, Schousboe M, Sykes K. (2010) An outbreak of Pontiac fever due to Legionella longbeachae serogroup 2 found in potting mix in a horticultural nursery in New Zealand. Epidemiol Infect. 138(1):15–20. pmid:19781115
40. Fliermans CB, Cherry Wb, Orrison LH, Smith SJ, Tison DL, Pope DH. Ecological distribution of Legionella pneumophila. Appl Environ Microbiol. 1981;41:9–16. pmid:7013702
41. Kao PM, Hsu BM, Chang TY, Hsu TK, Tzeng KJ, Huang YL. (2015) Seasonal variation of Legionella in Taiwan’s reservoir and its relationship with environmental factors. Environ Sci Pollut Res Int. 22(8):6104–11. pmid:25391236
42. Doleans A, Aurell H, Reyrolle M, Lina G, Freney J, Vandenesch F, et al. 2004. Clinical and environmental distributions of Legionella strains in France are different. J. Clin. Microbiol. 42:458–460. pmid:14715805
43. Yu VL, Plouffe JF, Pastoris MC, Stout JE, Schousboe M, Widmer A, et al. 2002. Distribution of Legionella species and serogroups isolated by culture in patients with sporadic community-acquired pneumonia: an international collaborative survey. J. Infect. Dis. 186:127–8. pmid:12089674
44. Karagiannis I, Brandsema P, Van Der Sande M. 2009. Warm, wet weather associated with increased Legionnaires’ disease incidence in The Netherlands. Epidemiol Infect 137:181–187. pmid:18631425
45. Faccini M, Russo AG, Bonini M, Tunesi S, et al. (2020) Large community-acquired Legionnaires’ disease outbreak caused by Legionella pneumophila serogroup 1, Italy, July to August 2018. Euro Surveill. 25:1900523. pmid:32458793
46. Han XY, Ihegword A, Evans SE, Zhang J, Li L, Cao H, et al. 2015. Microbiological and Clinical Studies of Legionellosis in 33 Patients with Cancer. J Clin Microbiol 53:2180–2187. pmid:25926494
47. North Carolina Department of Health and Human Services. Legionnaires’ disease outbreak associated with the North Carolina Mountain State Fair, 2019. https://epi.dph.ncdhhs.gov/cd/legionellosis/MSFOutbreakReport_FINAL.pdf?ver=1.1. Published January 30, 2020. Accessed February 18, 2020.
48. Smith AF, Huss A, Dorevitch S, Heijnen L, Arntzen VH, Davies M, et al. 2019. Multiple sources of the outbreak of Legionnaires’ disease in Genesee County, Michigan, in 2014 and 2015. Environ Health Perspect. 127:127001. pmid:31799878
49. Addiss DG, Davis JP, LaVenture M, Wand PJ, Hutchinson MA, McKinney RM. 1989. Community-acquired Legionnaires’ disease associated with a cooling tower: evidence for longer distance transport of Legionella pneumophila. Am J Epidemiol. 130:557–568. pmid:2764000
50. Lévesque S, Plante PL, Mendis N, Cantin P, Marchand G, Charest H, et al. 2014. Genomic characterization of a large outbreak of Legionella pneumophila serogroup 1 strains in Quebec City, 2012. PLoS One 9:e103852. pmid:25105285
51. Nguyen TM, Ilef D, Jarraud S, Rouil L, Campese C, Che D, et al. 2006. A community-wide outbreak of Legionnaires disease linked to industrial cooling towers–how far can contaminated aerosols spread? J Infect Dis. 193:102–111. pmid:16323138
52. https://www.epa.gov/sunsafety/sun-safety-monthly-average-uv-index, accessed March 27, 2020.
53. Villanueva D, Schepanski K. 2019. Investigation of atmospheric conditions fostering the spreading of Legionnaires’ disease in outbreaks related to cooling towers. Int J Biometeorol. 63:1347–1356. pmid:31342243
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
© 2021 Xiang Y. Han. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
Abstract
About the Authors: Xiang Y. Han Roles Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Project administration, Writing – original draft, Writing – review & editing * E-mail: [email protected] Affiliation: Department of Laboratory Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, United States of America ORCID logo https://orcid.org/0000-0001-8472-0870 Introduction Legionellosis is a pulmonary infection caused by the aquatic and soil bacteria Legionella pneumophila and other Legionella spp. In this context, we analyzed the legionellosis incidence rates in the US from 1999 to 2018 for correlation with concurrent temperature, precipitation, solar ultraviolet B (UVB) radiation, and vehicle mileage data in search of an explanation for the rapid rise in incidence. Data sources The legionellosis case data from 1999 to 2018 were from the annual summary of notifiable diseases from the Centers for Disease Control and Prevention (CDC) [23]. [...]proper interpretation of significant correlations between the incidence rates and explanatory variables and model identification/fitting required biological relevance for support.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer